Colon Cancer: Gene >> CPNE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000198765
Start	86529078:86529078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266T>C
AA Mutation	p.Leu89Pro(p.L89P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000198765
Start	86548434:86548434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781021543
CDS Mutation	c.1013C>T
AA Mutation	p.Ala338Val(p.A338V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000198765
Start	86554940:86554940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148215511
CDS Mutation	c.1210G>A
AA Mutation	p.Val404Met(p.V404M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000198765
Start	86551207:86551207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093T>G
AA Mutation	p.Phe365Val(p.F365V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000198765
Start	86529011:86529011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199T>A
AA Mutation	p.Tyr67Asn(p.Y67N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000198765
Start	86529059:86529059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143209735
CDS Mutation	c.247G>A
AA Mutation	p.Asp83Asn(p.D83N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000198765
Start	86551205:86551205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1091A>G
AA Mutation	p.Asn364Ser(p.N364S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000198765
Start	86528968:86528968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000198765
Start	86547755:86547755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000198765
Start	86558392:86558392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756944839
CDS Mutation	c.1596G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000198765
Start	86558293:86558293(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1500delA
AA Mutation	p.Glu501LysfsTer107(p.E501Kfs*107)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000198765
Start	86531168:86531169(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.327dupG
AA Mutation	p.Lys110GlufsTer24(p.K110Efs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000198765
Start	86546618:86546619(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs751554216
CDS Mutation	c.763dupA
AA Mutation	p.Arg255LysfsTer19(p.R255Kfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CPNE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000198765
Start	86556314:86556314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1467T>A
AA Mutation	p.Phe489Leu(p.F489L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000198765
Start	86551198:86551198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1084C>T
AA Mutation	p.Pro362Ser(p.P362S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000198765
Start	86554917:86554917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187A>C
AA Mutation	p.Asn396Thr(p.N396T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000198765
Start	86532521:86532521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400G>T
AA Mutation	p.Glu134Ter(p.E134*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript