Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGAAAAGAAGACAATTTGCTTACCC[A/G]TTTTATTGTCAAAAAATTTGATGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614766 | ||||||||||||||||||||
Literature Links: |
STRN3 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 |
STRN3 - striatin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001083893.1 | 2351 | Missense Mutation | ACG,ATG | T,M 712 | NP_001077362.1 | |
NM_014574.3 | 2351 | Missense Mutation | ACG,ATG | T,M 628 | NP_055389.3 | |
XM_005267569.3 | 2351 | Missense Mutation | ACG,ATG | T,M 675 | XP_005267626.1 | |
XM_005267570.3 | 2351 | Missense Mutation | ACG,ATG | T,M 665 | XP_005267627.1 |