Transcript #00000040 (NM_000057.2, BLM gene)

Transcript name Bloom syndrome, RecQ helicase-like
Gene name BLM (Bloom syndrome, RecQ helicase-like)
Chromosome 15
Transcript - NCBI ID NM_000057.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000048.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-05-11 13:11:54 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-5+16G>C r.(=) p.(=)
-?/. - c.-5+12429_-5+12430del r.(=) p.(=)
-?/. - c.11T>C r.(?) p.(Val4Ala)
-?/. - c.11T>C r.(?) p.(Val4Ala)
?/. - c.11T>C r.(?) p.(Val4Ala)
./. - c.11T>C r.(?) p.(Val4Ala)
./. - c.11T>C r.(?) p.(Val4Ala)
?/. - c.43C>T r.(?) p.(Arg15Cys)
+?/. - c.53_56del c.(53_56del) p.(Ala18Glufs*7)
?/. - c.61C>T r.(?) p.(Leu21Phe)
+/. - c.98+2dup r.spl p.?
+/. - c.98+3_98+6del r.spl p.?
+?/. - c.98+6T>G r.(=) p.(=)
?/. - c.178T>A r.(?) p.(Leu60Ile)
?/. - c.178T>A r.(?) p.(Leu60Ile)
-?/. - c.178T>A r.(?) p.(Leu60Ile)
?/. - c.186T>G r.(?) p.(Asn62Lys)
-?/. - c.186T>G r.(?) p.(Asn62Lys)
./. - c.191A>T r.(?) p.(Asp64Val)
?/. - c.205G>A r.(?) p.(Glu69Lys)
-?/. - c.254G>C r.(?) p.(Arg85Thr)
./. - c.254G>C r.(?) p.(Arg85Thr)
./. - c.274A>G r.(?) p.(Asn92Asp)
+/. - c.298_299del r.(?) p.(Gln100Glufs*42)
?/. - c.317C>A r.(?) p.(Ser106*)
?/. - c.320dup r.(?) p.(Leu107Phefs*36)
?/. - c.394C>T r.(?) p.(Arg132Trp)
-?/. - c.395G>A r.(?) p.(Arg132Gln)
-?/. - c.395G>A r.(?) p.(Arg132Gln)
./. - c.403G>T r.(?) p.(Ala135Ser)
-/. - c.410A>G r.(?) p.(Lys137Arg)
./. - c.410A>G r.(?) p.(Lys137Arg)
-/. - c.410A>G r.(?) p.(Lys137Arg)
./. - c.419A>G r.(?) p.(Glu140Gly)
-?/. - c.431C>T r.(?) p.(Ser144Leu)
-?/. - c.451A>G r.(?) p.(Ile151Val)
-?/. - c.465T>C r.(?) p.(Asp155=)
-?/. - c.465T>C r.(?) p.(Asp155=)
-?/. - c.465T>C r.(?) p.(Asp155=)
?/. - c.470T>C r.(?) p.(Met157Thr)
-?/. - c.480T>C r.(?) p.(Phe160=)
./. - c.550C>G r.(?) p.(Gln184Glu)
./. - c.617C>A r.(?) p.(Thr206Asn)
./. - c.715G>A r.(?) p.(Asp239Asn)
-?/. - c.715G>A r.(?) p.(Asp239Asn)
-?/. - c.777A>C r.(?) p.(Lys259Asn)
-?/. - c.808G>A r.(?) p.(Glu270Lys)
./. - c.811delAAG - -
./. - c.863G>A r.(?) p.(Cys288Tyr)
-/. - c.893C>T r.(?) p.(Thr298Met)
-?/. - c.893C>T r.(?) p.(Thr298Met)
-?/. - c.960-9dup r.(=) p.(=)
?/. - c.968A>G r.(?) p.(Lys323Arg)
./. - c.968A>G r.(?) p.(Lys323Arg)
./. - c.1006A>G r.(?) p.(Ser336Gly)
-?/. - c.1044G>A r.(?) p.(Met348Ile)
?/. - c.1045A>G r.(?) p.(Ser349Gly)
-?/. - c.1077A>G r.(?) p.(Thr359=)
-?/. - c.1086C>T r.(?) p.(Asp362=)
-?/. - c.1088-173G>T r.(=) p.(=)
?/. - c.1088-169C>A r.(=) p.(=)
-/. - c.1122T>C r.(?) p.(His374=)
?/. - c.1201C>T r.(?) p.(Leu401Phe)
?/. - c.1211G>A r.(?) p.(Arg404Gln)
-?/. - c.1221-11del r.(=) p.(=)
+/. - c.1284G>A r.(?) p.(Trp428Ter)
-?/. - c.1305T>C r.(?) p.(Leu435=)
-?/. - c.1467G>A r.(?) p.(Arg489=)
+/. - c.1479_1480del r.(?) p.(Thr494ProfsTer9)
?/. - c.1553C>G r.(?) p.(Ser518Cys)
-?/. - c.1601A>G r.(?) p.(Asn534Ser)
+?/. - c.1642C>T r.(?) p.(Gln548Ter)
./. - c.1642C>T r.(?) p.(Gln548*)
+/. - c.1642C>T r.(?) p.(Gln548Ter)
./. - c.1642C>T r.(?) p.(Gln548*)
+/. - c.1642C>T r.(?) p.(Gln548*)
+/. - c.1642C>T r.(?) p.(Gln548Ter)
+/. - c.1642C>T r.(?) p.(Gln548*)
+?/. - c.1642C>T r.(?) p.(Gln548*)
+?/. - c.1642C>T r.(?) p.(Gln548*)
-?/. - c.1722A>G r.(?) p.(Leu574=)
-/. - c.1722A>G r.(?) p.(Leu574=)
-/. - c.1722A>G r.(?) p.(Leu574=)
?/. - c.1762A>G r.(?) p.(Lys588Glu)
-?/. - c.1771C>G r.(?) p.(Arg591Gly)
?/. - c.1838C>T r.(?) p.(Thr613Ile)
./. - c.1838C>T r.(?) p.(Thr613Ile)
-?/. - c.1881T>C r.(?) p.(Thr627=)
-?/. - c.1928G>A r.(?) p.(Arg643His)
-?/. - c.1928G>A r.(?) p.(Arg643His)
-?/. 8 c.1928G>A r.(?) p.(Arg643His)
-/. - c.1928G>A r.(?) p.(Arg643His)
-/. - c.1928G>A r.(?) p.(Arg643His)
./. - c.1928G>A r.(?) p.(Arg643His)
./. - c.1928G>A r.(?) p.(Arg643His)
+/. - c.1933C>T r.(?) p.(Gln645Ter)
+/. - c.1933C>T r.(?) p.(Gln645Ter)
+/. - c.1933C>T r.(?) p.(Gln645Ter)
+/. - c.1933C>T r.(1933c>u) p.(Gln645Ter)
./. - c.1934A>G r.(?) p.(Gln645Arg)
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