リンチ症候群 - MGenReviews

リンチ症候群

腫瘍性疾患

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Type	Name	Gene Symbol	Clinical Significance	Chromosome	Start	Stop	Reference Allele	Alternate Allele	Review Status	Other IDs
Type	Name	Gene Symbol	Clinical Significance	Chromosome	(GRCh37)		Reference Allele	Alternate Allele	Review Status	Other IDs
Duplication	NM_000251.3(MSH2):c.352dup (p.Tyr118fs)	MSH2	Pathogenic	2	47635679	47635680	G	GT	reviewed by expert panel	ClinGen:CA331577
single nucleotide variant	NM_000251.3(MSH2):c.363T>G (p.Tyr121Ter)	MSH2	Pathogenic	2	47635691	47635691	T	G	reviewed by expert panel	ClinGen:CA021049
single nucleotide variant	NM_000251.3(MSH2):c.366+1G>T	MSH2	Likely pathogenic	2	47635695	47635695	G	T	reviewed by expert panel	ClinGen:CA021052
single nucleotide variant	NM_000251.3(MSH2):c.367-1G>A	MSH2	Likely pathogenic	2	47637232	47637232	G	A	reviewed by expert panel	ClinGen:CA021069
Deletion	NM_000251.3(MSH2):c.367-371_646-513del	MSH2	Pathogenic	2	47636841	47639019	TGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGCGCCTGTATTCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGATTGAACCCTTGAGGCAGAGGTTGCAGTGAGTTGAGATCGCACCATTGCACTCTAGCCTGGGTGACAGAGCAAGACTTCATCTCAAAAAAAAGAGAAAACATTTTATTAATAAGGTTCATAGAGTTTGGATTTTTCCTTTTTGCTTATAAAATTTTAAAGTATGTTCAAGAGTTTGTTAAATTTTTAAAATTTTATTTTTACTTAGGCTTCTCCTGGCAATCTCTCTCAGTTTGAAGACATTCTCTTTGGTAACAATGATATGTCAGCTTCCATTGGTGTTGTGGGTGTTAAAATGTCCGCAGTTGATGGCCAGAGACAGGTTGGAGTTGGGTATGTGGATTCCATACAGAGGAAACTAGGACTGTGTGAATTCCCTGATAATGATCAGTTCTCCAATCTTGAGGCTCTCCTCATCCAGATTGGACCAAAGGAATGTGTTTTACCCGGAGGAGAGACTGCTGGAGACATGGGGAAACTGAGACAGGTAAGCAAATTGAGTCTAGTGATAGAGGAGATTCCAGGCCTAGGAAAGGCTCTTTAATTGACATGATACTGTTTCATTTAAGGAAAAATAATAAAAAAACTCTTTTTTTTGTATCTAATTAAAATAATGTTCTGATGTTTACAGAAACTTTGTATATTTAATTGGACATTAGAACAAGCTGTTTGTTGTGTAAGATTTATTTTACCTCAGATCTTTTCTCCCCCCTTTCCTTTCTGTCTTGTGTTCCAAAAGAGTAATTATTACGGTAAATATTACTGTAATTATGGATTTATCAAATAAGATGCAGTTCTTTAGCATTTTTTGATAAATCGAGTGGAACTTTAGCCTGTTATTTTACTATTTGTTTTATTTTAACTAAATTCTGATTGTGTCATTTTTTTTTTTTTTTTTTGGGACCGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGTACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGGTGAGGTTTCACCATCTTGGCCAGGCTGGTCTTGAACTCCTCACCTCGTGATCCACCCACCTGGGCCTCCCAAAGTGCTGGGATTACAGCCATGAGCCACCATGCTCGGCTTTGATTGTGTCATTTGTATAGGCATGTGGTTTATTATTTAGTTATTTTTTTTTTTTTCTTTGAGGTGGAGTATCACTCTTGGTGCCCAGGCTGGAGTGTAATGGCGTGATCTCAGCTCACTGCAACCTCTACCTCCTGGGTTCAAGCAATTCTCCTGCCCCAGCAGGAGTAGCTTGGGATTACAGGCATGCCCCACCACACCTGGCCAATTTTGTGTTTTTAGTAGAGACAGGGTTCCACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCTGCCCACCTCAGCCTCCCAGAGTGCTGGGATTATAGGCATGAGCCACGGTGCCCAGCATATTTAGATTTTTTTTTTTTTGAGACTGAGTCTGACTCTGTCACCCAGGCTAGAGTGCAGTGGCACGATCCACGATCTTGGCTCACTGCAGCCTCCACCTTATGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACATGCCAACACGCCCGGCTTATTTTTGTATTTTTATAGAGACGGGGTTTCATCATATTGGTCAGGCTGGTCTCTAACTCCTGACCTTGTGATCCACCCGCCTTGGCCTCCCATAGTTCTGGGATTACAGGCATGAGCCACAGCGCCAGGCCTAGATGTTTCTTAAGGTATGTATCTCCCAAAGATTCTTTTTGTGGTCCTCAAGTACCATAAGCACCGCTGGAGATAACACATGTGATGGGCATTTTTAGCATAGATTGTATCTAAGCAACTTTCCACAAGTAATAGTTCTGTTAAGGGTTGTTATTGTGGCCGGGCGC	T	reviewed by expert panel	ClinGen:CA331581
Deletion	NM_000251.3(MSH2):c.367-452_646-722del	MSH2	Pathogenic	2	47636768	47638818	TTGGGATTACAGGCGTGAGCCACAGCACTCAGCCAGTTATTTTTTTATAAGAAAACATTTTACTGGCCAGGCCTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGCGCCTGTATTCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGATTGAACCCTTGAGGCAGAGGTTGCAGTGAGTTGAGATCGCACCATTGCACTCTAGCCTGGGTGACAGAGCAAGACTTCATCTCAAAAAAAAGAGAAAACATTTTATTAATAAGGTTCATAGAGTTTGGATTTTTCCTTTTTGCTTATAAAATTTTAAAGTATGTTCAAGAGTTTGTTAAATTTTTAAAATTTTATTTTTACTTAGGCTTCTCCTGGCAATCTCTCTCAGTTTGAAGACATTCTCTTTGGTAACAATGATATGTCAGCTTCCATTGGTGTTGTGGGTGTTAAAATGTCCGCAGTTGATGGCCAGAGACAGGTTGGAGTTGGGTATGTGGATTCCATACAGAGGAAACTAGGACTGTGTGAATTCCCTGATAATGATCAGTTCTCCAATCTTGAGGCTCTCCTCATCCAGATTGGACCAAAGGAATGTGTTTTACCCGGAGGAGAGACTGCTGGAGACATGGGGAAACTGAGACAGGTAAGCAAATTGAGTCTAGTGATAGAGGAGATTCCAGGCCTAGGAAAGGCTCTTTAATTGACATGATACTGTTTCATTTAAGGAAAAATAATAAAAAAACTCTTTTTTTTGTATCTAATTAAAATAATGTTCTGATGTTTACAGAAACTTTGTATATTTAATTGGACATTAGAACAAGCTGTTTGTTGTGTAAGATTTATTTTACCTCAGATCTTTTCTCCCCCCTTTCCTTTCTGTCTTGTGTTCCAAAAGAGTAATTATTACGGTAAATATTACTGTAATTATGGATTTATCAAATAAGATGCAGTTCTTTAGCATTTTTTGATAAATCGAGTGGAACTTTAGCCTGTTATTTTACTATTTGTTTTATTTTAACTAAATTCTGATTGTGTCATTTTTTTTTTTTTTTTTTGGGACCGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGTACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGGTGAGGTTTCACCATCTTGGCCAGGCTGGTCTTGAACTCCTCACCTCGTGATCCACCCACCTGGGCCTCCCAAAGTGCTGGGATTACAGCCATGAGCCACCATGCTCGGCTTTGATTGTGTCATTTGTATAGGCATGTGGTTTATTATTTAGTTATTTTTTTTTTTTTCTTTGAGGTGGAGTATCACTCTTGGTGCCCAGGCTGGAGTGTAATGGCGTGATCTCAGCTCACTGCAACCTCTACCTCCTGGGTTCAAGCAATTCTCCTGCCCCAGCAGGAGTAGCTTGGGATTACAGGCATGCCCCACCACACCTGGCCAATTTTGTGTTTTTAGTAGAGACAGGGTTCCACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCTGCCCACCTCAGCCTCCCAGAGTGCTGGGATTATAGGCATGAGCCACGGTGCCCAGCATATTTAGATTTTTTTTTTTTTGAGACTGAGTCTGACTCTGTCACCCAGGCTAGAGTGCAGTGGCACGATCCACGATCTTGGCTCACTGCAGCCTCCACCTTATGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACATGCCAACACGCCCGGCTTATTTTTGTATTTTTATAGAGACGGGGTTTCATCATATTGGTCAGGCTGGTCTCTAACTCCTGACCTTGTGATCCACCCGCCTTGGCCTCCCATAGTTC	T	reviewed by expert panel	ClinGen:CA331582
Deletion	NM_000251.3(MSH2):c.367-466_645+658del	MSH2	Pathogenic	2	47636753	47638155	TGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACAGCACTCAGCCAGTTATTTTTTTATAAGAAAACATTTTACTGGCCAGGCCTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGCGCCTGTATTCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGATTGAACCCTTGAGGCAGAGGTTGCAGTGAGTTGAGATCGCACCATTGCACTCTAGCCTGGGTGACAGAGCAAGACTTCATCTCAAAAAAAAGAGAAAACATTTTATTAATAAGGTTCATAGAGTTTGGATTTTTCCTTTTTGCTTATAAAATTTTAAAGTATGTTCAAGAGTTTGTTAAATTTTTAAAATTTTATTTTTACTTAGGCTTCTCCTGGCAATCTCTCTCAGTTTGAAGACATTCTCTTTGGTAACAATGATATGTCAGCTTCCATTGGTGTTGTGGGTGTTAAAATGTCCGCAGTTGATGGCCAGAGACAGGTTGGAGTTGGGTATGTGGATTCCATACAGAGGAAACTAGGACTGTGTGAATTCCCTGATAATGATCAGTTCTCCAATCTTGAGGCTCTCCTCATCCAGATTGGACCAAAGGAATGTGTTTTACCCGGAGGAGAGACTGCTGGAGACATGGGGAAACTGAGACAGGTAAGCAAATTGAGTCTAGTGATAGAGGAGATTCCAGGCCTAGGAAAGGCTCTTTAATTGACATGATACTGTTTCATTTAAGGAAAAATAATAAAAAAACTCTTTTTTTTGTATCTAATTAAAATAATGTTCTGATGTTTACAGAAACTTTGTATATTTAATTGGACATTAGAACAAGCTGTTTGTTGTGTAAGATTTATTTTACCTCAGATCTTTTCTCCCCCCTTTCCTTTCTGTCTTGTGTTCCAAAAGAGTAATTATTACGGTAAATATTACTGTAATTATGGATTTATCAAATAAGATGCAGTTCTTTAGCATTTTTTGATAAATCGAGTGGAACTTTAGCCTGTTATTTTACTATTTGTTTTATTTTAACTAAATTCTGATTGTGTCATTTTTTTTTTTTTTTTTTGGGACCGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGTACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGGTGAGGTTTCACCATCTTGGCCAGGCTGGTCTTGAACTCCTCACCTCGTGATCCACCCACCTG	T	reviewed by expert panel	ClinGen:CA331583
