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TGCTTGAGGTTGTCATGCAGAATAG[A/T]ATCCTTCACGTCACGGAAAACAAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604406 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GNA13 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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GNA13 - G protein subunit alpha 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282425.1 | 992 | Missense Mutation | ACT,TCT | T,S 270 | NP_001269354.1 | |
NM_006572.5 | 992 | Missense Mutation | ACT,TCT | T,S 365 | NP_006563.2 | |
XM_011524202.1 | 992 | Intron | XP_011522504.1 |