Variant #0000003675 (NC_000023.10:-, EMD(NM_000117.2):c.3G>A)

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type hence would abolish this as a start codon.
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID EMD_00006 See all 2 reported entries
Frequency -
Variant remarks a G to A transition at nucleotide 61
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EMD NM_000117.2 ./. 01 c.3G>A - P.Met1Ile