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See other BAIAP2L1 GT Assays ›
SNP ID:
rs7791321
Gene
BAIAP2L1 BRI3
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.7: 98314813 - 98314813 on Build GRCh38
Polymorphism:
C/G, Transversion substitution
Context Sequence [VIC/FAM]:

CCGCTGGGACTCACCAGCAGCCATG[C/G]TGAAGACACTGATGCTGAGGACACA

Assay ID C___2618865_10
Size
Availability Made To Order
Catalog # 4351379
Price
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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
C (0.27)
(0.73)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
C (0.26)
(0.74)
African American - Not Available YRI (Yoruba)
C (0.14)
(0.86)
SAS
C (0.16)
(0.84)
Chinese - Not Available JPT (Japanese)
C (0.13)
(0.87)
AFR
C (0.15)
(0.85)
Japanese - Not Available CHB (Han Chinese)
C (0.14)
(0.86)
EUR
C (0.48)
(0.52)
AMR
C (0.34)
(0.66)
BAIAP2L1 - BAI1 associated protein 2 like 1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_018842.4 Intron NP_061330.2
BRI3 - brain protein I3
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001159491.1 Intron NP_001152963.1
NM_015379.4 Intron NP_056194.1
XM_017011931.1 Intron XP_016867420.1
XM_017011932.1 Intron XP_016867421.1
XM_017011933.1 Intron XP_016867422.1
XM_017011934.1 Intron XP_016867423.1
XM_017011935.1 Intron XP_016867424.1
XM_017011936.1 Intron XP_016867425.1

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