Colon Cancer: Gene >> LARS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265537
Start	45516118:45516118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs398123036
CDS Mutation	c.1886C>T
AA Mutation	p.Thr629Met(p.T629M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265537
Start	45394650:45394650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149789249
CDS Mutation	c.197G>A
AA Mutation	p.Arg66Gln(p.R66Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265537
Start	45491635:45491635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1358G>T
AA Mutation	p.Arg453Leu(p.R453L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265537
Start	45394591:45394591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138G>T
AA Mutation	p.Lys46Asn(p.K46N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265537
Start	45516139:45516139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575606480
CDS Mutation	c.1907C>T
AA Mutation	p.Thr636Met(p.T636M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265537
Start	45516171:45516171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539920212
CDS Mutation	c.1939G>A
AA Mutation	p.Gly647Arg(p.G647R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265537
Start	45500561:45500561(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1747delA
AA Mutation	p.Met583TrpfsTer51(p.M583Wfs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LARS2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265537
Start	45400250:45400250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368047098
CDS Mutation	c.240G>A
Mutation Classification	Silent
Feature Type	Transcript