Variant #0000436204 (NC_000002.11:g.69615232C>T, NM_001244710.1:c.-1029G>A (GFPT1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.69615232C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID GFPT1_000026
Variant remarks Variant Error [EREF/ERANGE]: This genomic variant does not match the reference sequence; the transcript variant also has an error. Please fix this entry and then remove this message.
Reference -
ClinVar ID -
dbSNP ID rs6546511
Origin Germline
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 2018-11-11 17:31:52 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GFPT1 NM_001244710.1 ?/. - c.-1029G>A r.(=) p.(=)


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