Variant #0000553846 (NC_000015.9:g.29561828C>G, NM_138704.3:c.82G>C (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.29561828C>G
DNA change (hg38) g.29269624C>G
Published as NDNL2(NM_138704.3):c.82G>C (p.(Gly28Arg))
ISCN -
DB-ID FAM189A1_000006
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM189A1 NM_015307.1 ?/. - c.277-17146G>C r.(=) p.(=)
NDNL2 NM_138704.3 ?/. - c.82G>C r.(?) p.(Gly28Arg)


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