Variant #0000696948 (NC_000017.10:g.18024278G>T, NM_016239.3:c.2164G>T (MYO15A))

Chromosome 17
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.18024278G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYO15A_000341
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
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 2020-10-05 18:15:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MYO15A NM_016239.3 ?/. - c.2164G>T r.(?) p.(Val722Leu) -


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