Variant #0001003666 (NC_000017.10:g.7360008C>T, NM_000747.2:c.1472C>T (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.7360008C>T
DNA change (hg38) -
Published as CHRNB1(NM_000747.2):c.1472C>T (p.(Thr491Met))
ISCN -
DB-ID CHRNB1_000044
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 2024-08-28 13:16:32 +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     
CHRNB1 NM_000747.2 ?/. - c.1472C>T r.(?) p.(Thr491Met)
SLC35G6 NM_001102614.1 ?/. - c.-24828C>T r.(?) p.(=)
ZBTB4 NM_020899.3 ?/. - c.*5251G>A r.(=) p.(=)


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