Variant #0000262961 (NC_000003.11:g.93754302del, ARL13B(NM_182896.2):c.486+22del)

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.93754302del
DNA change (hg38) g.94035458del
Published as ARL13B(NM_001174150.1):c.486+22delT
ISCN -
DB-ID ARL13B_000008
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STX19 NM_001001850.2 -/. - c.-7090del r.(?) p.(=)
ARL13B NM_182896.2 -/. - c.486+22del r.(=) p.(=)