Variant #0001030034 (NC_000002.11:g.29498088C>T, NM_004304.4:c.1918G>A (ALK))

Chromosome 2
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.29498088C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ALK_000108
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs144453491
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-03-24 16:47:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALK NM_004304.4 ?/. - c.1918G>A r.(?) p.(Gly640Arg)


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