Colon Cancer: Gene >> ABCC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50669175:50669175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1973C>A
AA Mutation	p.Ala658Asp(p.A658D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50663773:50663773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762463467
CDS Mutation	c.1091C>T
AA Mutation	p.Ser364Leu(p.S364L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50683686:50683686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3884C>T
AA Mutation	p.Ser1295Phe(p.S1295F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50676530:50676530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3320G>A
AA Mutation	p.Ser1107Asn(p.S1107N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50669487:50669487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2200G>A
AA Mutation	p.Glu734Lys(p.E734K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50663739:50663739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763074343
CDS Mutation	c.1057G>A
AA Mutation	p.Ala353Thr(p.A353T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50667582:50667582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1460G>A
AA Mutation	p.Arg487His(p.R487H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50667581:50667581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577213087
CDS Mutation	c.1459C>T
AA Mutation	p.Arg487Cys(p.R487C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50657049:50657049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352C>A
AA Mutation	p.Leu118Met(p.L118M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50663748:50663748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1066A>G
AA Mutation	p.Met356Val(p.M356V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50668903:50668903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1921C>A
AA Mutation	p.Pro641Thr(p.P641T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50665237:50665237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543738423
CDS Mutation	c.1423G>A
AA Mutation	p.Ala475Thr(p.A475T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50658168:50658168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50655919:50655919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50678180:50678180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754055850
CDS Mutation	c.3666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50656737:50656737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746009186
CDS Mutation	c.258G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50667895:50667895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775482973
CDS Mutation	c.1668C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50687677:50687677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4422C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50677881:50677881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3516C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000285238
Start	50675920:50675921(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2901dupG
AA Mutation	p.Leu968AlafsTer31(p.L968Afs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ABCC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50656744:50656744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265T>G
AA Mutation	p.Phe89Val(p.F89V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50676399:50676399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3189A>G
Mutation Classification	Silent
Feature Type	Transcript