Variant #0000343081 (NC_000001.10:g.155154372C>T, NM_001204285.1:c.*4239G>A (MUC1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.155154372C>T
DNA change (hg38) g.155181896C>T
Published as -
ISCN -
DB-ID TRIM46_000002
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
MUC1 NM_001204285.1 ?/. - c.*4239G>A - r.(=) p.(=)
TRIM46 NM_025058.4 ?/. - c.1633C>T - r.(?) p.(Arg545Trp)
KRTCAP2 NM_173852.3 ?/. - c.-8594G>A - r.(?) p.(=)


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