Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAGCGGGGCGCATGCCAGGCGGGG[G/T]TCCTCAGGGCGCCCCAGCCGCCGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 605210 | ||||||||||||||||||||
Literature Links: |
DISC1 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 |
DISC1 - disrupted in schizophrenia 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012957.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001012975.1 | |
NM_001012958.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001012976.1 | |
NM_001012959.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001012977.1 | |
NM_001164537.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158009.1 | |
NM_001164538.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158010.1 | |
NM_001164539.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158011.1 | |
NM_001164540.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158012.1 | |
NM_001164541.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158013.1 | |
NM_001164542.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158014.1 | |
NM_001164544.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158016.1 | |
NM_001164545.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158017.1 | |
NM_001164546.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158018.1 | |
NM_001164547.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158019.1 | |
NM_001164548.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158020.1 | |
NM_001164549.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158021.1 | |
NM_001164550.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158022.1 | |
NM_001164551.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158023.1 | |
NM_001164552.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158024.1 | |
NM_001164553.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158025.1 | |
NM_001164554.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158026.1 | |
NM_001164555.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158027.1 | |
NM_001164556.1 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_001158028.1 | |
NM_018662.2 | 67 | Missense Mutation | GGT,GTT | G,V 5 | NP_061132.2 |
TSNAX-DISC1 - TSNAX-DISC1 readthrough (NMD candidate) | ||||||
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There are no transcripts associated with this gene. |