Variant #0000560559 (NC_000017.10:g.18023897G>A, NM_016239.3:c.1783G>A (MYO15A))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18023897G>A
DNA change (hg38) g.18120583G>A
Published as MYO15A(NM_016239.3):c.1783G>A (p.A595T), MYO15A(NM_016239.4):c.1783G>A (p.A595T)
ISCN -
DB-ID MYO15A_000043 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.45373 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.1783G>A r.(?) p.(Ala595Thr) -


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