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GCGGGCGGAGGGCCGAAAGTCCAGT[A/T]TGTGGGTCCAGGGTCACTCTTCTAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605790 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM221A 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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FAM221A - family with sequence similarity 221 member A | ||||||
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There are no transcripts associated with this gene. |
STK31 - serine/threonine kinase 31 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001260504.1 | 120 | Intron | NP_001247433.1 | |||
NM_001260505.1 | 120 | Missense Mutation | ATG,TTG | M,L 1 | NP_001247434.1 | |
NM_031414.4 | 120 | Missense Mutation | ATG,TTG | M,L 1 | NP_113602.2 | |
NM_032944.3 | 120 | Intron | NP_116562.2 | |||
XM_006715758.3 | 120 | Missense Mutation | ATG,TTG | M,L 1 | XP_006715821.1 | |
XM_011515449.2 | 120 | Intron | XP_011513751.2 | |||
XM_011515450.1 | 120 | Intron | XP_011513752.1 | |||
XM_011515452.2 | 120 | Intron | XP_011513754.2 |