Variant #0000810752 (NC_000017.10:g.18023337C>T, NM_016239.3:c.1223C>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.18023337C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYO15A_000072 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs191710555
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-09-17 18:24:01 +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.1223C>T r.(?) p.(Ala408Val) -


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