Variant #0000688188 (NC_000001.10:g.45796881G>A, NM_001128425.1:c.1449C>T (MUTYH))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45796881G>A
DNA change (hg38) -
Published as MUTYH(NM_001128425.1):c.1449C>T (p.T483=), MUTYH(NM_001128425.2):c.1449C>T (p.T483=)
ISCN -
DB-ID MUTYH_000261 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00296 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 -/. - c.1449C>T r.(?) p.(Thr483=) -
TOE1 NM_025077.3 -/. - c.-9044G>A r.(?) p.(=) -
HPDL NM_032756.2 -/. - c.*2945G>A r.(=) p.(=) -


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