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CTCCACACCACCCTGGTTGTCACGA[C/T]GAAACTGGTGCTCCCGACCCCTGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 612730 | ||||||||||||||||||||
Literature Links: |
SLC9A8 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SLC9A8 - solute carrier family 9 member A8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001260491.1 | 164 | Missense Mutation | ACG,ATG | T,M 31 | NP_001247420.1 | |
NM_015266.2 | 164 | Missense Mutation | ACG,ATG | T,M 31 | NP_056081.1 | |
XM_006723756.1 | 164 | Missense Mutation | ACG,ATG | T,M 31 | XP_006723819.1 | |
XM_011528736.1 | 164 | Missense Mutation | ACG,ATG | T,M 31 | XP_011527038.1 | |
XM_011528737.1 | 164 | Missense Mutation | ACG,ATG | T,M 31 | XP_011527039.1 | |
XM_011528738.1 | 164 | Missense Mutation | ACG,ATG | T,M 31 | XP_011527040.1 | |
XM_011528739.1 | 164 | Missense Mutation | ACG,ATG | T,M 31 | XP_011527041.1 | |
XM_011528740.1 | 164 | Missense Mutation | ACG,ATG | T,M 31 | XP_011527042.1 | |
XM_011528741.1 | 164 | Missense Mutation | ACG,ATG | T,M 31 | XP_011527043.1 | |
XM_011528742.1 | 164 | UTR 5 | XP_011527044.1 | |||
XM_011528743.2 | 164 | Intron | XP_011527045.1 | |||
XM_011528744.2 | 164 | Intron | XP_011527046.1 | |||
XM_011528745.1 | 164 | Missense Mutation | ACG,ATG | T,M 31 | XP_011527047.1 | |
XM_017027754.1 | 164 | Missense Mutation | ACG,ATG | T,M 31 | XP_016883243.1 | |
XM_017027755.1 | 164 | UTR 5 | XP_016883244.1 | |||
XM_017027756.1 | 164 | UTR 5 | XP_016883245.1 |