Variant #0000266556 (NC_000017.10:g.32612894G>A, CCL11(NM_002986.2):c.67G>A)

Chromosome 17
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.32612894G>A
DNA change (hg38) g.34285875G>A
Published as CCL11(NM_002986.3):c.67G>A (p.A23T)
ISCN -
DB-ID CCL11_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.16428 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCL11 NM_002986.2 -/. - c.67G>A r.(?) p.(Ala23Thr)