Colon Cancer: Gene >> RERGL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229002
Start	18081320:18081320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489G>T
AA Mutation	p.Met163Ile(p.M163I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229002
Start	18084529:18084529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563526809
CDS Mutation	c.323G>A
AA Mutation	p.Ser108Asn(p.S108N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229002
Start	18084535:18084535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317A>G
AA Mutation	p.Gln106Arg(p.Q106R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229002
Start	18081381:18081381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428T>C
AA Mutation	p.Leu143Pro(p.L143P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229002
Start	18081385:18081385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>A
AA Mutation	p.Ala142Thr(p.A142T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000229002
Start	18081430:18081430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768331335
CDS Mutation	c.379C>A
AA Mutation	p.Leu127Ile(p.L127I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229002
Start	18085677:18085677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000229002
Start	18081373:18081373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753937969
CDS Mutation	c.436C>T
AA Mutation	p.Arg146Ter(p.R146*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RERGL

No Mutation Annotation!