Colon Cancer: Gene >> CCNA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36433141:36433141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217C>A
AA Mutation	p.Pro73Thr(p.P73T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36440160:36440160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748235047
CDS Mutation	c.1075G>A
AA Mutation	p.Val359Ile(p.V359I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36438733:36438733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.759G>T
AA Mutation	p.Glu253Asp(p.E253D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36438728:36438728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754G>T
AA Mutation	p.Val252Leu(p.V252L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36438788:36438788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814C>A
AA Mutation	p.Leu272Met(p.L272M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36433205:36433205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.281G>T
AA Mutation	p.Arg94Met(p.R94M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000255465
Start	36432729:36432729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108G>T
AA Mutation	p.Gln36His(p.Q36H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36432671:36432671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.50G>A
AA Mutation	p.Gly17Asp(p.G17D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36441136:36441136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117C>A
AA Mutation	p.Leu373Ile(p.L373I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36441135:36441135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116T>A
AA Mutation	p.Ser372Arg(p.S372R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36437693:36437693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362C>A
AA Mutation	p.Ala121Glu(p.A121E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36440050:36440050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140946240
CDS Mutation	c.965G>A
AA Mutation	p.Arg322Gln(p.R322Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36432665:36432665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44T>C
AA Mutation	p.Ile15Thr(p.I15T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36441121:36441121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749179710
CDS Mutation	c.1102G>A
AA Mutation	p.Val368Ile(p.V368I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36432685:36432685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.64T>A
AA Mutation	p.Tyr22Asn(p.Y22N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36432659:36432659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38C>T
AA Mutation	p.Ser13Phe(p.S13F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255465
Start	36437838:36437838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255465
Start	36442176:36442176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255465
Start	36433183:36433183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255465
Start	36437763:36437763(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.436delG
AA Mutation	p.Asp146ThrfsTer19(p.D146Tfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000255465
Start	36438162:36438162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640G>T
AA Mutation	p.Glu214Ter(p.E214*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCNA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255465
Start	36432650:36432650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29A>G
AA Mutation	p.Tyr10Cys(p.Y10C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255465
Start	36439991:36439991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000255465
Start	36433105:36433105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Ter(p.R61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript