Variant #0000890719 (NC_000012.11:g.58201129C>T, NM_001172696.1:c.*10763C>T (TSFM))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.58201129C>T
DNA change (hg38) -
Published as AVIL(NM_006576.3):c.1476G>A (p.K492=)
ISCN -
DB-ID AVIL_000015
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) 0.00182 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 2022-11-01 13:01:21 +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     
TSFM NM_001172696.1 -/. - c.*10763C>T r.(=) p.(=)
AVIL NM_006576.3 -/. - c.1476G>A r.(?) p.(Lys492=)


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