Transcript #00001535 (NM_004327.3, BCR gene)

Transcript name transcript variant 1
Gene name BCR (breakpoint cluster region)
Chromosome 22
Transcript - NCBI ID NM_004327.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_004318.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

295 entries on 3 pages. Showing entries 1 - 100.
Legend   How to query   « First ‹ Prev     1 2 3     Next › Last »

Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-9G>A r.(=) p.(=)
?/? c.-1C>A r.(=) p.(=)
?/? c.48G>C r.(=) p.(=)
?/? c.65G>T r.(?) p.(Arg22Leu)
?/? c.86G>A r.(?) p.(Gly29Asp)
?/? c.96G>T r.(?) p.(Glu32Asp)
?/? c.117G>A r.(=) p.(=)
?/? c.138G>T r.(?) p.(Glu46Asp)
?/? c.149A>G r.(?) p.(Asn50Ser)
?/? c.162C>T r.(=) p.(=)
?/? c.215G>C r.(?) p.(Arg72Pro)
?/? c.455C>T r.(?) p.(Ala152Val)
?/? c.459G>T r.(=) p.(=)
?/? c.468C>T r.(=) p.(=)
?/? c.483C>A r.(=) p.(=)
?/? c.497G>A r.(?) p.(Gly166Asp)
?/? c.513C>T r.(=) p.(=)
?/? c.562C>T r.(=) p.(=)
?/? c.598A>G r.(?) p.(Ile200Val)
?/? c.606C>T r.(=) p.(=)
?/? c.636C>T r.(=) p.(=)
?/? c.645C>T r.(=) p.(=)
?/? c.684G>A r.(=) p.(=)
?/? c.693C>T r.(=) p.(=)
?/? c.723C>T r.(=) p.(=)
?/? c.760C>T r.(?) p.(Arg254Cys)
?/? c.765C>T r.(=) p.(=)
?/? c.822G>A r.(=) p.(=)
?/? c.824A>C r.(?) p.(Glu275Ala)
?/? c.825G>A r.(=) p.(=)
?/? c.828C>T r.(=) p.(=)
?/? c.834C>G r.(=) p.(=)
?/? c.843C>G r.(?) p.(Ser281Arg)
?/? c.884C>A r.(?) p.(Pro295Gln)
?/? c.922C>T r.(?) p.(Arg308Cys)
?/? c.954C>T r.(=) p.(=)
?/? c.983A>G r.(?) p.(Tyr328Cys)
?/? c.1023C>T r.(=) p.(=)
?/? c.1035_1037del r.(?) p.(Ser347del)
?/? c.1037C>T r.(?) p.(Ser346Phe)
?/? c.1062C>G r.(=) p.(=)
?/? c.1109C>T r.(?) p.(Pro370Leu)
?/? c.1111T>C r.(?) p.(Ser371Pro)
?/? c.1121C>G r.(?) p.(Ser374Trp)
?/? c.1127A>C r.(?) p.(Gln376Pro)
?/? c.1142G>A r.(?) p.(Ser381Asn)
?/? c.1151C>T r.(?) p.(Pro384Leu)
?/? c.1184G>T r.(?) p.(Cys395Phe)
?/? c.1187C>T r.(?) p.(Pro396Leu)
?/? c.1195G>C r.(?) p.(Val399Leu)
?/? c.1206C>T r.(=) p.(=)
?/? c.1228A>G r.(?) p.(Thr410Ala)
?/? c.1239C>G r.(?) p.(Ile413Met)
?/? c.1275C>G r.(?) p.(Asp425Glu)
?/? c.1279+40G>T r.(=) p.(=)
?/? c.1279+15988T>G r.(=) p.(=)
?/? c.1279+16014G>A r.(=) p.(=)
?/? c.1279+16019C>T r.(=) p.(=)
?/? c.1279+16025G>A r.(=) p.(=)
?/? c.1279+16084G>A r.(=) p.(=)
?/? c.1279+16089G>A r.(=) p.(=)
?/? c.1279+16096G>A r.(=) p.(=)
?/? c.1279+16164G>A r.(=) p.(=)
?/? c.1279+16183A>G r.(=) p.(=)
?/? c.1279+16999A>G r.(=) p.(=)
?/? c.1279+17002C>T r.(=) p.(=)
?/? c.1279+17014C>T r.(=) p.(=)
?/? c.1279+17024G>C r.(=) p.(=)
?/? c.1279+17062C>T r.(=) p.(=)
?/? c.1279+17066G>T r.(=) p.(=)
?/? c.1279+17088G>A r.(=) p.(=)
?/? c.1279+17095C>T r.(=) p.(=)
?/? c.1279+17102T>C r.(=) p.(=)
?/? c.1279+17106C>T r.(=) p.(=)
?/? c.1279+17110C>T r.(=) p.(=)
?/? c.1279+17111C>G r.(=) p.(=)
?/? c.1279+17123G>T r.(=) p.(=)
?/? c.1279+17139C>T r.(=) p.(=)
?/? c.1279+17148G>C r.(=) p.(=)
?/? c.1280-9C>T r.(=) p.(=)
?/? c.1283G>A r.(?) p.(Gly428Asp)
?/? c.1290C>T r.(=) p.(=)
?/? c.1308C>T r.(=) p.(=)
?/? c.1325G>A r.(?) p.(Arg442Gln)
?/? c.1339C>T r.(?) p.(Arg447Cys)
?/? c.1343G>A r.(?) p.(Arg448Gln)
?/? c.1368T>C r.(=) p.(=)
?/? c.1413G>A r.(=) p.(=)
?/? c.1427C>T r.(?) p.(Ala476Val)
?/? c.1428G>A r.(=) p.(=)
?/? c.1461+561A>G r.(=) p.(=)
?/? c.1461+565C>T r.(=) p.(=)
?/? c.1461+589_1461+590insCC r.(=) p.(=)
?/? c.1461+589_1461+590insC r.(=) p.(=)
?/? c.1461+596C>G r.(=) p.(=)
?/? c.1461+596_1461+597insG r.(=) p.(=)
?/? c.1462-108A>C r.(=) p.(=)
?/? c.1462-98C>G r.(=) p.(=)
?/? c.1462-90_1462-88del r.(=) p.(=)
?/? c.1462-77C>G r.(=) p.(=)
Legend   How to query   « First ‹ Prev     1 2 3     Next › Last »