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GGTCTCTTGCCAACGGGTTGTGGTG[A/G]GGGCTGCTGCTGTGGGTGCCCCAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 612163 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TPCN2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
TPCN2 - two pore segment channel 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_139075.3 | Intron | NP_620714.2 | ||||
XM_005273824.3 | Intron | XP_005273881.1 | ||||
XM_005273826.3 | Intron | XP_005273883.1 | ||||
XM_005273830.3 | Intron | XP_005273887.1 | ||||
XM_005273831.3 | Intron | XP_005273888.1 | ||||
XM_005273832.3 | Intron | XP_005273889.1 | ||||
XM_011544802.2 | Intron | XP_011543104.1 | ||||
XM_011544805.1 | Intron | XP_011543107.1 | ||||
XM_011544806.1 | Intron | XP_011543108.1 | ||||
XM_011544807.2 | Intron | XP_011543109.1 | ||||
XM_011544808.2 | Intron | XP_011543110.1 | ||||
XM_017017328.1 | Intron | XP_016872817.1 | ||||
XM_017017329.1 | Intron | XP_016872818.1 | ||||
XM_017017330.1 | Intron | XP_016872819.1 | ||||
XM_017017331.1 | Intron | XP_016872820.1 | ||||
XM_017017332.1 | Intron | XP_016872821.1 | ||||
XM_017017333.1 | Intron | XP_016872822.1 | ||||
XM_017017334.1 | Intron | XP_016872823.1 | ||||
XM_017017335.1 | Intron | XP_016872824.1 | ||||
XM_017017336.1 | Intron | XP_016872825.1 |