Variant #0000273127 (NC_000013.10:g.25458236_25458238del, NC_000013.10(NM_018451.3):c.3704-14_3704-12del (CENPJ))

Chromosome 13
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.25458236_25458238del
DNA change (hg38) g.24884098_24884100del
Published as CENPJ(NM_018451.4):c.3704-14_3704-12delAAC, CENPJ(NM_018451.5):c.3704-14_3704-12delAAC
ISCN -
DB-ID CENPJ_000001 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF17 NM_001184993.1 -/. - c.*4372_*4374del r.(=) p.(=)
CENPJ NM_018451.3 -/. - c.3704-14_3704-12del r.(=) p.(=)


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