Variant #0000914335 (NC_000015.9:g.59453379C>T, NM_004998.3:c.2678G>A (MYO1E))

Chromosome 15
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.59453379C>T
DNA change (hg38) -
Published as MYO1E(NM_004998.3):c.2678G>A (p.G893D)
ISCN -
DB-ID MYO1E_000017 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) 0.00037 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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     
MYO1E NM_004998.3 -?/. - c.2678G>A r.(?) p.(Gly893Asp)
LDHAL6B NM_033195.2 -?/. - c.-45761C>T r.(?) p.(=)


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