Variant #0001044367 (NC_000023.10:g.48825549C>A, NM_020137.3:c.*5056G>T (GRIPAP1))

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.48825549C>A
DNA change (hg38) -
Published as KCND1(NM_004979.6):c.1121+9G>T
ISCN -
DB-ID KCND1_000024
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) 0.0016 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
KCND1 NM_004979.4 -?/. - c.1121+9G>T r.(=) p.(=)
GRIPAP1 NM_020137.3 -?/. - c.*5056G>T r.(=) p.(=)


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