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GGTGATGGGCCAAGGCCCTGGGGTA[C/T]AGTGAGCTTTTAGGTGGCCTCAGCC
Species: |
Human | |||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606205 | |||||||||||||||||||||||||||||
Literature Links: |
SLC6A7 PubMed Links | |||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
SLC6A7 - solute carrier family 6 member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014228.4 | 521 | Intron | NP_055043.2 | |||
XM_017009767.1 | 521 | Intron | XP_016865256.1 | |||
XM_017009768.1 | 521 | Intron | XP_016865257.1 | |||
XM_017009769.1 | 521 | UTR 5 | XP_016865258.1 | |||
XM_017009770.1 | 521 | Intron | XP_016865259.1 |
Set Membership: |
HapMap |