Variant #0001050282 (NC_000001.10:g.155161642G>C, NC_000001.10(NM_001204285.1):c.434+57C>G (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.155161642G>C
DNA change (hg38) -
Published as MUC1(NM_001371720.1):c.518C>G (p.(Thr173Ser))
ISCN -
DB-ID THBS3_000014
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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.434+57C>G - r.(=) p.(=)
THBS3 NM_007112.4 ?/. - c.*3990C>G - r.(=) p.(=)
TRIM46 NM_025058.4 ?/. - c.*4976G>C - r.(=) p.(=)


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