Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCAGCGTGTAGGCCAGACCCCAG[C/G]GAGCCCTGCCGCGGCTGGCCCCGGG
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 |
---|---|---|
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 |
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 | 2125 | Missense Mutation | CCC,CGC | P,R 638 | NP_001136089.1 | |
NM_001142618.1 | 2125 | Missense Mutation | CCC,CGC | P,R 638 | NP_001136090.1 | |
NM_001142619.1 | 2125 | Missense Mutation | CCC,CGC | P,R 629 | NP_001136091.1 | |
NM_001142620.1 | 2125 | Intron | NP_001136092.1 | |||
NM_001199040.1 | 2125 | Missense Mutation | CCC,CGC | P,R 675 | NP_001185969.1 | |
NM_001199041.1 | 2125 | Missense Mutation | CCC,CGC | P,R 653 | NP_001185970.1 | |
NM_001199042.1 | 2125 | Missense Mutation | CCC,CGC | P,R 677 | NP_001185971.1 | |
NM_022369.3 | 2125 | Missense Mutation | CCC,CGC | P,R 638 | NP_071764.3 | |
XM_011521883.1 | 2125 | Missense Mutation | CCC,CGC | P,R 638 | XP_011520185.1 | |
XM_011521884.1 | 2125 | Missense Mutation | CCC,CGC | P,R 575 | XP_011520186.1 | |
XM_011521885.2 | 2125 | Intron | XP_011520187.1 | |||
XM_017022478.1 | 2125 | Missense Mutation | CCC,CGC | P,R 654 | XP_016877967.1 | |
XM_017022479.1 | 2125 | Missense Mutation | CCC,CGC | P,R 638 | XP_016877968.1 | |
XM_017022480.1 | 2125 | Missense Mutation | CCC,CGC | P,R 575 | XP_016877969.1 |