Variant #0000259637 (NC_000006.11:g.24495214T>C, ALDH5A1(NM_001080.3):c.-11T>C)

Chromosome 6
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.24495214T>C
DNA change (hg38) g.24494986T>C
Published as ALDH5A1(NM_170740.1):c.-11T>C
ISCN -
DB-ID ALDH5A1_000116
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH5A1 NM_001080.3 ?/. - c.-11T>C r.(?) p.(=)
GPLD1 NM_001503.3 ?/. - c.-5475A>G r.(?) p.(=)
ALDH5A1 NM_170740.1 ?/. - c.-11T>C r.(?) p.(=)