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ACATGAATACTGACATCAGTTCTCT[A/G]CGTACATTAAGAAGCTCCTCTTCTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604105 | ||||||||||||||||||||
Literature Links: |
SYCP2 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 |
SYCP2 - synaptonemal complex protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014258.3 | 4727 | Silent Mutation | CGC,CGT | R,R 1514 | NP_055073.2 | |
XM_011528487.2 | 4727 | Silent Mutation | CGC,CGT | R,R 1521 | XP_011526789.1 | |
XM_011528488.2 | 4727 | Silent Mutation | CGC,CGT | R,R 1521 | XP_011526790.1 | |
XM_011528489.2 | 4727 | Silent Mutation | CGC,CGT | R,R 1514 | XP_011526791.1 | |
XM_011528490.2 | 4727 | Silent Mutation | CGC,CGT | R,R 1513 | XP_011526792.1 | |
XM_011528493.2 | 4727 | Silent Mutation | CGC,CGT | R,R 1349 | XP_011526795.1 | |
XM_017027586.1 | 4727 | Silent Mutation | CGC,CGT | R,R 1521 | XP_016883075.1 | |
XM_017027587.1 | 4727 | Silent Mutation | CGC,CGT | R,R 1520 | XP_016883076.1 | |
XM_017027588.1 | 4727 | Silent Mutation | CGC,CGT | R,R 1469 | XP_016883077.1 | |
XM_017027589.1 | 4727 | Silent Mutation | CGC,CGT | R,R 1464 | XP_016883078.1 | |
XM_017027590.1 | 4727 | Silent Mutation | CGC,CGT | R,R 1349 | XP_016883079.1 | |
XM_017027591.1 | 4727 | Silent Mutation | CGC,CGT | R,R 1038 | XP_016883080.1 | |
XM_017027592.1 | 4727 | Intron | XP_016883081.1 |