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Search Thermo Fisher Scientific
AGGAGTTTCCCGGTCTTCAGCCCGC[C/T]GGGGCCCCCACGGAAGCCCCCCGCG
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 |
---|---|---|
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 |
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 | 261 | Missense Mutation | CCG,CTG | P,L 47 | NP_001180451.1 | |
NM_001193523.1 | 261 | Missense Mutation | CCG,CTG | P,L 63 | NP_001180452.1 | |
NM_001193524.1 | 261 | Missense Mutation | CCG,CTG | P,L 57 | NP_001180453.1 | |
NM_024519.3 | 261 | Missense Mutation | CCG,CTG | P,L 43 | NP_078795.2 | |
XM_011523321.1 | 261 | Missense Mutation | CCG,CTG | P,L 63 | XP_011521623.1 | |
XM_011523322.1 | 261 | Missense Mutation | CCG,CTG | P,L 63 | XP_011521624.1 | |
XM_011523324.2 | 261 | Missense Mutation | CCG,CTG | P,L 57 | XP_011521626.1 | |
XM_011523325.1 | 261 | Missense Mutation | CCG,CTG | P,L 43 | XP_011521627.1 | |
XM_011523326.1 | 261 | Missense Mutation | CCG,CTG | P,L 43 | XP_011521628.1 | |
XM_017023663.1 | 261 | Missense Mutation | CCG,CTG | P,L 63 | XP_016879152.1 | |
XM_017023664.1 | 261 | UTR 5 | XP_016879153.1 |
LOC100505942 - uncharacterized LOC100505942 | ||||||
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There are no transcripts associated with this gene. |