Product Details

SNP ID

rs200132653

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:227330691 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGGCAGAAATTAGTCGAATTCAGT[A/G]CGAAATGGAATATACTGAAGGCATT

Phenotype

MIM: 614785

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LOC654841 PubMed Links

Gene Details

Gene

LOC654841

Gene Name

uncharacterized LOC654841

There are no transcripts associated with this gene.

Gene

MFF

Gene Name

mitochondrial fission factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001277061.1	617	Intron			NP_001263990.1
NM_001277062.1	617	Intron			NP_001263991.1
NM_001277063.1	617	Intron			NP_001263992.1
NM_001277064.1	617	Intron			NP_001263993.1
NM_001277065.1	617	Intron			NP_001263994.1
NM_001277066.1	617	Intron			NP_001263995.1
NM_001277067.1	617	Intron			NP_001263996.1
NM_001277068.1	617	Intron			NP_001263997.1
NM_020194.5	617	Intron			NP_064579.3
XM_005246681.3	617	Intron			XP_005246738.1
XM_005246682.1	617	Intron			XP_005246739.1
XM_005246683.1	617	Intron			XP_005246740.1
XM_005246684.1	617	Intron			XP_005246741.1
XM_005246685.3	617	Intron			XP_005246742.1
XM_005246686.3	617	Intron			XP_005246743.1
XM_005246687.3	617	Intron			XP_005246744.1
XM_005246688.1	617	Intron			XP_005246745.1
XM_006712637.1	617	Intron			XP_006712700.1
XM_006712638.1	617	Intron			XP_006712701.1
XM_006712639.2	617	Intron			XP_006712702.1
XM_011511500.1	617	Intron			XP_011509802.1
XM_011511501.1	617	Intron			XP_011509803.1
XM_017004512.1	617	Missense Mutation	TAC,TGC	Y35C	XP_016860001.1
XM_017004513.1	617	Intron			XP_016860002.1
XM_017004514.1	617	Intron			XP_016860003.1
XM_017004515.1	617	Intron			XP_016860004.1

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