Product Details

SNP ID
rs359925
Assay Type
Functionally Tested
NCBI dbSNP Submissions
45
Location
Chr.1:89530777 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAGCGGGTGGACAACCCCAACGGCC[A/G]GTCCCTCCGTACCTTTCCATTTTGC
Phenotype
MIM: 612888
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
LRRC8B PubMed Links

Gene Details

Gene
LRRC8B
Gene Name
leucine rich repeat containing 8 family member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001134476.1 Intron NP_001127948.1
NM_015350.2 Intron NP_056165.1
XM_005270701.4 Intron XP_005270758.1
XM_005270702.4 Intron XP_005270759.1
XM_005270703.4 Intron XP_005270760.1
XM_011541143.2 Intron XP_011539445.1
XM_011541144.2 Intron XP_011539446.1
XM_011541145.2 Intron XP_011539447.1
XM_011541146.2 Intron XP_011539448.1
XM_011541148.2 Intron XP_011539450.1
XM_017000883.1 Intron XP_016856372.1
XM_017000884.1 Intron XP_016856373.1
XM_017000885.1 Intron XP_016856374.1
XM_017000886.1 Intron XP_016856375.1

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