Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGACCAAGGCTGCCGCCTCCAGGC[C/T]GGCCTCCAGGAAGTAGGGCAGGTAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 114019 | ||||||||||||||||||||
Literature Links: |
CDH15 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 |
CDH15 - cadherin 15 | ||||||
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There are no transcripts associated with this gene. |
SLC22A31 - solute carrier family 22 member 31 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242757.1 | 2475 | Missense Mutation | AGC,GGC | S,G 158 | NP_001229686.1 | |
XM_011522897.2 | 2475 | Missense Mutation | AGC,GGC | S,G 158 | XP_011521199.1 | |
XM_011522899.2 | 2475 | Missense Mutation | AGC,GGC | S,G 158 | XP_011521201.1 | |
XM_017022962.1 | 2475 | Missense Mutation | AGC,GGC | S,G 191 | XP_016878451.1 | |
XM_017022963.1 | 2475 | Missense Mutation | AGC,GGC | S,G 165 | XP_016878452.1 | |
XM_017022964.1 | 2475 | Missense Mutation | AGC,GGC | S,G 165 | XP_016878453.1 | |
XM_017022965.1 | 2475 | Missense Mutation | AGC,GGC | S,G 165 | XP_016878454.1 | |
XM_017022966.1 | 2475 | Missense Mutation | AGC,GGC | S,G 165 | XP_016878455.1 |
ZNF778 - zinc finger protein 778 | ||||||
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There are no transcripts associated with this gene. |