Colon Cancer: Gene >> TBX22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80026774:80026774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704T>A
AA Mutation	p.Leu235Gln(p.L235Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80030606:80030606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1058G>A
AA Mutation	p.Ser353Asn(p.S353N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80025763:80025763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619G>A
AA Mutation	p.Asp207Asn(p.D207N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80026849:80026849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104894943
CDS Mutation	c.779C>T
AA Mutation	p.Thr260Met(p.T260M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80023119:80023119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.235G>A
AA Mutation	p.Gly79Ser(p.G79S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80030747:80030747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199C>A
AA Mutation	p.Ser400Tyr(p.S400Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80022330:80022330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61A>C
AA Mutation	p.Lys21Gln(p.K21Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80030863:80030863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315T>C
AA Mutation	p.Ser439Pro(p.S439P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80022348:80022348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79C>A
AA Mutation	p.Pro27Thr(p.P27T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373294
Start	80028069:80028069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373294
Start	80025684:80025684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374171441
CDS Mutation	c.540G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373294
Start	80028063:80028063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376686839
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373294
Start	80026745:80026745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770012858
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000373294
Start	80026737:80026737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Ter(p.R223*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TBX22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80022330:80022330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61A>G
AA Mutation	p.Lys21Glu(p.K21E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80030726:80030726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178G>T
AA Mutation	p.Arg393Ile(p.R393I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373294
Start	80030942:80030942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756809972
CDS Mutation	c.1394G>T
AA Mutation	p.Ser465Ile(p.S465I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000373294
Start	80030637:80030637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1089C>G
AA Mutation	p.Tyr363Ter(p.Y363*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript