Colon Cancer: Gene >> RPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1880627:1880627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>T
AA Mutation	p.Val393Leu(p.V393L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1875747:1875747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.541C>G
AA Mutation	p.Gln181Glu(p.Q181E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1888793:1888793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1493A>G
AA Mutation	p.Tyr498Cys(p.Y498C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1888838:1888838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143105728
CDS Mutation	c.1538G>A
AA Mutation	p.Arg513His(p.R513H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1879311:1879311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55800538
CDS Mutation	c.856G>A
AA Mutation	p.Val286Ile(p.V286I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1844643:1844643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229T>C
AA Mutation	p.Cys77Arg(p.C77R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1880685:1880685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764606507
CDS Mutation	c.1235G>A
AA Mutation	p.Arg412His(p.R412H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1844629:1844629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215C>A
AA Mutation	p.Ser72Tyr(p.S72Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1883928:1883928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358T>C
AA Mutation	p.Leu453Pro(p.L453P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1883879:1883879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1309G>T
AA Mutation	p.Gly437Trp(p.G437W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1888715:1888715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774947057
CDS Mutation	c.1415G>A
AA Mutation	p.Arg472His(p.R472H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000254719
Start	1883870:1883870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201226474
CDS Mutation	c.1300G>A
AA Mutation	p.Gly434Arg(p.G434R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254719
Start	1888770:1888770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1470G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254719
Start	1879567:1879567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370063869
CDS Mutation	c.960C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254719
Start	1879272:1879272(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.821delA
AA Mutation	p.Asn274MetfsTer5(p.N274Mfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000254719
Start	1895096:1895096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745884794
CDS Mutation	c.1746+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RPA1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254719
Start	1891838:1891838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1557T>C
Mutation Classification	Silent
Feature Type	Transcript