Product Details

SNP ID
rs55779592
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:140361149 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGGAGCAAGTTCATTGGCCCTGGC[A/G]TTCTGAGACTCCCAGAAGGGAAAGG
Phenotype
MIM: 610207
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC4A9 PubMed Links

Gene Details

Gene
SLC4A9
Gene Name
solute carrier family 4 member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001258426.1 Intron NP_001245355.1
NM_001258427.1 Intron NP_001245356.1
NM_001258428.1 Intron NP_001245357.1
NM_031467.2 Intron NP_113655.2
XM_005268521.3 Intron XP_005268578.2
XM_011537694.2 Intron XP_011535996.1
XM_017009933.1 Intron XP_016865422.1
XM_017009934.1 Intron XP_016865423.1
XM_017009935.1 Intron XP_016865424.1
XM_017009936.1 Intron XP_016865425.1
XM_017009937.1 Intron XP_016865426.1
XM_017009938.1 Intron XP_016865427.1
XM_017009939.1 Intron XP_016865428.1
XM_017009940.1 Intron XP_016865429.1
XM_017009941.1 Intron XP_016865430.1
XM_017009942.1 Intron XP_016865431.1
XM_017009943.1 Intron XP_016865432.1

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