Variant #0000611829 (NC_000009.11:g.119460300G>A, NM_012210.3:c.279G>A (TRIM32))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.119460300G>A
DNA change (hg38) g.116698021G>A
Published as TRIM32(NM_012210.3):c.279G>A (p.E93=)
ISCN -
DB-ID ASTN2_000032
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-25 17:54:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM32 NM_012210.3 -?/. - c.279G>A r.(?) p.(Glu93=)
ASTN2 NM_014010.4 -?/. - c.2653+27750C>T r.(=) p.(=)


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