Variant #0000332760 (NC_000009.11:g.119460500_119460501insA, NM_012210.3:c.479_480insA (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.119460500_119460501insA
DNA change (hg38) g.116698221_116698222insA
Published as TRIM32(NM_012210.3):c.479_480insA (p.(Met160IlefsTer23))
ISCN -
DB-ID TRIM32_000026
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 2020-06-25 17:54:09 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM32 NM_012210.3 ?/. - c.479_480insA r.(?) p.(Met160IlefsTer23)
ASTN2 NM_014010.4 ?/. - c.2653+27549_2653+27550insT r.(=) p.(=)


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