Variant #0000994510 (NC_000004.11:g.96051106A>G, NM_001203.2:c.679A>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.96051106A>G
DNA change (hg38) -
Published as BMPR1B(NM_001203.2):c.679A>G (p.(Lys227Glu))
ISCN -
DB-ID BMPR1B_000030
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) 1.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
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.679A>G r.(?) p.(Lys227Glu)
BMPR1B NM_001256792.1 -?/. - c.679A>G r.(?) p.(Lys227Glu)
BMPR1B NM_001256793.1 -?/. - c.769A>G r.(?) p.(Lys257Glu)
BMPR1B NM_001256794.1 -?/. - c.679A>G r.(?) p.(Lys227Glu)


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