Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTGCTCTCCCACTGCAGGCCTCTT[C/T]GGCACAGGAATTCGGTCCTACTTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605828 MIM: 605829 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TMC6 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
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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
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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TMC6 - transmembrane channel like 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127198.2 | 2170 | Intron | NP_001120670.1 | |||
NM_001321185.1 | 2170 | Intron | NP_001308114.1 | |||
NM_007267.7 | 2170 | UTR 5 | NP_009198.4 | |||
XM_005256995.1 | 2170 | Intron | XP_005257052.1 | |||
XM_011524255.1 | 2170 | Intron | XP_011522557.1 | |||
XM_011524256.1 | 2170 | Intron | XP_011522558.1 | |||
XM_011524257.2 | 2170 | Intron | XP_011522559.1 | |||
XM_011524258.1 | 2170 | Intron | XP_011522560.1 | |||
XM_017024107.1 | 2170 | Intron | XP_016879596.1 | |||
XM_017024108.1 | 2170 | Intron | XP_016879597.1 | |||
XM_017024109.1 | 2170 | Intron | XP_016879598.1 |
TMC8 - transmembrane channel like 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152468.4 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | NP_689681.2 | |
XM_011524402.2 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_011522704.1 | |
XM_011524403.2 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_011522705.1 | |
XM_011524404.2 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_011522706.1 | |
XM_011524406.2 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_011522708.1 | |
XM_011524409.2 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_011522711.1 | |
XM_011524410.2 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_011522712.1 | |
XM_011524411.2 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_011522713.1 | |
XM_017024238.1 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_016879727.1 | |
XM_017024239.1 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_016879728.1 | |
XM_017024240.1 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_016879729.1 | |
XM_017024241.1 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_016879730.1 | |
XM_017024242.1 | 2170 | Intron | XP_016879731.1 | |||
XM_017024243.1 | 2170 | Intron | XP_016879732.1 | |||
XM_017024244.1 | 2170 | Silent Mutation | TTC,TTT | F,F 102 | XP_016879733.1 |