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SNP ID:
rs145709687
Gene
DCLK2 LRBA
Gene Name
Set Membership:
-
Chromosome Location:
Chr.4: 150265730 - 150265730 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

ATGTACAGCTGTCACCATCAGTAGC[A/G]GGTTTGGTATTCATGATGCCACCGG

Assay ID C_170548215_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 613166 MIM: 606453

Literature Links:

 DCLK2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
DCLK2 - doublecortin like kinase 2
There are no transcripts associated with this gene.
LRBA - LPS responsive beige-like anchor protein
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001199282.2 9038 Missense Mutation CGC,TGC R,C 2850 NP_001186211.2
NM_006726.4 9038 Missense Mutation CGC,TGC R,C 2862 NP_006717.2
XM_005263372.3 9038 Missense Mutation CGC,TGC R,C 2867 XP_005263429.1
XM_005263373.2 9038 Missense Mutation CGC,TGC R,C 2867 XP_005263430.1
XM_005263374.3 9038 Missense Mutation CGC,TGC R,C 2856 XP_005263431.1
XM_005263375.3 9038 Missense Mutation CGC,TGC R,C 2851 XP_005263432.1
XM_011532434.2 9038 Missense Mutation CGC,TGC R,C 2862 XP_011530736.1
XM_017008872.1 9038 Missense Mutation CGC,TGC R,C 2856 XP_016864361.1
XM_017008873.1 9038 Missense Mutation CGC,TGC R,C 757 XP_016864362.1
XM_017008874.1 9038 Missense Mutation CGC,TGC R,C 755 XP_016864363.1

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