Variant #0001034739 (NC_000004.11:g.96035971C>T, NM_001203.2:c.244C>T (BMPR1B))

Chromosome 4
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.96035971C>T
DNA change (hg38) -
Published as BMPR1B(NM_001203.3):c.244C>T (p.(Arg82Trp))
ISCN -
DB-ID BMPR1B_000032
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMPR1B NM_001203.2 ?/. - c.244C>T r.(?) p.(Arg82Trp)
BMPR1B NM_001256792.1 ?/. - c.244C>T r.(?) p.(Arg82Trp)
BMPR1B NM_001256793.1 ?/. - c.334C>T r.(?) p.(Arg112Trp)
BMPR1B NM_001256794.1 ?/. - c.244C>T r.(?) p.(Arg82Trp)


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