Variant #0001034741 (NC_000004.11:g.96046214T>C, NM_001203.2:c.527T>C (BMPR1B))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.96046214T>C
DNA change (hg38) -
Published as BMPR1B(NM_001203.3):c.527T>C (p.(Leu176Pro))
ISCN -
DB-ID BMPR1B_000033
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) 2.0E-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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMPR1B NM_001203.2 +?/. - c.527T>C r.(?) p.(Leu176Pro)
BMPR1B NM_001256792.1 +?/. - c.527T>C r.(?) p.(Leu176Pro)
BMPR1B NM_001256793.1 +?/. - c.617T>C r.(?) p.(Leu206Pro)
BMPR1B NM_001256794.1 +?/. - c.527T>C r.(?) p.(Leu176Pro)


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