Variant #0000609698 (NC_000005.9:g.35876251A>C, NM_002185.3:c.1043A>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.35876251A>C
DNA change (hg38) g.35876149A>C
Published as IL7R(NM_002185.2):c.1043A>C (p.N348T), IL7R(NM_002185.3):c.1043A>C (p.(Asn348Thr))
ISCN -
DB-ID IL7R_000011 See all 3 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) 0.01028 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +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     
IL7R NM_002185.3 -?/. - c.1043A>C r.(?) p.(Asn348Thr)


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