Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACGTAGCCCCCATAGTTAGGTAAA[A/G]GACCCAGGTTCTGAGGGTATGTTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611053 | ||||||||||||||||||||
Literature Links: |
FAM166B 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 |
FAM166B - family with sequence similarity 166 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099951.3 | 781 | Silent Mutation | TCC,TCT | S,S 214 | NP_001093421.1 | |
NM_001164310.2 | 781 | Missense Mutation | CCT,CTT | P,L 237 | NP_001157782.1 | |
NM_001287238.1 | 781 | Missense Mutation | CCT,CTT | P,L 225 | NP_001274167.1 | |
NM_001287239.1 | 781 | Missense Mutation | CTT,TTT | L,F 222 | NP_001274168.1 | |
XM_011518028.2 | 781 | Missense Mutation | CTT,TTT | L,F 217 | XP_011516330.1 |
RUSC2 - RUN and SH3 domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135999.1 | 781 | Intron | NP_001129471.1 | |||
XM_006716896.2 | 781 | Intron | XP_006716959.1 |