Variant #0000536313 (NC_000009.11:g.130502158G>A, NM_130459.3:c.-4609C>T (TOR2A))

Chromosome 9
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.130502158G>A
DNA change (hg38) g.127739879G>A
Published as SH2D3C(NM_170600.2):c.2210C>T (p.P737L)
ISCN -
DB-ID TOR2A_000003
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SH2D3C NM_005489.2 ?/. - c.1739C>T r.(?) p.(Pro580Leu)
TOR2A NM_130459.3 ?/. - c.-4609C>T r.(?) p.(=)
TTC16 NM_144965.1 ?/. - c.*8474G>A r.(=) p.(=)


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