Variant #0000909267 (NC_000005.9:g.137206519C>G, MYOT(NM_006790.2):c.179C>G)

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.137206519C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYOT_000007 See all 20 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121908458
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-12-28 13:19:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYOT NM_006790.2 +/. - c.179C>G r.(?) p.(Ser60Cys)