Colon Cancer: Gene >> SLC7A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380752
Start	29536143:29536143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.46C>T
AA Mutation	p.Arg16Trp(p.R16W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380752
Start	29532967:29532967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386C>T
AA Mutation	p.Ala129Val(p.A129V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380752
Start	29524179:29524179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.779C>T
AA Mutation	p.Ala260Val(p.A260V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380752
Start	29535852:29535852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337A>G
AA Mutation	p.Thr113Ala(p.T113A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380752
Start	29517582:29517582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1501A>G
AA Mutation	p.Ser501Gly(p.S501G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380752
Start	29532953:29532953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400G>A
AA Mutation	p.Ala134Thr(p.A134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380752
Start	29535968:29535968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221C>T
AA Mutation	p.Ala74Val(p.A74V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380752
Start	29519477:29519477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138868586
CDS Mutation	c.1262C>T
AA Mutation	p.Ser421Leu(p.S421L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000380752
Start	29536145:29536145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44G>A
AA Mutation	p.Arg15Gln(p.R15Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380752
Start	29522375:29522375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574126039
CDS Mutation	c.1131C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380752
Start	29523445:29523445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145011879
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380752
Start	29523301:29523301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1014A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380752
Start	29523388:29523388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.927G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380752
Start	29524187:29524187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202146685
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380752
Start	29517766:29517766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1317G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380752
Start	29522435:29522435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1071C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000380752
Start	29532980:29532981(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.372_373delTA
AA Mutation	p.Thr125PhefsTer37(p.T125Ffs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380752
Start	29517777:29517777(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1306delC
AA Mutation	p.Gln436SerfsTer15(p.Q436Sfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC7A1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380752
Start	29530675:29530675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380752
Start	29532945:29532945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144196494
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380752
Start	29523454:29523454(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.861delC
AA Mutation	p.Val288TrpfsTer8(p.V288Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript