Variant #0000993833 (NC_000003.11:g.53906434C>A, NM_018725.3:c.*7099C>A (IL17RB))

Chromosome 3
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.53906434C>A
DNA change (hg38) -
Published as ACTR8(NM_022899.4):c.1279G>T (p.(Ala427Ser))
ISCN -
DB-ID ACTR8_000004
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) 0.00034 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL17RB NM_018725.3 -?/. - c.*7099C>A r.(=) p.(=)
ACTR8 NM_022899.4 -?/. - c.1279G>T r.(?) p.(Ala427Ser)


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