Variant #0000536140 (NC_000009.11:g.119461243C>T, NM_012210.3:c.1222C>T (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.119461243C>T
DNA change (hg38) g.116698964C>T
Published as TRIM32(NM_001379048.1):c.1222C>T (p.R408C), TRIM32(NM_012210.3):c.1222C>T (p.R408C), TRIM32(NM_012210.4):c.1222C>T (p.R408C)
ISCN -
DB-ID TRIM32_000032 See all 20 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) 0.0015 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +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.1222C>T r.(?) p.(Arg408Cys)
ASTN2 NM_014010.4 ?/. - c.2653+26807G>A r.(=) p.(=)


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