Variant #0000535506 (NC_000008.10:g.95888726C>T, NC_000008.10(NM_017864.3):c.2871+9C>T (INTS8))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.95888726C>T
DNA change (hg38) g.94876498C>T
Published as INTS8(NM_017864.4):c.2871+9C>T
ISCN -
DB-ID CCNE2_000004
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) 2.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
INTS8 NM_017864.3 -?/. - c.2871+9C>T r.(=) p.(=)
CCNE2 NM_057749.2 -?/. - c.*5134G>A r.(=) p.(=)


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