Variant #0000960179 (NC_000001.10:g.171605441T>G, NM_000261.1:c.1139A>C (MYOC))

Chromosome 1
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.171605441T>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYOC_000027
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2102944632
Origin CLASSIFICATION record
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 2024-02-20 16:33:01 +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     
MYOC NM_000261.1 +/. - c.1139A>C r.(?) p.(Asp380Ala)


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