Colon Cancer: Gene >> PLOD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000196061
Start	11964257:11964257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1285G>A
AA Mutation	p.Ala429Thr(p.A429T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000196061
Start	11957876:11957876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144226170
CDS Mutation	c.776G>A
AA Mutation	p.Arg259His(p.R259H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000196061
Start	11963581:11963581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147G>T
AA Mutation	p.Ala383Ser(p.A383S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000196061
Start	11956949:11956949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>A
AA Mutation	p.Val226Met(p.V226M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000196061
Start	11964297:11964297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199567720
CDS Mutation	c.1325G>A
AA Mutation	p.Arg442His(p.R442H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000196061
Start	11949890:11949890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763494719
CDS Mutation	c.286A>G
AA Mutation	p.Ile96Val(p.I96V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000196061
Start	11964219:11964219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138586136
CDS Mutation	c.1247C>T
AA Mutation	p.Ser416Leu(p.S416L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000196061
Start	11970700:11970700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149654030
CDS Mutation	c.1786G>A
AA Mutation	p.Val596Met(p.V596M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000196061
Start	11963555:11963555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121G>A
AA Mutation	p.Ser374Asn(p.S374N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000196061
Start	11949826:11949826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000196061
Start	11965506:11965506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1497G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000196061
Start	11958596:11958596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000196061
Start	11972940:11972940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1971T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000196061
Start	11970817:11970817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1902+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PLOD1

No Mutation Annotation!