Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACAGCACTAAGCGGCTTCAGTCACA[C/T]GCTTTTCAGGTGAATCACTCCAAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609841 MIM: 609666 | ||||||||||||||||||||
Literature Links: |
MIR6762 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 |
MIR6762 - microRNA 6762 | ||||||
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There are no transcripts associated with this gene. |
SLC8B1 - solute carrier family 8 member B1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_006719607.2 | 2364 | Missense Mutation | ATG,GTG | M,V 389 | XP_006719670.1 | |
XM_011538749.2 | 2364 | Missense Mutation | ATG,GTG | M,V 584 | XP_011537051.1 | |
XM_011538750.2 | 2364 | Missense Mutation | ATG,GTG | M,V 528 | XP_011537052.1 | |
XM_011538752.2 | 2364 | Missense Mutation | ATG,GTG | M,V 389 | XP_011537054.1 | |
XM_017019978.1 | 2364 | Intron | XP_016875467.1 |
TPCN1 - two pore segment channel 1 | ||||||
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There are no transcripts associated with this gene. |