Unique variants in gene ALOX5AP

Information The variants shown are described using the NM_001629.3 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. 1 - c.-21764_-21763insGTGT likely benign r.(?) p.(=) g.31287979_31287980insGTGT - ALOX5AP(NM_001204406.1):c.116_116+1insGTGT (p.?) - ALOX5AP_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
-?/. 1 - c.-21763_-21762insAT likely benign r.(?) p.(=) g.31287980_31287981insAT - ALOX5AP(NM_001204406.1):c.116+1_116+2insTA - ALOX5AP_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
-/. 1 - c.-21753_-21750dup benign r.(?) p.(=) g.31287990_31287993dup - ALOX5AP(NM_001204406.1):c.117_116+2insTGTG - ALOX5AP_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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