Variant #0000892914 (NC_000016.9:g.30017956_30017957insT, NM_003586.2:c.920_921insA (DOC2A))

Chromosome 16
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.30017956_30017957insT
DNA change (hg38) -
Published as DOC2A(NM_003586.3):c.920_921insA (p.C308Vfs*12)
ISCN -
DB-ID DOC2A_000008
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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOC2A NM_003586.2 ?/. - c.920_921insA r.(?) p.(Cys308Valfs*12)
INO80E NM_173618.1 ?/. - c.*1193_*1194insT r.(=) p.(=)


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