Transcript #00024232 (NM_000118.3, ENG gene)

Transcript name transcript variant 2
Gene name ENG (endoglin)
Chromosome 9
Transcript - NCBI ID NM_000118.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000109.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2017-03-03 11:58:58 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. 1 c.-35A>G r.(=) p.(=)
-/. 1 c.-35A>G r.(?) p.(=)
+/. - c.-10C>T r.(?) p.(=)
-?/. - c.-9G>A r.(?) p.(=)
-?/. - c.-9G>A r.(?) p.(=)
?/. - c.-9G>A r.(?) p.(=)
+/. - c.1A>G r.(?) p.(Met1?)
+/. - c.2T>C r.(?) p.(Met1?)
+/. - c.2T>G r.(?) p.(Met1?)
-?/. - c.7C>T r.(?) p.(Arg3Cys)
?/. - c.14C>A r.(?) p.(Thr5Lys)
-/. - c.14C>T r.(?) p.(Thr5Met)
-/. - c.14C>T r.(?) p.(Thr5Met)
-/. - c.14C>T r.(?) p.(Thr5Met)
-?/. - c.14C>T r.(?) p.(Thr5Met)
-/. - c.14C>T r.(?) p.(Thr5Met)
-?/. - c.48C>G r.(?) p.(Ser16Arg)
+/. - c.67+1G>A r.spl? p.?
+/. - c.67+1G>A r.spl? p.?
+/. - c.67+1G>A r.spl? p.?
+/. - c.67+3A>G r.spl? p.?
+/. - c.67+5G>A r.spl? p.?
-?/. - c.68-18C>T r.(=) p.(=)
-?/. - c.68-9C>G r.(=) p.(=)
?/. - c.68-3C>G r.spl? p.?
-?/. - c.116G>A r.(?) p.(Arg39Lys)
-/. - c.120C>T r.(?) p.(Gly40=)
-?/. - c.120C>T r.(?) p.(Gly40=)
-?/. - c.120C>T r.(?) p.(Gly40=)
-/. - c.120C>T r.(?) p.(Gly40=)
-?/. - c.120C>T r.(?) p.(Gly40=)
-?/. - c.120C>T r.(?) p.(Gly40=)
+/. - c.142C>T r.(?) p.(Gln48Ter)
+/. - c.154G>C r.(?) p.(Gly52Arg)
+/. - c.159C>A r.(?) p.(Cys53Ter)
-/. - c.159C>T r.(?) p.(Cys53=)
-?/. - c.179C>A r.(?) p.(Ala60Asp)
?/. - c.179C>T r.(?) p.(Ala60Val)
-/. - c.207G>A r.(?) p.(Leu69=)
+/. - c.219G>A r.(?) p.(Thr73=)
-?/. - c.219+22C>T r.(=) p.(=)
+/. - c.220-2A>G r.spl? p.?
-?/. - c.224C>T r.(?) p.(Pro75Leu)
-?/. - c.225G>A r.(?) p.(Pro75=)
+/. - c.229C>T r.(?) p.(Gln77Ter)
-?/. - c.234G>A r.(?) p.(Leu78=)
+/. - c.247C>T r.(?) p.(Gln83Ter)
+/. - c.247C>T r.(?) p.(Gln83Ter)
+/. - c.277C>T r.(?) p.(Arg93Ter)
+?/. - c.296T>A r.(?) p.(Leu99His)
?/. - c.302T>A r.(?) p.(Val101Glu)
-?/. - c.321G>T r.(?) p.(Leu107=)
-?/. - c.322C>T r.(?) p.(His108Tyr)
-?/. - c.322C>T r.(?) p.(His108Tyr)
-?/. - c.322C>T r.(?) p.(His108Tyr)
+/. - c.328C>T r.(?) p.(Gln110Ter)
+/. - c.360C>A r.(?) p.(Tyr120Ter)
+/. - c.360+1G>A r.spl? p.?
+/. - c.360+2T>C r.spl? p.?
+/. - c.360+5G>A r.spl? p.?
?/. - c.360+5G>T r.spl? p.?
+/. - c.361-2A>G r.spl? p.?
-?/. - c.388C>T r.(?) p.(Pro130Ser)
-/. - c.392C>T r.(?) p.(Pro131Leu)
-?/. - c.392C>T r.(?) p.(Pro131Leu)
-?/. - c.393G>C r.(?) p.(Pro131=)
-?/. - c.412C>T r.(?) p.(Leu138=)
?/. - c.475G>C r.(?) p.(Ala159Pro)
?/. - c.503T>A r.(?) p.(Ile168Asn)
+/. - c.503T>C r.(?) p.(Ile168Thr)
+/. - c.511C>T r.(?) p.(Arg171Ter)
+/. - c.512G>C r.(?) p.(Arg171Pro)
+/. - c.523+1G>T r.spl? p.?
-/. - c.524-15C>T r.(=) p.(=)
+/. - c.526C>T r.(?) p.(Gln176Ter)
+/. - c.533C>G r.(?) p.(Ser178Ter)
+/. - c.553G>T r.(?) p.(Glu185Ter)
+/. - c.562C>T r.(?) p.(Gln188Ter)
-/. - c.572G>A r.(?) p.(Gly191Asp)
-?/. - c.572G>A r.(?) p.(Gly191Asp)
-/. - c.572G>A r.(?) p.(Gly191Asp)
-?/. - c.572G>A r.(?) p.(Gly191Asp)
-/. - c.572G>A r.(?) p.(Gly191Asp)
-?/. - c.572G>A r.(?) p.(Gly191Asp)
-/. 5 c.572G>A r.(?) p.(Gly191Asp)
?/. - c.583G>A r.(?) p.(Glu195Lys)
?/. - c.583G>A r.(?) p.(Glu195Lys)
?/. - c.589C>T r.(?) p.(Arg197Trp)
-?/. - c.595C>T r.(?) p.(Arg199Cys)
+/. 5 c.617dup r.(?) p.(Cys207Leufs*127)
-?/. - c.627G>C r.(?) p.(Leu209Phe)
-?/. - c.636G>C r.(?) p.(Val212=)
?/. - c.640G>A r.(?) p.(Gly214Ser)
+/. 5 c.640_643del r.(?) p.(Gly214Thrfs*7)
?/. - c.653C>A r.(?) p.(Ala218Glu)
+/. - c.689+2T>C r.spl? p.?
-?/. - c.690-19C>T r.(=) p.(=)
-?/. - c.690-19del r.(=) p.(=)
-?/. - c.690-17C>T r.(=) p.(=)
-?/. - c.690-4_690-3dup r.spl? p.?
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