Variant #0000325285 (NC_000017.10:g.18918512_18918529dup, NC_000017.10(NM_152351.4):c.1289_1289+17dup (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.18918512_18918529dup
DNA change (hg38) g.19015199_19015216dup
Published as SLC5A10(NM_001042450.1):c.1239_1240insCGGTACGGGGGTGGGGGC (p.?)
ISCN -
DB-ID SLC5A10_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-13 10:52:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM83G NM_001039999.2 ?/. - c.-10635_-10618dup r.(?) p.(=)
GRAP NM_006613.3 ?/. - c.*6744_*6761dup r.(=) p.(=)
SLC5A10 NM_152351.4 ?/. - c.1289_1289+17dup r.spl? p.?


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