Colon Cancer: Gene >> TBL1X

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217964
Start	9714998:9714998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702G>A
AA Mutation	p.Gly568Ser(p.G568S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217964
Start	9691587:9691587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625G>A
AA Mutation	p.Ala209Thr(p.A209T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217964
Start	9691648:9691648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370618515
CDS Mutation	c.686G>A
AA Mutation	p.Arg229Gln(p.R229Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217964
Start	9716238:9716238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746301021
CDS Mutation	c.1726C>T
AA Mutation	p.Arg576Trp(p.R576W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217964
Start	9711670:9711670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752103477
CDS Mutation	c.1499C>T
AA Mutation	p.Thr500Met(p.T500M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000217964
Start	9692220:9692220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857C>T
AA Mutation	p.Pro286Leu(p.P286L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217964
Start	9714994:9714994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771230797
CDS Mutation	c.1698C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217964
Start	9688070:9688070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145411823
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217964
Start	9692188:9692188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217964
Start	9693184:9693184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142039049
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217964
Start	9654249:9654249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200551470
CDS Mutation	c.138G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217964
Start	9711755:9711755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745779471
CDS Mutation	c.1584C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000217964
Start	9692162:9692162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.803delG
AA Mutation	p.Gly268AlafsTer7(p.G268Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TBL1X

No Mutation Annotation!