Product Details
- SNP ID
-
rs11582369
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
23
- Location
-
Chr.1:228212098 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGCAGGTGGACGCGGAGGCCGCGTG[C/T]GCCGAGCAGGCGCCGCACTTCCTGC
- Phenotype
-
MIM: 608616
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
C1orf145
PubMed Links
Gene Details
- Gene
- C1orf145
- Gene Name
- chromosome 1 open reading frame 145
There are no transcripts associated with this gene.
- Gene
- OBSCN
- Gene Name
- obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001098623.2 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
NP_001092093.2 |
NM_001271223.2 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
NP_001258152.2 |
NM_052843.3 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
NP_443075.3 |
XM_005273287.4 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_005273344.1 |
XM_005273291.4 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_005273348.1 |
XM_005273298.4 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_005273355.1 |
XM_005273307.4 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_005273364.1 |
XM_006711822.3 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_006711885.1 |
XM_006711823.3 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_006711886.1 |
XM_006711827.3 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_006711890.1 |
XM_006711829.3 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_006711892.1 |
XM_011544297.2 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_011542599.1 |
XM_011544299.2 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_011542601.1 |
XM_017002443.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857932.1 |
XM_017002444.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857933.1 |
XM_017002445.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857934.1 |
XM_017002446.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857935.1 |
XM_017002447.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857936.1 |
XM_017002448.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857937.1 |
XM_017002449.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857938.1 |
XM_017002450.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857939.1 |
XM_017002451.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857940.1 |
XM_017002452.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857941.1 |
XM_017002453.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857942.1 |
XM_017002454.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857943.1 |
XM_017002455.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857944.1 |
XM_017002456.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857945.1 |
XM_017002457.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857946.1 |
XM_017002458.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857947.1 |
XM_017002459.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857948.1 |
XM_017002460.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857949.1 |
XM_017002461.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857950.1 |
XM_017002462.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857951.1 |
XM_017002463.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857952.1 |
XM_017002464.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857953.1 |
XM_017002465.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857954.1 |
XM_017002466.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857955.1 |
XM_017002467.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857956.1 |
XM_017002468.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857957.1 |
XM_017002469.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857958.1 |
XM_017002470.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857959.1 |
XM_017002471.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857960.1 |
XM_017002472.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857961.1 |
XM_017002473.1 |
468 |
Silent Mutation |
TGC,TGT |
C105C |
XP_016857962.1 |
View Full Product Details