Variant #0000296226 (NC_000015.9:g.59548475C>T, NC_000015.9(NM_004998.3):c.332+8G>A (MYO1E))

Chromosome 15
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.59548475C>T
DNA change (hg38) g.59256276C>T
Published as MYO1E(NM_004998.4):c.332+8G>A
ISCN -
DB-ID MYO1E_000015 See all 2 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) 0.99534 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO1E NM_004998.3 -/. - c.332+8G>A r.(=) p.(=)
LDHAL6B NM_033195.2 -/. - c.*48190C>T r.(=) p.(=)


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