Variant #0000523575 (NC_000004.11:g.95972917A>G, NC_000004.11(NM_001203.2):c.-17-52642A>G (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.95972917A>G
DNA change (hg38) g.95051766A>G
Published as BMPR1B(NM_001256793.1):c.67A>G (p.(Thr23Ala))
ISCN -
DB-ID BMPR1B_000012
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) 0.00038 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 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.-17-52642A>G r.(=) p.(=)
BMPR1B NM_001256792.1 -?/. - c.-17-52642A>G r.(=) p.(=)
BMPR1B NM_001256793.1 -?/. - c.67A>G r.(?) p.(Thr23Ala)
BMPR1B NM_001256794.1 -?/. - c.-39879A>G r.(?) p.(=)


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