Colon Cancer: Gene >> CTC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8235929:8235929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771759195
CDS Mutation	c.1108G>A
AA Mutation	p.Ala370Thr(p.A370T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8228598:8228598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3419T>A
AA Mutation	p.Met1140Lys(p.M1140K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8228533:8228533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3484G>A
AA Mutation	p.Glu1162Lys(p.E1162K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8230415:8230415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2812G>A
AA Mutation	p.Ala938Thr(p.A938T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8235188:8235188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1304C>T
AA Mutation	p.Ser435Phe(p.S435F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8234649:8234649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1624C>T
AA Mutation	p.Arg542Trp(p.R542W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8229943:8229943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202138550
CDS Mutation	c.2959C>T
AA Mutation	p.Arg987Trp(p.R987W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8231748:8231748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772328631
CDS Mutation	c.2453G>A
AA Mutation	p.Arg818Gln(p.R818Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8235113:8235113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200619397
CDS Mutation	c.1379G>A
AA Mutation	p.Arg460His(p.R460H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8234519:8234519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1754A>G
AA Mutation	p.Gln585Arg(p.Q585R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8248021:8248021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16G>A
AA Mutation	p.Ala6Thr(p.A6T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000315684
Start	8230294:8230294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2933G>T
AA Mutation	p.Arg978Ile(p.R978I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8232915:8232915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780151711
CDS Mutation	c.1936C>T
AA Mutation	p.Arg646Trp(p.R646W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000315684
Start	8236059:8236059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561782597
CDS Mutation	c.1076C>T
AA Mutation	p.Ser359Leu(p.S359L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000315684
Start	8229306:8229306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758206104
CDS Mutation	c.3152G>A
AA Mutation	p.Arg1051Gln(p.R1051Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315684
Start	8231464:8231464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2481A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315684
Start	8228534:8228534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315684
Start	8238407:8238407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315684
Start	8232913:8232913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1938G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315684
Start	8234545:8234545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78320653
CDS Mutation	c.1728G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315684
Start	8232065:8232065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2223C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315684
Start	8230609:8230609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2712A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315684
Start	8230396:8230396(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs199473677
CDS Mutation	c.2831delC
AA Mutation	p.Pro944LeufsTer7(p.P944Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000315684
Start	8238451:8238451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376C>T
AA Mutation	p.Gln126Ter(p.Q126*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000315684
Start	8237377:8237377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790C>T
AA Mutation	p.Gln264Ter(p.Q264*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000315684
Start	8230653:8230653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2670-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CTC1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315684
Start	8238569:8238569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369789111
CDS Mutation	c.258G>A
Mutation Classification	Silent
Feature Type	Transcript