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
Deletion	NM_000251.3(MSH2):c.759del (p.Met253fs)	MSH2	Pathogenic	2	47639666	47639666	TG	T	reviewed by expert panel	ClinGen:CA022195
Deletion	NM_000251.3(MSH2):c.761del (p.Asn254fs)	MSH2	Pathogenic	2	47639667	47639667	GA	G	reviewed by expert panel	ClinGen:CA022201
Indel	NM_000251.3(MSH2):c.763_766delinsTT (p.Ser255fs)	MSH2	Pathogenic	2	47639670	47639673	AGTG	TT	reviewed by expert panel	ClinGen:CA022212
Duplication	NM_000251.3(MSH2):c.767_768dup (p.Val257fs)	MSH2	Pathogenic	2	47639673	47639674	G	GCT	reviewed by expert panel	ClinGen:CA331679
Deletion	NM_000251.3(MSH2):c.788_789del (p.Asn263fs)	MSH2	Pathogenic	2	47639695	47639696	AAT	A	reviewed by expert panel	ClinGen:CA022259
single nucleotide variant	NM_000251.3(MSH2):c.792+1G>A	MSH2	Pathogenic	2	47639700	47639700	G	A	reviewed by expert panel	ClinGen:CA022273
Deletion	NM_000251.3(MSH2):c.792+10_943-448del	MSH2	Pathogenic	2	47639707	47642985	GGATTATAAATGTGAATTACAATATATATAATGTAAATATGTAATATATAATAAATAATATGTAAACTATAGTGACTTTTTAGAAGGATATTTCTGTCATATTTATCTCAAAACCTAAACTGTGTATCAATGATATTAAGCTTTTTTTTTTTTTTGAGACAGAGTTTCACTTTTGTTGCCCAGGCTGGAGTACAATGGCGCGATCTTGGCTCACCACATCCTCTGCCTCCCAGGTTCAAGTGATCCTCCTGCCTTGGCCTCCTGAGTAGCTGGGATTACAGGCATGTGCCACCACGCCTGGCTCATCTTTTTTGTATTTTTAGTAGAGATGGGGTTTCTCTATGTTGGTCAGGCTGGTCTCAAACTCCTGAACCTCAGGTGATCCGCCCGCCTCGGGCTTCCAAAGCGCTGAGATTGCAGGCATGAGCCACTGTGTCTGGCCTATTTTTATAGTTTATGTACTTGGAATTATATAATATATTCTGCCTAGCTTCTTTCATTCAATATTTGTAAGATTTATCCATATTATTGAGTGTAGTTGTGGATTTTTGCATTTATATTTCATAGCACGAGCATGTCAGAATTTATCCATTTTACTTCCCTTCTGCCCGCCACTGCTACTCTCCCCATTTTACCTTTTTTTTTGTTTTTTTGAGATGGAGTCTCAGAATTTCGCTCTGTCGCCCAGGCTGGAGTGCTGTGGCACGGTCTCAGCTCACTGCAACTTCTGCCTCTGGGTTCAGCTGCACGCCACCATGCCTGGCTAATTTTTGTATTTTCAGTAGAGGGGATTTTGCTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCACCCACCTTGGCCTGCCAGAGTGCTGTGATTACAGGCGTGAACCACCGTGCCCGACCCCCATTCTAATTTTGATGGACATTTGGGTAATTTTCATTTTTGGCTGTTATAAATACTGCTGCAATTACAGTTAATTTTCACAGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGGTGAGTTTCGCTCTTGTTGCTCAGGCTGGAGTGCAGTGGTGCGATCTCAGCCCACTGCAACCTTCACCTTCTGGATTCAAGCAATTCTCCTTTCTCATCTCCTAAGTAGCTGGGGTTTACAGGCATGTGCCACCATGCCCAGCTAATTTTTGTATTTTAATTTCACAGTTCTGGAGGCTGGGAAGTTCAGAATTAAGGCACTGGCTGATCTGTTGTCTGGTGAGGGCCCACTTGTTCATAGATAACCATTTTCTCACTCTAACCTCACAAGGTTGAAAGGGCCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACTATGTTGGCTAGGCTGGTCTCAAACTCCTAGCCTCGAGTCATCCACCCGCCTCGTCCTCCCGGAGTGCTTGGATTACAGCATGAGCCACTGCGCCCGGCCCCCATTTTAGTTTTGATGGACATTTGGGTAATTTTCTTTTTTGGCTATTCTAAATAATGCTGCAATTACTGTTAATTTTCACCTTGTAAAAACCATTTTCAAATCTCAAGAGATTAACCTTTAGTTTTCTTGGTTTGGATTGGGAAGGAACACCAAGGAAAATGAGGGACTTCAGAATTTATTTTCATTTTGCATTTGTTTTTTAAAATCTTTAGAACTGGATCCAGTGGTATAGAAATCTTCGATTTTTAAATTCTTAATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGTGCCCAGCCTACTTTTTACTTTTTTAGAGACTGGGCTTGGTGGAGTGAAGTGGCAAGATCATAGCTCACTGCAGTATTGAACTCCTGGGCTCAAGCGATCTTCCTGCTTCAACCTCATGAGTAGCTGGGTCTACAGGCACAAGCCACCATGCTTGCCTAATTTTAAAATTTTTGCAGAGTTGGAGTTTCACAGTGTTGCCCAGGATGTTCGCTCACTCCTGACTTCAAGTGATTCTTCTGCCTTAGCCTCTAGAGTGGTAGCTGGGATTACAGGCATGAACCACCATGCTCTGCTATTTTTTTTCAAGGTTTTTTTTTTTTTTTTTTTTTTTGAGAGACTGGTATGACTATGTATGCTCCCTAGGCTGGAGTGCAGTGGCTATTCACAGGAAGTGCCATCAGAGTGTACTACAGCTTCAAACTCCTGGGCTCAAGCACTTCTATCATAGTCTCCAAAGTAGCTGGGACTACGAGTGTGTCTCATTGTGCCTTGCTCTCGAATTGCTTTTTTTTTTTTTTTCTGGTTTCAAGCTATCTATGTGGTATTAGTCCTCACTTTATGAATAATTTTGTATACTACTAATAGCAATTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCATTCTTGTCGCCCAGGCTGGAGTGCAGTGGTGTGATCTTAGCTCACTGCAACCTCTGCCTCTCCGGTTTGGGCAATTAGCTGGGATTAGAGGCGCCTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGACATGGGGTTTCATCTTGTTGGCTAGGCTGGACTCTAACTCCAGGTGATCTGCCTGCCTCGGCCTCCCAAATTGATGGGATTACAGGTGTAAACCACTGGGCCTGGCCTAGCAATTTAAAATGACATTCTAAGAAGTTTTATGTCTAAATCTGCAGTAAGTGGCTGGGTGACGTGGCTCATGCCTGTAATCCCAACGCTTTGGGAGTCCAGGGTGGGAGGAT	G	reviewed by expert panel	ClinGen:CA331682
single nucleotide variant	NM_000251.3(MSH2):c.793-2A>C	MSH2	Likely pathogenic	2	47641406	47641406	A	C	reviewed by expert panel	ClinGen:CA022304
Deletion	NM_000251.3(MSH2):c.793-6_942+450del	MSH2	Pathogenic	2	47641402	47642007	ATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGT	A	reviewed by expert panel	ClinGen:CA331685
Deletion	NM_000251.3(MSH2):c.(792+1_793-1)_(1076+1_1077-1)del (p.Val265Ilefs*29)	MSH2	Pathogenic	2	47639700	47656880	na	na	reviewed by expert panel	LOVD 3:MSH2_001276