Colon Cancer: Gene >> ZHX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122953384:122953384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1874C>A
AA Mutation	p.Ser625Tyr(p.S625Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122952280:122952280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770A>C
AA Mutation	p.Lys257Thr(p.K257T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122952558:122952558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375789703
CDS Mutation	c.1048G>A
AA Mutation	p.Ala350Thr(p.A350T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122952906:122952906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779513082
CDS Mutation	c.1396G>A
AA Mutation	p.Asp466Asn(p.D466N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122953369:122953369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1859C>T
AA Mutation	p.Ala620Val(p.A620V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122953327:122953327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565561893
CDS Mutation	c.1817C>T
AA Mutation	p.Ala606Val(p.A606V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122953065:122953065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137944558
CDS Mutation	c.1555G>A
AA Mutation	p.Gly519Ser(p.G519S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122951776:122951776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266A>T
AA Mutation	p.Asn89Ile(p.N89I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122952912:122952912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1402G>A
AA Mutation	p.Glu468Lys(p.E468K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122953878:122953878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148101741
CDS Mutation	c.2368G>A
AA Mutation	p.Val790Ile(p.V790I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122953165:122953165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1655C>A
AA Mutation	p.Ser552Tyr(p.S552Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122953530:122953530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2020C>T
AA Mutation	p.Arg674Cys(p.R674C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314393
Start	122953934:122953934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2424A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314393
Start	122953631:122953631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186468091
CDS Mutation	c.2121C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314393
Start	122952338:122952338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140865098
CDS Mutation	c.828G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314393
Start	122953713:122953713(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2207delA
AA Mutation	p.Lys736SerfsTer11(p.K736Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314393
Start	122953560:122953560(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2053delA
AA Mutation	p.Thr685ArgfsTer4(p.T685Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314393
Start	122953653:122953653(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2145delC
AA Mutation	p.Met716TrpfsTer31(p.M716Wfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314393
Start	122953096:122953096(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1591delC
AA Mutation	p.Gln531ArgfsTer19(p.Q531Rfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000314393
Start	122953260:122953260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1750C>T
AA Mutation	p.Arg584Ter(p.R584*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314393
Start	122952743:122952744(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1237dupC
AA Mutation	p.Gln413ProfsTer31(p.Q413Pfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZHX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122952499:122952499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989G>A
AA Mutation	p.Arg330Gln(p.R330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314393
Start	122951848:122951848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338C>T
AA Mutation	p.Ala113Val(p.A113V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript