Variant #0000545069 (NC_000011.9:g.66109703C>T, NM_006876.2:c.*3817G>A (B3GNT1))

Chromosome 11
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.66109703C>T
DNA change (hg38) g.66342232C>T
Published as BRMS1(NM_001024957.1):c.3G>A (p.(Met1?))
ISCN -
DB-ID B3GNT1_000005
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 18:25:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B3GNT1 NM_006876.2 ?/. - c.*3817G>A r.(=) p.(=)
BRMS1 NM_015399.3 ?/. - c.3G>A r.(?) p.(Met1?)


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