Variant #0000262216 (NC_000001.10:g.19228963C>G, NM_001161504.1:c.-11894G>C (ALDH4A1))

Chromosome 1
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.19228963C>G
DNA change (hg38) g.18902469C>G
Published as ALDH4A1(NM_003748.4):c.55G>C (p.G19R)
ISCN -
DB-ID ALDH4A1_000018
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFFO2 NM_001136265.1 -?/. - c.*6092G>C r.(=) p.(=)
ALDH4A1 NM_001161504.1 -?/. - c.-11894G>C r.(?) p.(=)


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