Colon Cancer: Gene >> PTPN6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318974
Start	6957744:6957744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782346134
CDS Mutation	c.1165G>A
AA Mutation	p.Glu389Lys(p.E389K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318974
Start	6952008:6952008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370939978
CDS Mutation	c.157C>T
AA Mutation	p.Arg53Trp(p.R53W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318974
Start	6960893:6960893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1761G>T
AA Mutation	p.Lys587Asn(p.K587N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000318974
Start	6960090:6960090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1432C>A
AA Mutation	p.Leu478Met(p.L478M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318974
Start	6954863:6954863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385G>A
AA Mutation	p.Glu129Lys(p.E129K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318974
Start	6955263:6955263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367551491
CDS Mutation	c.629G>A
AA Mutation	p.Arg210Gln(p.R210Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318974
Start	6951689:6951689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89G>A
AA Mutation	p.Arg30Gln(p.R30Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000318974
Start	6952054:6952054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203A>C
AA Mutation	p.Lys68Thr(p.K68T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318974
Start	6960146:6960146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200112594
CDS Mutation	c.1488G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318974
Start	6960161:6960161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782495635
CDS Mutation	c.1503G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318974
Start	6960830:6960830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1698C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318974
Start	6959930:6959930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370019783
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318974
Start	6959936:6959936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782284633
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318974
Start	6958047:6958047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375270811
CDS Mutation	c.1335C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000318974
Start	6956502:6956502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1008G>A
AA Mutation	p.Trp336Ter(p.W336*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PTPN6

No Mutation Annotation!