Variant #0000001120 (NC_000007.13:g.94248112_94248113delCT, SGCE(NM_001099401.1):c.619_620delAG)

Individual ID 00001120
Chromosome 7
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94248112_94248113delCT
Reference Korten JJ, Notermans SL, Frenken CW, Gabreels FJ, Joosten EM.(1974)
DB-ID SGCE_000011
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
SGCE NM_001099401.1 ./. 5 c.619_620delAG r.(?) p.(Arg207Glyfs*9) VariO:0141 DNA deletion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001120 ? ? SGCE 1 Y Yang