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CTTGATGCGGTGGGAGCGGCGCGTC[C/A]CAGCCGGCTTCAGGGAGCTGGTCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM172A PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
FAM172A - family with sequence similarity 172 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001163417.1 | 1019 | Missense Mutation | GGG,GTG | G,V 358 | NP_001156889.1 | |
NM_001163418.1 | 1019 | Missense Mutation | GGG,GTG | G,V 294 | NP_001156890.1 | |
NM_032042.5 | 1019 | Missense Mutation | GGG,GTG | G,V 404 | NP_114431.2 | |
XM_005272103.3 | 1019 | Intron | XP_005272160.1 | |||
XM_005272105.3 | 1019 | Missense Mutation | GGG,GTG | G,V 340 | XP_005272162.1 | |
XM_005272106.3 | 1019 | Missense Mutation | GGG,GTG | G,V 331 | XP_005272163.1 | |
XM_005272108.3 | 1019 | Missense Mutation | GGG,GTG | G,V 321 | XP_005272165.1 | |
XM_005272109.4 | 1019 | Intron | XP_005272166.1 | |||
XM_005272110.3 | 1019 | Missense Mutation | GGG,GTG | G,V 285 | XP_005272167.1 | |
XM_005272111.4 | 1019 | Intron | XP_005272168.1 | |||
XM_006714717.3 | 1019 | Missense Mutation | GGG,GTG | G,V 404 | XP_006714780.1 | |
XM_006714718.3 | 1019 | Missense Mutation | GGG,GTG | G,V 321 | XP_006714781.1 | |
XM_006714719.3 | 1019 | Missense Mutation | GGG,GTG | G,V 321 | XP_006714782.1 | |
XM_011543668.2 | 1019 | Intron | XP_011541970.1 | |||
XM_011543670.2 | 1019 | Intron | XP_011541972.1 | |||
XM_011543671.2 | 1019 | Intron | XP_011541973.1 | |||
XM_011543672.2 | 1019 | Missense Mutation | GGG,GTG | G,V 358 | XP_011541974.1 | |
XM_011543673.2 | 1019 | Missense Mutation | GGG,GTG | G,V 321 | XP_011541975.1 | |
XM_011543674.2 | 1019 | Intron | XP_011541976.1 | |||
XM_017009952.1 | 1019 | Missense Mutation | GGG,GTG | G,V 382 | XP_016865441.1 | |
XM_017009953.1 | 1019 | Missense Mutation | GGG,GTG | G,V 382 | XP_016865442.1 | |
XM_017009954.1 | 1019 | Intron | XP_016865443.1 | |||
XM_017009955.1 | 1019 | Missense Mutation | GGG,GTG | G,V 358 | XP_016865444.1 | |
XM_017009956.1 | 1019 | Missense Mutation | GGG,GTG | G,V 358 | XP_016865445.1 | |
XM_017009957.1 | 1019 | Missense Mutation | GGG,GTG | G,V 321 | XP_016865446.1 | |
XM_017009958.1 | 1019 | Missense Mutation | GGG,GTG | G,V 321 | XP_016865447.1 | |
XM_017009959.1 | 1019 | Intron | XP_016865448.1 | |||
XM_017009960.1 | 1019 | Missense Mutation | GGG,GTG | G,V 257 | XP_016865449.1 | |
XM_017009961.1 | 1019 | Intron | XP_016865450.1 | |||
XM_017009962.1 | 1019 | Intron | XP_016865451.1 |
MIR2277 - microRNA 2277 | ||||||
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There are no transcripts associated with this gene. |