Varaico: Literature-Extracted Genetic Variants

Gene:AFG3L2
Variant:p.M666V

AFG3L2

272 papers

RefSeq Summary

This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene ...

Pfam Domains

FtsH_extaa 146–242UCSCFtsH Extracellular
AAAaa 344–477UCSCATPase family associated with various cellular activities (AAA)
AAA_lid_3aa 505–547UCSCAAA+ lid domain
Peptidase_M41aa 561–744UCSCPeptidase family M41

Gene Aliases

HGNC Name

AFG3 like matrix AAA peptidase subunit 2

HGNC Previous Symbol

SCA28

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
13 papers
NM_006796.3
p.M666V
c.1996A>G
Surrounding Variants
15 papers
NM_006796.3
p.M666R
c.1997T>G
8 papers
NM_006796.3
p.M666T
c.1997T>C
1 paper
NM_006796.3
p.M666I
c.1998G>T
1 paper
NM_006796.3
p.G665V
c.1994G>T
1 paper
NM_006796.3
p.M666I
c.1998G>C
1 paper
NM_006796.3
p.M666I
c.1998G>A
1 paper
NM_006796.3
p.N667I
c.2000A>T
3 papers
NM_006796.3
p.F664S
c.1991T>C
4 papers
NM_006796.3
p.G671W
c.2011G>T
15 papers
NM_006796.3
p.G671R
c.2011G>C
15 papers
NM_006796.3
p.G671R
c.2011G>A
9 papers
NM_006796.3
p.G671E
c.2012G>A
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