Variant #0000806477 (NC_000014.8:g.74527350G>A, NM_005589.2:c.1603C>T (ALDH6A1))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74527350G>A
DNA change (hg38) -
Published as ALDH6A1(NM_001278594.1):c.1141C>T (p.R381C)
ISCN -
DB-ID ALDH6A1_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) 1.0E-5 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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH6A1 NM_005589.2 -?/. - c.1603C>T r.(?) p.(Arg535Cys)
ALDH6A1 XM_005267686.1 -?/. - c.1141C>T r.(?) p.(Arg381Cys)


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