Variant #0000536132 (NC_000009.11:g.119460579G>C, NM_012210.3:c.558G>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.119460579G>C
DNA change (hg38) g.116698300G>C
Published as ASTN2(NM_014010.5):c.2653+27471C>G, TRIM32(NM_001099679.1):c.558G>C (p.Q186H, p.(Gln186His)), TRIM32(NM_012210.3):c.558G>C (p.Q186H), TRIM32(NM_01...)
ISCN -
DB-ID TRIM32_000030 See all 17 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) 0.0019 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.558G>C r.(?) p.(Gln186His)
ASTN2 NM_014010.4 -?/. - c.2653+27471C>G r.(=) p.(=)


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