Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCAGGGTCACCAAGGGTCCAGTT[G/T]CAGTCTTTGGAGACCCAGTCTGAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM200A 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 |
FAM200A - family with sequence similarity 200 member A | ||||||
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There are no transcripts associated with this gene. |
ZNF655 - zinc finger protein 655 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001009958.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | NP_001009958.1 | |
NM_001009960.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | NP_001009960.1 | |
NM_001083956.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | NP_001077425.1 | |
NM_001085366.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | NP_001078835.1 | |
NM_001085367.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | NP_001078836.1 | |
NM_001085368.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | NP_001078837.1 | |
NM_024061.3 | 288 | Missense Mutation | TTG,TTT | L,F 17 | NP_076966.1 | |
NM_138494.2 | 288 | Missense Mutation | TTG,TTT | L,F 17 | NP_612503.1 | |
XM_017012598.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868087.1 | |
XM_017012599.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868088.1 | |
XM_017012600.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868089.1 | |
XM_017012601.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868090.1 | |
XM_017012602.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868091.1 | |
XM_017012603.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868092.1 | |
XM_017012604.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868093.1 | |
XM_017012605.1 | 288 | UTR 5 | XP_016868094.1 | |||
XM_017012606.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868095.1 | |
XM_017012607.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868096.1 | |
XM_017012608.1 | 288 | UTR 5 | XP_016868097.1 | |||
XM_017012609.1 | 288 | UTR 5 | XP_016868098.1 | |||
XM_017012610.1 | 288 | UTR 5 | XP_016868099.1 | |||
XM_017012611.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868100.1 | |
XM_017012612.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868101.1 | |
XM_017012613.1 | 288 | Missense Mutation | TTG,TTT | L,F 17 | XP_016868102.1 |