Variant #0000620399 (NC_000001.10:g.154437622G>A, NM_000565.3:c.1173G>A (IL6R))

Chromosome 1
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.154437622G>A
DNA change (hg38) g.154465146G>A
Published as IL6R(NM_181359.2):c.1079G>A (p.R360H)
ISCN -
DB-ID IL6R_000003
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL6R NM_000565.3 -?/. - c.1173G>A r.(?) p.(Thr391=)
SHE NM_001010846.2 -?/. - c.*19003C>T r.(=) p.(=)
TDRD10 NM_182499.3 -?/. - c.-37911G>A r.(?) p.(=)


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