Variant #0000436200 (NC_000002.11:g.69586446A>G, NM_001244710.1:c.362T>C (GFPT1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.69586446A>G
DNA change (hg38) g.69359314A>G
Published as -
ISCN -
DB-ID GFPT1_000013 See all 3 reported entries
Variant remarks normal protein localisation
Reference PubMed: Senderek 2011
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-07-29 19:51:26 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GFPT1 NM_001244710.1 -?/. 5 c.362T>C r.(?) p.Ile121Thr


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