Product Details
- SNP ID
-
rs200032264
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:49633022 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCCCCCCCCCCACCCAGAGGGCCCT[A/G]TGGAGTGAGCATGTGGCCCCAGATG
- Phenotype
-
MIM: 616288
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FMNL3
PubMed Links
Gene Details
- Gene
- FMNL3
- Gene Name
- formin like 3
There are no transcripts associated with this gene.
- Gene
- PRPF40B
- Gene Name
- pre-mRNA processing factor 40 homolog B
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001031698.2 |
1588 |
Silent Mutation |
CTA,CTG |
L119L |
NP_001026868.2 |
| NM_012272.2 |
1588 |
Silent Mutation |
CTA,CTG |
L91L |
NP_036404.1 |
| XM_006719324.3 |
1588 |
Silent Mutation |
CTA,CTG |
L181L |
XP_006719387.1 |
| XM_006719325.3 |
1588 |
Silent Mutation |
CTA,CTG |
L181L |
XP_006719388.1 |
| XM_011538135.2 |
1588 |
Silent Mutation |
CTA,CTG |
L181L |
XP_011536437.1 |
| XM_011538136.2 |
1588 |
Silent Mutation |
CTA,CTG |
L181L |
XP_011536438.1 |
| XM_011538137.2 |
1588 |
Silent Mutation |
CTA,CTG |
L154L |
XP_011536439.1 |
| XM_011538138.2 |
1588 |
Intron |
|
|
XP_011536440.1 |
| XM_011538139.2 |
1588 |
Silent Mutation |
CTA,CTG |
L119L |
XP_011536441.1 |
| XM_011538140.2 |
1588 |
Silent Mutation |
CTA,CTG |
L119L |
XP_011536442.1 |
| XM_011538141.1 |
1588 |
Silent Mutation |
CTA,CTG |
L97L |
XP_011536443.1 |
| XM_011538143.2 |
1588 |
Silent Mutation |
CTA,CTG |
L92L |
XP_011536445.1 |
| XM_011538144.2 |
1588 |
Intron |
|
|
XP_011536446.1 |
| XM_017019135.1 |
1588 |
Silent Mutation |
CTA,CTG |
L91L |
XP_016874624.1 |
| XM_017019136.1 |
1588 |
Intron |
|
|
XP_016874625.1 |
| XM_017019137.1 |
1588 |
Intron |
|
|
XP_016874626.1 |
| XM_017019138.1 |
1588 |
Silent Mutation |
CTA,CTG |
L181L |
XP_016874627.1 |
| XM_017019139.1 |
1588 |
UTR 5 |
|
|
XP_016874628.1 |
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