Variant #0001026958 (NC_000017.10:g.4802641_4802643dup, NM_000080.3:c.1077_1079dup (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.4802641_4802643dup
DNA change (hg38) -
Published as CHRNE(NM_000080.4):c.1077_1079dupGCC (p.P360dup)
ISCN -
DB-ID C17orf107_000026
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNE NM_000080.3 ?/. - c.1077_1079dup r.(?) p.(Pro360dup)
C17orf107 NM_001145536.1 ?/. - c.-417_-415dup r.(?) p.(=)
MINK1 NM_015716.4 ?/. - c.*2059_*2061dup r.(=) p.(=)


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