Colon Cancer: Gene >> PACS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105381978:105381978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1333C>T
AA Mutation	p.Arg445Trp(p.R445W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105368484:105368484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782690320
CDS Mutation	c.686T>C
AA Mutation	p.Val229Ala(p.V229A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105394649:105394649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368316410
CDS Mutation	c.2647G>A
AA Mutation	p.Gly883Arg(p.G883R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105379789:105379789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010G>A
AA Mutation	p.Ser337Asn(p.S337N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105384905:105384905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782754114
CDS Mutation	c.1906C>T
AA Mutation	p.Arg636Cys(p.R636C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105383390:105383390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782813009
CDS Mutation	c.1645G>A
AA Mutation	p.Val549Met(p.V549M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105348566:105348566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.193G>A
AA Mutation	p.Ala65Thr(p.A65T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105384395:105384395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782813839
CDS Mutation	c.1811G>A
AA Mutation	p.Arg604His(p.R604H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105352424:105352424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254G>A
AA Mutation	p.Ser85Asn(p.S85N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105367354:105367354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781868356
CDS Mutation	c.565G>A
AA Mutation	p.Gly189Ser(p.G189S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000325438
Start	105382540:105382540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1465G>A
AA Mutation	p.Glu489Lys(p.E489K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325438
Start	105367302:105367302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325438
Start	105376890:105376890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146162539
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325438
Start	105382524:105382524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113443045
CDS Mutation	c.1449C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325438
Start	105382815:105382815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782027893
CDS Mutation	c.1515C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325438
Start	105391221:105391221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2046A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325438
Start	105391686:105391686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782232270
CDS Mutation	c.2130G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000325438
Start	105352458:105352460(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.290_292delCCT
AA Mutation	p.Ser97del(p.S97del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PACS2

No Mutation Annotation!