Product Details
- SNP ID
-
rs140611432
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
3
- Location
-
Chr.1:231818360 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ATTTCTGGACGGCTAAAGACCTCAC[C/T]GAGGAGATTAGATCATTAACATCAG
- Phenotype
-
MIM: 605210
MIM: 606271
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
DISC1
PubMed Links
Gene Details
- Gene
- DISC1
- Gene Name
- disrupted in schizophrenia 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001012957.1 |
669 |
Silent Mutation |
ACC,ACT |
T608T |
NP_001012975.1 |
NM_001012958.1 |
669 |
Intron |
|
|
NP_001012976.1 |
NM_001012959.1 |
669 |
Silent Mutation |
ACC,ACT |
T608T |
NP_001012977.1 |
NM_001164537.1 |
669 |
Silent Mutation |
ACC,ACT |
T640T |
NP_001158009.1 |
NM_001164538.1 |
669 |
Silent Mutation |
ACC,ACT |
T608T |
NP_001158010.1 |
NM_001164539.1 |
669 |
Silent Mutation |
ACC,ACT |
T608T |
NP_001158011.1 |
NM_001164540.1 |
669 |
Silent Mutation |
ACC,ACT |
T486T |
NP_001158012.1 |
NM_001164541.1 |
669 |
Silent Mutation |
ACC,ACT |
T608T |
NP_001158013.1 |
NM_001164542.1 |
669 |
Silent Mutation |
ACC,ACT |
T608T |
NP_001158014.1 |
NM_001164544.1 |
669 |
Silent Mutation |
ACC,ACT |
T608T |
NP_001158016.1 |
NM_001164545.1 |
669 |
Missense Mutation |
CCG,CTG |
P574L |
NP_001158017.1 |
NM_001164546.1 |
669 |
Intron |
|
|
NP_001158018.1 |
NM_001164547.1 |
669 |
Intron |
|
|
NP_001158019.1 |
NM_001164548.1 |
669 |
UTR 3 |
|
|
NP_001158020.1 |
NM_001164549.1 |
669 |
Intron |
|
|
NP_001158021.1 |
NM_001164550.1 |
669 |
Intron |
|
|
NP_001158022.1 |
NM_001164551.1 |
669 |
Intron |
|
|
NP_001158023.1 |
NM_001164552.1 |
669 |
Intron |
|
|
NP_001158024.1 |
NM_001164553.1 |
669 |
Intron |
|
|
NP_001158025.1 |
NM_001164554.1 |
669 |
Intron |
|
|
NP_001158026.1 |
NM_001164555.1 |
669 |
Intron |
|
|
NP_001158027.1 |
NM_001164556.1 |
669 |
UTR 3 |
|
|
NP_001158028.1 |
NM_018662.2 |
669 |
Silent Mutation |
ACC,ACT |
T608T |
NP_061132.2 |
- Gene
- DISC2
- Gene Name
- disrupted in schizophrenia 2 (non-protein coding)
There are no transcripts associated with this gene.
- Gene
- TSNAX-DISC1
- Gene Name
- TSNAX-DISC1 readthrough (NMD candidate)
There are no transcripts associated with this gene.
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