Transcript #00000058 (NM_000548.4, TSC2 gene)

Transcript name transcript variant 1
Gene name TSC2 (TSC complex subunit 2)
Chromosome 16
Transcript - NCBI ID NM_000548.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000539.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

28 entries on 1 page. Showing entries 1 - 28.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
+/. 1-15 c.1_1716del - r.? p.? - -
+/. 3 c.266T>A - r.(?) p.(Leu89*) - -
+/. 7 c.705dupC - r.(?) p.(Leu236Profs*102) - -
+/. 8 c.826_827delAT - r.(?) p.(Met276Valfs*61) - ClinVar
./. 8 c.833A>C - r.(?) p.(His278Pro) - ClinVar
./. 9 c.856A>G - r.(?) p.(Met286Val) - ClinVar
-/. 10 c.1100G>A - r.(?) p.(Arg367Gln) - ClinVar
./. 21i c.1361+1G>A - r.spl? p.? - ClinVar
+/. 15 c.1714C>T - r.(?) p.(Gln572*) - -
?/. 16 c.1825A>G - r.(?) p.(Ser609Gly) - ClinVar
./. 18 c.2032G>A - r.(?) p.(Ala678Thr) - ClinVar
+/. 23 c.2656_2657insGT - r.(?) p.(Val886Glyfs*9) - -
+/. 26-31 c.2967_3883del - r.(?) p.(Ser989Argfs*27) - -
+/. 26-31 c.2967_3883del - r.(?) p.(Ser989Argfs*27) - -
+/. 27 c.3230C>A - r.(?) p.(Thr1077Asn) - -
./. 29 c.3581G>A - r.(?) p.(Trp1194*) - ClinVar
?/. 29 c.3595G>A - r.(?) p.(Val1199Ile) - ClinVar
+/. 29 c.3596T>C - r.(?) p.(Val1199Ala) - -
?/. 30 c.3755C>A - r.(?) p.(Ser1252*) - ClinVar
+/. 30 c.3755C>A - r.(?) p.(Ser1252*) - ClinVar
+/. 32-41 c.3884_5424del - r.? p.? - -
+/. 32-41 c.3884_5424del - r.? p.? - -
+/. 32 c.3999C>A - r.(?) p.(Tyr1333*) - ClinVar
+/. 33 c.4344_4345insC - r.(?) p.(Ser1449Leufs*75) - -
+/. 37 c.4925G>A - r.(?) p.(Gly1642Asp) - ClinVar
+/. 38 c.4993C>T - r.(?) p.(Gln1665*) - ClinVar
+/. 39 c.5074_5075insG - r.(?) p.(Glu1692Glyfs*14) - -
+/. 40 c.5228G>A - r.(?) p.(Arg1743Gln) - ClinVar
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