Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCAGGCCGATTCCGAGCAGCTGTG[C/T]CCAGTGGGGCTTCCACGGGTATCTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 131370 MIM: 176610 MIM: 610431 MIM: 610056 | ||||||||||||||||||||
Literature Links: |
ENO3 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 |
ENO3 - enolase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193503.1 | 630 | Intron | NP_001180432.1 | |||
NM_001976.4 | 630 | Intron | NP_001967.3 | |||
NM_053013.3 | 630 | Intron | NP_443739.3 | |||
XM_005256521.2 | 630 | Missense Mutation | CCC,TCC | P,S 45 | XP_005256578.1 | |
XM_011523729.1 | 630 | Missense Mutation | CCC,TCC | P,S 36 | XP_011522031.1 | |
XM_017024346.1 | 630 | Missense Mutation | CCC,TCC | P,S 36 | XP_016879835.1 |
PFN1 - profilin 1 | ||||||
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There are no transcripts associated with this gene. |
RNF167 - ring finger protein 167 | ||||||
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There are no transcripts associated with this gene. |
SPAG7 - sperm associated antigen 7 | ||||||
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There are no transcripts associated with this gene. |