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TTATTACAGACCTAGAGTCCTGACT[G/T]TGATGATTCATTGTTCTCAGATGTT
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 4391 | Missense Mutation | CAA,CAC | Q,H 1402 | NP_055073.2 | |
XM_011528487.2 | 4391 | Missense Mutation | CAA,CAC | Q,H 1409 | XP_011526789.1 | |
XM_011528488.2 | 4391 | Missense Mutation | CAA,CAC | Q,H 1409 | XP_011526790.1 | |
XM_011528489.2 | 4391 | Missense Mutation | CAA,CAC | Q,H 1402 | XP_011526791.1 | |
XM_011528490.2 | 4391 | Missense Mutation | CAA,CAC | Q,H 1401 | XP_011526792.1 | |
XM_011528493.2 | 4391 | Missense Mutation | CAA,CAC | Q,H 1237 | XP_011526795.1 | |
XM_017027586.1 | 4391 | Missense Mutation | CAA,CAC | Q,H 1409 | XP_016883075.1 | |
XM_017027587.1 | 4391 | Missense Mutation | CAA,CAC | Q,H 1408 | XP_016883076.1 | |
XM_017027588.1 | 4391 | Missense Mutation | CAA,CAC | Q,H 1357 | XP_016883077.1 | |
XM_017027589.1 | 4391 | Missense Mutation | CAA,CAC | Q,H 1352 | XP_016883078.1 | |
XM_017027590.1 | 4391 | Missense Mutation | CAA,CAC | Q,H 1237 | XP_016883079.1 | |
XM_017027591.1 | 4391 | Missense Mutation | CAA,CAC | Q,H 926 | XP_016883080.1 | |
XM_017027592.1 | 4391 | Intron | XP_016883081.1 |