Product Details

SNP ID
rs143060842
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:49632604 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTCTTTCTTCGGCAGACGGCTCC[A/G]GGTGCGGACACCGCCAGCTGTGAGT
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_001031698.2 300 Silent Mutation CCA,CCG P101P NP_001026868.2
NM_012272.2 300 Silent Mutation CCA,CCG P73P NP_036404.1
XM_006719324.3 300 Intron XP_006719387.1
XM_006719325.3 300 Intron XP_006719388.1
XM_011538135.2 300 Intron XP_011536437.1
XM_011538136.2 300 Intron XP_011536438.1
XM_011538137.2 300 Intron XP_011536439.1
XM_011538138.2 300 Intron XP_011536440.1
XM_011538139.2 300 Silent Mutation CCA,CCG P101P XP_011536441.1
XM_011538140.2 300 Silent Mutation CCA,CCG P101P XP_011536442.1
XM_011538141.1 300 Silent Mutation CCA,CCG P79P XP_011536443.1
XM_011538143.2 300 Silent Mutation CCA,CCG P74P XP_011536445.1
XM_011538144.2 300 Silent Mutation CCA,CCG P79P XP_011536446.1
XM_017019135.1 300 Silent Mutation CCA,CCG P73P XP_016874624.1
XM_017019136.1 300 Silent Mutation CCA,CCG P79P XP_016874625.1
XM_017019137.1 300 Silent Mutation CCA,CCG P79P XP_016874626.1
XM_017019138.1 300 Intron XP_016874627.1
XM_017019139.1 300 Intron XP_016874628.1

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