Colon Cancer: Gene >> PARP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287196
Start	72260602:72260602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764588650
CDS Mutation	c.632G>A
AA Mutation	p.Arg211His(p.R211H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287196
Start	72266750:72266750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769021644
CDS Mutation	c.76G>A
AA Mutation	p.Val26Ile(p.V26I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287196
Start	72242187:72242187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1675C>T
AA Mutation	p.Arg559Trp(p.R559W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000287196
Start	72265169:72265169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.240G>T
AA Mutation	p.Glu80Asp(p.E80D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287196
Start	72242658:72242658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1603C>A
AA Mutation	p.Leu535Met(p.L535M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287196
Start	72265945:72265945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128A>G
AA Mutation	p.Asp43Gly(p.D43G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287196
Start	72241528:72241528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375825095
CDS Mutation	c.1820A>G
AA Mutation	p.Asn607Ser(p.N607S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287196
Start	72242171:72242171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1691T>C
AA Mutation	p.Ile564Thr(p.I564T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000287196
Start	72254472:72254472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174A>G
AA Mutation	p.Ile392Val(p.I392V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287196
Start	72257390:72257390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370713698
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287196
Start	72241536:72241536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546050509
CDS Mutation	c.1812C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287196
Start	72257409:72257409(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.938delT
AA Mutation	p.Phe313SerfsTer34(p.F313Sfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287196
Start	72259613:72259614(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.804_805insTTTCCTTCTACCATTA
AA Mutation	p.Val269PhefsTer21(p.V269Ffs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PARP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287196
Start	72256560:72256560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030G>A
AA Mutation	p.Ala344Thr(p.A344T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287196
Start	72266752:72266752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.74G>C
AA Mutation	p.Gly25Ala(p.G25A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript