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Search Thermo Fisher Scientific
TTGTTTGGCAAATTCTTTGGCTTCC[A/G]GCGTGTCCCCCAGGCAGGAACGGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612064 MIM: 139390 | ||||||||||||||||||||
Literature Links: |
GIGYF1 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 |
GIGYF1 - GRB10 interacting GYF protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022574.4 | 3636 | Missense Mutation | CCG,CTG | P,L 949 | NP_072096.2 | |
XM_005250532.1 | 3636 | Missense Mutation | CCG,CTG | P,L 949 | XP_005250589.1 | |
XM_011516472.1 | 3636 | Missense Mutation | CCG,CTG | P,L 949 | XP_011514774.1 | |
XM_011516477.1 | 3636 | Missense Mutation | CCG,CTG | P,L 948 | XP_011514779.1 | |
XM_017012526.1 | 3636 | Missense Mutation | CCG,CTG | P,L 949 | XP_016868015.1 | |
XM_017012527.1 | 3636 | Missense Mutation | CCG,CTG | P,L 949 | XP_016868016.1 | |
XM_017012528.1 | 3636 | Missense Mutation | CCG,CTG | P,L 949 | XP_016868017.1 | |
XM_017012529.1 | 3636 | Missense Mutation | CCG,CTG | P,L 949 | XP_016868018.1 | |
XM_017012530.1 | 3636 | Missense Mutation | CCG,CTG | P,L 949 | XP_016868019.1 | |
XM_017012531.1 | 3636 | Missense Mutation | CCG,CTG | P,L 847 | XP_016868020.1 |
GNB2 - G protein subunit beta 2 | ||||||
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There are no transcripts associated with this gene. |