Colon Cancer: Gene >> TGM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38139456:38139456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142184177
CDS Mutation	c.1298G>A
AA Mutation	p.Arg433Gln(p.R433Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38155978:38155978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540320021
CDS Mutation	c.302C>T
AA Mutation	p.Ser101Leu(p.S101L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38141307:38141307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1074C>A
AA Mutation	p.Asp358Glu(p.D358E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38130317:38130317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1966C>T
AA Mutation	p.Pro656Ser(p.P656S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38142110:38142110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781011976
CDS Mutation	c.949C>T
AA Mutation	p.Arg317Cys(p.R317C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38142167:38142167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751214792
CDS Mutation	c.892G>A
AA Mutation	p.Val298Met(p.V298M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38132470:38132470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148045565
CDS Mutation	c.1646A>G
AA Mutation	p.Glu549Gly(p.E549G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38155910:38155910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>T
AA Mutation	p.Gly124Cys(p.G124C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38146789:38146789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746351550
CDS Mutation	c.787C>T
AA Mutation	p.Arg263Cys(p.R263C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38146834:38146834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742G>A
AA Mutation	p.Gly248Ser(p.G248S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38146872:38146872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704G>T
AA Mutation	p.Gly235Val(p.G235V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38139529:38139529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368135396
CDS Mutation	c.1225G>A
AA Mutation	p.Asp409Asn(p.D409N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38138277:38138277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1451A>T
AA Mutation	p.Asn484Ile(p.N484I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361475
Start	38139539:38139539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1215C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361475
Start	38139650:38139650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772874225
CDS Mutation	c.1104G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361475
Start	38131170:38131170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752256099
CDS Mutation	c.1836G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361475
Start	38132463:38132463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761336603
CDS Mutation	c.1653C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361475
Start	38146775:38146775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749547512
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361475
Start	38138330:38138330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1398C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361475
Start	38130273:38130273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113631627
CDS Mutation	c.2010C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361475
Start	38146832:38146832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369988859
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361475
Start	38139590:38139590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756405757
CDS Mutation	c.1164C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TGM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38141290:38141290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091A>G
AA Mutation	p.Lys364Arg(p.K364R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38131204:38131204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1802G>A
AA Mutation	p.Arg601His(p.R601H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361475
Start	38132469:38132469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1647G>T
AA Mutation	p.Glu549Asp(p.E549D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript