Variant #0000621436 (NC_000004.11:g.96052652T>A, NM_001203.2:c.1065T>A (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.96052652T>A
DNA change (hg38) g.95131501T>A
Published as BMPR1B(NM_001203.2):c.1065T>A (p.V355=)
ISCN -
DB-ID BMPR1B_000017
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) 0.00061 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-06-16 13:37:48 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMPR1B NM_001203.2 -?/. - c.1065T>A r.(?) p.(Val355=)
BMPR1B NM_001256792.1 -?/. - c.1065T>A r.(?) p.(Val355=)
BMPR1B NM_001256793.1 -?/. - c.1155T>A r.(?) p.(Val385=)
BMPR1B NM_001256794.1 -?/. - c.1065T>A r.(?) p.(Val355=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.