Colon Cancer: Gene >> PTPN11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112489068:112489068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397507541
CDS Mutation	c.1492C>T
AA Mutation	p.Arg498Trp(p.R498W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112453325:112453325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463G>A
AA Mutation	p.Asp155Asn(p.D155N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112450387:112450387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.207G>T
AA Mutation	p.Glu69Asp(p.E69D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112489084:112489084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397507546
CDS Mutation	c.1508G>T
AA Mutation	p.Gly503Val(p.G503V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112489111:112489111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1535G>A
AA Mutation	p.Arg512Gln(p.R512Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112502165:112502165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186919241
CDS Mutation	c.1621G>A
AA Mutation	p.Glu541Lys(p.E541K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112450406:112450406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121918464
CDS Mutation	c.226G>A
AA Mutation	p.Glu76Lys(p.E76K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112482143:112482143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749523268
CDS Mutation	c.1162G>A
AA Mutation	p.Val388Ile(p.V388I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112450385:112450385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205G>A
AA Mutation	p.Glu69Lys(p.E69K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112488456:112488456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1393C>T
AA Mutation	p.Arg465Trp(p.R465W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351677
Start	112486483:112486483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351677
Start	112486552:112486552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777895575
CDS Mutation	c.1302C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351677
Start	112477682:112477682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351677
Start	112453204:112453204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTPN11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112453325:112453325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463G>T
AA Mutation	p.Asp155Tyr(p.D155Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112488466:112488466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121918457
CDS Mutation	c.1403C>T
AA Mutation	p.Thr468Met(p.T468M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112504718:112504718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1736T>G
AA Mutation	p.Val579Gly(p.V579G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112504746:112504746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1764G>T
AA Mutation	p.Gln588His(p.Q588H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112489084:112489084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397507546
CDS Mutation	c.1508G>T
AA Mutation	p.Gly503Val(p.G503V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112453231:112453231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755619262
CDS Mutation	c.369G>T
AA Mutation	p.Glu123Asp(p.E123D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000351677
Start	112454635:112454635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597G>T
AA Mutation	p.Lys199Asn(p.K199N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript