Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCTCTGAGAACGGGGCTTTCAGCC[A/G]CAGCACTCCGTGCTCCAGGTCGATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ITFG2 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 |
ITFG2 - integrin alpha FG-GAP repeat containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018463.3 | 798 | Intron | NP_060933.3 | |||
XM_005253707.4 | 798 | Intron | XP_005253764.1 | |||
XM_005253709.4 | 798 | Intron | XP_005253766.1 | |||
XM_017019641.1 | 798 | Intron | XP_016875130.1 |
LOC100507424 - uncharacterized LOC100507424 | ||||||
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There are no transcripts associated with this gene. |
NRIP2 - nuclear receptor interacting protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_031474.2 | 798 | Missense Mutation | CGG,TGG | R,W 262 | NP_113662.1 | |
XM_005253797.3 | 798 | Missense Mutation | CGG,TGG | R,W 262 | XP_005253854.1 | |
XM_005253798.3 | 798 | Intron | XP_005253855.1 | |||
XM_011521031.2 | 798 | Missense Mutation | CGG,TGG | R,W 212 | XP_011519333.1 | |
XM_017020000.1 | 798 | UTR 3 | XP_016875489.1 | |||
XM_017020001.1 | 798 | Intron | XP_016875490.1 |