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TGTGTGCGATGGTACCTGTGGCAAG[A/G]GCGAGGGCAGTCCCAGTGAGAACTC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605458 | |||||||||||||||||||||||
Literature Links: |
ACTR8 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 - 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 |
ACTR8 - ARP8 actin-related protein 8 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022899.4 | 1139 | Intron | NP_075050.3 | |||
XM_005265587.4 | 1139 | Intron | XP_005265644.1 | |||
XM_011534249.2 | 1139 | Intron | XP_011532551.1 |
IL17RB - interleukin 17 receptor B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018725.3 | 1139 | Missense Mutation | AGC,GGC | S,G 411 | NP_061195.2 | |
XM_005265310.4 | 1139 | Missense Mutation | AGC,GGC | S,G 440 | XP_005265367.1 | |
XM_005265311.4 | 1139 | Missense Mutation | AGC,GGC | S,G 424 | XP_005265368.1 | |
XM_005265312.4 | 1139 | Missense Mutation | AGC,GGC | S,G 395 | XP_005265369.1 | |
XM_011533941.2 | 1139 | UTR 3 | XP_011532243.1 | |||
XM_017006804.1 | 1139 | Missense Mutation | AGC,GGC | S,G 323 | XP_016862293.1 | |
XM_017006805.1 | 1139 | Missense Mutation | AGC,GGC | S,G 307 | XP_016862294.1 | |
XM_017006806.1 | 1139 | Missense Mutation | AGC,GGC | S,G 294 | XP_016862295.1 | |
XM_017006807.1 | 1139 | UTR 3 | XP_016862296.1 |