Variant #0001000751 (NC_000014.8:g.105417452C>G, NM_138420.2:c.4336G>C (AHNAK2))

Chromosome 14
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.105417452C>G
DNA change (hg38) -
Published as AHNAK2(NM_138420.4):c.4336G>C (p.E1446Q)
ISCN -
DB-ID AHNAK2_000326
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AHNAK2 NM_138420.2 ?/. - c.4336G>C r.(?) p.(Glu1446Gln)


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