Variant #0000536121 (NC_000009.11:g.119449030T>C, NM_012210.3:c.-712T>C (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.119449030T>C
DNA change (hg38) g.116686751T>C
Published as ASTN2(NM_198186.3):c.55A>G (p.(Ser19Gly))
ISCN -
DB-ID ASTN2_000020
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) 0.00029 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.-712T>C r.(?) p.(=)
ASTN2 NM_014010.4 -?/. - c.2654-34958A>G r.(=) p.(=)


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