Variant #0000332766 (NC_000009.11:g.120176941_120176946dup, NM_012210.3:c.*714958_*714963dup (TRIM32))

Chromosome 9
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.120176941_120176946dup
DNA change (hg38) g.117414663_117414668dup
Published as ASTN2(NM_014010.4):c.279_280insGCTGGG (p.(Ala92_Gly93dup))
ISCN -
DB-ID ASTN2_000017
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 2018-01-15 20:58:59 +01:00 (CET)
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     
TRIM32 NM_012210.3 ?/. - c.*714958_*714963dup r.(=) p.(=)
ASTN2 NM_014010.4 ?/. - c.274_279dup r.(?) p.(Ala92_Gly93dup)


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