Variant #0001035087 (NC_000005.9:g.171765648T>C, NM_001017995.2:c.2461A>G (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.171765648T>C
DNA change (hg38) -
Published as SH3PXD2B(NM_001017995.3):c.2461A>G (p.(Lys821Glu))
ISCN -
DB-ID SH3PXD2B_000060
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SH3PXD2B NM_001017995.2 ?/. - c.2461A>G r.(?) p.(Lys821Glu)


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