Variant #0000857872 (NC_000002.11:g.175614925del, NC_000002.11(NM_001039523.2):c.854-12del (CHRNA1))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.175614925del
DNA change (hg38) -
Published as CHRNA1(NM_000079.3):c.779-14del (p.(=)), CHRNA1(NM_001039523.3):c.854-12delT
ISCN -
DB-ID CHRNA1_000049 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) 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNA1 NM_000079.3 -/. - c.779-12del r.(=) p.(=)
CHRNA1 NM_001039523.2 -/. - c.854-12del r.(=) p.(=)


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