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Search Thermo Fisher Scientific
CGCTGCTCCCAGAGTAGGCACCCAG[A/G]CCTGGGAGGATGCCGATACATACTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604206 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CPNE2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
CPNE2 - copine 2 | ||||||
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There are no transcripts associated with this gene. |
FAM192A - family with sequence similarity 192 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024946.2 | 901 | Silent Mutation | GGC,GGT | G,G 214 | NP_079222.1 | |
XM_005256156.4 | 901 | Silent Mutation | GGC,GGT | G,G 260 | XP_005256213.1 | |
XM_005256158.3 | 901 | Silent Mutation | GGC,GGT | G,G 220 | XP_005256215.1 | |
XM_005256160.2 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_005256217.1 | |
XM_005256163.2 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_005256220.1 | |
XM_005256164.3 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_005256221.1 | |
XM_005256165.2 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_005256222.1 | |
XM_006721275.3 | 901 | Silent Mutation | GGC,GGT | G,G 240 | XP_006721338.2 | |
XM_011523343.2 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_011521645.1 | |
XM_017023681.1 | 901 | Silent Mutation | GGC,GGT | G,G 220 | XP_016879170.1 | |
XM_017023682.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879171.1 | |
XM_017023683.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879172.1 | |
XM_017023684.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879173.1 | |
XM_017023685.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879174.1 | |
XM_017023686.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879175.1 | |
XM_017023687.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879176.1 | |
XM_017023688.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879177.1 | |
XM_017023689.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879178.1 | |
XM_017023690.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879179.1 | |
XM_017023691.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879180.1 | |
XM_017023692.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879181.1 | |
XM_017023693.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879182.1 | |
XM_017023694.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879183.1 | |
XM_017023695.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879184.1 | |
XM_017023696.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879185.1 | |
XM_017023697.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879186.1 | |
XM_017023698.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879187.1 | |
XM_017023699.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879188.1 | |
XM_017023700.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879189.1 | |
XM_017023701.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879190.1 | |
XM_017023702.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879191.1 | |
XM_017023703.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879192.1 | |
XM_017023704.1 | 901 | Silent Mutation | GGC,GGT | G,G 214 | XP_016879193.1 |