Variant #0000563640 (NC_000017.10:g.79096276G>T, NM_004920.2:c.1151C>A (AATK))

Chromosome 17
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.79096276G>T
DNA change (hg38) g.81122476G>T
Published as AATK(NM_001080395.2):c.1460C>A (p.A487E)
ISCN -
DB-ID AATK_000011
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 2019-07-18 18:22:55 +02:00 (CEST)
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     
BAIAP2 NM_001144888.1 ?/. - c.*6637G>T r.(=) p.(=)
AATK NM_004920.2 ?/. - c.1151C>A r.(?) p.(Ala384Glu)


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