Variant #0000523576 (NC_000004.11:g.96025586G>A, NM_001203.2:c.11G>A (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.96025586G>A
DNA change (hg38) g.95104435G>A
Published as BMPR1B(NM_001203.2):c.11G>A (p.(Arg4Gln))
ISCN -
DB-ID BMPR1B_000013
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) 0.00037 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMPR1B NM_001203.2 ?/. - c.11G>A r.(?) p.(Arg4Gln)
BMPR1B NM_001256792.1 ?/. - c.11G>A r.(?) p.(Arg4Gln)
BMPR1B NM_001256793.1 ?/. - c.101G>A r.(?) p.(Arg34Gln)
BMPR1B NM_001256794.1 ?/. - c.11G>A r.(?) p.(Arg4Gln)


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