Variant #0001003820 (NC_000017.10:g.79094438A>C, NM_004920.2:c.2989T>G (AATK))

Chromosome 17
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.79094438A>C
DNA change (hg38) -
Published as AATK(NM_001080395.2):c.3298T>G (p.(Phe1100Val))
ISCN -
DB-ID AATK_000016
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 2024-08-28 13:16:32 +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     
BAIAP2 NM_001144888.1 -?/. - c.*4799A>C r.(=) p.(=)
AATK NM_004920.2 -?/. - c.2989T>G r.(?) p.(Phe997Val)


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