Linked Data
ClinVar Variation Id:
237128
ClinVar RCV Id:
RCV000234680
RCV000445727
RCV001290648
RCV000759841
RCV001082552
RCV004532832
RCV003998706
dbSNP Id:
rs1042819
ExAC:
2:48026289 C / T
gnomAD v2:
2-48026289-C-T
gnomAD v3:
2-47799150-C-T
gnomAD v4:
2-47799150-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47799150C>T , CM000664.2:g.47799150C>T | GRCh38 |
| NC_000002.11:g.48026289C>T , CM000664.1:g.48026289C>T | GRCh37 |
| NC_000002.10:g.47879793C>T | NCBI36 |
| NG_007111.1:g.21004C>T , LRG_219:g.21004C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.870C>T (MSH6) | ENSP00000406248.2:p.Pro290= | |
| ENST00000420813.6:c.870C>T (MSH6) | ENSP00000390382.2:p.Pro290= | |
| ENST00000455383.6:c.870C>T (MSH6) | ENSP00000397484.2:p.Pro290= | |
| ENST00000700004.2:c.1167C>T (MSH6) | ENSP00000514752.2:p.Pro389= | |
| ENST00000699999.1:n.1251C>T (MSH6) | ||
| ENST00000700000.1:c.1167C>T (MSH6) | ENSP00000514749.1:p.Pro389= | |
| ENST00000700002.1:c.1173C>T (MSH6) | ENSP00000514750.1:p.Pro391= | |
| ENST00000700003.1:c.627+3087C>T (MSH6) | ENSP00000514751.1:n.627+3087C>T | |
| ENST00000700004.1:c.324C>T (MSH6) | ENSP00000514752.1:p.Pro108= | |
| ENST00000234420.11:c.1167C>T (MSH6) MANE Select | ENSP00000234420.5:p.Pro389= | |
| ENST00000540021.6:c.777C>T (MSH6) | ENSP00000446475.1:p.Pro259= | |
| ENST00000652107.1:c.870C>T (MSH6) | ENSP00000498629.1:p.Pro290= | |
| ENST00000673637.1:c.870C>T (MSH6) | ENSP00000501310.1:p.Pro290= | |
| ENST00000234420.9:c.1167C>T (MSH6) | ENSP00000234420.4:p.Pro389= | |
| ENST00000405808.5:c.169+9045G>A (FBXO11) | ENSP00000385127.1:n.169+9045G>A | |
| ENST00000434234.5:c.*124+8844G>A (FBXO11) | ENSP00000402692.1:n.*124+8844G>A | |
| ENST00000445503.5:c.*514C>T (MSH6) | ENSP00000405294.1:n.*514C>T | |
| ENST00000538136.1:c.261C>T (MSH6) | ENSP00000438580.1:p.Pro87= | |
| ENST00000540021.5:c.777C>T (MSH6) | ENSP00000446475.1:p.Pro259= | |
| ENST00000614496.4:c.261C>T (MSH6) | ENSP00000477844.1:p.Pro87= | |
| ENST00000616033.4:c.1164C>T (MSH6) | ENSP00000480261.1:p.Pro388= | |
| ENST00000622629.4:c.-1930C>T (MSH6) | ENSP00000482078.1:n.-1930C>T | |
| NM_000179.2:c.1167C>T , LRG_219t1:c.1167C>T (MSH6) | NP_000170.1:p.Pro389= | |
| NM_001281492.1:c.777C>T (MSH6) | NP_001268421.1:p.Pro259= | |
| NM_001281493.1:c.261C>T (MSH6) | NP_001268422.1:p.Pro87= | |
| NM_001281494.1:c.261C>T (MSH6) | NP_001268423.1:p.Pro87= | |
| XM_005264271.1:c.870C>T (MSH6) | XP_005264328.1:p.Pro290= | |
| XM_011532798.1:c.984C>T (MSH6) | XP_011531100.1:p.Pro328= | |
| XM_011532799.1:c.870C>T (MSH6) | XP_011531101.1:p.Pro290= | |
| XM_011532800.1:c.870C>T (MSH6) | XP_011531102.1:p.Pro290= | |
| XM_024452819.1:c.1167C>T (MSH6) | XP_024308587.1:p.Pro389= | |
| XM_024452820.1:c.984C>T (MSH6) | XP_024308588.1:p.Pro328= | |
| XM_024452821.1:c.870C>T (MSH6) | XP_024308589.1:p.Pro290= | |
| XM_024452822.1:c.261C>T (MSH6) | XP_024308590.1:p.Pro87= | |
| NM_000179.3:c.1167C>T (MSH6) MANE Select | NP_000170.1:p.Pro389= | |
| NM_001281492.2:c.777C>T (MSH6) | NP_001268421.1:p.Pro259= | |
| NM_001281493.2:c.261C>T (MSH6) | NP_001268422.1:p.Pro87= | |
| NM_001281494.2:c.261C>T (MSH6) | NP_001268423.1:p.Pro87= |