Variant #0000991269 (NC_000001.10:g.40235516G>T, NC_000001.10(NM_001720.3):c.673+4464C>A (BMP8B))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.40235516G>T
DNA change (hg38) -
Published as OXCT2(NM_022120.1):c.1412C>A (p.(Ala471Asp))
ISCN -
DB-ID BMP8B_000014
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) Retrieve
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 13:07:21 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMP8B NM_001720.3 ?/. - c.673+4464C>A r.(=) p.(=)
OXCT2 NM_022120.1 ?/. - c.1412C>A r.(?) p.(Ala471Asp)


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