Variant #0000967792 (NC_000015.9:g.48431335del, NM_205850.2:c.1041del (SLC24A5))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48431335del
DNA change (hg38) -
Published as SLC24A5(NM_205850.3):c.1041delA (p.F348Lfs*11)
ISCN -
DB-ID MYEF2_000017
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
MYEF2 NM_016132.3 +/. - c.*3770del r.(?) p.(=)
SLC24A5 NM_205850.2 +/. - c.1041del r.(?) p.(Phe348Leufs*11)


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