Variant #0000693739 (NC_000023.10:g.73962294C>G, NM_001008537.2:c.2098G>C (KIAA2022))

Chromosome X
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.73962294C>G
DNA change (hg38) -
Published as KIAA2022(NM_001008537.2):c.2098G>C (p.V700L), NEXMIF(NM_001008537.3):c.2098G>C (p.V700L)
ISCN -
DB-ID KIAA2022_000013 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) 0.00042 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA2022 NM_001008537.2 -?/. - c.2098G>C r.(?) p.(Val700Leu)


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