Variant #0000329464 (NC_000003.11:g.53911753C>T, NM_018725.3:c.*12418C>T (IL17RB))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.53911753C>T
DNA change (hg38) g.53877726C>T
Published as ACTR8(NM_022899.4):c.431G>A (p.(Arg144Gln))
ISCN -
DB-ID ACTR8_000002
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 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL17RB NM_018725.3 ?/. - c.*12418C>T r.(=) p.(=)
ACTR8 NM_022899.4 ?/. - c.431G>A r.(?) p.(Arg144Gln)


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