Variant #0000570238 (NC_000020.10:g.61978149C>T, NM_000744.6:c.1825G>A (CHRNA4))

Chromosome 20
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.61978149C>T
DNA change (hg38) g.63346797C>T
Published as CHRNA4(NM_000744.6):c.1825G>A (p.V609I), CHRNA4(NM_000744.7):c.1825G>A (p.V609I)
ISCN -
DB-ID CHRNA4_000046 See all 2 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) 9.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNA4 NM_000744.6 ?/. - c.1825G>A r.(?) p.(Val609Ile)


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