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CTGGAGGGCGAGCGTCTGTGCAAGG[C/T]GGGCGACTTCAAGACAGGCGTGGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609491 | ||||||||||||||||||||
Literature Links: |
DKFZP434A062 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 |
DKFZP434A062 - uncharacterized LOC26102 | ||||||
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There are no transcripts associated with this gene. |
GPSM1 - G-protein signaling modulator 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145638.2 | 342 | Missense Mutation | GCG,GTG | A,V 41 | NP_001139110.2 | |
NM_001145639.1 | 342 | Intron | NP_001139111.1 | |||
NM_001200003.1 | 342 | Intron | NP_001186932.1 | |||
NM_015597.5 | 342 | Missense Mutation | GCG,GTG | A,V 41 | NP_056412.5 | |
XM_011518498.2 | 342 | Missense Mutation | GCG,GTG | A,V 73 | XP_011516800.1 | |
XM_017014598.1 | 342 | Missense Mutation | GCG,GTG | A,V 18 | XP_016870087.1 | |
XM_017014599.1 | 342 | Intron | XP_016870088.1 |