Variant #0000563051 (NC_000017.10:g.7358597C>G, NC_000017.10(NM_000747.2):c.1045-6C>G (CHRNB1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7358597C>G
DNA change (hg38) g.7455278C>G
Published as CHRNB1(NM_000747.3):c.1045-6C>G
ISCN -
DB-ID CHRNB1_000024
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) 0.00403 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.1045-6C>G r.(=) p.(=)
SLC35G6 NM_001102614.1 -?/. - c.-26239C>G r.(?) p.(=)
ZBTB4 NM_020899.3 -?/. - c.*6662G>C r.(=) p.(=)


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