Variant #0000910785 (NC_000001.10:g.155158650G>A, NM_001204285.1:c.1389C>T (MUC1))

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.155158650G>A
DNA change (hg38) -
Published as MUC1(NM_001204286.1):c.1416C>T (p.Y472=)
ISCN -
DB-ID KRTCAP2_000001
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) 0.00055 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
MUC1 NM_001204285.1 -?/. - c.1389C>T - r.(?) p.(Tyr463=)
TRIM46 NM_025058.4 -?/. - c.*1984G>A - r.(=) p.(=)
KRTCAP2 NM_173852.3 -?/. - c.-12872C>T - r.(?) p.(=)


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