Linked Data
ClinVar Variation Id:
234074
dbSNP Id:
rs759654665
ExAC:
1:45805888 T / A
gnomAD v2:
1-45805888-T-A
gnomAD v3:
1-45340216-T-A
gnomAD v4:
1-45340216-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45340216T>A , CM000663.2:g.45340216T>A | GRCh38 |
| NC_000001.10:g.45805888T>A , CM000663.1:g.45805888T>A | GRCh37 |
| NC_000001.9:g.45578475T>A | NCBI36 |
| NG_008189.1:g.5255A>T , LRG_220:g.5255A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412971.6:c.36+3A>T (MUTYH) | ENSP00000410263.2:n.36+3A>T | |
| ENST00000529892.6:c.36+3A>T (MUTYH) | ENSP00000432528.2:n.36+3A>T | |
| ENST00000710952.2:c.36+3A>T (MUTYH) MANE Plus Clinical | ENSP00000518552.2:n.36+3A>T | |
| ENST00000672818.3:c.36+3A>T (MUTYH) | ENSP00000500891.1:n.36+3A>T | |
| ENST00000372090.6:c.-37T>A (TOE1) MANE Select | ENSP00000361162.5:n.-37T>A | |
| ENST00000450313.6:c.36+3A>T (MUTYH) | ENSP00000408176.2:n.36+3A>T | |
| ENST00000461495.6:c.36+3A>T (MUTYH) | ENSP00000437166.1:n.36+3A>T | |
| ENST00000671856.1:n.14+3A>T (MUTYH) | ||
| ENST00000671898.1:c.541-5705A>T | ENSP00000499896.1:n.541-5705A>T | |
| ENST00000672011.1:c.36+3A>T (MUTYH) | ENSP00000500418.1:n.36+3A>T | |
| ENST00000672818.2:c.36+3A>T (MUTYH) | ENSP00000500891.1:n.36+3A>T | |
| ENST00000372090.5:c.-37T>A (TOE1) | ENSP00000361162.5:n.-37T>A | |
| ENST00000372098.7:c.36+3A>T (MUTYH) | ENSP00000361170.3:n.36+3A>T | |
| ENST00000372110.7:c.36+3A>T (MUTYH) | ENSP00000361182.3:n.36+3A>T | |
| ENST00000372115.7:c.36+3A>T (MUTYH) | ENSP00000361187.3:n.36+3A>T | |
| ENST00000412971.5:c.36+3A>T (MUTYH) | ENSP00000410263.1:n.36+3A>T | |
| ENST00000450313.5:c.36+3A>T (MUTYH) | ENSP00000408176.1:n.36+3A>T | |
| ENST00000461495.5:c.36+3A>T (MUTYH) | ENSP00000437166.1:n.36+3A>T | |
| ENST00000462387.5:n.214+3A>T (MUTYH) | ||
| ENST00000467940.5:c.39A>T (MUTYH) | ENSP00000436478.1:p.Val13= | |
| ENST00000471337.5:n.42T>A (TOE1) | ||
| ENST00000476789.5:n.214+3A>T (MUTYH) | ||
| ENST00000477731.5:n.165T>A (TOE1) | ||
| ENST00000481139.5:n.197+3A>T (MUTYH) | ||
| ENST00000481571.5:c.36+3A>T (MUTYH) | ENSP00000436597.1:n.36+3A>T | |
| ENST00000483642.5:n.175+7A>T (MUTYH) | ||
| ENST00000525160.5:c.36+3A>T (MUTYH) | ENSP00000431568.1:n.36+3A>T | |
| ENST00000529984.5:c.-7+3A>T (MUTYH) | ENSP00000437093.1:n.-7+3A>T | |
| ENST00000534453.1:n.20A>T (MUTYH) | ||
| NM_001048171.1:c.36+3A>T (MUTYH) | NP_001041636.1:n.36+3A>T | |
| NM_001128425.1:c.36+3A>T , LRG_220t1:c.36+3A>T (MUTYH) | NP_001121897.1:n.36+3A>T | |
| NM_001293190.1:c.36+3A>T (MUTYH) | NP_001280119.1:n.36+3A>T | |
