Variant #0000280190 (NC_000001.10:g.45799074C>T, NC_000001.10(NM_001128425.1):c.348+11G>A (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.45799074C>T
DNA change (hg38) g.45333402C>T
Published as MUTYH(NM_001048171.1):c.306+11G>A (p.(=)), MUTYH(NM_001128425.2):c.348+11G>A
ISCN -
DB-ID MUTYH_000108 See all 4 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) 0.00167 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.348+11G>A r.(=) p.(=) -
TOE1 NM_025077.3 -/. - c.-6851C>T r.(?) p.(=) -
HPDL NM_032756.2 -/. - c.*5138C>T r.(=) p.(=) -


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