Variant #0000001074 (NC_000022.10:, SPECC1L(NM_015330.5):chr22:g.24718197A>C)

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference -
DB-ID SPECC1L_000001
Frequency -
Variant remarks de novo
ClassClinical -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner qingting114
Database submission license No license selected
Created by qingting114




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPECC1L NM_015330.5 ?/? 17 chr22:g.24718197A>C c.1249A>C p.T417P