Variant #0000410669 (NC_000012.11:g.102224453T>C, NM_024312.4:c.1A>G (GNPTAB))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.102224453T>C
DNA change (hg38) g.101830675T>C
Published as -
ISCN -
DB-ID GNPTAB_000293
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Renata Voltolini Velho
Database submission license No license selected
Created by Renata Voltolini Velho
Date created 2018-10-30 16:53:45 +01:00 (CET)
Date last edited 2020-07-02 17:54:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +/+? 1 c.1A>G r.(?) p.(Met1?)


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