Colon Cancer: Gene >> ACSL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131960562:131960562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1842G>C
AA Mutation	p.Lys614Asn(p.K614N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131966429:131966429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1625G>A
AA Mutation	p.Gly542Glu(p.G542E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131971599:131971599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1310C>T
AA Mutation	p.Pro437Leu(p.P437L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131990877:131990877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286T>C
AA Mutation	p.Phe96Leu(p.F96L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131968023:131968023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200649165
CDS Mutation	c.1438G>A
AA Mutation	p.Val480Ile(p.V480I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131989456:131989456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.428A>T
AA Mutation	p.Lys143Ile(p.K143I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131988858:131988858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524T>C
AA Mutation	p.Val175Ala(p.V175A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379264
Start	132011538:132011538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16C>A
AA Mutation	p.Leu6Ile(p.L6I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131994168:131994168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58C>A
AA Mutation	p.Gln20Lys(p.Q20K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131990952:131990952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151127186
CDS Mutation	c.211C>T
AA Mutation	p.Arg71Trp(p.R71W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131971567:131971567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1342G>A
AA Mutation	p.Ala448Thr(p.A448T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379240
Start	131966466:131966466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1588C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379240
Start	131962607:131962607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370745130
CDS Mutation	c.1710C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ACSL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379240
Start	131970140:131970140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1420G>T
AA Mutation	p.Asp474Tyr(p.D474Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript