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TCCTCATTCCTAAAGTGGGGATATT[A/C]GCTAAGATAGGATTTTTCAACAGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609666 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IQCD PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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IQCD - IQ motif containing D | ||||||
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There are no transcripts associated with this gene. |
TPCN1 - two pore segment channel 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143819.2 | Intron | NP_001137291.1 | ||||
NM_001301214.1 | Intron | NP_001288143.1 | ||||
NM_017901.5 | Intron | NP_060371.2 | ||||
XM_005253906.4 | Intron | XP_005253963.1 | ||||
XM_011538490.2 | Intron | XP_011536792.1 | ||||
XM_011538492.2 | Intron | XP_011536794.1 | ||||
XM_011538493.2 | Intron | XP_011536795.1 | ||||
XM_017019480.1 | Intron | XP_016874969.1 | ||||
XM_017019481.1 | Intron | XP_016874970.1 | ||||
XM_017019482.1 | Intron | XP_016874971.1 |