Variant #0000852818 (NC_000011.9:g.126318993A>G, NM_032531.3:c.908T>C (KIRREL3))

Chromosome 11
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.126318993A>G
DNA change (hg38) -
Published as KIRREL3(NM_032531.3):c.908T>C (p.V303A), KIRREL3(NM_032531.4):c.908T>C (p.V303A)
ISCN -
DB-ID KIRREL3_000006 See all 2 reported entries
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) 0.00043 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +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     
KIRREL3 NM_032531.3 ?/. - c.908T>C r.(?) p.(Val303Ala)


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