Variant #0000554515 (NC_000015.9:g.48413341del, NM_205850.2:c.100del (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.48413341del
DNA change (hg38) g.48121144del
Published as SLC24A5(NM_205850.3):c.100delC (p.Q34Nfs*37)
ISCN -
DB-ID MYEF2_000002
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 2019-07-18 18:22:55 +02:00 (CEST)
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     
MYEF2 NM_016132.3 +/. - c.*21767del r.(?) p.(=)
SLC24A5 NM_205850.2 +/. - c.100del r.(?) p.(Gln34AsnfsTer37)


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