Variant #0000255961 (NC_000012.11:g.40154010A>C, NM_052885.3:c.1765T>G (SLC2A13))

Chromosome 12
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.40154010A>C
DNA change (hg38) g.39760208A>C
Published as SLC2A13(NM_052885.4):c.1765T>G (p.F589V)
ISCN -
DB-ID SLC2A13_000001
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) 0 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
C12orf40 NM_001031748.2 ?/. - c.*38957A>C r.(=) p.(=)
SLC2A13 NM_052885.3 ?/. - c.1765T>G r.(?) p.(Phe589Val)


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