Variant #0000656161 (NC_000008.10:g.95863831G>C, NM_017864.3:c.1558G>C (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.95863831G>C
DNA change (hg38) g.94851603G>C
Published as INTS8(NM_017864.3):c.1558G>C (p.V520L)
ISCN -
DB-ID CCNE2_000005
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 2020-03-23 16:13:27 +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     
INTS8 NM_017864.3 -?/. - c.1558G>C r.(?) p.(Val520Leu)
CCNE2 NM_057749.2 -?/. - c.*30029C>G r.(=) p.(=)


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