Variant #0000972226 (NC_000016.9:g.21693151G>A, NC_000016.9(NM_144672.3):c.267+5G>A (OTOA))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.21693151G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID OTOA_000087
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1310241377
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-04-10 11:56:02 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OTOA NM_144672.3 ?/. - c.267+5G>A r.(?) p.(?)


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