Variant #0001035005 (NC_000005.9:g.148408101A>G, NM_024577.3:c.1194T>C (SH3TC2))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.148408101A>G
DNA change (hg38) -
Published as SH3TC2(NM_024577.3):c.1194T>C (p.G398=), SH3TC2(NM_024577.4):c.1194T>C (p.G398=)
ISCN -
DB-ID SH3TC2_000055 See all 3 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) 0.44009 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SH3TC2 NM_024577.3 -/. - c.1194T>C r.(?) p.(Gly398=)


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