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GGACTTGGAATCAGTGTCTCTCTTG[C/T]TGATGAGCACCTCCAGGAGCCTCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613299 MIM: 613300 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM13A 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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FAM13A - family with sequence similarity 13 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001015045.2 | 4961 | Missense Mutation | AAC,AGC | N,S 688 | NP_001015045.1 | |
NM_001265578.1 | 4961 | Missense Mutation | AAC,AGC | N,S 674 | NP_001252507.1 | |
NM_001265579.1 | 4961 | Missense Mutation | AAC,AGC | N,S 660 | NP_001252508.1 | |
NM_001265580.1 | 4961 | Missense Mutation | AAC,AGC | N,S 660 | NP_001252509.1 | |
NM_014883.3 | 4961 | Missense Mutation | AAC,AGC | N,S 1014 | NP_055698.2 | |
XM_005262681.2 | 4961 | Missense Mutation | AAC,AGC | N,S 1000 | XP_005262738.1 | |
XM_005262682.2 | 4961 | Missense Mutation | AAC,AGC | N,S 994 | XP_005262739.1 | |
XM_005262683.2 | 4961 | Missense Mutation | AAC,AGC | N,S 986 | XP_005262740.1 | |
XM_005262684.3 | 4961 | Missense Mutation | AAC,AGC | N,S 805 | XP_005262741.1 | |
XM_006714057.3 | 4961 | Missense Mutation | AAC,AGC | N,S 825 | XP_006714120.1 | |
XM_011531516.1 | 4961 | Missense Mutation | AAC,AGC | N,S 1014 | XP_011529818.1 | |
XM_011531517.1 | 4961 | Missense Mutation | AAC,AGC | N,S 986 | XP_011529819.1 | |
XM_011531518.1 | 4961 | Missense Mutation | AAC,AGC | N,S 828 | XP_011529820.1 | |
XM_011531519.2 | 4961 | Missense Mutation | AAC,AGC | N,S 828 | XP_011529821.1 | |
XM_017007624.1 | 4961 | Missense Mutation | AAC,AGC | N,S 972 | XP_016863113.1 | |
XM_017007625.1 | 4961 | Missense Mutation | AAC,AGC | N,S 959 | XP_016863114.1 | |
XM_017007626.1 | 4961 | Missense Mutation | AAC,AGC | N,S 837 | XP_016863115.1 | |
XM_017007627.1 | 4961 | Missense Mutation | AAC,AGC | N,S 805 | XP_016863116.1 | |
XM_017007628.1 | 4961 | Missense Mutation | AAC,AGC | N,S 763 | XP_016863117.1 | |
XM_017007629.1 | 4961 | Missense Mutation | AAC,AGC | N,S 742 | XP_016863118.1 | |
XM_017007630.1 | 4961 | Missense Mutation | AAC,AGC | N,S 742 | XP_016863119.1 | |
XM_017007631.1 | 4961 | Missense Mutation | AAC,AGC | N,S 728 | XP_016863120.1 | |
XM_017007632.1 | 4961 | Missense Mutation | AAC,AGC | N,S 728 | XP_016863121.1 | |
XM_017007633.1 | 4961 | Missense Mutation | AAC,AGC | N,S 693 | XP_016863122.1 | |
XM_017007634.1 | 4961 | Missense Mutation | AAC,AGC | N,S 646 | XP_016863123.1 |
FAM13A-AS1 - FAM13A antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |