Variant #0000964693 (NC_000007.13:g.86556240_86556257dup, NC_000007.13(NM_152748.3):c.589-22_589-5dup (KIAA1324L))

Chromosome 7
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.86556240_86556257dup
DNA change (hg38) -
Published as ELAPOR2(NM_001142749.3):c.1090-22_1090-5dupTTTTTTTTTTTTTTTTTT
ISCN -
DB-ID KIAA1324L_000008
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA1324L NM_152748.3 -/. - c.589-22_589-5dup r.spl? p.?


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