Variant #0000001569 (NC_000007.14:g.22727089G>C, NM_000600.4:c.-174G>C (IL6))

Individual ID 00000336
Chromosome 7
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.22727089G>C
Published as -
Reference K H Chua et al. (2009), ClinVar
DB-ID IL6_000001 See all 2 reported entries
dbSNP ID -
Frequency 3/100
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-01-07 11:53:16 +08:00 (CST)
Date last edited 2021-01-14 12:50:29 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
IL6 NM_000600.4 +/. - c.-174G>C - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000351 DNA PCR IL6 2 Nuur Athirah Binti Mohd Daud