Variant #0000320758 (NC_000001.10:g.40228259_40228260insC, NC_000001.10(NM_001720.3):c.1059+504_1059+505insG (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.40228259_40228260insC
DNA change (hg38) g.39762587_39762588insC
Published as PPIE(NM_001195007.1):c.908_909insC (p.(Trp303CysfsTer8))
ISCN -
DB-ID BMP8B_000004
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) 0.00068 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 2018-01-15 20:58:59 +01:00 (CET)
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.1059+504_1059+505insG r.(=) p.(=)
PPIE NM_006112.3 ?/. - c.*9232_*9233insC r.(=) p.(=)
OXCT2 NM_022120.1 ?/. - c.*7114_*7115insG r.(=) p.(=)


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