Variant #0000507393 (NC_000001.10:g.40235710G>C, NC_000001.10(NM_001720.3):c.673+4270C>G (BMP8B))

Chromosome 1
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.40235710G>C
DNA change (hg38) g.39770038G>C
Published as OXCT2(NM_022120.1):c.1218C>G (p.(Asp406Glu))
ISCN -
DB-ID BMP8B_000008
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) 0.00189 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMP8B NM_001720.3 -?/. - c.673+4270C>G r.(=) p.(=)
OXCT2 NM_022120.1 -?/. - c.1218C>G r.(?) p.(Asp406Glu)


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