Variant #0000614135 (NC_000012.11:g.40114729C>A, NM_052885.3:c.*39099G>T (SLC2A13))

Chromosome 12
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.40114729C>A
DNA change (hg38) g.39720927C>A
Published as C12orf40(NM_001031748.4):c.1635C>A (p.D545E)
ISCN -
DB-ID C12orf40_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) 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 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     
C12orf40 NM_001031748.2 -?/. - c.1635C>A r.(?) p.(Asp545Glu)
SLC2A13 NM_052885.3 -?/. - c.*39099G>T r.(=) p.(=)


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