Variant #0000322326 (NC_000011.9:g.66108808C>A, NM_006876.2:c.*4712G>T (B3GNT1))

Chromosome 11
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.66108808C>A
DNA change (hg38) g.66341337C>A
Published as BRMS1(NM_001024957.1):c.231-4G>T (p.?)
ISCN -
DB-ID BRMS1_000001
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-30 18:25:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RIN1 NM_004292.2 -?/. - c.-4935G>T r.(?) p.(=)
B3GNT1 NM_006876.2 -?/. - c.*4712G>T r.(=) p.(=)
BRMS1 NM_015399.3 -?/. - c.231-4G>T r.spl? p.?


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