Variant #0000616774 (NC_000017.10:g.6596546_6596549dup, NC_000017.10(NM_177550.3):c.1157-20_1157-17dup (SLC13A5))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6596546_6596549dup
DNA change (hg38) g.6693227_6693230dup
Published as SLC13A5(NM_177550.4):c.1157-22_1157-19dupGTGT
ISCN -
DB-ID SLC13A5_000020
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC13A5 NM_177550.3 -/. - c.1157-20_1157-17dup r.(=) p.(=)


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