Transcript #00018855 (NM_001017995.2, SH3PXD2B gene)

Transcript name SH3 and PX domains 2B
Gene name SH3PXD2B (SH3 and PX domains 2B)
Chromosome 5
Transcript - NCBI ID NM_001017995.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001017995.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

65 entries on 1 page. Showing entries 1 - 65.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.75+1G>A r.spl? p.?
-?/. - c.80A>C r.(?) p.(Tyr27Ser)
?/. - c.85A>G r.(?) p.(Ile29Val)
-?/. - c.89G>A r.(?) p.(Arg30Gln)
-/. - c.105C>T r.(?) p.(Ser35=)
+/. - c.115G>T r.(?) p.(Glu39Ter)
-?/. - c.222C>A r.(?) p.(Pro74=)
-?/. - c.232+4G>A r.spl? p.?
+/. - c.280C>G r.(?) p.(Arg94Gly)
-?/. - c.339T>C r.(?) p.(Ser113=)
?/. - c.395C>A r.(?) p.(Pro132His)
+/. - c.400G>T r.(?) p.(Glu134Ter)
-?/. - c.410T>C r.(?) p.(Ile137Thr)
?/. - c.410T>C r.(?) p.(Ile137Thr)
?/. - c.430G>T r.(?) p.(Gly144Cys)
-/. - c.522C>T r.(?) p.(Ser174=)
-?/. - c.522C>T r.(?) p.(Ser174=)
-/. - c.563-11T>C r.(=) p.(=)
?/. - c.611C>T r.(?) p.(Thr204Met)
-?/. - c.667+4G>A r.spl? p.?
?/. - c.814G>A r.(?) p.(Ala272Thr)
?/. - c.814G>A r.(?) p.(Ala272Thr)
-?/. - c.884C>A r.(?) p.(Pro295Gln)
-/. - c.884C>A r.(?) p.(Pro295Gln)
+/. - c.969del r.(?) p.(Arg324Glyfs*19)
-?/. - c.970C>T r.(?) p.(Arg324Trp)
?/. - c.970C>T r.(?) p.(Arg324Trp)
-?/. - c.986C>T r.(?) p.(Pro329Leu)
-/. - c.986C>T r.(?) p.(Pro329Leu)
-?/. - c.994G>A r.(?) p.(Asp332Asn)
-?/. - c.997G>A r.(?) p.(Gly333Ser)
-?/. - c.1050G>A r.(?) p.(Arg350=)
-?/. - c.1063-7G>T r.(=) p.(=)
-?/. - c.1063-7G>T r.(=) p.(=)
?/. - c.1088C>T r.(?) p.(Pro363Leu)
?/. - c.1283C>T r.(?) p.(Thr428Met)
-?/. - c.1284G>C r.(?) p.(=)
?/. - c.1403G>A r.(?) p.(Arg468Gln)
?/. - c.1405C>T r.(?) p.(Pro469Ser)
?/. - c.1504A>G r.(?) p.(Met502Val)
-?/. - c.1543G>A r.(?) p.(Asp515Asn)
-?/. - c.1546A>G r.(?) p.(Met516Val)
-?/. - c.1602G>A r.(?) p.(Gly534=)
-?/. - c.1624_1629del r.(?) p.(Glu542_Arg543del)
?/. - c.1705A>T r.(?) p.(Ile569Phe)
-?/. - c.1712C>T r.(?) p.(Pro571Leu)
?/. - c.1837C>T r.(?) p.(Arg613Trp)
?/. - c.1882G>T r.(?) p.(Asp628Tyr)
?/. - c.1984G>A r.(?) p.(Asp662Asn)
?/. - c.1988T>C r.(?) p.(Ile663Thr)
?/. - c.2027A>C r.(?) p.(Gln676Pro)
?/. - c.2122C>T r.(?) p.(Arg708Cys)
-?/. - c.2128C>G r.(?) p.(Gln710Glu)
-?/. - c.2227G>A r.(?) p.(Val743Met)
-?/. - c.2227G>A r.(?) p.(Val743Met)
?/. - c.2279G>A r.(?) p.(Arg760His)
?/. - c.2386C>T r.(?) p.(Arg796Cys)
?/. - c.2395_2397del r.(?) p.(Leu799del)
?/. - c.2395_2397del r.(?) p.(Leu799del)
?/. - c.2461A>G r.(?) p.(Lys821Glu)
-?/. - c.2577C>T r.(?) p.(Ala859=)
-?/. - c.2664C>T r.(?) p.(Phe888=)
?/. - c.2680G>A r.(?) p.(Gly894Arg)
?/. - c.2687C>T r.(?) p.(Pro896Leu)
?/. - c.*12988G>A r.(=) p.(=)
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