Variant #0000760960 (NC_000017.10:g.18024134C>T, NM_016239.3:c.2020C>T (MYO15A))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18024134C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYO15A_000372 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs557225435
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0072 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-04-02 11:51:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MYO15A NM_016239.3 -?/. - c.2020C>T r.(?) p.(Pro674Ser) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.