Variant #0001003828 (NC_000017.10:g.79214927C>T, NM_001086521.1:c.*111C>T (C17orf89))

Chromosome 17
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.79214927C>T
DNA change (hg38) -
Published as C17ORF89(NM_001086521.1):c.*111C>T (p.?)
ISCN -
DB-ID C17orf89_000005
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) 0.00663 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 2024-08-28 13:16:32 +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     
C17orf89 NM_001086521.1 -?/. - c.*111C>T r.(=) p.(=)
SLC38A10 NM_138570.2 -?/. - c.*10088G>A r.(=) p.(=)


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