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Search Thermo Fisher Scientific
TTCTGGATAAATACCCCAGGAATGA[A/T]TACCTAGAAAATCAAAGACACAAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
TMEM161B 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 |
TMEM161B - transmembrane protein 161B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289007.1 | 1296 | Missense Mutation | AAT,ATT | N,I 397 | NP_001275936.1 | |
NM_001289008.1 | 1296 | Missense Mutation | AAT,ATT | N,I 386 | NP_001275937.1 | |
NM_153354.4 | 1296 | Intron | NP_699185.1 | |||
XM_006714553.1 | 1296 | Intron | XP_006714616.1 | |||
XM_006714554.3 | 1296 | Intron | XP_006714617.1 | |||
XM_006714555.3 | 1296 | Intron | XP_006714618.1 | |||
XM_006714556.3 | 1296 | Missense Mutation | AAT,ATT | N,I 270 | XP_006714619.2 | |
XM_011543201.2 | 1296 | Intron | XP_011541503.1 | |||
XM_011543202.2 | 1296 | Missense Mutation | AAT,ATT | N,I 270 | XP_011541504.2 | |
XM_011543203.2 | 1296 | Missense Mutation | AAT,ATT | N,I 252 | XP_011541505.2 | |
XM_011543204.2 | 1296 | Missense Mutation | AAT,ATT | N,I 215 | XP_011541506.2 | |
XM_017009093.1 | 1296 | Missense Mutation | AAT,ATT | N,I 397 | XP_016864582.1 | |
XM_017009094.1 | 1296 | Missense Mutation | AAT,ATT | N,I 386 | XP_016864583.1 | |
XM_017009095.1 | 1296 | Missense Mutation | AAT,ATT | N,I 397 | XP_016864584.1 | |
XM_017009096.1 | 1296 | Missense Mutation | AAT,ATT | N,I 270 | XP_016864585.1 | |
XM_017009097.1 | 1296 | Missense Mutation | AAT,ATT | N,I 270 | XP_016864586.1 | |
XM_017009098.1 | 1296 | Missense Mutation | AAT,ATT | N,I 270 | XP_016864587.1 | |
XM_017009099.1 | 1296 | Missense Mutation | AAT,ATT | N,I 270 | XP_016864588.1 | |
XM_017009100.1 | 1296 | Missense Mutation | ATC,TTC | I,F 354 | XP_016864589.1 | |
XM_017009101.1 | 1296 | Missense Mutation | AAT,ATT | N,I 215 | XP_016864590.1 | |
XM_017009102.1 | 1296 | Missense Mutation | AAT,ATT | N,I 215 | XP_016864591.1 | |
XM_017009103.1 | 1296 | Intron | XP_016864592.1 | |||
XM_017009104.1 | 1296 | Missense Mutation | AAT,ATT | N,I 118 | XP_016864593.1 | |
XM_017009105.1 | 1296 | Intron | XP_016864594.1 | |||
XM_017009106.1 | 1296 | Intron | XP_016864595.1 | |||
XM_017009107.1 | 1296 | Intron | XP_016864596.1 | |||
XM_017009108.1 | 1296 | Intron | XP_016864597.1 | |||
XM_017009109.1 | 1296 | Missense Mutation | ATC,TTC | I,F 238 | XP_016864598.1 | |
XM_017009110.1 | 1296 | Missense Mutation | ATC,TTC | I,F 238 | XP_016864599.1 |