Variant #0000304562 (NC_000016.9:g.67919722C>A, NM_014329.4:c.*1671C>A (EDC4))

Chromosome 16
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.67919722C>A
DNA change (hg38) g.67885819C>A
Published as NRN1L(NM_198443.2):c.177C>A (p.S59R)
ISCN -
DB-ID NRN1L_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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EDC4 NM_014329.4 ?/. - c.*1671C>A r.(=) p.(=)
NRN1L NM_198443.1 ?/. - c.177C>A r.(?) p.(Ser59Arg)


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