Variant #0000892186 (NC_000015.9:g.59455376T>C, NM_004998.3:c.2607A>G (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.59455376T>C
DNA change (hg38) -
Published as MYO1E(NM_004998.3):c.2607A>G (p.L869=)
ISCN -
DB-ID LDHAL6B_000020
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) 2.0E-5 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 2022-11-01 13:41:49 +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.2607A>G r.(?) p.(Leu869=)
LDHAL6B NM_033195.2 -?/. - c.-43764T>C r.(?) p.(=)


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