Colon Cancer: Gene >> SH2B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322610
Start	28873792:28873792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2243C>T
AA Mutation	p.Ala748Val(p.A748V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322610
Start	28866521:28866521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755239754
CDS Mutation	c.427A>G
AA Mutation	p.Thr143Ala(p.T143A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322610
Start	28866561:28866561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467G>A
AA Mutation	p.Arg156His(p.R156H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322610
Start	28872541:28872541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1733G>A
AA Mutation	p.Arg578His(p.R578H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322610
Start	28872540:28872540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1732C>T
AA Mutation	p.Arg578Cys(p.R578C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322610
Start	28866390:28866390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144126859
CDS Mutation	c.296C>T
AA Mutation	p.Ala99Val(p.A99V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322610
Start	28873599:28873599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2050G>T
AA Mutation	p.Gly684Cys(p.G684C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322610
Start	28873742:28873742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2193G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322610
Start	28873601:28873601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748376807
CDS Mutation	c.2052C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322610
Start	28866155:28866155(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.65delC
AA Mutation	p.Pro22ArgfsTer74(p.P22Rfs*74)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322610
Start	28866803:28866803(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.713delG
AA Mutation	p.Gly238AlafsTer3(p.G238Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SH2B1

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322610
Start	28869316:28869316(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1242delC
AA Mutation	p.Ser415ArgfsTer128(p.S415Rfs*128)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript