Colon Cancer: Gene >> NARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256854
Start	57607247:57607247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754289689
CDS Mutation	c.888G>T
AA Mutation	p.Leu296Phe(p.L296F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256854
Start	57607278:57607278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.857A>C
AA Mutation	p.Lys286Thr(p.K286T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256854
Start	57615700:57615700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283C>A
AA Mutation	p.Leu95Met(p.L95M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256854
Start	57601734:57601734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1565G>A
AA Mutation	p.Arg522Gln(p.R522Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256854
Start	57615720:57615720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263G>T
AA Mutation	p.Ser88Ile(p.S88I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256854
Start	57605884:57605884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1224A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256854
Start	57602818:57602818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1377T>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256854
Start	57615844:57615844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.225G>A
AA Mutation	p.Met75Ile(p.M75I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256854
Start	57615704:57615704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279G>T
AA Mutation	p.Lys93Asn(p.K93N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256854
Start	57606727:57606727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026T>C
Mutation Classification	Silent
Feature Type	Transcript