Variant #0000858636 (NC_000002.11:g.69581393_69581394del, NM_001244710.1:c.738_739del (GFPT1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.69581393_69581394del
DNA change (hg38) -
Published as GFPT1(NM_001244710.1):c.738_739del (p.(Gly247GlnfsTer33))
ISCN -
DB-ID GFPT1_000066
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GFPT1 NM_001244710.1 +?/. - c.738_739del r.(?) p.(Gly247GlnfsTer33)


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