Product Details
- SNP ID
-
rs111932354
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:176313722 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACTCTGCCTGGGCGAGTCCTTTTCC[C/T]GCGTTATGTCGTTCAGACCCTAGAA
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SIMC1
PubMed Links
Gene Details
- Gene
- SIMC1
- Gene Name
- SUMO interacting motifs containing 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001308195.1 |
1724 |
Missense Mutation |
CCG,CTG |
P589L |
NP_001295124.1 |
NM_001308196.1 |
1724 |
Missense Mutation |
CCG,CTG |
P570L |
NP_001295125.1 |
NM_001308200.1 |
1724 |
Missense Mutation |
CCG,CTG |
P31L |
NP_001295129.1 |
NM_198567.5 |
1724 |
Missense Mutation |
CCG,CTG |
P155L |
NP_940969.3 |
XM_011534553.2 |
1724 |
Missense Mutation |
CCG,CTG |
P593L |
XP_011532855.1 |
XM_011534554.2 |
1724 |
Missense Mutation |
CCG,CTG |
P593L |
XP_011532856.1 |
XM_011534556.2 |
1724 |
Missense Mutation |
CCG,CTG |
P566L |
XP_011532858.1 |
XM_017009454.1 |
1724 |
Missense Mutation |
CCG,CTG |
P570L |
XP_016864943.1 |
XM_017009455.1 |
1724 |
Missense Mutation |
CCG,CTG |
P481L |
XP_016864944.1 |
XM_017009456.1 |
1724 |
Missense Mutation |
CCG,CTG |
P481L |
XP_016864945.1 |
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