Variant #0001030175 (NC_000022.10:g.24621571C>T, NM_004121.2:c.1279G>A (GGT5))

Chromosome 22
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.24621571C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID GGT5_000002
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2047734271
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-04-02 11:53:01 +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     
GGT5 NM_004121.2 ?/. - c.1279G>A r.(?) p.(Glu427Lys)


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