Variant #0000725137 (NC_000015.9:g.48426691_48426694dup, NM_205850.2:c.445_448dup (SLC24A5))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48426691_48426694dup
DNA change (hg38) -
Published as SLC24A5(NM_205850.3):c.445_448dupAATC (p.L150Qfs*14)
ISCN -
DB-ID MYEF2_000013
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYEF2 NM_016132.3 +?/. - c.*8411_*8414dup r.(=) p.(=)
SLC24A5 NM_205850.2 +?/. - c.445_448dup r.(?) p.(Leu150Glnfs*14)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.