Variant #0000308038 (NC_000005.9:g.171765715_171765717del, NM_001017995.2:c.2395_2397del (SH3PXD2B))

Chromosome 5
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.171765715_171765717del
DNA change (hg38) g.172338711_172338713del
Published as SH3PXD2B(NM_001017995.2):c.2395_2397del (p.(Leu799del)), SH3PXD2B(NM_001017995.2):c.2395_2397delCTC (p.L799del)
ISCN -
DB-ID SH3PXD2B_000003 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) Retrieve
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 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SH3PXD2B NM_001017995.2 ?/. - c.2395_2397del r.(?) p.(Leu799del)


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