Variant #0000888318 (NC_000008.10:g.27319168G>T, NM_000742.3:c.1568C>A (CHRNA2))

Chromosome 8
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.27319168G>T
DNA change (hg38) -
Published as CHRNA2(NM_000742.3):c.1568C>A (p.P523Q, p.(Pro523Gln))
ISCN -
DB-ID CHRNA2_000036 See all 3 reported entries
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) 1.0E-5 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNA2 NM_000742.3 ?/. - c.1568C>A r.(?) p.(Pro523Gln)
PTK2B NM_004103.4 ?/. - c.*3142G>T r.(=) p.(=)


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