Transcript #00011835 (NM_006610.3, MASP2 gene)

Transcript name transcript variant 1
Gene name MASP2 (mannan-binding lectin serine peptidase 2)
Chromosome 1
Transcript - NCBI ID NM_006610.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_006601.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

63 entries on 1 page. Showing entries 1 - 63.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-1592736_*1886941del r.0? p.0?
-?/. - c.231C>T r.(?) p.(Val77=)
-?/. - c.234+6G>A r.(=) p.(=)
-?/. - c.234+13C>T r.(=) p.(=)
+?/. - c.242C>A r.(?) p.(Ser81Ter)
?/. - c.242C>A r.(?) p.(Ser81Ter)
?/. - c.352C>T r.(?) p.(Arg118Cys)
?/. - c.352C>T r.(?) p.(Arg118Cys)
?/. - c.359A>G r.(?) p.(Asp120Gly)
?/. - c.359A>G r.(?) p.(Asp120Gly)
-/. - c.359A>G r.(?) p.(Asp120Gly)
-?/. - c.383C>T r.(?) p.(Thr128Met)
-/. - c.408C>T r.(?) p.(Ala136=)
-?/. - c.446C>T r.(?) p.(Ala149Val)
?/. - c.467G>A r.(?) p.(Cys156Tyr)
-/. - c.470A>G r.(?) p.(His157Arg)
?/. - c.659G>A r.(?) p.(Gly220Glu)
-/. - c.742-12C>T r.(=) p.(=)
?/. - c.791C>T r.(?) p.(Pro264Leu)
-?/. - c.828C>G r.(?) p.(Ile276Met)
-?/. - c.828C>G r.(?) p.(Ile276Met)
-/. - c.881C>T r.(?) p.(Thr294Met)
-/. - c.881C>T r.(?) p.(Thr294Met)
-/. - c.1111G>T r.(?) p.(Asp371Tyr)
?/. - c.1142C>T r.(?) p.(Thr381Ile)
?/. - c.1142C>T r.(?) p.(Thr381Ile)
?/. - c.1187G>A r.(?) p.(Cys396Tyr)
-?/. - c.1204A>G r.(?) p.(Thr402Ala)
-?/. - c.1207A>C r.(?) p.(Met403Leu)
-/. - c.1243G>A r.(?) p.(Asp415Asn)
./. - c.1244_1246del r.(?) p.(Asp415del)
-?/. - c.1276T>C r.(?) p.(Ser426Pro)
-?/. - c.1287C>G r.(?) p.(Val429=)
+?/. - c.1289_1293del r.(?) p.(Cys430Serfs*24)
?/. - c.1361G>A r.(?) p.(Gly454Asp)
?/. - c.1366T>C r.(?) p.(Phe456Leu)
-/. - c.1479C>T r.(?) p.(Ser493=)
+?/. - c.1538G>A r.(?) p.(Trp513*)
-/. - c.1617T>C r.(?) p.(Asn539=)
?/. - c.1656_1659del r.(?) p.(Leu553Glnfs*9)
?/. - c.1727C>T r.(?) p.(Thr576Ile)
-/. - c.1731A>C r.(?) p.(Gln577His)
-?/. - c.1731A>C r.(?) p.(Gln577His)
-?/. - c.1733G>C r.(?) p.(Arg578Thr)
-?/. - c.1834G>T r.(?) p.(Val612Leu)
+?/. - c.*4329T>C r.(=) p.(=)
+?/. - c.*4329T>C r.(=) p.(=)
+?/. - c.*4329T>C r.(=) p.(=)
-?/. - c.*4378G>C r.(=) p.(=)
-?/. - c.*4378G>C r.(=) p.(=)
+/. - c.*4421T>C r.(=) p.(=)
+/. - c.*4421T>C r.(=) p.(=)
+?/. - c.*4421T>C r.(=) p.(=)
+/. - c.*4421T>C r.(=) p.(=)
+/. - c.*4448T>C r.(=) p.(=)
-?/. - c.*4501G>A r.(=) p.(=)
-?/. - c.*4531C>T r.(=) p.(=)
-?/. - c.*4531C>T r.(=) p.(=)
?/. - c.*4593C>A r.(=) p.(=)
+/. - c.*4595C>A r.(=) p.(=)
?/. - c.*4676T>C r.(=) p.(=)
+/. - c.*4689T>C r.(=) p.(=)
-/. - c.*4887del r.(?) p.(=)
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