Variant #0001042264 (NC_000017.10:g.79058672C>G, NM_004920.2:c.*33530G>C (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.79058672C>G
DNA change (hg38) -
Published as BAIAP2(NM_001144888.2):c.258C>G (p.(Ile86Met))
ISCN -
DB-ID AATK_000022
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BAIAP2 NM_001144888.1 ?/. - c.258C>G r.(?) p.(Ile86Met)
AATK NM_004920.2 ?/. - c.*33530G>C r.(=) p.(=)


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