Variant #0000369868 (NC_000016.9:g.1412140_1412168del, NC_000016.9(NM_032520.4):c.411+8_411+35del (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.1412140_1412168del
DNA change (hg38) -
Published as -
ISCN -
DB-ID GNPTG_000076
Variant remarks Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message.
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 2018-06-27 12:55:25 +02:00 (CEST)
Date last edited 2018-06-27 12:58:11 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTG NM_032520.4 +/+ 6i c.411+8_411+35del r.(=) p.Glu139Glyfs*75


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