Variant #0001050007 (NC_000001.10:g.24122489G>T, NM_000403.3:c.997C>A (GALE))

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.24122489G>T
DNA change (hg38) -
Published as GALE(NM_001008216.2):c.997C>A (p.(Leu333Ile))
ISCN -
DB-ID GALE_000023
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) 0.00018 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALE NM_000403.3 ?/. - c.997C>A r.(?) p.(Leu333Ile)
GALE NM_001008216.2 ?/. - c.997C>A r.(?) p.(Leu333Ile)
LYPLA2 NM_007260.2 ?/. - c.*1267G>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.