Colon Cancer: Gene >> PDCD6IP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307296
Start	33855209:33855209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2069A>T
AA Mutation	p.Lys690Ile(p.K690I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307296
Start	33836258:33836258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1049A>C
AA Mutation	p.Lys350Thr(p.K350T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307296
Start	33825317:33825317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593T>C
AA Mutation	p.Val198Ala(p.V198A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307296
Start	33821982:33821982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362G>A
AA Mutation	p.Ser121Asn(p.S121N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307296
Start	33845557:33845557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1610C>T
AA Mutation	p.Ala537Val(p.A537V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000307296
Start	33825338:33825338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.614G>T
AA Mutation	p.Arg205Ile(p.R205I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307296
Start	33852505:33852505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1659A>T
AA Mutation	p.Lys553Asn(p.K553N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307296
Start	33865284:33865284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2286G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307296
Start	33866393:33866393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756528890
CDS Mutation	c.2475G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307296
Start	33844147:33844147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1395T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307296
Start	33836259:33836260(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1050_1051insAATCC
AA Mutation	p.Phe351AsnfsTer37(p.F351Nfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PDCD6IP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307296
Start	33838243:33838243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097C>G
AA Mutation	p.Ser366Cys(p.S366C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307296
Start	33836174:33836174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.965G>A
AA Mutation	p.Arg322Gln(p.R322Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307296
Start	33844151:33844151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1399G>T
AA Mutation	p.Asp467Tyr(p.D467Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307296
Start	33825319:33825319(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781474699
CDS Mutation	c.602delT
AA Mutation	p.Leu201Ter(p.L201*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000307296
Start	33825241:33825241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757821681
CDS Mutation	c.517C>T
AA Mutation	p.Arg173Ter(p.R173*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript