Variant #0000680188 (NC_000015.9:g.48434479T>C, NM_205850.2:c.1434T>C (SLC24A5))

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.48434479T>C
DNA change (hg38) -
Published as SLC24A5(NM_205850.2):c.1434T>C (p.L478=)
ISCN -
DB-ID MYEF2_000012
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYEF2 NM_016132.3 -?/. - c.*626A>G r.(=) p.(=)
SLC24A5 NM_205850.2 -?/. - c.1434T>C r.(?) p.(Leu478=)


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