Variant #0000720054 (NC_000004.11:g.9892363_9892364dup, NC_000004.11(NM_001001290.1):c.1027-17_1027-16dup (SLC2A9))

Chromosome 4
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.9892363_9892364dup
DNA change (hg38) -
Published as SLC2A9(NM_020041.3):c.1114-17_1114-16dupCT
ISCN -
DB-ID SLC2A9_000015
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 2021-02-08 18:36:18 +01:00 (CET)
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     
SLC2A9 NM_001001290.1 -?/. - c.1027-17_1027-16dup r.(=) p.(=)


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