Variant #0000857036 (NC_000001.10:g.155160270C>T, NM_001204285.1:c.1009G>A (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.155160270C>T
DNA change (hg38) -
Published as MUC1(NM_001204286.1):c.1036G>A (p.V346M)
ISCN -
DB-ID TRIM46_000004
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) 0.00297 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 2022-05-09 15:51:19 +02:00 (CEST)
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.1009G>A - r.(?) p.(Val337Met)
TRIM46 NM_025058.4 -?/. - c.*3604C>T - r.(=) p.(=)


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