Variant #0000555169 (NC_000015.9:g.65943145_65943147del, NM_004727.2:c.2658_2660del (SLC24A1))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65943145_65943147del
DNA change (hg38) g.65650807_65650809del
Published as SLC24A1(NM_004727.3):c.2658_2660delGGA (p.E890del)
ISCN -
DB-ID DENND4A_000015 See all 2 reported entries
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 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC24A1 NM_004727.2 -/. - c.2658_2660del r.(?) p.(Glu890del)
DENND4A NM_005848.3 -/. - c.*11059_*11061del r.(=) p.(=)


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