Transcript #00000310

Transcript name transcript variant 1
Gene name SPG7 (spastic paraplegia 7 (pure and complicated autosomal recessive))
Chromosome 16
Transcript - NCBI ID NM_003119.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_003110.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

90 entries on 1 page. Showing entries 1 - 90.
Legend  

Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.1A>G p.? - - - -
./. - - c.7_8insTGC p.(Leu8dup) - - - -
./. - - c.9G>T p.(=) - - - -
./. - - c.80C>G p.(Pro27Arg) - - - -
./. - - c.120G>A p.(=) - - - -
./. - - c.144T>G p.(=) - - - -
./. - - c.185G>A p.(Ser62Asn) - - - -
./. - - c.220G>A p.(Gly74Arg) - - - -
./. - - c.233T>A p.(Leu78*) - - - -
./. - - c.338A>G p.(Lys113Arg) - - - -
./. - - c.376+1G>T p.? - - - -
./. - - c.377-6G>A p.(=) - - - -
./. - - c.413A>C p.(Tyr138Ser) - - - -
./. - - c.470_471del p.(Leu158Glnfs*30) - - - -
./. - - c.558G>C p.(=) - - - -
./. - - c.568G>A p.(Asp190Asn) - - - -
./. - - c.584A>G p.(Tyr195Cys) - - - -
./. - - c.618+3_618+60del p.(=) - - - -
./. - - c.618+12T>C p.(=) - - - -
./. - - c.637C>T p.(Arg213*) - - - -
./. - - c.656T>C p.(Ile219Thr) - - - -
./. - - c.771_772del p.(Val258Glyfs*30) - - - -
./. - - c.850_851delinsC p.(Phe284Profs*45) - - - -
./. - - c.857_858insT p.(Asn288*) - - - -
./. - - c.861+1G>C p.? - - - -
./. - - c.861+1G>T p.? - - - -
./. - - c.898G>A p.(Gly300Arg) - - - -
./. - - c.932T>A p.(Val311Glu) - - - -
./. - - c.973_987del p.? - - - -
./. - - c.983T>C p.(Leu328Pro) - - - -
./. - - c.987+5A>G p.? - - - -
./. - - c.988-1G>A p.? - - - -
./. - - c.1032C>T p.(=) - - - -
./. - - c.1033G>C p.(Ala345Pro) - - - -
./. - - c.1045G>A p.(Gly349Ser) - - - -
./. - - c.1045_1046delinsAGC p.(Gly349Serfs*47) - - - -
./. - - c.1045_1073del p.(Pro350Glnfs*36) - - - -
./. - - c.1046_1047insC p.(Gly352Argfs*44) - - - -
./. - - c.1049C>A p.(Pro350His) - - - -
./. - - c.1055G>C p.(Gly352Ala) - - - -
./. - - c.1067C>T p.(Thr356Met) - - - -
./. - - c.1101del p.(Val368Cysfs*71) - - - -
./. - - c.1151-8C>T p.(=) - - - -
./. - - c.1175G>A p.(Ser392Asn) - - - -
./. - - c.1213G>A p.(Val405Ile) - - - -
./. - - c.1242C>G p.(=) - - - -
./. - - c.1325-6C>T p.(=) - - - -
./. - - c.1408C>T p.(Arg470*) - - - -
./. - - c.1420C>T p.(His474Tyr) - - - -
./. - - c.1457G>A p.(Arg486Gln) - - - -
./. - - c.1507A>G p.(Thr503Ala) - - - -
./. - - c.1523G>A p.(Arg508His) - - - -
./. - - c.1553-2A>G p.? - - - -
./. - - c.1555G>C p.(Ala519Pro) - - - -
./. - - c.1625_1626del p.(Leu543Glnfs*32) - - - -
./. - - c.1644C>T p.(=) - - - -
./. - - c.1653C>T p.(=) - - - -
./. - - c.1654G>A p.(Val552Ile) - - - -
./. - - c.1672A>T p.(Lys558*) - - - -
./. - - c.1675A>T p.(Lys559*) - - - -
./. - - c.1715C>T p.(Ala572Val) - - - -
./. - - c.1729G>A p.(Gly577Ser) - - - -
./. - - c.1749G>C p.(Trp583Cys) - - - -
./. - - c.1770C>T p.(=) - - - -
./. - - c.1830C>T p.(=) - - - -
./. - - c.1904C>T p.(Ser635Leu) - - - -
./. - - c.1933T>A p.(Ser645Thr) - - - -
./. - - c.1937-2A>G p.? - - - -
./. - - c.1948G>A p.(Asp650Asn) - - - -
./. - - c.1996G>A p.(Gly666Arg) - - - -
./. - - c.1996G>C p.(Gly666Arg) - - - -
./. - - c.2014G>A p.(Gly672Arg) - - - -
./. - - c.2037G>A p.(=) - - - -
./. - - c.2063G>A p.(Arg688Gln) - - - -
./. - - c.2066G>A p.(Arg689His) - - - -
./. - - c.2075G>C p.(Ser692Thr) - - - -
./. - - c.2084T>C p.(Leu695Pro) - - - -
./. - - c.2095_2096insT p.(Met699Ilefs*4) - - - -
./. - - c.2113_2129del p.(Leu706Glnfs*30) - - - -
./. - - c.2120delinsCCAAGTCTGTA p.(Val707Alafs*38) - - - -
./. - - c.2142C>T p.(=) - - - -
./. - - c.2188A>G p.(Asn730Asp) - - - -
./. - - c.2228T>C p.(Ile743Thr) - - - -
./. - - c.2249C>T p.(Pro750Leu) - - - -
./. - - c.2271del p.(Met757Ilefs*66) - - - -
./. - - c.2275G>A p.(Ala759Thr) - - - -
./. - - c.2280G>A p.(=) - - - -
./. - - c.2292C>T p.(=) - - - -
./. - - c.2295C>T p.(=) - - - -
./. - - c.2365G>A p.(Glu789Lys) - - - -
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