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See other BAIAP2L1 GT Assays ›
SNP ID:
rs958117
Gene
BAIAP2L1 BRI3
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.7: 98310567 - 98310567 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

GGGGGGCATCTTTGGTGAGCATTTA[A/G]AAAGGGTGTCGTAATCTTTCCTAAC

Assay ID C___8324779_30
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 611877 MIM: 615628

Literature Links:

 BAIAP2L1 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 JPT (Japanese)
A (0.01)
(0.99)
AFR - Not Available Japanese - Not Available CHB (Han Chinese)
A (0.01)
(0.99)
EUR - Not Available
AMR - Not Available
BAIAP2L1 - BAI1 associated protein 2 like 1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_018842.4 1096 Missense Mutation TCT,TTT S,F 278 NP_061330.2
BRI3 - brain protein I3
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001159491.1 1096 Intron NP_001152963.1
NM_015379.4 1096 Intron NP_056194.1
XM_017011931.1 1096 Intron XP_016867420.1
XM_017011932.1 1096 Intron XP_016867421.1
XM_017011933.1 1096 Intron XP_016867422.1
XM_017011934.1 1096 Intron XP_016867423.1
XM_017011935.1 1096 Intron XP_016867424.1
XM_017011936.1 1096 Intron XP_016867425.1

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