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CTTCCCCGACCAGGGTCTCCAGAGC[A/G]ACCTGCCCCTCACGCCAGAGCAGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602243 MIM: 614177 MIM: 609059 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CD151 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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CD151 - CD151 molecule (Raph blood group) | ||||||
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There are no transcripts associated with this gene. |
CRACR2B - calcium release activated channel regulator 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286606.1 | 1228 | Missense Mutation | AAC,GAC | N,D 60 | NP_001273535.1 | |
NM_173584.4 | 1228 | Missense Mutation | AAC,GAC | N,D 60 | NP_775855.3 | |
XM_011520011.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_011518313.1 | |
XM_011520019.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_011518321.1 | |
XM_017017581.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873070.1 | |
XM_017017582.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873071.1 | |
XM_017017583.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873072.1 | |
XM_017017584.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873073.1 | |
XM_017017585.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873074.1 | |
XM_017017586.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873075.1 | |
XM_017017587.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873076.1 | |
XM_017017588.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873077.1 | |
XM_017017589.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873078.1 | |
XM_017017590.1 | 1228 | Missense Mutation | AAC,GAC | N,D 60 | XP_016873079.1 | |
XM_017017591.1 | 1228 | Missense Mutation | AAC,GAC | N,D 60 | XP_016873080.1 | |
XM_017017592.1 | 1228 | Missense Mutation | AAC,GAC | N,D 60 | XP_016873081.1 | |
XM_017017593.1 | 1228 | Missense Mutation | AAC,GAC | N,D 60 | XP_016873082.1 | |
XM_017017594.1 | 1228 | Missense Mutation | AAC,GAC | N,D 60 | XP_016873083.1 | |
XM_017017595.1 | 1228 | Missense Mutation | AAC,GAC | N,D 60 | XP_016873084.1 | |
XM_017017596.1 | 1228 | Missense Mutation | AAC,GAC | N,D 60 | XP_016873085.1 | |
XM_017017597.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873086.1 | |
XM_017017598.1 | 1228 | Silent Mutation | GCA,GCG | A,A 50 | XP_016873087.1 | |
XM_017017599.1 | 1228 | Missense Mutation | AAC,GAC | N,D 60 | XP_016873088.1 |
PNPLA2 - patatin like phospholipase domain containing 2 | ||||||
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There are no transcripts associated with this gene. |