Colon Cancer: Gene >> XRRA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340360
Start	74927420:74927420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759144221
CDS Mutation	c.469G>A
AA Mutation	p.Val157Met(p.V157M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340360
Start	74852025:74852025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369302102
CDS Mutation	c.1204G>A
AA Mutation	p.Val402Ile(p.V402I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340360
Start	74843330:74843330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2249C>T
AA Mutation	p.Thr750Ile(p.T750I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340360
Start	74845245:74845245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1731C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340360
Start	74940870:74940870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75258704
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340360
Start	74936947:74936947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340360
Start	74848274:74848274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368615662
CDS Mutation	c.1545G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340360
Start	74852026:74852026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188659360
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340360
Start	74843867:74843868(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2111_2112delCA
AA Mutation	p.Thr704ArgfsTer62(p.T704Rfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000340360
Start	74851147:74851147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773580583
CDS Mutation	c.1297C>T
AA Mutation	p.Arg433Ter(p.R433*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> XRRA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340360
Start	74851146:74851146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1298G>A
AA Mutation	p.Arg433Gln(p.R433Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340360
Start	74937048:74937048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115G>T
AA Mutation	p.Val39Phe(p.V39F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340360
Start	74859258:74859258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046C>A
AA Mutation	p.Pro349His(p.P349H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340360
Start	74907209:74907209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697C>T
Mutation Classification	Silent
Feature Type	Transcript