Linked Data
ClinVar Variation Id:
418902
ClinVar RCV Id:
RCV000485755
dbSNP Id:
rs752857771
ExAC:
2:48032771 T / C
gnomAD v2:
2-48032771-T-C
gnomAD v4:
2-47805632-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47805632T>C , CM000664.2:g.47805632T>C | GRCh38 |
| NC_000002.11:g.48032771T>C , CM000664.1:g.48032771T>C | GRCh37 |
| NC_000002.10:g.47886275T>C | NCBI36 |
| NG_007111.1:g.27486T>C , LRG_219:g.27486T>C | |
| NG_008397.1:g.105044A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000411819.2:c.3274T>C (MSH6) | ENSP00000406248.2:p.Phe1092Leu | |
| ENST00000420813.6:c.3274T>C (MSH6) | ENSP00000390382.2:p.Phe1092Leu | |
| ENST00000455383.6:c.3274T>C (MSH6) | ENSP00000397484.2:p.Phe1092Leu | |
| ENST00000700004.2:c.3187T>C (MSH6) | ENSP00000514752.2:p.Phe1063Leu | |
| ENST00000699999.1:n.4245T>C (MSH6) | ||
| ENST00000700000.1:c.2005T>C (MSH6) | ENSP00000514749.1:p.Phe669Leu | |
| ENST00000700002.1:c.3577T>C (MSH6) | ENSP00000514750.1:p.Phe1193Leu | |
| ENST00000700003.1:c.1026T>C (MSH6) | ENSP00000514751.1:n.1026T>C | |
| ENST00000700004.1:c.2344T>C (MSH6) | ENSP00000514752.1:p.Phe782Leu | |
| ENST00000700005.1:n.2422T>C (MSH6) | ||
| ENST00000700006.1:n.4233T>C (MSH6) | ||
| ENST00000700007.1:n.2166T>C (MSH6) | ||
| ENST00000700008.1:n.1740T>C (MSH6) | ||
| ENST00000700009.1:n.1739T>C (MSH6) | ||
| ENST00000700010.1:n.980T>C (MSH6) | ||
| ENST00000700011.1:n.2865T>C (MSH6) | ||
| ENST00000234420.11:c.3571T>C (MSH6) MANE Select | ENSP00000234420.5:p.Phe1191Leu | |
| ENST00000540021.6:c.3181T>C (MSH6) | ENSP00000446475.1:p.Phe1061Leu | |
| ENST00000652107.1:c.3274T>C (MSH6) | ENSP00000498629.1:p.Phe1092Leu | |
| ENST00000673637.1:c.3274T>C (MSH6) | ENSP00000501310.1:p.Phe1092Leu | |
| ENST00000234420.9:c.3571T>C (MSH6) | ENSP00000234420.4:p.Phe1191Leu | |
| ENST00000405808.5:c.169+2563A>G (FBXO11) | ENSP00000385127.1:n.169+2563A>G | |
| ENST00000434234.5:c.*124+2362A>G (FBXO11) | ENSP00000402692.1:n.*124+2362A>G | |
| ENST00000445503.5:c.*2918T>C (MSH6) | ENSP00000405294.1:n.*2918T>C | |
| ENST00000538136.1:c.2665T>C (MSH6) | ENSP00000438580.1:p.Phe889Leu | |
| ENST00000540021.5:c.3181T>C (MSH6) | ENSP00000446475.1:p.Phe1061Leu | |
| ENST00000614496.4:c.2665T>C (MSH6) | ENSP00000477844.1:p.Phe889Leu | |
| ENST00000622629.4:c.475T>C (MSH6) | ENSP00000482078.1:p.Phe159Leu | |
| NM_000179.2:c.3571T>C , LRG_219t1:c.3571T>C (MSH6) | NP_000170.1:p.Phe1191Leu | |
| NM_001281492.1:c.3181T>C (MSH6) | NP_001268421.1:p.Phe1061Leu | |
| NM_001281493.1:c.2665T>C (MSH6) | NP_001268422.1:p.Phe889Leu | |
| NM_001281494.1:c.2665T>C (MSH6) | NP_001268423.1:p.Phe889Leu | |
| XM_005264271.1:c.3274T>C (MSH6) | XP_005264328.1:p.Phe1092Leu | |
| XM_011532798.1:c.3388T>C (MSH6) | XP_011531100.1:p.Phe1130Leu | |
| XM_011532799.1:c.3274T>C (MSH6) | XP_011531101.1:p.Phe1092Leu | |
| XM_011532800.1:c.3274T>C (MSH6) | XP_011531102.1:p.Phe1092Leu | |
| XM_024452819.1:c.3571T>C (MSH6) | XP_024308587.1:p.Phe1191Leu | |
| XM_024452820.1:c.3388T>C (MSH6) | XP_024308588.1:p.Phe1130Leu | |
| XM_024452821.1:c.3274T>C (MSH6) | XP_024308589.1:p.Phe1092Leu | |
| XM_024452822.1:c.2665T>C (MSH6) | XP_024308590.1:p.Phe889Leu | |
| NM_000179.3:c.3571T>C (MSH6) MANE Select | NP_000170.1:p.Phe1191Leu | |
| NM_001281492.2:c.3181T>C (MSH6) | NP_001268421.1:p.Phe1061Leu | |
| NM_001281493.2:c.2665T>C (MSH6) | NP_001268422.1:p.Phe889Leu | |
| NM_001281494.2:c.2665T>C (MSH6) | NP_001268423.1:p.Phe889Leu |