Variant #0001053938 (NC_000011.9:g.66103233C>T, NM_015399.3:c.*2120G>A (BRMS1))

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.66103233C>T
DNA change (hg38) -
Published as RIN1(NM_004292.3):c.382G>A (p.(Gly128Ser))
ISCN -
DB-ID BRMS1_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 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RIN1 NM_004292.2 ?/. - c.382G>A r.(?) p.(Gly128Ser)
BRMS1 NM_015399.3 ?/. - c.*2120G>A r.(=) p.(=)


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