Variant #0000852567 (NC_000010.10:g.73887894T>A, NM_001198800.3:c.903A>T (ASCC1))

Chromosome 10
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.73887894T>A
DNA change (hg38) -
Published as ASCC1(NM_001369085.1):c.969A>T (p.E323D)
ISCN -
DB-ID ANAPC16_000006
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) 0.00309 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 2022-05-09 15:40:45 +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     
ASCC1 NM_001198800.3 -/. - c.903A>T r.(?) p.(Glu301Asp)
ANAPC16 NM_173473.3 -/. - c.-88030T>A r.(?) p.(=)


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