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TTGGAAAGCCGATGTTCTGGACAGT[C/T]TCCTCATGGACAGGCTGTCCCCTCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608961 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRPM3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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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
|
TRPM3 - transient receptor potential cation channel subfamily M member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007470.1 | 8179 | Intron | NP_001007471.1 | |||
NM_001007471.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1692 | NP_001007472.2 | |
NM_020952.4 | 8179 | Missense Mutation | AAA,AGA | K,R 1539 | NP_066003.3 | |
NM_024971.5 | 8179 | Missense Mutation | AAA,AGA | K,R 1551 | NP_079247.5 | |
NM_206944.3 | 8179 | Missense Mutation | AAA,AGA | K,R 1529 | NP_996827.3 | |
NM_206945.3 | 8179 | Missense Mutation | AAA,AGA | K,R 1541 | NP_996828.3 | |
NM_206946.3 | 8179 | Missense Mutation | AAA,AGA | K,R 1564 | NP_996829.3 | |
NM_206947.3 | 8179 | Missense Mutation | AAA,AGA | K,R 1554 | NP_996830.3 | |
NM_206948.2 | 8179 | Intron | NP_996831.1 | |||
XM_011519035.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1731 | XP_011517337.1 | |
XM_011519036.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1729 | XP_011517338.1 | |
XM_011519037.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1719 | XP_011517339.1 | |
XM_011519038.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1717 | XP_011517340.1 | |
XM_011519039.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1707 | XP_011517341.1 | |
XM_011519040.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1706 | XP_011517342.1 | |
XM_011519041.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1704 | XP_011517343.1 | |
XM_011519042.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1696 | XP_011517344.1 | |
XM_011519043.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1694 | XP_011517345.1 | |
XM_011519044.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1694 | XP_011517346.1 | |
XM_011519045.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1684 | XP_011517347.1 | |
XM_011519046.2 | 8179 | Missense Mutation | AAA,AGA | K,R 1682 | XP_011517348.1 | |
XM_011519047.2 | 8179 | Intron | XP_011517349.1 | |||
XM_017015141.1 | 8179 | Missense Mutation | AAA,AGA | K,R 1721 | XP_016870630.1 | |
XM_017015142.1 | 8179 | Missense Mutation | AAA,AGA | K,R 1719 | XP_016870631.1 | |
XM_017015143.1 | 8179 | Missense Mutation | AAA,AGA | K,R 1709 | XP_016870632.1 | |
XM_017015144.1 | 8179 | Missense Mutation | AAA,AGA | K,R 1576 | XP_016870633.1 | |
XM_017015145.1 | 8179 | Missense Mutation | AAA,AGA | K,R 1576 | XP_016870634.1 | |
XM_017015146.1 | 8179 | Missense Mutation | AAA,AGA | K,R 1576 | XP_016870635.1 | |
XM_017015147.1 | 8179 | Missense Mutation | AAA,AGA | K,R 1576 | XP_016870636.1 | |
XM_017015148.1 | 8179 | Intron | XP_016870637.1 | |||
XM_017015149.1 | 8179 | Intron | XP_016870638.1 | |||
XM_017015150.1 | 8179 | Intron | XP_016870639.1 | |||
XM_017015151.1 | 8179 | Intron | XP_016870640.1 | |||
XM_017015152.1 | 8179 | Intron | XP_016870641.1 | |||
XM_017015153.1 | 8179 | Intron | XP_016870642.1 | |||
XM_017015154.1 | 8179 | Intron | XP_016870643.1 | |||
XM_017015155.1 | 8179 | Intron | XP_016870644.1 | |||
XM_017015156.1 | 8179 | Missense Mutation | AAA,AGA | K,R 1275 | XP_016870645.1 | |
XM_017015157.1 | 8179 | Intron | XP_016870646.1 | |||
XM_017015158.1 | 8179 | Intron | XP_016870647.1 | |||
XM_017015159.1 | 8179 | Intron | XP_016870648.1 | |||
XM_017015160.1 | 8179 | Intron | XP_016870649.1 | |||
XM_017015161.1 | 8179 | Intron | XP_016870650.1 |