Variant #0000553844 (NC_000015.9:g.29561738G>A, NM_138704.3:c.172C>T (NDNL2))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.29561738G>A
DNA change (hg38) g.29269534G>A
Published as NSMCE3(NM_138704.3):c.172C>T (p.Q58*)
ISCN -
DB-ID FAM189A1_000004
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-06 09:35:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM189A1 NM_015307.1 +/. - c.277-17056C>T r.(=) p.(=)
NDNL2 NM_138704.3 +/. - c.172C>T r.(?) p.(Gln58Ter)


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