Variant #0000952502 (NC_000002.11:g.29436847C>G, NC_000002.11(NM_004304.4):c.3743+3G>C (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.29436847C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID ALK_000101
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1669532102
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-12-10 21:40:01 +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.3743+3G>C r.(?) p.(?)


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