Variant #0000982589 (NC_000017.10:g.4798459C>T, NM_000080.3:c.*3572G>A (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.4798459C>T
DNA change (hg38) -
Published as MINK1(NM_153827.5):c.3007C>T (p.(Arg1003Trp))
ISCN -
DB-ID C17orf107_000021
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.*3572G>A r.(=) p.(=)
C17orf107 NM_001145536.1 ?/. - c.-4599C>T r.(?) p.(=)
MINK1 NM_015716.4 ?/. - c.2896C>T r.(?) p.(Arg966Trp)


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