Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGGCTCCAGGAAAGACCAGCCACC[C/T]TGTTCGAAGAAGCCCTCAGGGTCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 605446 MIM: 605012 | ||||||||||||||||||||
Literature Links: |
RPGRIP1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
RPGRIP1 - retinitis pigmentosa GTPase regulator interacting protein 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
SUPT16H - SPT16 homolog, facilitates chromatin remodeling subunit | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007192.3 | 3096 | Silent Mutation | CAA,CAG | Q,Q 919 | NP_009123.1 | |
XM_011536381.2 | 3096 | Intron | XP_011534683.1 |