Variant #0000263726 (NC_000008.10:g.22049596G>A, NM_006129.4:c.1112G>A (BMP1))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.22049596G>A
DNA change (hg38) g.22192083G>A
Published as BMP1(NM_001199.3):c.1112G>A (p.(Arg371His)), BMP1(NM_006129.4):c.1112G>A (p.R371H), BMP1(NM_006129.5):c.1112G>A (p.R371H)
ISCN -
DB-ID BMP1_000018 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference PubMed: Fahiminiya 2014
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00413 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMP1 NM_006129.4 -/. - c.1112G>A r.(?) p.(Arg371His)


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