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ATTCCCAGTGGGAGGGCGCACCTTC[A/G]TCTTCCTCCCCTGGTCTGAGGCTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602059 MIM: 610745 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ISLR 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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ISLR - immunoglobulin superfamily containing leucine rich repeat | ||||||
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There are no transcripts associated with this gene. |
STRA6 - stimulated by retinoic acid 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142617.1 | 2048 | Silent Mutation | GAC,GAT | D,D 612 | NP_001136089.1 | |
NM_001142618.1 | 2048 | Silent Mutation | GAC,GAT | D,D 612 | NP_001136090.1 | |
NM_001142619.1 | 2048 | Silent Mutation | GAC,GAT | D,D 603 | NP_001136091.1 | |
NM_001142620.1 | 2048 | Intron | NP_001136092.1 | |||
NM_001199040.1 | 2048 | Silent Mutation | GAC,GAT | D,D 649 | NP_001185969.1 | |
NM_001199041.1 | 2048 | Silent Mutation | GAC,GAT | D,D 627 | NP_001185970.1 | |
NM_001199042.1 | 2048 | Silent Mutation | GAC,GAT | D,D 651 | NP_001185971.1 | |
NM_022369.3 | 2048 | Silent Mutation | GAC,GAT | D,D 612 | NP_071764.3 | |
XM_011521883.1 | 2048 | Silent Mutation | GAC,GAT | D,D 612 | XP_011520185.1 | |
XM_011521884.1 | 2048 | Silent Mutation | GAC,GAT | D,D 549 | XP_011520186.1 | |
XM_011521885.2 | 2048 | Intron | XP_011520187.1 | |||
XM_017022478.1 | 2048 | Silent Mutation | GAC,GAT | D,D 628 | XP_016877967.1 | |
XM_017022479.1 | 2048 | Silent Mutation | GAC,GAT | D,D 612 | XP_016877968.1 | |
XM_017022480.1 | 2048 | Silent Mutation | GAC,GAT | D,D 549 | XP_016877969.1 |