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Search Thermo Fisher Scientific
CCTCTCCCCCAGCAAGTCAAGTCCA[C/T]TGAACGCTTCCTGCGACGACTGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM65A 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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FAM65A - family with sequence similarity 65 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193522.1 | 507 | Missense Mutation | ACT,ATT | T,I 129 | NP_001180451.1 | |
NM_001193523.1 | 507 | Missense Mutation | ACT,ATT | T,I 145 | NP_001180452.1 | |
NM_001193524.1 | 507 | Missense Mutation | ACT,ATT | T,I 139 | NP_001180453.1 | |
NM_024519.3 | 507 | Missense Mutation | ACT,ATT | T,I 125 | NP_078795.2 | |
XM_011523321.1 | 507 | Missense Mutation | ACT,ATT | T,I 145 | XP_011521623.1 | |
XM_011523322.1 | 507 | Missense Mutation | ACT,ATT | T,I 145 | XP_011521624.1 | |
XM_011523324.2 | 507 | Missense Mutation | ACT,ATT | T,I 139 | XP_011521626.1 | |
XM_011523325.1 | 507 | Missense Mutation | ACT,ATT | T,I 125 | XP_011521627.1 | |
XM_011523326.1 | 507 | Missense Mutation | ACT,ATT | T,I 125 | XP_011521628.1 | |
XM_017023663.1 | 507 | Missense Mutation | ACT,ATT | T,I 145 | XP_016879152.1 | |
XM_017023664.1 | 507 | UTR 5 | XP_016879153.1 |