Variant #0000302950 (NC_000015.9:g.29561562G>C, NM_138704.3:c.348C>G (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.29561562G>C
DNA change (hg38) g.29269358G>C
Published as NDNL2(NM_138704.3):c.348C>G (p.I116M)
ISCN -
DB-ID FAM189A1_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.277-16880C>G r.(=) p.(=)
NDNL2 NM_138704.3 ?/. - c.348C>G r.(?) p.(Ile116Met)


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