Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTGTAAATGAAGTTTCAAGATGAG[A/C]TCTCGAATATCTTCCCGTTTGGTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607056 MIM: 612846 | ||||||||||||||||||||
Literature Links: |
IMPG2 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 |
IMPG2 - interphotoreceptor matrix proteoglycan 2 | ||||||
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There are no transcripts associated with this gene. |
SENP7 - SUMO1/sentrin specific peptidase 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077203.2 | 3205 | Missense Mutation | GAG,GAT | E,D 970 | NP_001070671.1 | |
NM_001282801.1 | 3205 | Missense Mutation | GAG,GAT | E,D 969 | NP_001269730.1 | |
NM_001282802.1 | 3205 | Missense Mutation | GAG,GAT | E,D 1002 | NP_001269731.1 | |
NM_001282803.1 | 3205 | Missense Mutation | GAG,GAT | E,D 871 | NP_001269732.1 | |
NM_001282804.1 | 3205 | Intron | NP_001269733.1 | |||
NM_020654.4 | 3205 | Missense Mutation | GAG,GAT | E,D 1035 | NP_065705.3 | |
XM_005247662.4 | 3205 | Missense Mutation | GAG,GAT | E,D 904 | XP_005247719.1 | |
XM_011513038.2 | 3205 | Missense Mutation | GAG,GAT | E,D 1036 | XP_011511340.1 | |
XM_011513039.2 | 3205 | Missense Mutation | GAG,GAT | E,D 1003 | XP_011511341.1 | |
XM_011513040.2 | 3205 | Missense Mutation | GAG,GAT | E,D 971 | XP_011511342.1 | |
XM_011513041.2 | 3205 | Missense Mutation | GAG,GAT | E,D 970 | XP_011511343.1 | |
XM_011513042.2 | 3205 | Missense Mutation | GAG,GAT | E,D 905 | XP_011511344.1 | |
XM_011513045.2 | 3205 | Intron | XP_011511347.1 | |||
XM_017006924.1 | 3205 | Missense Mutation | GAG,GAT | E,D 1003 | XP_016862413.1 | |
XM_017006925.1 | 3205 | Missense Mutation | GAG,GAT | E,D 1002 | XP_016862414.1 | |
XM_017006926.1 | 3205 | Missense Mutation | GAG,GAT | E,D 937 | XP_016862415.1 | |
XM_017006927.1 | 3205 | Missense Mutation | GAG,GAT | E,D 936 | XP_016862416.1 | |
XM_017006928.1 | 3205 | Intron | XP_016862417.1 | |||
XM_017006929.1 | 3205 | Intron | XP_016862418.1 |