Colon Cancer: Gene >> THBD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377103
Start	23047961:23047961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1544C>T
AA Mutation	p.Ser515Leu(p.S515L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377103
Start	23048501:23048501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004C>T
AA Mutation	p.Pro335Leu(p.P335L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377103
Start	23048322:23048322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183G>A
AA Mutation	p.Ala395Thr(p.A395T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377103
Start	23049188:23049188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764904057
CDS Mutation	c.317G>A
AA Mutation	p.Arg106His(p.R106H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377103
Start	23047841:23047841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1664C>T
AA Mutation	p.Ala555Val(p.A555V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377103
Start	23049377:23049377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768321291
CDS Mutation	c.128C>T
AA Mutation	p.Ala43Val(p.A43V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377103
Start	23049406:23049406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377103
Start	23047843:23047843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1662C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377103
Start	23048302:23048302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1203G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377103
Start	23048500:23048500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377103
Start	23048071:23048071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377103
Start	23048018:23048018(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1487delC
AA Mutation	p.Pro496ArgfsTer10(p.P496Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> THBD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377103
Start	23049129:23049129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376G>A
AA Mutation	p.Asp126Asn(p.D126N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377103
Start	23048592:23048592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.913T>C
AA Mutation	p.Ser305Pro(p.S305P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript