Variant #0000722231 (NC_000009.11:g.119461129del, NM_012210.3:c.1108del (TRIM32))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.119461129del
DNA change (hg38) -
Published as TRIM32(NM_001099679.1):c.1108del (p.(Met370Cysfs*10))
ISCN -
DB-ID ASTN2_000036
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM32 NM_012210.3 +?/. - c.1108del r.(?) p.(Met370Cysfs*10)
ASTN2 NM_014010.4 +?/. - c.2653+26922del r.(=) p.(=)


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