Transcript #00016305 (NM_002661.3, PLCG2 gene)

Transcript name phospholipase C, gamma 2 (phosphatidylinositol-specific)
Gene name PLCG2 (phospholipase C, gamma 2 (phosphatidylinositol-specific))
Chromosome 16
Transcript - NCBI ID NM_002661.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_002652.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

253 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-47-8C>T r.(=) p.(=)
-?/. - c.32C>T r.(?) p.(Ala11Val)
?/. - c.37T>G r.(?) p.(Tyr13Asp)
-?/. - c.57G>A r.(?) p.(Lys19=)
?/. - c.77C>T r.(?) p.(Thr26Met)
-?/. - c.77C>T r.(?) p.(Thr26Met)
-?/. - c.82A>T r.(?) p.(Met28Leu)
-/. - c.82A>T r.(?) p.(Met28Leu)
-?/. - c.96C>T r.(?) p.(Ser32=)
-?/. - c.114C>G r.(?) p.(Pro38=)
?/. - c.146C>T r.(?) p.(Thr49Met)
?/. - c.149G>T r.(?) p.(Arg50Leu)
?/. - c.157G>A r.(?) p.(Ala53Thr)
?/. - c.157G>A r.(?) p.(Ala53Thr)
?/. - c.157G>A r.(?) p.(Ala53Thr)
-?/. - c.164G>C r.(?) p.(Ser55Thr)
-/. - c.174= r.(=) p.(Ala58=)
-?/. - c.183C>T r.(?) p.(Ile61=)
-?/. - c.183C>T r.(?) p.(Ile61=)
-/. - c.193+25T>C r.(=) p.(=)
-/. - c.194-128G>C r.(=) p.(=)
?/. - c.202A>T r.(?) p.(Met68Leu)
-/. - c.297A>G r.(?) p.(Leu99=)
-/. - c.297A>G r.(?) p.(Leu99=)
-?/. - c.337+7G>T r.(=) p.(=)
-?/. - c.337+9A>C r.(=) p.(=)
-/. - c.338-173_338-167del r.(=) p.(=)
-?/. - c.398C>T r.(?) p.(Ala133Val)
-?/. - c.421A>G r.(?) p.(Ile141Val)
-?/. - c.421A>G r.(?) p.(Ile141Val)
-/. - c.431+81_431+83del r.(=) p.(=)
-/. - c.431+82G>A r.(=) p.(=)
-/. - c.431+87A>C r.(=) p.(=)
-/. - c.431+92_431+95del r.(=) p.(=)
-/. - c.432-13T>A r.(=) p.(=)
-/. - c.432-13T>A r.(=) p.(=)
-/. - c.432-13T>A r.(=) p.(=)
-?/. - c.432-3C>T r.spl? p.?
-?/. - c.432-3C>T r.spl? p.?
-?/. - c.485G>C r.(?) p.(Ser162Thr)
-?/. - c.485G>C r.(?) p.(Ser162Thr)
-/. - c.540C>G r.(?) p.(Ala180=)
-?/. - c.564+8T>A r.(=) p.(=)
-?/. - c.565-84_565-83insT r.(=) p.(=)
-?/. - c.565-83_565-82insT r.(=) p.(=)
-/. - c.565-82C>A r.(=) p.(=)
-/. - c.565-82C>T r.(=) p.(=)
-/. - c.565-10A>G r.(=) p.(=)
-?/. - c.577C>G r.(?) p.(His193Asp)
?/. - c.579C>G r.(?) p.(His193Gln)
?/. - c.579C>G r.(?) p.(His193Gln)
?/. - c.579C>G r.(?) p.(His193Gln)
-/. - c.579C>G r.(?) p.(His193Gln)
?/. - c.579C>G r.(?) p.(His193Gln)
?/. - c.594C>G r.(?) p.(Ser198Arg)
?/. - c.594C>G r.(?) p.(Ser198Arg)
-?/. - c.652C>A r.(?) p.(Leu218Ile)
-?/. - c.675G>A r.(?) p.(Ser225=)
-?/. - c.688C>T r.(?) p.(Leu230=)
-?/. - c.688C>T r.(?) p.(Leu230=)
-?/. - c.707C>T r.(?) p.(Pro236Leu)
?/. - c.707C>T r.(?) p.(Pro236Leu)
-?/. - c.714C>T r.(?) p.(Ala238=)
-?/. - c.714C>T r.(?) p.(Ala238=)
-/. - c.731A>G r.(?) p.(His244Arg)
-/. - c.731A>G r.(?) p.(His244Arg)
?/. - c.743G>A r.(?) p.(Arg248Lys)
-/. - c.770A>T r.(?) p.(His257Leu)
-?/. - c.770A>T r.(?) p.(His257Leu)
-?/. - c.771T>C r.(?) p.(His257=)
-?/. - c.771T>C r.(?) p.(His257=)
-/. - c.802C>T r.(?) p.(Arg268Trp)
-/. - c.802C>T r.(?) p.(Arg268Trp)
-?/. - c.804G>A r.(?) p.(Arg268=)
-?/. - c.810A>T r.(?) p.(Thr270=)
?/. - c.832C>T r.(?) p.(Arg278Cys)
?/. - c.832C>T r.(?) p.(Arg278Cys)
-?/. - c.855G>A r.(?) p.(Leu285=)
-/. - c.868-18C>T r.(=) p.(=)
?/. - c.901A>G r.(?) p.(Ile301Val)
-?/. - c.921C>T r.(?) p.(Asp307=)
-?/. - c.923C>T r.(?) p.(Ala308Val)
-?/. - c.923C>T r.(?) p.(Ala308Val)
?/. - c.958C>T r.(?) p.(His320Tyr)
-/. - c.986+45C>T r.(=) p.(=)
-?/. - c.986+175C>T r.(=) p.(=)
-?/. - c.987G>A r.(?) p.(Thr329=)
-?/. - c.987G>A r.(?) p.(Thr329=)
-?/. - c.987G>A r.(?) p.(Thr329=)
?/. - c.1072+5G>A r.spl? p.?
?/. - c.1072+5G>A r.spl? p.?
-?/. - c.1072+8G>A r.(=) p.(=)
-/. - c.1072+17T>C r.(=) p.(=)
-?/. - c.1073-8C>G r.(=) p.(=)
-?/. - c.1073-5T>C r.spl? p.?
-?/. - c.1092C>T r.(?) p.(Pro364=)
?/. - c.1096G>A r.(?) p.(Gly366Arg)
-?/. - c.1107C>T r.(?) p.(Val369=)
-/. - c.1146T>C r.(?) p.(Phe382=)
-/. - c.1146T>C r.(?) p.(Phe382=)
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