Variant #0001001267 (NC_000015.9:g.29415639G>A, NM_138704.3:c.*145356C>T (NDNL2))

Chromosome 15
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.29415639G>A
DNA change (hg38) -
Published as FAM189A1(NM_015307.1):c.1523C>T (p.(Ala508Val))
ISCN -
DB-ID FAM189A1_000017
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM189A1 NM_015307.1 ?/. - c.1523C>T r.(?) p.(Ala508Val)
NDNL2 NM_138704.3 ?/. - c.*145356C>T r.(=) p.(=)


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