Variant #0000560631 (NC_000017.10:g.18872390_18872393del, NM_152351.4:c.479_482del (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.18872390_18872393del
DNA change (hg38) g.18969077_18969080del
Published as SLC5A10(NM_152351.4):c.476_479del (p.(Phe160CysfsTer32))
ISCN -
DB-ID FAM83G_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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-13 10:51:28 +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.*2282_*2285del r.(=) p.(=)
GRAP NM_006613.3 ?/. - c.*52882_*52885del r.(=) p.(=)
SLC5A10 NM_152351.4 ?/. - c.479_482del r.(?) p.(Phe160CysfsTer32)


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