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GAGTCCCTGCTGCAGGTGGGCGTCA[C/T]GCAGCGCTTTATTGATGATGTCGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604627 | ||||||||||||||||||||
Literature Links: |
GRPEL2-AS1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
GRPEL2-AS1 - GRPEL2 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |
IL17B - interleukin 17B | ||||||
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There are no transcripts associated with this gene. |
PCYOX1L - prenylcysteine oxidase 1 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301054.1 | 664 | Missense Mutation | ACG,ATG | T,M 184 | NP_001287983.1 | |
NM_001301057.1 | 664 | Intron | NP_001287986.1 | |||
NM_024028.3 | 664 | Missense Mutation | ACG,ATG | T,M 201 | NP_076933.3 | |
XM_011537680.1 | 664 | Missense Mutation | ACG,ATG | T,M 83 | XP_011535982.1 | |
XM_011537681.1 | 664 | Missense Mutation | ACG,ATG | T,M 83 | XP_011535983.1 | |
XM_011537682.2 | 664 | Intron | XP_011535984.1 |