Transcript #00016342 (NM_020631.4, PLEKHG5 gene)

Transcript name transcript variant 1
Gene name PLEKHG5 (pleckstrin homology domain containing, family G (with RhoGef domain) member 5)
Chromosome 1
Transcript - NCBI ID NM_020631.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_065682.2
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

160 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-28234G>A r.(?) p.(=)
-/. - c.-28044C>G r.(?) p.(=)
-/. - c.-27998G>A r.(?) p.(=)
-/. - c.-27912C>G r.(?) p.(=)
-/. - c.-27501T>C r.(?) p.(=)
-/. - c.-5400T>G r.(?) p.(=)
+/. _1 c.-4984del r.(?) p.(=)
?/. - c.-4976C>T r.(?) p.(=)
-?/. - c.-4976C>T r.(?) p.(=)
-/. - c.-88+6188G>A r.(=) p.(=)
-/. - c.-88+6307T>A r.(=) p.(=)
-/. - c.-88+6328C>T r.(=) p.(=)
+/. _1 - r.(?) p.(=)
+/. _1 - r.(?) p.(=)
+/. - - r.(?) p.(=)
-/. - c.30C>T r.(?) p.(Asp10=)
-?/. - c.33T>C r.(?) p.(Leu11=)
?/. - c.34C>A r.(?) p.(Pro12Thr)
+/. - c.38del r.(?) p.(Pro13Hisfs*45)
+/. - c.38del r.(?) p.(Pro13Hisfs*45)
+?/. - c.43+1G>A r.spl? p.?
-/. - c.43+13G>A r.(=) p.(=)
-/. - c.43+14_43+20del r.(=) p.(=)
-?/. - c.43+14_43+20del r.(=) p.(=)
+/. - c.58del r.(?) p.(Arg20Glyfs*38)
+?/. - c.59G>A r.(?) p.(Arg20Gln)
-?/. - c.87G>A r.(?) p.(Pro29=)
?/. - c.88C>T r.(?) p.(Arg30Cys)
-?/. - c.186G>A r.(?) p.(Lys62=)
-/. - c.260T>C r.(?) p.(Ile87Thr)
?/. - c.269A>G r.(?) p.(Glu90Gly)
?/. - c.274G>A r.(?) p.(Val92Ile)
?/. - c.292_294del r.(?) p.(Lys98del)
-?/. - c.307G>A r.(?) p.(Val103Met)
?/. - c.307G>A r.(?) p.(Val103Met)
?/. - c.307G>A r.(?) p.(Val103Met)
?/. - c.335G>T r.(?) p.(Gly112Val)
?/. - c.335G>T r.(?) p.(Gly112Val)
-/. - c.414C>T r.(?) p.(Phe138=)
?/. - c.431G>T r.(?) p.(Arg144Leu)
?/. - c.431G>T r.(?) p.(Arg144Leu)
-?/. - c.439+12C>G r.(=) p.(=)
-?/. - c.440-6A>G r.(=) p.(=)
-?/. - c.440-6A>G r.(=) p.(=)
?/. - c.532G>A r.(?) p.(Gly178Arg)
-?/. - c.558C>T r.(?) p.(Asp186=)
-/. - c.592-14C>T r.(=) p.(=)
-?/. - c.691G>A r.(?) p.(Gly231Ser)
-/. - c.713C>G r.(?) p.(Thr238Ser)
?/. - c.719A>G r.(?) p.(Asp240Gly)
?/. - c.719A>G r.(?) p.(Asp240Gly)
-?/. - c.768C>T r.(?) p.(Ser256=)
-?/. - c.768C>T r.(?) p.(Ser256=)
-/. - c.795+8G>A r.(=) p.(=)
?/. - c.865C>T r.(?) p.(Pro289Ser)
-?/. - c.882C>T r.(?) p.(=)
?/. - c.912_918dup r.(?) p.(Glu307Ter)
+/. - c.912_918dup r.(?) p.(Glu307*)
+/. - c.912_918dup r.(?) p.(Glu307*)
+/. - c.912_918dup r.(?) p.(Glu307*)
+/. - c.912_918dup r.(?) p.(Glu307Ter)
-?/. - c.918C>T r.(?) p.(Asp306=)
-?/. - c.918C>T r.(?) p.(Asp306=)
?/. - c.928G>A r.(?) p.(Asp310Asn)
-?/. - c.928G>A r.(?) p.(Asp310Asn)
+/. - c.982G>T r.(?) p.(Glu328*)
-?/. - c.985-56C>T r.(=) p.(=)
?/. - c.994C>T r.(?) p.(Arg332Trp)
?/. - c.994C>T r.(?) p.(Arg332Trp)
?/. - c.994C>T r.(?) p.(Arg332Trp)
-?/. - c.997C>A r.(?) p.(Arg333=)
-?/. - c.1023G>A r.(?) p.(=)
-?/. - c.1080+13T>C r.(=) p.(=)
-/. - c.1081-98G>A r.(=) p.(=)
?/. - c.1106T>C r.(?) p.(Leu369Pro)
?/. - c.1112A>C r.(?) p.(Glu371Ala)
+?/. - c.1133T>G r.(?) p.(Val378Gly)
-/. - c.1179G>A r.(?) p.(Leu393=)
-?/. - c.1236G>A r.(?) p.(Thr412=)
-/. - c.1240G>A r.(?) p.(Ala414Thr)
-/. - c.1254C>G r.(?) p.(Pro418=)
-?/. - c.1254C>G r.(?) p.(Pro418=)
-/. - c.1318A>G r.(?) p.(Met440Val)
-/. - c.1393-22dup r.(=) p.(=)
?/. 14 c.1405C>T r.(?) p.(His469Tyr)
+/. - c.1417C>T r.(?) p.(Gln473*)
+?/. - c.1438A>C r.(?) p.(Met480Leu)
?/. - c.1514C>T r.(?) p.(Pro505Leu)
-?/. - c.1543-44_1543-40dup r.(=) p.(=)
+?/. - c.1549_1550del r.(?) p.(Ser517Argfs*137)
?/. - c.1576A>G r.(?) p.(Asn526Asp)
+/. - c.1604_1629del r.(?) p.(Arg535Profs*111)
?/. - c.1639G>A r.(?) p.(Ala547Thr)
-?/. - c.1680+19G>A r.(=) p.(=)
-/. - c.1681-20T>C r.(=) p.(=)
-?/. - c.1681-8G>C r.(=) p.(=)
?/. - c.1705G>A r.(?) p.(Asp569Asn)
?/. - c.1709T>C r.(?) p.(Leu570Ser)
-?/. - c.1724C>T r.(?) p.(Pro575Leu)
-/. - c.1800+107C>T r.(=) p.(=)
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