Colon Cancer: Gene >> BANP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286122
Start	87975131:87975131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16G>A
AA Mutation	p.Asp6Asn(p.D6N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286122
Start	88033166:88033166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097C>T
AA Mutation	p.Pro366Leu(p.P366L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286122
Start	88033179:88033179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110C>A
AA Mutation	p.His370Gln(p.H370Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286122
Start	88018490:88018490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694G>A
AA Mutation	p.Ala232Thr(p.A232T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286122
Start	88033183:88033183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757034546
CDS Mutation	c.1114G>A
AA Mutation	p.Ala372Thr(p.A372T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286122
Start	88018551:88018551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755C>T
AA Mutation	p.Ala252Val(p.A252V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000286122
Start	88072093:88072093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776799978
CDS Mutation	c.1369G>A
AA Mutation	p.Ala457Thr(p.A457T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000286122
Start	88018580:88018580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784C>T
AA Mutation	p.Arg262Cys(p.R262C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000286122
Start	88072181:88072181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1457C>T
AA Mutation	p.Ala486Val(p.A486V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286122
Start	88006135:88006135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746913650
CDS Mutation	c.501G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286122
Start	88018637:88018637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286122
Start	88027586:88027586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.975C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286122
Start	88018456:88018456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752382664
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286122
Start	87981041:87981041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747772558
CDS Mutation	c.76T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286122
Start	88033167:88033167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752840012
CDS Mutation	c.1098G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BANP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286122
Start	88006187:88006187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764132919
CDS Mutation	c.553G>A
AA Mutation	p.Asp185Asn(p.D185N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000286122
Start	87981098:87981098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133G>T
AA Mutation	p.Glu45Ter(p.E45*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286122
Start	88027647:88027648(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1036_1037insG
AA Mutation	p.Ser346CysfsTer145(p.S346Cfs*145)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript