Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGGTCCGAGCTTCTTCTTCCAATC[A/G]TGGGGCTCCATATCCGCCACGGGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615659 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TMEM131 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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TMEM131 - transmembrane protein 131 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015348.1 | 5997 | Missense Mutation | NP_056163.1 | |||
XM_005263909.1 | 5997 | Missense Mutation | XP_005263966.1 | |||
XM_005263910.1 | 5997 | Missense Mutation | XP_005263967.1 | |||
XM_005263911.1 | 5997 | Missense Mutation | XP_005263968.1 | |||
XM_005263912.3 | 5997 | Missense Mutation | XP_005263969.1 | |||
XM_011510869.1 | 5997 | Missense Mutation | XP_011509171.1 |