| NM_001293192.1:c.-219+3A>T (MUTYH) | NP_001280121.1:n.-219+3A>T | |
| NM_012222.2:c.36+3A>T (MUTYH) | NP_036354.1:n.36+3A>T | |
| NM_025077.3:c.-37T>A (TOE1) | NP_079353.3:n.-37T>A | |
| XM_005270412.2:c.-37T>A (TOE1) | XP_005270469.1:n.-37T>A | |
| XM_011541503.1:c.36+3A>T (MUTYH) | XP_011539805.1:n.36+3A>T | |
| XM_011541505.1:c.-80+3A>T (MUTYH) | XP_011539807.1:n.-80+3A>T | |
| XR_246230.2:n.241T>A (TOE1) | ||
| XR_426587.2:n.43T>A (TOE1) | ||
| XR_946532.1:n.43T>A (TOE1) | ||
| XR_946658.1:n.83+3A>T (MUTYH) | ||
| NM_001350650.1:c.-278+3A>T (MUTYH) | NP_001337579.1:n.-278+3A>T | |
| NM_001350651.1:c.-214+3A>T (MUTYH) | NP_001337580.1:n.-214+3A>T | |
| NR_146882.1:n.252+3A>T (MUTYH) | ||
| XM_005270412.4:c.-37T>A (TOE1) | XP_005270469.1:n.-37T>A | |
| XM_005270413.5:c.-413T>A (TOE1) | XP_005270470.1:n.-413T>A | |
| XM_011540569.3:c.-321T>A (TOE1) | XP_011538871.1:n.-321T>A | |
| XM_011541503.2:c.36+3A>T (MUTYH) | XP_011539805.1:n.36+3A>T | |
| XM_011541505.2:c.-80+3A>T (MUTYH) | XP_011539807.1:n.-80+3A>T | |
| XM_017001331.1:c.-20A>T (MUTYH) | XP_016856820.1:n.-20A>T | |
| XM_017001332.1:c.-7+7A>T (MUTYH) | XP_016856821.1:n.-7+7A>T | |
| XM_017001335.1:c.-232A>T (MUTYH) | XP_016856824.1:n.-232A>T | |
| XM_017001336.1:c.-311+3A>T (MUTYH) | XP_016856825.1:n.-311+3A>T | |
| XM_024447244.1:c.-320+3A>T (MUTYH) | XP_024303012.1:n.-320+3A>T | |
| XM_024447248.1:c.-278+3A>T (MUTYH) | XP_024303016.1:n.-278+3A>T | |
| XM_024447249.1:c.-774+7A>T (MUTYH) | XP_024303017.1:n.-774+7A>T | |
| XM_024447250.1:c.-790A>T (MUTYH) | XP_024303018.1:n.-790A>T | |
| XM_024452837.1:c.-413T>A (TOE1) | XP_024308605.1:n.-413T>A | |
| XR_001736951.2:n.151T>A (TOE1) | ||
| XR_001737190.1:n.103+3A>T (MUTYH) | ||
| XR_002956643.1:n.211+3A>T (MUTYH) | ||
| XR_002956644.1:n.229+3A>T (MUTYH) | ||
| XR_002959287.1:n.466T>A (TOE1) | ||
| XR_246230.4:n.151T>A (TOE1) | ||
| XR_426587.4:n.43T>A (TOE1) | ||
| XR_946532.3:n.43T>A (TOE1) | ||
| XR_946658.2:n.97+3A>T (MUTYH) | ||
| NM_025077.4:c.-37T>A (TOE1) MANE Select | NP_079353.3:n.-37T>A | |
| NM_001048171.2:c.-7+3A>T (MUTYH) | NP_001041636.2:n.-7+3A>T | |
| NM_001128425.2:c.36+3A>T (MUTYH) MANE Plus Clinical | NP_001121897.1:n.36+3A>T | |
| NM_001293190.2:c.36+3A>T (MUTYH) | NP_001280119.1:n.36+3A>T | |
| NM_001293192.2:c.-219+3A>T (MUTYH) | NP_001280121.1:n.-219+3A>T | |
| NM_001350650.2:c.-278+3A>T (MUTYH) | NP_001337579.1:n.-278+3A>T | |
| NM_001350651.2:c.-214+3A>T (MUTYH) | NP_001337580.1:n.-214+3A>T | |
| NM_012222.3:c.36+3A>T (MUTYH) | NP_036354.1:n.36+3A>T | |
| NR_146882.2:n.222+3A>T (MUTYH) |