Variant #0000854781 (NC_000017.10:g.18925387C>T, NM_152351.4:c.*1643C>T (SLC5A10))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.18925387C>T
DNA change (hg38) -
Published as GRAP(NM_006613.3):c.539G>A (p.R180H)
ISCN -
DB-ID FAM83G_000008
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) 0.00018 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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     
FAM83G NM_001039999.2 ?/. - c.-17494G>A r.(?) p.(=)
GRAP NM_006613.3 ?/. - c.539G>A r.(?) p.(Arg180His)
SLC5A10 NM_152351.4 ?/. - c.*1643C>T r.(=) p.(=)


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