Variant #0000369809 (NC_000016.9:g.1412038G>C, NC_000016.9(NM_032520.4):c.318-1G>C (GNPTG))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1412038G>C
DNA change (hg38) g.1362037G>C
Published as IVS5-1G>C
ISCN -
DB-ID GNPTG_000050 See all 2 reported entries
Variant remarks -
Reference Journal: Raas-Rothschild 2004
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Renata Voltolini Velho
Database submission license No license selected
Created by Renata Voltolini Velho
Date created 2018-06-26 14:47:17 +02:00 (CEST)
Date last edited 2020-07-07 12:46:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTG NM_032520.4 +/+ 5i c.318-1G>C r.spl? p.?


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