Variant #0000925190 (NC_000010.10:g.73887886T>C, NM_001198800.3:c.911A>G (ASCC1))

Chromosome 10
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.73887886T>C
DNA change (hg38) -
Published as ASCC1(NM_001369085.1):c.977A>G (p.Y326C)
ISCN -
DB-ID ANAPC16_000007
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) 0.00166 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 2023-04-16 21:50:28 +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.911A>G r.(?) p.(Tyr304Cys)
ANAPC16 NM_173473.3 -?/. - c.-88038T>C r.(?) p.(=)


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