Product Details
- SNP ID
-
rs4406193
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:71887034 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGCAGGCCACGAAAATGTCCTCGG[A/C]CGTGGGGCCCCGCGGTCCTCGCCCA
- Phenotype
-
MIM: 606629
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
RIMS1
PubMed Links
Gene Details
- Gene
- RIMS1
- Gene Name
- regulating synaptic membrane exocytosis 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001168407.1 |
268 |
Intron |
|
|
NP_001161879.1 |
NM_001168408.1 |
268 |
Intron |
|
|
NP_001161880.1 |
NM_001168409.1 |
268 |
Intron |
|
|
NP_001161881.1 |
NM_001168410.1 |
268 |
Intron |
|
|
NP_001161882.1 |
NM_001168411.1 |
268 |
Intron |
|
|
NP_001161883.1 |
NM_014989.5 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
NP_055804.2 |
XM_005248688.3 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_005248745.1 |
XM_011535604.2 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_011533906.2 |
XM_011535611.2 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_011533913.2 |
XM_011535615.2 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_011533917.2 |
XM_017010516.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866005.1 |
XM_017010517.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866006.1 |
XM_017010518.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866007.1 |
XM_017010519.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866008.1 |
XM_017010520.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866009.1 |
XM_017010521.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866010.1 |
XM_017010522.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866011.1 |
XM_017010523.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866012.1 |
XM_017010524.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866013.1 |
XM_017010525.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866014.1 |
XM_017010526.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866015.1 |
XM_017010527.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866016.1 |
XM_017010528.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866017.1 |
XM_017010529.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866018.1 |
XM_017010530.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866019.1 |
XM_017010531.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866020.1 |
XM_017010532.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866021.1 |
XM_017010533.1 |
268 |
Missense Mutation |
GAC,GCC |
D4A |
XP_016866022.1 |
XM_017010534.1 |
268 |
Intron |
|
|
XP_016866023.1 |
XM_017010535.1 |
268 |
Intron |
|
|
XP_016866024.1 |
XM_017010536.1 |
268 |
Intron |
|
|
XP_016866025.1 |
XM_017010537.1 |
268 |
Intron |
|
|
XP_016866026.1 |
XM_017010538.1 |
268 |
Intron |
|
|
XP_016866027.1 |
XM_017010539.1 |
268 |
Intron |
|
|
XP_016866028.1 |
XM_017010540.1 |
268 |
Intron |
|
|
XP_016866029.1 |
XM_017010541.1 |
268 |
Intron |
|
|
XP_016866030.1 |
XM_017010542.1 |
268 |
Intron |
|
|
XP_016866031.1 |
XM_017010543.1 |
268 |
Intron |
|
|
XP_016866032.1 |
XM_017010544.1 |
268 |
Intron |
|
|
XP_016866033.1 |
XM_017010545.1 |
268 |
Intron |
|
|
XP_016866034.1 |
XM_017010546.1 |
268 |
Intron |
|
|
XP_016866035.1 |
XM_017010547.1 |
268 |
Intron |
|
|
XP_016866036.1 |
XM_017010548.1 |
268 |
Intron |
|
|
XP_016866037.1 |
XM_017010549.1 |
268 |
Intron |
|
|
XP_016866038.1 |
XM_017010550.1 |
268 |
Intron |
|
|
XP_016866039.1 |
XM_017010551.1 |
268 |
Intron |
|
|
XP_016866040.1 |
XM_017010552.1 |
268 |
Intron |
|
|
XP_016866041.1 |
XM_017010553.1 |
268 |
Intron |
|
|
XP_016866042.1 |
XM_017010554.1 |
268 |
Intron |
|
|
XP_016866043.1 |
XM_017010555.1 |
268 |
Intron |
|
|
XP_016866044.1 |
XM_017010556.1 |
268 |
Intron |
|
|
XP_016866045.1 |
XM_017010557.1 |
268 |
Intron |
|
|
XP_016866046.1 |
XM_017010558.1 |
268 |
Intron |
|
|
XP_016866047.1 |
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