Colon Cancer: Gene >> LAMP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265598
Start	183154043:183154043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398C>T
AA Mutation	p.Ser133Leu(p.S133L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265598
Start	183152460:183152460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151059567
CDS Mutation	c.803C>T
AA Mutation	p.Thr268Met(p.T268M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265598
Start	183153897:183153897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774368709
CDS Mutation	c.544G>A
AA Mutation	p.Gly182Ser(p.G182S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265598
Start	183135765:183135765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069G>A
AA Mutation	p.Asp357Asn(p.D357N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265598
Start	183140583:183140583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901T>C
AA Mutation	p.Tyr301His(p.Y301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265598
Start	183153898:183153898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759259053
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265598
Start	183153703:183153703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265598
Start	183154327:183154327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.114A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265598
Start	183154291:183154291(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.150delA
AA Mutation	p.Lys50AsnfsTer15(p.K50Nfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LAMP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265598
Start	183153923:183153923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115806403
CDS Mutation	c.518C>T
AA Mutation	p.Ser173Leu(p.S173L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript