Variant #0000534566 (NC_000008.10:g.22054188C>T, NC_000008.10(NM_006129.4):c.1766-5C>T (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.22054188C>T
DNA change (hg38) g.22196675C>T
Published as BMP1(NM_001199.3):c.1766-5C>T (p.?), BMP1(NM_006129.5):c.1766-5C>T
ISCN -
DB-ID BMP1_000039 See all 2 reported entries
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) 0.0072 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.1766-5C>T r.spl? p.?


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