Variant #0000263735 (NC_000004.11:g.96052380G>A, NM_001203.2:c.793G>A (BMPR1B))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.96052380G>A
DNA change (hg38) g.95131229G>A
Published as BMPR1B(NM_001203.2):c.793G>A (p.D265N)
ISCN -
DB-ID BMPR1B_000007
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMPR1B NM_001203.2 +/. - c.793G>A r.(?) p.(Asp265Asn)
BMPR1B NM_001256792.1 +/. - c.793G>A r.(?) p.(Asp265Asn)
BMPR1B NM_001256793.1 +/. - c.883G>A r.(?) p.(Asp295Asn)
BMPR1B NM_001256794.1 +/. - c.793G>A r.(?) p.(Asp265Asn)


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