Product Details

SNP ID
rs115287651
Assay Type
Functionally tested
NCBI dbSNP Submissions
9
Location
Chr.1:240013920 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCCTTCACCTATCTTGCAAAATGG[A/G]CATTATCTTATTCTTCTTGCTATCT
Phenotype
MIM: 606373
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FMN2 PubMed Links

Gene Details

Gene
FMN2
Gene Name
formin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001305424.1 145 Intron NP_001292353.1
NM_020066.4 145 Intron NP_064450.3
XM_011544237.2 145 Intron XP_011542539.1
XM_017001837.1 145 Intron XP_016857326.1
XM_017001838.1 145 Intron XP_016857327.1
XM_017001839.1 145 UTR 5 XP_016857328.1
XM_017001840.1 145 Intron XP_016857329.1
XM_017001841.1 145 Intron XP_016857330.1
XM_017001842.1 145 Intron XP_016857331.1
XM_017001843.1 145 Intron XP_016857332.1
Gene
RPS7P5
Gene Name
ribosomal protein S7 pseudogene 5
There are no transcripts associated with this gene.

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