Variant #0000968723 (NC_000017.10:g.18043906C>T, NM_016239.3:c.5287C>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.18043906C>T
DNA change (hg38) -
Published as MYO15A(NM_016239.3):c.5287C>T (p.R1763W), MYO15A(NM_016239.4):c.5287C>T (p.R1763W)
ISCN -
DB-ID MYO15A_000129 See all 5 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) 0.0018 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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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.5287C>T r.(?) p.(Arg1763Trp) -


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