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GCTCTCCAGTCTCCTGGTCGCTGGG[C/G]TTGGGGGGCCCAAGGTCCACAGCCT
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 | |||
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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
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FAM129B - family with sequence similarity 129 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001035534.2 | 2170 | Silent Mutation | AAC,AAG | N,K 700 | NP_001030611.1 | |
NM_022833.3 | 2170 | Silent Mutation | AAC,AAG | N,K 713 | NP_073744.2 | |
XM_005252135.2 | 2170 | Missense Mutation | AAC,AAG | N,K 738 | XP_005252192.2 | |
XM_011518925.1 | 2170 | Missense Mutation | AAC,AAG | N,K 743 | XP_011517227.1 |
LRSAM1 - leucine rich repeat and sterile alpha motif containing 1 | ||||||
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There are no transcripts associated with this gene. |