Product Details
- SNP ID
-
rs34819224
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:144168385 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGTGCCCTGTGCTCCCTCGGGGAGG[C/T]GCGGCCGGTGGAGACGCTCCGTGCC
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
MROH1
PubMed Links
Gene Details
- Gene
- MROH1
- Gene Name
- maestro heat like repeat family member 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001099280.2 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
NP_001092750.1 |
NM_001099281.2 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
NP_001092751.1 |
NM_001288814.1 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
NP_001275743.1 |
NM_032450.2 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
NP_115826.2 |
XM_011517270.2 |
350 |
Missense Mutation |
GCG,GTG |
A131V |
XP_011515572.1 |
XM_011517271.2 |
350 |
Missense Mutation |
GCG,GTG |
A131V |
XP_011515573.1 |
XM_011517272.2 |
350 |
Missense Mutation |
GCG,GTG |
A131V |
XP_011515574.1 |
XM_011517273.2 |
350 |
Missense Mutation |
GCG,GTG |
A131V |
XP_011515575.1 |
XM_011517274.2 |
350 |
Missense Mutation |
GCG,GTG |
A131V |
XP_011515576.1 |
XM_011517275.2 |
350 |
Missense Mutation |
GCG,GTG |
A131V |
XP_011515577.1 |
XM_011517276.2 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
XP_011515578.1 |
XM_011517277.1 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
XP_011515579.1 |
XM_011517278.1 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
XP_011515580.1 |
XM_011517279.2 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
XP_011515581.1 |
XM_011517281.1 |
350 |
UTR 5 |
|
|
XP_011515583.1 |
XM_011517282.1 |
350 |
UTR 5 |
|
|
XP_011515584.1 |
XM_011517283.2 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
XP_011515585.1 |
XM_011517285.1 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
XP_011515587.1 |
XM_011517286.2 |
350 |
Missense Mutation |
GCG,GTG |
A131V |
XP_011515588.1 |
XM_017013802.1 |
350 |
Missense Mutation |
GCG,GTG |
A131V |
XP_016869291.1 |
XM_017013803.1 |
350 |
Missense Mutation |
GCG,GTG |
A131V |
XP_016869292.1 |
XM_017013804.1 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
XP_016869293.1 |
XM_017013805.1 |
350 |
Missense Mutation |
GCG,GTG |
A38V |
XP_016869294.1 |
XM_017013806.1 |
350 |
Intron |
|
|
XP_016869295.1 |
XM_017013807.1 |
350 |
Missense Mutation |
GCG,GTG |
A131V |
XP_016869296.1 |
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