Variant #0001003829 (NC_000017.10:g.79219937T>C, NM_001086521.1:c.*5121T>C (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.79219937T>C
DNA change (hg38) -
Published as SLC38A10(NM_001037984.1):c.2779A>G (p.(Lys927Glu))
ISCN -
DB-ID C17orf89_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) 0.00294 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.*5121T>C r.(=) p.(=)
SLC38A10 NM_138570.2 -?/. - c.*5078A>G r.(=) p.(=)


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