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TAGCCATGTTCATGAAAAACTGGGC[C/G]CTTGTTGTTACTCAATGCTTCCACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 300311 | ||||||||||||||||||||
Literature Links: |
TEX11 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 |
TEX11 - testis expressed 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003811.1 | 2819 | Missense Mutation | CGC,GGC | R,G 927 | NP_001003811.1 | |
NM_031276.2 | 2819 | Missense Mutation | CGC,GGC | R,G 912 | NP_112566.2 | |
XM_011530994.1 | 2819 | Intron | XP_011529296.1 | |||
XM_011530996.1 | 2819 | Missense Mutation | CGC,GGC | R,G 602 | XP_011529298.1 | |
XM_017029649.1 | 2819 | Intron | XP_016885138.1 | |||
XM_017029650.1 | 2819 | Intron | XP_016885139.1 | |||
XM_017029651.1 | 2819 | Intron | XP_016885140.1 | |||
XM_017029652.1 | 2819 | Intron | XP_016885141.1 |