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GCACCTGGCTGGGAAAAGGCTAAAG[A/G]TCCTTGAAGCCTGTGCTTAGCACCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
11 submissions
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Phenotype: |
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Literature Links: |
SLC9C2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SLC9C2 - solute carrier family 9 member C2 (putative) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | 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 |