Variant #0000798814 (NC_000001.10:g.155161689C>G, NC_000001.10(NM_001204285.1):c.434+10G>C (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.155161689C>G
DNA change (hg38) -
Published as MUC1(NM_001204286.1):c.461+10G>C
ISCN -
DB-ID THBS3_000006
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +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.434+10G>C - r.(=) p.(=)
THBS3 NM_007112.4 -?/. - c.*3943G>C - r.(=) p.(=)
TRIM46 NM_025058.4 -?/. - c.*5023C>G - r.(=) p.(=)


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