Variant #0000806714 (NC_000015.9:g.48433400T>C, NM_205850.2:c.1169T>C (SLC24A5))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48433400T>C
DNA change (hg38) -
Published as SLC24A5(NM_205850.2):c.1169T>C (p.V390A)
ISCN -
DB-ID MYEF2_000015
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.*1705A>G r.(=) p.(=)
SLC24A5 NM_205850.2 ?/. - c.1169T>C r.(?) p.(Val390Ala)


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