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CCGAAGTTTCTTTCGAATCCTTTTC[C/T]TTTCTTCTCTCATTTCCTGGAGGTG
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 |
---|---|---|
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 |
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 | 4805 | Missense Mutation | AAG,AGG | K,R 636 | NP_001015045.1 | |
NM_001265578.1 | 4805 | Missense Mutation | AAG,AGG | K,R 622 | NP_001252507.1 | |
NM_001265579.1 | 4805 | Missense Mutation | AAG,AGG | K,R 608 | NP_001252508.1 | |
NM_001265580.1 | 4805 | Missense Mutation | AAG,AGG | K,R 608 | NP_001252509.1 | |
NM_014883.3 | 4805 | Missense Mutation | AAG,AGG | K,R 962 | NP_055698.2 | |
XM_005262681.2 | 4805 | Missense Mutation | AAG,AGG | K,R 948 | XP_005262738.1 | |
XM_005262682.2 | 4805 | Missense Mutation | AAG,AGG | K,R 942 | XP_005262739.1 | |
XM_005262683.2 | 4805 | Missense Mutation | AAG,AGG | K,R 934 | XP_005262740.1 | |
XM_005262684.3 | 4805 | Missense Mutation | AAG,AGG | K,R 753 | XP_005262741.1 | |
XM_006714057.3 | 4805 | Missense Mutation | AAG,AGG | K,R 773 | XP_006714120.1 | |
XM_011531516.1 | 4805 | Missense Mutation | AAG,AGG | K,R 962 | XP_011529818.1 | |
XM_011531517.1 | 4805 | Missense Mutation | AAG,AGG | K,R 934 | XP_011529819.1 | |
XM_011531518.1 | 4805 | Missense Mutation | AAG,AGG | K,R 776 | XP_011529820.1 | |
XM_011531519.2 | 4805 | Missense Mutation | AAG,AGG | K,R 776 | XP_011529821.1 | |
XM_017007624.1 | 4805 | Missense Mutation | AAG,AGG | K,R 920 | XP_016863113.1 | |
XM_017007625.1 | 4805 | Missense Mutation | AAG,AGG | K,R 907 | XP_016863114.1 | |
XM_017007626.1 | 4805 | Missense Mutation | AAG,AGG | K,R 785 | XP_016863115.1 | |
XM_017007627.1 | 4805 | Missense Mutation | AAG,AGG | K,R 753 | XP_016863116.1 | |
XM_017007628.1 | 4805 | Missense Mutation | AAG,AGG | K,R 711 | XP_016863117.1 | |
XM_017007629.1 | 4805 | Missense Mutation | AAG,AGG | K,R 690 | XP_016863118.1 | |
XM_017007630.1 | 4805 | Missense Mutation | AAG,AGG | K,R 690 | XP_016863119.1 | |
XM_017007631.1 | 4805 | Missense Mutation | AAG,AGG | K,R 676 | XP_016863120.1 | |
XM_017007632.1 | 4805 | Missense Mutation | AAG,AGG | K,R 676 | XP_016863121.1 | |
XM_017007633.1 | 4805 | Missense Mutation | AAG,AGG | K,R 641 | XP_016863122.1 | |
XM_017007634.1 | 4805 | Missense Mutation | AAG,AGG | K,R 594 | XP_016863123.1 |
FAM13A-AS1 - FAM13A antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |