Linked Data
ClinVar Variation Id:
237198
dbSNP Id:
rs63750554
ExAC:
2:48033468 C / G
gnomAD v2:
2-48033468-C-G
gnomAD v3:
2-47806329-C-G
gnomAD v4:
2-47806329-C-G
PubMed:
PMID:28874130
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47806329C>G , CM000664.2:g.47806329C>G | GRCh38 |
| NC_000002.11:g.48033468C>G , CM000664.1:g.48033468C>G | GRCh37 |
| NC_000002.10:g.47886972C>G | NCBI36 |
| NG_007111.1:g.28183C>G , LRG_219:g.28183C>G | |
| NG_008397.1:g.104347G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.3475C>G (MSH6) | ENSP00000406248.2:p.Gln1159Glu | |
| ENST00000420813.6:c.3475C>G (MSH6) | ENSP00000390382.2:p.Gln1159Glu | |
| ENST00000455383.6:c.3475C>G (MSH6) | ENSP00000397484.2:p.Gln1159Glu | |
| ENST00000700004.2:c.3388C>G (MSH6) | ENSP00000514752.2:p.Gln1130Glu | |
| ENST00000699999.1:n.4446C>G (MSH6) | ||
| ENST00000700000.1:c.2206C>G (MSH6) | ENSP00000514749.1:p.Gln736Glu | |
| ENST00000700002.1:c.3778C>G (MSH6) | ENSP00000514750.1:p.Gln1260Glu | |
| ENST00000700003.1:c.1227C>G (MSH6) | ENSP00000514751.1:n.1227C>G | |
| ENST00000700004.1:c.2545C>G (MSH6) | ENSP00000514752.1:p.Gln849Glu | |
| ENST00000700005.1:n.2623C>G (MSH6) | ||
| ENST00000700006.1:n.4930C>G (MSH6) | ||
| ENST00000700007.1:n.2367C>G (MSH6) | ||
| ENST00000700008.1:n.1941C>G (MSH6) | ||
| ENST00000700009.1:n.2436C>G (MSH6) | ||
| ENST00000700010.1:n.1181C>G (MSH6) | ||
| ENST00000700011.1:n.3066C>G (MSH6) | ||
| ENST00000682451.1:n.4419G>C (FBXO11) | ||
| ENST00000684712.1:n.4681G>C (FBXO11) | ||
| ENST00000234420.11:c.3772C>G (MSH6) MANE Select | ENSP00000234420.5:p.Gln1258Glu | |
| ENST00000540021.6:c.3382C>G (MSH6) | ENSP00000446475.1:p.Gln1128Glu | |
| ENST00000652107.1:c.3475C>G (MSH6) | ENSP00000498629.1:p.Gln1159Glu | |
| ENST00000673637.1:c.3475C>G (MSH6) | ENSP00000501310.1:p.Gln1159Glu | |
| ENST00000234420.9:c.3772C>G (MSH6) | ENSP00000234420.4:p.Gln1258Glu | |
| ENST00000405808.5:c.169+1866G>C (FBXO11) | ENSP00000385127.1:n.169+1866G>C | |
| ENST00000434234.5:c.*124+1665G>C (FBXO11) | ENSP00000402692.1:n.*124+1665G>C | |
| ENST00000445503.5:c.*3119C>G (MSH6) | ENSP00000405294.1:n.*3119C>G | |
| ENST00000538136.1:c.2866C>G (MSH6) | ENSP00000438580.1:p.Gln956Glu | |
| ENST00000540021.5:c.3382C>G (MSH6) | ENSP00000446475.1:p.Gln1128Glu | |
| ENST00000614496.4:c.2866C>G (MSH6) | ENSP00000477844.1:p.Gln956Glu | |
| ENST00000622629.4:c.674C>G (MSH6) | ENSP00000482078.1:p.Ser225Ter | |
| NM_000179.2:c.3772C>G , LRG_219t1:c.3772C>G (MSH6) | NP_000170.1:p.Gln1258Glu | |
| NM_001281492.1:c.3382C>G (MSH6) | NP_001268421.1:p.Gln1128Glu | |
| NM_001281493.1:c.2866C>G (MSH6) | NP_001268422.1:p.Gln956Glu | |
| NM_001281494.1:c.2866C>G (MSH6) | NP_001268423.1:p.Gln956Glu | |
| XM_005264271.1:c.3475C>G (MSH6) | XP_005264328.1:p.Gln1159Glu | |
| XM_011532798.1:c.3589C>G (MSH6) | XP_011531100.1:p.Gln1197Glu | |
| XM_011532799.1:c.3475C>G (MSH6) | XP_011531101.1:p.Gln1159Glu | |
| XM_011532800.1:c.3475C>G (MSH6) | XP_011531102.1:p.Gln1159Glu | |
| XM_024452819.1:c.3772C>G (MSH6) | XP_024308587.1:p.Gln1258Glu | |
| XM_024452820.1:c.3589C>G (MSH6) | XP_024308588.1:p.Gln1197Glu | |
| XM_024452821.1:c.3475C>G (MSH6) | XP_024308589.1:p.Gln1159Glu | |
| XM_024452822.1:c.2866C>G (MSH6) | XP_024308590.1:p.Gln956Glu | |
| NM_000179.3:c.3772C>G (MSH6) MANE Select | NP_000170.1:p.Gln1258Glu | |
| NM_001281492.2:c.3382C>G (MSH6) | NP_001268421.1:p.Gln1128Glu | |
| NM_001281493.2:c.2866C>G (MSH6) | NP_001268422.1:p.Gln956Glu | |
| NM_001281494.2:c.2866C>G (MSH6) | NP_001268423.1:p.Gln956Glu |