Variant #0000317050 (NC_000009.11:g.119460518G>A, NM_012210.3:c.497G>A (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.119460518G>A
DNA change (hg38) g.116698239G>A
Published as TRIM32(NM_001099679.1):c.497G>A (p.(Arg166Gln)), TRIM32(NM_012210.3):c.497G>A (p.R166Q)
ISCN -
DB-ID TRIM32_000027 See all 4 reported entries
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +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.497G>A r.(?) p.(Arg166Gln)
ASTN2 NM_014010.4 ?/. - c.2653+27532C>T r.(=) p.(=)


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