Linked Data
ClinVar Variation Id:
127572
ClinVar RCV Id:
RCV000115392
RCV000195931
RCV000212667
RCV000412127
RCV001193702
RCV001354925
RCV003460814
RCV003997241
dbSNP Id:
rs587779925
ExAC:
2:48027633 C / G
gnomAD v2:
2-48027633-C-G
gnomAD v3:
2-47800494-C-G
gnomAD v4:
2-47800494-C-G
PubMed:
PMID:25186627
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47800494C>G , CM000664.2:g.47800494C>G | GRCh38 |
| NC_000002.11:g.48027633C>G , CM000664.1:g.48027633C>G | GRCh37 |
| NC_000002.10:g.47881137C>G | NCBI36 |
| NG_007111.1:g.22348C>G , LRG_219:g.22348C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.2214C>G (MSH6) | ENSP00000406248.2:p.His738Gln | |
| ENST00000420813.6:c.2214C>G (MSH6) | ENSP00000390382.2:p.His738Gln | |
| ENST00000455383.6:c.2214C>G (MSH6) | ENSP00000397484.2:p.His738Gln | |
| ENST00000700004.2:c.2511C>G (MSH6) | ENSP00000514752.2:p.His837Gln | |
| ENST00000699999.1:n.2595C>G (MSH6) | ||
| ENST00000700000.1:c.1606+905C>G (MSH6) | ENSP00000514749.1:n.1606+905C>G | |
| ENST00000700002.1:c.2517C>G (MSH6) | ENSP00000514750.1:p.His839Gln | |
| ENST00000700003.1:c.628-2926C>G (MSH6) | ENSP00000514751.1:n.628-2926C>G | |
| ENST00000700004.1:c.1668C>G (MSH6) | ENSP00000514752.1:p.His556Gln | |
| ENST00000234420.11:c.2511C>G (MSH6) MANE Select | ENSP00000234420.5:p.His837Gln | |
| ENST00000540021.6:c.2121C>G (MSH6) | ENSP00000446475.1:p.His707Gln | |
| ENST00000652107.1:c.2214C>G (MSH6) | ENSP00000498629.1:p.His738Gln | |
| ENST00000673637.1:c.2214C>G (MSH6) | ENSP00000501310.1:p.His738Gln | |
| ENST00000234420.9:c.2511C>G (MSH6) | ENSP00000234420.4:p.His837Gln | |
| ENST00000405808.5:c.169+7701G>C (FBXO11) | ENSP00000385127.1:n.169+7701G>C | |
| ENST00000434234.5:c.*124+7500G>C (FBXO11) | ENSP00000402692.1:n.*124+7500G>C | |
| ENST00000445503.5:c.*1858C>G (MSH6) | ENSP00000405294.1:n.*1858C>G | |
| ENST00000538136.1:c.1605C>G (MSH6) | ENSP00000438580.1:p.His535Gln | |
| ENST00000540021.5:c.2121C>G (MSH6) | ENSP00000446475.1:p.His707Gln | |
| ENST00000614496.4:c.1605C>G (MSH6) | ENSP00000477844.1:p.His535Gln | |
| ENST00000616033.4:c.2508C>G (MSH6) | ENSP00000480261.1:p.His836Gln | |
| ENST00000622629.4:c.-586C>G (MSH6) | ENSP00000482078.1:n.-586C>G | |
| NM_000179.2:c.2511C>G , LRG_219t1:c.2511C>G (MSH6) | NP_000170.1:p.His837Gln | |
| NM_001281492.1:c.2121C>G (MSH6) | NP_001268421.1:p.His707Gln | |
| NM_001281493.1:c.1605C>G (MSH6) | NP_001268422.1:p.His535Gln | |
| NM_001281494.1:c.1605C>G (MSH6) | NP_001268423.1:p.His535Gln | |
| XM_005264271.1:c.2214C>G (MSH6) | XP_005264328.1:p.His738Gln | |
| XM_011532798.1:c.2328C>G (MSH6) | XP_011531100.1:p.His776Gln | |
| XM_011532799.1:c.2214C>G (MSH6) | XP_011531101.1:p.His738Gln | |
| XM_011532800.1:c.2214C>G (MSH6) | XP_011531102.1:p.His738Gln | |
| XM_024452819.1:c.2511C>G (MSH6) | XP_024308587.1:p.His837Gln | |
| XM_024452820.1:c.2328C>G (MSH6) | XP_024308588.1:p.His776Gln | |
| XM_024452821.1:c.2214C>G (MSH6) | XP_024308589.1:p.His738Gln | |
| XM_024452822.1:c.1605C>G (MSH6) | XP_024308590.1:p.His535Gln | |
| NM_000179.3:c.2511C>G (MSH6) MANE Select | NP_000170.1:p.His837Gln | |
| NM_001281492.2:c.2121C>G (MSH6) | NP_001268421.1:p.His707Gln | |
| NM_001281493.2:c.1605C>G (MSH6) | NP_001268422.1:p.His535Gln | |
| NM_001281494.2:c.1605C>G (MSH6) | NP_001268423.1:p.His535Gln |