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CTGAAGTTCTCCAGGAGGGCGGCAA[A/C]CTCGGCGTCATTTAGCACTTGGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300369 MIM: 300574 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACRC 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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ACRC - acidic repeat containing | ||||||
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There are no transcripts associated with this gene. |
CXCR3 - C-X-C motif chemokine receptor 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142797.1 | 112 | Missense Mutation | GTT,TTT | V,F 63 | NP_001136269.1 | |
NM_001504.1 | 112 | Missense Mutation | GTT,TTT | V,F 16 | NP_001495.1 | |
XM_005262256.3 | 112 | Missense Mutation | GTT,TTT | V,F 26 | XP_005262313.1 | |
XM_005262257.3 | 112 | Missense Mutation | GTT,TTT | V,F 26 | XP_005262314.1 | |
XM_017029435.1 | 112 | Missense Mutation | GTT,TTT | V,F 63 | XP_016884924.1 | |
XM_017029436.1 | 112 | Missense Mutation | GTT,TTT | V,F 16 | XP_016884925.1 |