Variant #0000576289 (NC_000023.10:g.48814651G>A, KCND1(NM_004979.4):c.*5191C>T)

Chromosome X
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.48814651G>A
DNA change (hg38) g.48957389G>A
Published as OTUD5(NM_017602.3):c.182C>T (p.P61L)
ISCN -
DB-ID OTUD5_000013
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) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCND1 NM_004979.4 ?/. - c.*5191C>T r.(=) p.(=)
OTUD5 NM_017602.3 ?/. - c.182C>T r.(?) p.(Pro61Leu)