Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGGCGGACTTCGCTGGGCCGTCTT[C/T]TGCCGGCCGCAAGGCCGGGGCTCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 601749 MIM: 611476 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GLMN 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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GLMN - glomulin, FKBP associated protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319683.1 | 135 | Intron | NP_001306612.1 | |||
NM_053274.2 | 135 | Intron | NP_444504.1 | |||
XM_005270401.3 | 135 | Intron | XP_005270458.1 | |||
XM_006710309.2 | 135 | Intron | XP_006710372.1 | |||
XM_011540546.2 | 135 | Intron | XP_011538848.1 | |||
XM_017000137.1 | 135 | Intron | XP_016855626.1 | |||
XM_017000138.1 | 135 | Intron | XP_016855627.1 | |||
XM_017000139.1 | 135 | Intron | XP_016855628.1 | |||
XM_017000140.1 | 135 | Intron | XP_016855629.1 | |||
XM_017000141.1 | 135 | Intron | XP_016855630.1 | |||
XM_017000142.1 | 135 | Intron | XP_016855631.1 | |||
XM_017000143.1 | 135 | Intron | XP_016855632.1 | |||
XM_017000144.1 | 135 | Intron | XP_016855633.1 |
RPAP2 - RNA polymerase II associated protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024813.2 | 135 | Missense Mutation | TCT,TTT | S,F 9 | NP_079089.2 | |
XM_005271223.2 | 135 | Missense Mutation | TCT,TTT | S,F 9 | XP_005271280.1 | |
XM_011542167.2 | 135 | Missense Mutation | TCT,TTT | S,F 9 | XP_011540469.1 | |
XM_017002362.1 | 135 | Missense Mutation | TCT,TTT | S,F 9 | XP_016857851.1 | |
XM_017002363.1 | 135 | Missense Mutation | TCT,TTT | S,F 9 | XP_016857852.1 | |
XM_017002364.1 | 135 | Missense Mutation | TCT,TTT | S,F 9 | XP_016857853.1 |