Variant #0001037153 (NC_000009.11:g.119459650A>G, NC_000009.11(NM_012210.3):c.-81-291A>G (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.119459650A>G
DNA change (hg38) -
Published as TRIM32(NM_001379048.1):c.-142-2A>G
ISCN -
DB-ID ASTN2_000047
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 2025-05-05 21:14:00 +02:00 (CEST)
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.-81-291A>G r.(=) p.(=)
ASTN2 NM_014010.4 -?/. - c.2653+28400T>C r.(=) p.(=)


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