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TTCCCGCTGCCCGCGGGGCCCATGA[C/T]CAGCTGCGCATACCGAGGCATGTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM216A 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 |
FAM216A - family with sequence similarity 216 member A | ||||||
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There are no transcripts associated with this gene. |
GPN3 - GPN-loop GTPase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164372.1 | 558 | Intron | NP_001157844.1 | |||
NM_001164373.1 | 558 | Missense Mutation | ATC,GTC | I,V 8 | NP_001157845.1 | |
NM_016301.3 | 558 | Missense Mutation | ATC,GTC | I,V 8 | NP_057385.3 | |
XM_005253896.4 | 558 | Missense Mutation | ATC,GTC | I,V 181 | XP_005253953.3 | |
XM_017019394.1 | 558 | Intron | XP_016874883.1 |