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GCTCTAGACTAAGGGGACAGACTTA[C/T]CCCACCCCTGATGCTGCTGTTGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616309 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FRMD5 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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FRMD5 - FERM domain containing 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286490.1 | 2489 | UTR 3 | NP_001273419.1 | |||
NM_001286491.1 | 2489 | UTR 3 | NP_001273420.1 | |||
NM_001322949.1 | 2489 | Intron | NP_001309878.1 | |||
NM_001322950.1 | 2489 | UTR 3 | NP_001309879.1 | |||
NM_001322951.1 | 2489 | Intron | NP_001309880.1 | |||
NM_032892.4 | 2489 | UTR 3 | NP_116281.2 | |||
XM_005254730.3 | 2489 | Missense Mutation | GAT,GGT | D,G 511 | XP_005254787.1 |
PIN4P1 - peptidylprolyl cis/trans isomerase, NIMA-interacting 4 pseudogene 1 | ||||||
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There are no transcripts associated with this gene. |
WDR76 - WD repeat domain 76 | ||||||
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There are no transcripts associated with this gene. |