Colon Cancer: Gene >> ARR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307959
Start	70278124:70278124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.753C>A
AA Mutation	p.Phe251Leu(p.F251L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307959
Start	70277404:70277404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746178806
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Trp(p.R162W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307959
Start	70280809:70280809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057C>T
AA Mutation	p.Pro353Ser(p.P353S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307959
Start	70276259:70276259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323A>G
AA Mutation	p.Asn108Ser(p.N108S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307959
Start	70281707:70281707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108C>T
AA Mutation	p.Arg370Trp(p.R370W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307959
Start	70269890:70269890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745442722
CDS Mutation	c.87G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307959
Start	70277439:70277439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758684137
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307959
Start	70277782:70277782(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.682delA
AA Mutation	p.Ile228SerfsTer16(p.I228Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000307959
Start	70270138:70270138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Ter(p.R47*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ARR3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307959
Start	70269872:70269872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.69C>T
Mutation Classification	Silent
Feature Type	Transcript