Variant #0000680555 (NC_000016.9:g.31499367G>A, NM_003041.3:c.894G>A (SLC5A2))

Chromosome 16
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.31499367G>A
DNA change (hg38) -
Published as SLC5A2(NM_003041.3):c.894G>A (p.V298=)
ISCN -
DB-ID SLC5A2_000032
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC5A2 NM_003041.3 -?/. - c.894G>A r.(?) p.(Val298=)
C16orf58 NM_022744.2 -?/. - c.*2789C>T r.(=) p.(=)


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