Product Details
- SNP ID
-
rs146048989
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:197791284 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGAGTGTTGTCGGCTGGGAAATGGC[A/G]GCCGCGGGCTTGGTCGCTGTGGCAG
- Phenotype
-
MIM: 616933
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FYTTD1
PubMed Links
Gene Details
- Gene
- FYTTD1
- Gene Name
- forty-two-three domain containing 1
There are no transcripts associated with this gene.
- Gene
- LRCH3
- Gene Name
- leucine rich repeats and calponin homology domain containing 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_032773.3 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
NP_116162.1 |
XM_005269362.2 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_005269419.1 |
XM_005269363.2 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_005269420.1 |
XM_005269365.2 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_005269422.1 |
XM_005269367.2 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_005269424.1 |
XM_006713791.3 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_006713854.1 |
XM_006713792.3 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_006713855.1 |
XM_006713793.2 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_006713856.1 |
XM_011513242.2 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_011511544.1 |
XM_011513243.2 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_011511545.1 |
XM_017007350.1 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_016862839.1 |
XM_017007351.1 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_016862840.1 |
XM_017007352.1 |
59 |
Silent Mutation |
GCA,GCG |
A2A |
XP_016862841.1 |
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