Product Details

SNP ID
rs16846001
Assay Type
Functionally tested
NCBI dbSNP Submissions
11
Location
Chr.1:173502345 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCACCTGGCTGGGAAAAGGCTAAAG[A/G]TCCTTGAAGCCTGTGCTTAGCACCA
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC9C2 PubMed Links

Gene Details

Gene
SLC9C2
Gene Name
solute carrier family 9 member C2 (putative)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_178527.3 Intron NP_848622.2
XM_011509426.1 Intron XP_011507728.1
XM_017001065.1 Intron XP_016856554.1
XM_017001066.1 Intron XP_016856555.1
XM_017001067.1 Intron XP_016856556.1
XM_017001068.1 Intron XP_016856557.1
XM_017001069.1 Intron XP_016856558.1
XM_017001070.1 Intron XP_016856559.1
XM_017001071.1 Intron XP_016856560.1
XM_017001072.1 Intron XP_016856561.1
XM_017001073.1 Intron XP_016856562.1
XM_017001074.1 Intron XP_016856563.1
XM_017001075.1 Intron XP_016856564.1
XM_017001076.1 Intron XP_016856565.1

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