Variant #0000883429 (NC_000001.10:g.36025917C>G, NC_000001.10(NM_014284.2):c.175-10C>G (NCDN))

Chromosome 1
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.36025917C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID KIAA0319L_000002
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NCDN NM_014284.2 ?/. - c.175-10C>G r.(=) p.(=)
KIAA0319L NM_024874.4 ?/. - c.-3138G>C r.(?) p.(=)


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