Colon Cancer: Gene >> NSUN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264670
Start	6620130:6620130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200539341
CDS Mutation	c.791G>A
AA Mutation	p.Arg264Gln(p.R264Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264670
Start	6609855:6609855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1294T>C
AA Mutation	p.Ser432Pro(p.S432P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264670
Start	6600188:6600188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2042G>A
AA Mutation	p.Arg681Gln(p.R681Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264670
Start	6632753:6632753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100T>C
AA Mutation	p.Trp34Arg(p.W34R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264670
Start	6620283:6620283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638C>T
AA Mutation	p.Ala213Val(p.A213V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264670
Start	6625664:6625664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365C>A
AA Mutation	p.Pro122His(p.P122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264670
Start	6610973:6610973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1208C>T
AA Mutation	p.Ala403Val(p.A403V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264670
Start	6625668:6625668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361T>C
AA Mutation	p.Tyr121His(p.Y121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264670
Start	6625612:6625612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201206063
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264670
Start	6611077:6611077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1104G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264670
Start	6609880:6609880(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1269delT
AA Mutation	p.Phe423LeufsTer6(p.F423Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264670
Start	6616733:6616733(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1015delA
AA Mutation	p.Ser339ValfsTer17(p.S339Vfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264670
Start	6605401:6605401(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1609delT
AA Mutation	p.Tyr537MetfsTer10(p.Y537Mfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NSUN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264670
Start	6620262:6620262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146332265
CDS Mutation	c.659G>A
AA Mutation	p.Arg220His(p.R220H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264670
Start	6625569:6625569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460G>A
AA Mutation	p.Glu154Lys(p.E154K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264670
Start	6607308:6607308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1400A>C
AA Mutation	p.Asp467Ala(p.D467A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript