Variant #0000947253 (NC_000001.10:g.45795043G>T, NM_001128425.1:c.1585C>A (MUTYH))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45795043G>T
DNA change (hg38) -
Published as MUTYH(NM_001048171.1):c.1543C>A (p.(Leu515Met))
ISCN -
DB-ID MUTYH_000177 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) 0.00342 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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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.1585C>A r.(?) p.(Leu529Met) -
TOE1 NM_025077.3 -?/. - c.-10882G>T r.(?) p.(=) -
HPDL NM_032756.2 -?/. - c.*1107G>T r.(=) p.(=) -


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