Product Details

SNP ID

rs1350896

Assay Type

Functionally tested

NCBI dbSNP Submissions

40

Location

Chr.1:240018896 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAGGGTTCAGGAGATGGATGGTGG[C/T]GATAGTGACACATTATGAATGTATT

Phenotype

MIM: 606373

Polymorphism

C/T, 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		Intron			NP_001292353.1
NM_020066.4		Intron			NP_064450.3
XM_011544237.2		Intron			XP_011542539.1
XM_017001837.1		Intron			XP_016857326.1
XM_017001838.1		Intron			XP_016857327.1
XM_017001839.1		Intron			XP_016857328.1
XM_017001840.1		Intron			XP_016857329.1
XM_017001841.1		Intron			XP_016857330.1
XM_017001842.1		Intron			XP_016857331.1
XM_017001843.1		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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