Variant #0000334826 (NC_000023.10:g.86919941C>T, KLHL4(NM_019117.4):c.2097+6C>T)

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.86919941C>T
DNA change (hg38) g.87664941C>T
Published as KLHL4(NM_019117.4):c.2097+6C>T (p.(=))
ISCN -
DB-ID KLHL4_000019
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KLHL4 NM_019117.4 -?/. - c.2097+6C>T r.(=) p.(=)