Deletion	NM_000251.3(MSH2):c.367-681_646-956del	MSH2	Pathogenic	2	47636551	47638596	TGGAGTGCAGTGGCGCCATCTGGGCTCACTGCAAACTCTGACTCCCTGGTTCAAGCTTTTCTCCCGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCATGCTGCAACACCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGACGGTCTCGATCTCCTGACCTCGTGATCCGCCTGCCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACAGCACTCAGCCAGTTATTTTTTTATAAGAAAACATTTTACTGGCCAGGCCTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGCGCCTGTATTCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGATTGAACCCTTGAGGCAGAGGTTGCAGTGAGTTGAGATCGCACCATTGCACTCTAGCCTGGGTGACAGAGCAAGACTTCATCTCAAAAAAAAGAGAAAACATTTTATTAATAAGGTTCATAGAGTTTGGATTTTTCCTTTTTGCTTATAAAATTTTAAAGTATGTTCAAGAGTTTGTTAAATTTTTAAAATTTTATTTTTACTTAGGCTTCTCCTGGCAATCTCTCTCAGTTTGAAGACATTCTCTTTGGTAACAATGATATGTCAGCTTCCATTGGTGTTGTGGGTGTTAAAATGTCCGCAGTTGATGGCCAGAGACAGGTTGGAGTTGGGTATGTGGATTCCATACAGAGGAAACTAGGACTGTGTGAATTCCCTGATAATGATCAGTTCTCCAATCTTGAGGCTCTCCTCATCCAGATTGGACCAAAGGAATGTGTTTTACCCGGAGGAGAGACTGCTGGAGACATGGGGAAACTGAGACAGGTAAGCAAATTGAGTCTAGTGATAGAGGAGATTCCAGGCCTAGGAAAGGCTCTTTAATTGACATGATACTGTTTCATTTAAGGAAAAATAATAAAAAAACTCTTTTTTTTGTATCTAATTAAAATAATGTTCTGATGTTTACAGAAACTTTGTATATTTAATTGGACATTAGAACAAGCTGTTTGTTGTGTAAGATTTATTTTACCTCAGATCTTTTCTCCCCCCTTTCCTTTCTGTCTTGTGTTCCAAAAGAGTAATTATTACGGTAAATATTACTGTAATTATGGATTTATCAAATAAGATGCAGTTCTTTAGCATTTTTTGATAAATCGAGTGGAACTTTAGCCTGTTATTTTACTATTTGTTTTATTTTAACTAAATTCTGATTGTGTCATTTTTTTTTTTTTTTTTTGGGACCGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGTACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGGTGAGGTTTCACCATCTTGGCCAGGCTGGTCTTGAACTCCTCACCTCGTGATCCACCCACCTGGGCCTCCCAAAGTGCTGGGATTACAGCCATGAGCCACCATGCTCGGCTTTGATTGTGTCATTTGTATAGGCATGTGGTTTATTATTTAGTTATTTTTTTTTTTTTCTTTGAGGTGGAGTATCACTCTTGGTGCCCAGGCTGGAGTGTAATGGCGTGATCTCAGCTCACTGCAACCTCTACCTCCTGGGTTCAAGCAATTCTCCTGCCCCAGCAGGAGTAGCTTGGGATTACAGGCATGCCCCACCACACCTGGCCAATTTTGTGTTTTTAGTAGAGACAGGGTTCCACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCTGCCCACCTCAGCCTCCCAGAGTGCTGGGATTATAGGCATGAGCCACGGTGCCCAGCATATTTAGATTTTTTTTTTTTTGAGACTGAGTCTGACTCTGTCACCCAGGCTA	T	reviewed by expert panel	ClinGen:CA331584
Deletion	NM_000251.3(MSH2):c.368del (p.Ala123fs)	MSH2	Pathogenic	2	47637234	47637234	GC	G	reviewed by expert panel	ClinGen:CA021083
Deletion	NM_000251.3(MSH2):c.380_381del (p.Asn127fs)	MSH2	Pathogenic	2	47637246	47637247	AAT	A	reviewed by expert panel	ClinGen:CA021090