Variant #0001014138 (NC_000005.9:g.55243438_55243445del, NC_000005.9(NM_002184.3):c.1841-11_1841-4del (IL6ST))

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.55243438_55243445del
DNA change (hg38) -
Published as IL6ST(NM_002184.4):c.1841-11_1841-4delTTTTTTTT
ISCN -
DB-ID IL6ST_000031
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +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     
IL6ST NM_002184.3 -?/. - c.1841-11_1841-4del r.spl? p.?


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