Variant #0000322325 (NC_000011.9:g.66103565G>A, NM_015399.3:c.*1788C>T (BRMS1))

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.66103565G>A
DNA change (hg38) g.66336094G>A
Published as RIN1(NM_004292.3):c.151C>T (p.(Arg51Trp))
ISCN -
DB-ID RIN1_000003
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) 0.00557 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 2024-04-19 20:27:30 +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.151C>T r.(?) p.(Arg51Trp)
BRMS1 NM_015399.3 -?/. - c.*1788C>T r.(=) p.(=)


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