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CCCACACAGGATGTTCCGCTGGGAG[C/T]GCTCCATTCCCCTGCGAGGCTCGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602288 | ||||||||||||||||||||
Literature Links: |
C2orf81 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 |
C2orf81 - chromosome 2 open reading frame 81 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145054.1 | 89 | Intron | NP_001138526.1 | |||
NM_001316764.1 | 89 | Intron | NP_001303693.1 | |||
NM_001316765.1 | 89 | Intron | NP_001303694.1 | |||
NM_001316766.1 | 89 | Intron | NP_001303695.1 |
RTKN - rhotekin | ||||||
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There are no transcripts associated with this gene. |
WDR54 - WD repeat domain 54 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320823.1 | 89 | Missense Mutation | CGC,TGC | R,C 21 | NP_001307752.1 | |
NM_001320824.1 | 89 | Missense Mutation | CGC,TGC | R,C 6 | NP_001307753.1 | |
NM_001320825.1 | 89 | Intron | NP_001307754.1 | |||
NM_032118.3 | 89 | Missense Mutation | CGC,TGC | R,C 6 | NP_115494.1 | |
XM_017005064.1 | 89 | Intron | XP_016860553.1 |