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AGCAGTCGAAGCAGCTGGCCCACAA[C/G]AGGCAGCTCCTCAGGCCCAACTCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 243305 MIM: 616717 | ||||||||||||||||||||
Literature Links: |
INVS 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 |
INVS - inversin | ||||||
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There are no transcripts associated with this gene. |
TEX10 - testis expressed 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001161584.1 | 2279 | Missense Mutation | CTT,GTT | L,V 843 | NP_001155056.1 | |
NM_017746.3 | 2279 | Missense Mutation | CTT,GTT | L,V 859 | NP_060216.2 | |
XM_011518798.1 | 2279 | Missense Mutation | CTT,GTT | L,V 734 | XP_011517100.1 | |
XM_017014848.1 | 2279 | Missense Mutation | CTT,GTT | L,V 504 | XP_016870337.1 |