Product Details

SNP ID
rs147699386
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:110665376 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCCTGAAAACTTCAACATATATCT[C/T]CTGAGAATGAAGACCGTTTCATATA
Phenotype
MIM: 605977
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
IMMP2L PubMed Links

Gene Details

Gene
IMMP2L
Gene Name
inner mitochondrial membrane peptidase subunit 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001244606.1 Intron NP_001231535.1
NM_032549.3 Intron NP_115938.1
XM_005250630.3 Intron XP_005250687.1
XM_011516605.2 Intron XP_011514907.1
XM_011516608.2 Intron XP_011514910.1
XM_011516609.2 Intron XP_011514911.1
XM_011516611.2 Intron XP_011514913.1
XM_011516613.2 Intron XP_011514915.1
XM_017012699.1 Intron XP_016868188.1
XM_017012700.1 Intron XP_016868189.1
XM_017012701.1 Intron XP_016868190.1
XM_017012702.1 Intron XP_016868191.1
XM_017012703.1 Intron XP_016868192.1
XM_017012704.1 Intron XP_016868193.1
XM_017012705.1 Intron XP_016868194.1

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