Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATTCCCCAAGTTCAGGTACTGTAAG[C/G]CTTTGTCTGTGAACCGTCTGCAATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609080 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM185A 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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FAM185A - family with sequence similarity 185 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145268.1 | 1169 | Intron | NP_001138740.1 | |||
NM_001145269.1 | 1169 | Intron | NP_001138741.1 | |||
XM_006715896.3 | 1169 | Intron | XP_006715959.1 | |||
XM_011515922.2 | 1169 | Intron | XP_011514224.1 | |||
XM_011515923.2 | 1169 | Intron | XP_011514225.1 | |||
XM_011515924.2 | 1169 | Intron | XP_011514226.1 | |||
XM_011515925.2 | 1169 | Intron | XP_011514227.1 | |||
XM_011515926.2 | 1169 | Intron | XP_011514228.1 | |||
XM_017011846.1 | 1169 | Intron | XP_016867335.1 | |||
XM_017011847.1 | 1169 | Intron | XP_016867336.1 | |||
XM_017011848.1 | 1169 | Intron | XP_016867337.1 | |||
XM_017011849.1 | 1169 | UTR 3 | XP_016867338.1 |
FBXL13 - F-box and leucine rich repeat protein 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001111038.1 | 1169 | Missense Mutation | GCC,GGC | A,G 313 | NP_001104508.1 | |
NM_001287150.1 | 1169 | Missense Mutation | GCC,GGC | A,G 313 | NP_001274079.1 | |
NM_145032.3 | 1169 | Missense Mutation | GCC,GGC | A,G 313 | NP_659469.3 | |
XM_005250205.3 | 1169 | Missense Mutation | GCC,GGC | A,G 403 | XP_005250262.1 | |
XM_005250207.3 | 1169 | Missense Mutation | GCC,GGC | A,G 403 | XP_005250264.1 | |
XM_005250208.3 | 1169 | Missense Mutation | GCC,GGC | A,G 403 | XP_005250265.1 | |
XM_005250209.2 | 1169 | Missense Mutation | GCC,GGC | A,G 313 | XP_005250266.1 | |
XM_006715898.2 | 1169 | Missense Mutation | GCC,GGC | A,G 162 | XP_006715961.1 | |
XM_011515928.2 | 1169 | Missense Mutation | GCC,GGC | A,G 403 | XP_011514230.1 | |
XM_011515929.2 | 1169 | Missense Mutation | GCC,GGC | A,G 403 | XP_011514231.1 | |
XM_011515930.2 | 1169 | Missense Mutation | GCC,GGC | A,G 313 | XP_011514232.1 | |
XM_011515932.2 | 1169 | Missense Mutation | GCC,GGC | A,G 403 | XP_011514234.1 | |
XM_017011850.1 | 1169 | Missense Mutation | GCC,GGC | A,G 400 | XP_016867339.1 | |
XM_017011851.1 | 1169 | Missense Mutation | GCC,GGC | A,G 403 | XP_016867340.1 | |
XM_017011852.1 | 1169 | Missense Mutation | GCC,GGC | A,G 358 | XP_016867341.1 | |
XM_017011853.1 | 1169 | Missense Mutation | GCC,GGC | A,G 313 | XP_016867342.1 |
LRRC17 - leucine rich repeat containing 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031692.2 | 1169 | Intron | NP_001026862.1 | |||
NM_005824.2 | 1169 | Intron | NP_005815.2 | |||
XM_005250108.1 | 1169 | Intron | XP_005250165.1 |
Set Membership: |
HapMap |