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Search Thermo Fisher Scientific
CTTGTTTGCTTATAAGAACTTCAAG[A/G]AGCCTAAGCTTGGCTTTAATTTTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609371 MIM: 604669 | ||||||||||||||||||||
Literature Links: |
FAM13B 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 |
FAM13B - family with sequence similarity 13 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001101800.2 | 2120 | Silent Mutation | CTC,CTT | L,L 873 | NP_001095270.1 | |
NM_001101801.2 | 2120 | Silent Mutation | CTC,CTT | L,L 777 | NP_001095271.1 | |
NM_016603.3 | 2120 | Silent Mutation | CTC,CTT | L,L 901 | NP_057687.2 | |
XM_005272007.1 | 2120 | Silent Mutation | CTC,CTT | L,L 895 | XP_005272064.1 | |
XM_006714647.1 | 2120 | Silent Mutation | CTC,CTT | L,L 923 | XP_006714710.1 | |
XM_006714648.1 | 2120 | Silent Mutation | CTC,CTT | L,L 923 | XP_006714711.1 | |
XM_006714649.1 | 2120 | Silent Mutation | CTC,CTT | L,L 805 | XP_006714712.1 | |
XM_011543448.1 | 2120 | Silent Mutation | CTC,CTT | L,L 923 | XP_011541750.1 | |
XM_011543449.1 | 2120 | Silent Mutation | CTC,CTT | L,L 923 | XP_011541751.1 | |
XM_011543450.1 | 2120 | Silent Mutation | CTC,CTT | L,L 923 | XP_011541752.1 | |
XM_017009549.1 | 2120 | Silent Mutation | CTC,CTT | L,L 901 | XP_016865038.1 | |
XM_017009550.1 | 2120 | Silent Mutation | CTC,CTT | L,L 901 | XP_016865039.1 | |
XM_017009551.1 | 2120 | Silent Mutation | CTC,CTT | L,L 783 | XP_016865040.1 |
PKD2L2 - polycystin 2 like 2, transient receptor potential cation channel | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258448.1 | 2120 | UTR 3 | NP_001245377.1 | |||
NM_001258449.1 | 2120 | UTR 3 | NP_001245378.1 | |||
NM_001300921.1 | 2120 | Intron | NP_001287850.1 | |||
NM_014386.3 | 2120 | UTR 3 | NP_055201.2 | |||
XM_011543318.2 | 2120 | Intron | XP_011541620.1 | |||
XM_011543321.1 | 2120 | Intron | XP_011541623.1 | |||
XM_017009343.1 | 2120 | Intron | XP_016864832.1 | |||
XM_017009344.1 | 2120 | Intron | XP_016864833.1 | |||
XM_017009345.1 | 2120 | Intron | XP_016864834.1 |