Transcript #00000173

Transcript name MpV17 mitochondrial inner membrane protein
Gene name MPV17 (MpV17 mitochondrial inner membrane protein)
Chromosome 2
Transcript - NCBI ID NM_002437.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_002428.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

64 entries on 1 page. Showing entries 1 - 64.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-11G>C p.(=) - - - -
./. - - c.-6+8G>A p.(=) - - - -
./. - - c.22_23insC p.(Gln8Profs*24) - - - -
+/+ - - c.22_23insC p.(Gln8Profs*24) - - - -
./. - - c.27G>T p.(=) - - - -
+/+ - 2/8 c.70G>T p.(Gly24Trp) probably_damaging(0.998) missense_variant,splice_region_variant - deleterious(0)
./. - - c.70G>T p.(Gly24Trp) - - - -
+/+ - - c.70+5G>A p.? - - - -
./. - - c.70+5G>A p.? - - - -
./. - - c.106C>T p.(Gln36*) - - - -
./. - - c.122_147del p.(Arg41Profs*63) - - - -
./. - - c.135del p.(Glu45Aspfs*8) - - - -
+/+ - - c.116_141del p.(Arg41Profs*63) - - - -
./. - - c.148C>T p.(Arg50Trp) - - - -
+/+ - 3/8 c.148C>T p.(Arg50Trp) probably_damaging(0.992) missense_variant - deleterious(0)
+/+ - 3/8 c.149G>A p.(Arg50Gln) probably_damaging(0.92) missense_variant - deleterious(0.01)
./. - - c.149G>A p.(Arg50Gln) - - - -
./. - - c.164T>C p.(Val55Ala) - - - -
./. - - c.186+2T>C p.? - - - -
+/+ - - c.186+2T>C p.? - splice_donor_variant - -
./. - - c.191C>G p.(Pro64Arg) - - - -
./. - - c.206G>A p.(Trp69*) - - - -
+/+ - 4/8 c.206G>A p.(Trp69*) - stop_gained - -
./. - - c.234_242del p.(Gly79_Thr81del) - - - -
+/+ - - c.234_242del p.(Gly79_Thr81del) - - - -
./. - - c.262A>G p.(Lys88Glu) - - - -
+/+ - 4/8 c.262A>G p.(Lys88Glu) possibly_damaging(0.695) missense_variant - deleterious(0)
./. - - c.263_265del p.(Lys88del) - - - -
+/+ - - c.263_265del p.(Lys88del) - - - -
./. - - c.271_273del p.(Leu91del) - - - -
+/+ - - c.271_273del p.(Leu91del) - - - -
./. - - c.275A>G p.(Asp92Gly) - - - -
+/+ - 5/8 c.280G>C p.(Gly94Arg) possibly_damaging(0.707) missense_variant,splice_region_variant - tolerated(0.36)
./. - - c.280G>C p.(Gly94Arg) - - - -
./. - - c.284G>A p.(Gly95Asp) - - - -
./. - - c.284_285insG p.(Phe96Leufs*17) - - - -
./. - - c.293C>T p.(Pro98Leu) - - - -
+/+ - 5/8 c.293C>T p.(Pro98Leu) probably_damaging(0.995) missense_variant - deleterious(0)
./. - - c.293del p.(Pro98Argfs*4) - - - -
./. - - c.297T>A p.(Cys99*) - - - -
+/+ - 5/8 c.359G>A p.(Trp120*) - stop_gained - -
./. - - c.359G>A p.(Trp120*) - - - -
./. - - c.373C>T p.(Arg125Trp) - - - -
./. - - c.375G>A p.(=) - - - -
./. - - c.376-2A>C p.? - - - -
./. - - c.376-1G>A p.? - - - -
./. - - c.408+1G>A p.? - - - -
./. - - c.409-1G>C p.? - - - -
./. - - c.451_452insC p.(Leu151Profs*39) - - - -
+/+ - - c.451_452insC p.(Leu151Profs*39) - - - -
./. - - c.461G>T p.(Arg154Met) - - - -
+/+ - 8/8 c.485C>A p.(Ala162Asp) probably_damaging(0.921) missense_variant - deleterious(0)
./. - - c.485C>A p.(Ala162Asp) - - - -
+/+ - 8/8 c.498C>A p.(Asn166Lys) probably_damaging(0.977) missense_variant - deleterious(0)
./. - - c.498C>A p.(Asn166Lys) - - - -
./. - - c.509C>T p.(Ser170Phe) - - - -
+/+ - 8/8 c.509C>T p.(Ser170Phe) probably_damaging(0.975) missense_variant - deleterious(0.01)
./. - - c.*34G>A p.(=) - - - -
./. - - c.*80C>T p.(=) - - - -
./. - - c.*130G>T p.(=) - - - -
./. - - c.*194G>A p.(=) - - - -
./. - - c.*347C>T p.(=) - - - -
./. - - c.*360G>C p.(=) - - - -
./. - - c.*413A>C p.(=) - - - -
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