Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGGGCCCCCATGTGAGGACTCACCT[C/T]GGGAAGAGCTCCTGTGGTGGGTACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605926 MIM: 610409 | ||||||||||||||||||||
Literature Links: |
BAIAP2L2 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 |
BAIAP2L2 - BAI1 associated protein 2 like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_025045.5 | 1938 | Silent Mutation | CCA,CCG | P,P 504 | NP_079321.3 | |
XM_005261751.4 | 1938 | Silent Mutation | CCA,CCG | P,P 504 | XP_005261808.1 | |
XM_011530379.2 | 1938 | Silent Mutation | CCA,CCG | P,P 490 | XP_011528681.1 | |
XM_011530380.2 | 1938 | Silent Mutation | CCA,CCG | P,P 486 | XP_011528682.1 | |
XM_011530381.2 | 1938 | Silent Mutation | CCA,CCG | P,P 485 | XP_011528683.1 | |
XM_011530382.2 | 1938 | Silent Mutation | CCA,CCG | P,P 485 | XP_011528684.1 | |
XM_011530383.2 | 1938 | Silent Mutation | CCA,CCG | P,P 480 | XP_011528685.1 | |
XM_011530384.2 | 1938 | Silent Mutation | CCA,CCG | P,P 474 | XP_011528686.1 | |
XM_011530386.2 | 1938 | Silent Mutation | CCA,CCG | P,P 309 | XP_011528688.1 | |
XM_011530387.2 | 1938 | Silent Mutation | CCA,CCG | P,P 309 | XP_011528689.1 | |
XM_011530388.2 | 1938 | Silent Mutation | CCA,CCG | P,P 297 | XP_011528690.1 |
PICK1 - protein interacting with PRKCA 1 | ||||||
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There are no transcripts associated with this gene. |
SLC16A8 - solute carrier family 16 member 8 | ||||||
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There are no transcripts associated with this gene. |