Colon Cancer: Gene >> LARP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324052
Start	112653107:112653107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768746321
CDS Mutation	c.1447T>C
AA Mutation	p.Tyr483His(p.Y483H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324052
Start	112646606:112646606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374971073
CDS Mutation	c.322A>G
AA Mutation	p.Arg108Gly(p.R108G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324052
Start	112647340:112647340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788T>C
AA Mutation	p.Ile263Thr(p.I263T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000324052
Start	112647127:112647127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646G>A
AA Mutation	p.Glu216Lys(p.E216K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324052
Start	112654096:112654096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1605G>T
AA Mutation	p.Lys535Asn(p.K535N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324052
Start	112650519:112650519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765596788
CDS Mutation	c.1353C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324052
Start	112650567:112650567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324052
Start	112649598:112649598(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763740398
CDS Mutation	c.1213delA
AA Mutation	p.Thr405GlnfsTer5(p.T405Qfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324052
Start	112646388:112646389(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.246dupA
AA Mutation	p.Leu83IlefsTer4(p.L83Ifs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LARP7

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324052
Start	112646886:112646886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324052
Start	112649576:112649576(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1188delA
AA Mutation	p.Ala397LeufsTer6(p.A397Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript