Variant #0000886454 (NC_000004.11:g.96025646C>T, NM_001203.2:c.71C>T (BMPR1B))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.96025646C>T
DNA change (hg38) -
Published as BMPR1B(NM_001203.2):c.71C>T (p.(Thr24Ile))
ISCN -
DB-ID BMPR1B_000025
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 2022-11-01 13:01:21 +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     
BMPR1B NM_001203.2 -?/. - c.71C>T r.(?) p.(Thr24Ile)
BMPR1B NM_001256792.1 -?/. - c.71C>T r.(?) p.(Thr24Ile)
BMPR1B NM_001256793.1 -?/. - c.161C>T r.(?) p.(Thr54Ile)
BMPR1B NM_001256794.1 -?/. - c.71C>T r.(?) p.(Thr24Ile)


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