Variant #0000807128 (NC_000016.9:g.18805924T>G, NM_015161.1:c.490A>C (ARL6IP1))

Chromosome 16
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.18805924T>G
DNA change (hg38) -
Published as ARL6IP1(NM_015161.2):c.490A>C (p.I164L)
ISCN -
DB-ID ARL6IP1_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) 7.0E-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 2021-09-17 14:40:49 +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     
RPS15A NM_001019.4 ?/. - c.-4364A>C r.(?) p.(=)
ARL6IP1 NM_015161.1 ?/. - c.490A>C r.(?) p.(Ile164Leu)


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