Variant #0000436205 (NC_000002.11:g.69615794G>C, NM_001244710.1:c.-1591C>G (GFPT1))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.69615794G>C
DNA change (hg38) g.69388662G>C
Published as -1412C>G
ISCN -
DB-ID GFPT1_000027 See all 2 reported entries
Variant remarks functional reduced promoter activity; EMSA binding nuclear proteins
Reference PubMed: Burt 2005
ClinVar ID -
dbSNP ID rs67340771
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 2025-06-09 04:00:42 +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 +/. - c.-1591C>G r.(=) p.(=)


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