Colon Cancer: Gene >> LARP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299213
Start	70853961:70853961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128C>T
AA Mutation	p.Ala43Val(p.A43V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299213
Start	70853991:70853991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98A>G
AA Mutation	p.Asp33Gly(p.D33G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299213
Start	70832279:70832279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1249A>G
AA Mutation	p.Met417Val(p.M417V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299213
Start	70832132:70832132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201700915
CDS Mutation	c.1396G>A
AA Mutation	p.Val466Ile(p.V466I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299213
Start	70832111:70832111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1417A>G
AA Mutation	p.Arg473Gly(p.R473G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000299213
Start	70832221:70832221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372104696
CDS Mutation	c.1307G>A
AA Mutation	p.Arg436His(p.R436H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000299213
Start	70832354:70832354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561519879
CDS Mutation	c.1174G>A
AA Mutation	p.Val392Ile(p.V392I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299213
Start	70832318:70832318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1210C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299213
Start	70832283:70832283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1245G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299213
Start	70832355:70832355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1173C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299213
Start	70832919:70832919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766327224
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299213
Start	70836362:70836362(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.344delT
AA Mutation	p.Leu115CysfsTer2(p.L115Cfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LARP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299213
Start	70832593:70832593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770915412
CDS Mutation	c.935C>T
AA Mutation	p.Ala312Val(p.A312V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299213
Start	70832160:70832160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1368G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299213
Start	70832511:70832511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299213
Start	70832556:70832556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752044115
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299213
Start	70832739:70832739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371562863
CDS Mutation	c.789C>T
Mutation Classification	Silent
Feature Type	Transcript