Variant #0000302163 (NC_000017.10:g.6596540_6596549del, NC_000017.10(NM_177550.3):c.1157-26_1157-17del (SLC13A5))

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.6596540_6596549del
DNA change (hg38) g.6693221_6693230del
Published as SLC13A5(NM_177550.4):c.1157-26_1157-17delGTGTGTGTGT
ISCN -
DB-ID SLC13A5_000012
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 2018-01-15 20:58:59 +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.1157-26_1157-17del r.(=) p.(=)


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