Variant #0000404765 (NC_000012.11:g.102224384A>C, NM_024312.4:c.70T>G (GNPTAB))

Chromosome 12
Allele Parent #2
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.102224384A>C
DNA change (hg38) g.101830606A>C
Published as -
ISCN -
DB-ID GNPTAB_000009 See all 2 reported entries
Variant remarks Found in cis with the c.1000C>T.
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00032 View details
Owner Renata Voltolini Velho
Database submission license No license selected
Created by Renata Voltolini Velho
Date created 2018-08-26 17:31:19 +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     
GNPTAB NM_024312.4 +?/+? 1 c.70T>G r.(?) p.(Phe24Val)


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