Variant #0000555163 (NC_000015.9:g.65931911_65931912insAGGCCTG, NC_000015.9(NM_004727.2):c.1945-22_1945-21insAGGCCTG (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.65931911_65931912insAGGCCTG
DNA change (hg38) g.65639573_65639574insAGGCCTG
Published as SLC24A1(NM_004727.3):c.1945-22_1945-21insAGGCCTG
ISCN -
DB-ID DENND4A_000010
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC24A1 NM_004727.2 -/. - c.1945-22_1945-21insAGGCCTG r.(=) p.(=)
DENND4A NM_005848.3 -/. - c.*22280_*22281insGCCTCAG r.(=) p.(=)


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