Variant #0000624299 (NC_000022.10:g.38026176T>A, NM_013365.4:c.1330T>A (GGA1))

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.38026176T>A
DNA change (hg38) g.37630169T>A
Published as GGA1(NM_001363771.1):c.1381T>A (p.W461R)
ISCN -
DB-ID GGA1_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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GGA1 NM_013365.4 ?/. - c.1330T>A r.(?) p.(Trp444Arg)
SH3BP1 NM_018957.3 ?/. - c.-9619T>A r.(?) p.(=)


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