Variant #0000804653 (NC_000010.10:g.97376337A>G, NM_002860.3:c.1502T>C (ALDH18A1))

Chromosome 10
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.97376337A>G
DNA change (hg38) -
Published as ALDH18A1(NM_001323413.1):c.1502T>C (p.L501S), ALDH18A1(NM_002860.3):c.1502T>C (p.(Leu501Ser))
ISCN -
DB-ID ALDH18A1_000046 See all 2 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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH18A1 NM_002860.3 ?/. - c.1502T>C r.(?) p.(Leu501Ser)


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