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Search Thermo Fisher Scientific
CTACCTGCCCATCTTTGCGCACCAC[C/T]GCCTCTCACTGGACCTGCTGAGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614045 MIM: 610933 | ||||||||||||||||||||
Literature Links: |
FAM129B 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 |
FAM129B - family with sequence similarity 129 member B | ||||||
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There are no transcripts associated with this gene. |
LRSAM1 - leucine rich repeat and sterile alpha motif containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001005373.3 | 3151 | Missense Mutation | CGC,TGC | R,C 594 | NP_001005373.1 | |
NM_001005374.3 | 3151 | Missense Mutation | CGC,TGC | R,C 594 | NP_001005374.1 | |
NM_001190723.2 | 3151 | Missense Mutation | CGC,TGC | R,C 567 | NP_001177652.1 | |
NM_138361.5 | 3151 | Missense Mutation | CGC,TGC | R,C 594 | NP_612370.3 | |
XM_006717316.3 | 3151 | Missense Mutation | CGC,TGC | R,C 561 | XP_006717379.1 | |
XM_017015283.1 | 3151 | Missense Mutation | CGC,TGC | R,C 594 | XP_016870772.1 | |
XM_017015284.1 | 3151 | Missense Mutation | CGC,TGC | R,C 331 | XP_016870773.1 |