Transcript #00018840 (NM_003023.4, SH3BP2 gene)

Transcript name transcript variant 1
Gene name SH3BP2 (SH3-domain binding protein 2)
Chromosome 4
Transcript - NCBI ID NM_003023.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_003014.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-2749250_*540076del r.0? p.0?
-/. - c.-6654A>G r.(?) p.(=)
-?/. - c.-6586G>A r.(?) p.(=)
?/. - c.46G>A r.(?) p.(Gly16Ser)
-?/. - c.79G>A r.(?) p.(Val27Met)
-?/. - c.79G>A r.(?) p.(Val27Met)
-/. - c.123G>T r.(?) p.(Leu41=)
-?/. - c.136+7_136+18del r.(=) p.(=)
?/. - c.160C>A r.(?) p.(His54Asn)
-?/. - c.239G>A r.(?) p.(Arg80Gln)
-?/. - c.239G>A r.(?) p.(Arg80Gln)
?/. - c.239G>A r.(?) p.(Arg80Gln)
-?/. - c.239+10C>T r.(=) p.(=)
-/. - c.240-122_240-121insA r.(=) p.(=)
-?/. - c.247C>A r.(?) p.(Arg83=)
?/. - c.247C>T r.(?) p.(Arg83Trp)
-/. - c.276C>T r.(?) p.(Asn92=)
-?/. - c.299A>G r.(?) p.(His100Arg)
-?/. - c.299A>G r.(?) p.(His100Arg)
-?/. - c.299A>G r.(?) p.(His100Arg)
?/. - c.299A>G r.(?) p.(His100Arg)
-/. - c.300T>C r.(?) p.(His100=)
?/. - c.316C>T r.(?) p.(Arg106Cys)
?/. - c.322T>C r.(?) p.(Trp108Arg)
-?/. - c.334G>T r.(?) p.(Ala112Ser)
?/. - c.353G>A r.(?) p.(Arg118His)
-/. - c.357+15G>T r.(=) p.(=)
?/. - c.400G>A r.(?) p.(Glu134Lys)
-/. - c.417C>G r.(?) p.(Pro139=)
-/. - c.429-90C>T r.(=) p.(=)
-?/. - c.429-16G>T r.(=) p.(=)
-?/. - c.441G>A r.(?) p.(Ser147=)
-?/. - c.441G>A r.(?) p.(Ser147=)
-?/. - c.459C>T r.(?) p.(Tyr153=)
-?/. - c.459C>T r.(?) p.(Tyr153=)
-/. - c.464C>T r.(?) p.(Ala155Val)
-?/. - c.464C>T r.(?) p.(Ala155Val)
?/. - c.472C>T r.(?) p.(Arg158Trp)
-/. - c.518-18C>A r.(=) p.(=)
-/. - c.518-15C>G r.(=) p.(=)
?/. - c.524A>G r.(?) p.(Glu175Gly)
-?/. - c.528C>T r.(?) p.(His176=)
?/. - c.532G>A r.(?) p.(Asp178Asn)
-?/. - c.535G>A r.(?) p.(Glu179Lys)
-?/. - c.560A>G r.(?) p.(Asp187Gly)
-?/. - c.566C>T r.(?) p.(Pro189Leu)
-?/. - c.579G>C r.(?) p.(Arg193Ser)
?/. - c.584A>C r.(?) p.(Glu195Ala)
-?/. - c.586+15T>G r.(=) p.(=)
-?/. - c.600C>T r.(?) p.(His200=)
?/. - c.605C>T r.(?) p.(Pro202Leu)
-?/. - c.688G>T r.(?) p.(Gly230Cys)
?/. - c.713C>T r.(?) p.(Pro238Leu)
-?/. - c.720T>A r.(?) p.(Pro240=)
?/. - c.724del r.(?) p.(His242ThrfsTer36)
-/. - c.750T>G r.(?) p.(Ala250=)
-/. - c.750T>G r.(?) p.(Ala250=)
-?/. - c.756G>A r.(?) p.(Glu252=)
-/. - c.801C>T r.(?) p.(Cys267=)
-?/. - c.859A>T r.(?) p.(Thr287Ser)
-?/. - c.861C>T r.(?) p.(Thr287=)
-?/. - c.865C>T r.(?) p.(Pro289Ser)
-?/. - c.905G>A r.(?) p.(Ser302Asn)
-?/. - c.932G>A r.(?) p.(Gly311Asp)
-?/. - c.932G>A r.(?) p.(Gly311Asp)
-?/. - c.937G>A r.(?) p.(Gly313Arg)
?/. - c.937G>A r.(?) p.(Gly313Arg)
-?/. - c.950C>T r.(?) p.(Thr317Ile)
-?/. - c.1031C>A r.(?) p.(Pro344Gln)
-?/. - c.1084A>G r.(?) p.(Ile362Val)
?/. - c.1109del r.(?) p.(Glu370Glyfs*19)
-?/. - c.1122C>T r.(?) p.(Pro374=)
-?/. - c.1123G>A r.(?) p.(Gly375Arg)
-?/. - c.1141G>A r.(?) p.(Val381Met)
-?/. - c.1151G>A r.(?) p.(Arg384Gln)
-?/. - c.1164G>A r.(?) p.(Leu388=)
-?/. - c.1190C>G r.(?) p.(Ala397Gly)
-?/. - c.1203C>A r.(?) p.(Val401=)
-?/. - c.1223C>T r.(?) p.(Pro408Leu)
?/. - c.1227_1235dup r.(?) p.(Gln409_Pro411dup)
-?/. - c.1241+20G>T r.(=) p.(=)
-/. - c.1242-98C>T r.(=) p.(=)
-?/. - c.1281C>T r.(?) p.(Ser427=)
-?/. - c.1292C>T r.(?) p.(Pro431Leu)
?/. - c.1295G>A r.(?) p.(Arg432Gln)
-?/. - c.1313A>G r.(?) p.(Asp438Gly)
-?/. - c.1326C>T r.(?) p.(Asp442=)
?/. - c.1343A>T r.(?) p.(Tyr448Phe)
-?/. - c.1350+6G>A r.(=) p.(=)
-/. - c.1350+117C>T r.(=) p.(=)
-?/. - c.1351-13C>T r.(=) p.(=)
-?/. - c.1366T>C r.(?) p.(Ser456Pro)
-?/. - c.1366T>C r.(?) p.(Ser456Pro)
-?/. - c.1366T>C r.(?) p.(Ser456Pro)
?/. - c.1367C>T r.(?) p.(Ser456Leu)
-?/. - c.1367C>T r.(?) p.(Ser456Leu)
-?/. - c.1406+14C>A r.(=) p.(=)
-/. - c.1407-11T>A r.(=) p.(=)
-?/. - c.1429C>T r.(?) p.(Arg477Trp)
-/. - c.1429C>T r.(?) p.(Arg477Trp)
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