Variant #0000726670 (NC_000017.10:g.7351934G>A, NM_000747.2:c.647G>A (CHRNB1))

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.7351934G>A
DNA change (hg38) -
Published as CHRNB1(NM_000747.2):c.647G>A (p.R216Q), CHRNB1(NM_000747.3):c.647G>A (p.R216Q)
ISCN -
DB-ID CHRNB1_000020 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) 0.00016 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNB1 NM_000747.2 ?/. - c.647G>A r.(?) p.(Arg216Gln)
FGF11 NM_004112.2 ?/. - c.*5469G>A r.(=) p.(=)


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