Variant #0000692285 (NC_000017.10:g.18925246G>T, NM_152351.4:c.*1502G>T (SLC5A10))

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.18925246G>T
DNA change (hg38) -
Published as GRAP(NM_001330148.1):c.511C>A (p.R171=)
ISCN -
DB-ID FAM83G_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM83G NM_001039999.2 -?/. - c.-17353C>A r.(?) p.(=)
GRAP NM_006613.3 -?/. - c.*26C>A r.(=) p.(=)
SLC5A10 NM_152351.4 -?/. - c.*1502G>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.