Variant #0000285279 (NC_000005.9:g.35861068T>C, NM_002185.3:c.197T>C (IL7R))

Chromosome 5
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.35861068T>C
DNA change (hg38) g.35860966T>C
Published as IL7R(NM_002185.2):c.197T>C (p.I66T), IL7R(NM_002185.5):c.197T>C (p.I66T)
ISCN -
DB-ID IL7R_000004 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) 0.61892 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 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     
IL7R NM_002185.3 -?/. - c.197T>C r.(?) p.(Ile66Thr)


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