Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_000090.4(COL3A1):c.1997G>A (p.Gly666Asp) | COL3A1 | Likely pathogenic | 2 | 189863419 | 189863419 | G | A | criteria provided, single submitter | ClinGen:CA004844,UniProtKB:P02461#VAR_001777,OMIM:120180.0022 |
single nucleotide variant | NM_000090.4(COL3A1):c.3518G>A (p.Gly1173Glu) | COL3A1 | Likely pathogenic | 2 | 189872861 | 189872861 | G | A | criteria provided, single submitter | ClinGen:CA006567,UniProtKB:P02461#VAR_001801,OMIM:120180.0016 |
single nucleotide variant | NM_000090.4(COL3A1):c.3554G>A (p.Gly1185Asp) | COL3A1 | Likely pathogenic | 2 | 189873678 | 189873678 | G | A | criteria provided, single submitter | ClinGen:CA006649,UniProtKB:P02461#VAR_001804,OMIM:120180.0015 |
single nucleotide variant | NM_000090.4(COL3A1):c.746G>A (p.Gly249Asp) | COL3A1 | Likely pathogenic | 2 | 189855034 | 189855034 | G | A | criteria provided, single submitter | ClinGen:CA007350,UniProtKB:P02461#VAR_011105,OMIM:120180.0028 |
single nucleotide variant | NM_000090.4(COL3A1):c.2553+5G>T | COL3A1 | Likely pathogenic | 2 | 189867793 | 189867793 | G | T | criteria provided, single submitter | ClinGen:CA005487,OMIM:120180.0008 |