Variant #0000865342 (NC_000017.10:g.4802543C>G, NM_000080.3:c.1169G>C (CHRNE))

Chromosome 17
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.4802543C>G
DNA change (hg38) -
Published as CHRNE(NM_000080.4):c.1169G>C (p.R390P)
ISCN -
DB-ID C17orf107_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) 0.00012 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNE NM_000080.3 ?/. - c.1169G>C r.(?) p.(Arg390Pro)
C17orf107 NM_001145536.1 ?/. - c.-515C>G r.(?) p.(=)
MINK1 NM_015716.4 ?/. - c.*1961C>G r.(=) p.(=)


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