Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTTTGATTTTCAAGTCCTTCTGAAT[C/G]TTGGGGTCACAGGCTTGACTGAAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616695 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
STYXL1 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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STYXL1 - serine/threonine/tyrosine interacting-like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317785.1 | 732 | Missense Mutation | AAC,AAG | N,K 180 | NP_001304714.1 | |
NM_001317786.1 | 732 | Missense Mutation | AAC,AAG | N,K 180 | NP_001304715.1 | |
NM_001317787.1 | 732 | Missense Mutation | AAC,AAG | N,K 84 | NP_001304716.1 | |
NM_001317788.1 | 732 | Missense Mutation | AAC,AAG | N,K 84 | NP_001304717.1 | |
NM_001317789.1 | 732 | Missense Mutation | AAC,AAG | N,K 42 | NP_001304718.1 | |
NM_016086.2 | 732 | Missense Mutation | AAC,AAG | N,K 180 | NP_057170.1 | |
XM_011516292.2 | 732 | Missense Mutation | AAC,AAG | N,K 180 | XP_011514594.1 | |
XM_011516293.2 | 732 | Missense Mutation | AAC,AAG | N,K 180 | XP_011514595.1 | |
XM_011516300.1 | 732 | Missense Mutation | AAC,AAG | N,K 42 | XP_011514602.1 | |
XM_017012296.1 | 732 | Missense Mutation | AAC,AAG | N,K 218 | XP_016867785.1 | |
XM_017012297.1 | 732 | Missense Mutation | AAC,AAG | N,K 180 | XP_016867786.1 | |
XM_017012298.1 | 732 | Missense Mutation | AAC,AAG | N,K 180 | XP_016867787.1 | |
XM_017012299.1 | 732 | Missense Mutation | AAC,AAG | N,K 218 | XP_016867788.1 | |
XM_017012300.1 | 732 | Missense Mutation | AAC,AAG | N,K 102 | XP_016867789.1 | |
XM_017012301.1 | 732 | Missense Mutation | AAC,AAG | N,K 42 | XP_016867790.1 | |
XM_017012302.1 | 732 | Missense Mutation | AAC,AAG | N,K 42 | XP_016867791.1 |