Variant #0000609339 (NC_000004.11:g.96075691T>C, NC_000004.11(NM_001203.2):c.1384-8T>C (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.96075691T>C
DNA change (hg38) g.95154540T>C
Published as BMPR1B(NM_001203.2):c.1384-8T>C (p.(=))
ISCN -
DB-ID BMPR1B_000018
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) 0.00303 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 2019-12-04 15:24:38 +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.1384-8T>C r.(=) p.(=)
BMPR1B NM_001256792.1 -?/. - c.1384-8T>C r.(=) p.(=)
BMPR1B NM_001256793.1 -?/. - c.1474-8T>C r.(=) p.(=)
BMPR1B NM_001256794.1 -?/. - c.1384-8T>C r.(=) p.(=)


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