Variant #0000675878 (NC_000001.10:g.46532758C>T, NM_005727.3:c.-108465C>T (TSPAN1))

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.46532758C>T
DNA change (hg38) -
Published as LOC110117498-PIK3R3(NM_001303427.1):c.458G>A (p.G153E), PIK3R3(NM_003629.4):c.320G>A (p.G107E)
ISCN -
DB-ID PIK3R3_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIK3R3 NM_003629.3 ?/. - c.320G>A r.(?) p.(Gly107Glu)
TSPAN1 NM_005727.3 ?/. - c.-108465C>T r.(?) p.(=)


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