Colon Cancer: Gene >> BTK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101356215:101356215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1403G>A
AA Mutation	p.Arg468His(p.R468H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101362192:101362192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569C>A
AA Mutation	p.Pro190Gln(p.P190Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101359324:101359324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863G>A
AA Mutation	p.Arg288Gln(p.R288Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101356150:101356150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1468C>T
AA Mutation	p.Arg490Cys(p.R490C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101353295:101353295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1807A>G
AA Mutation	p.Asn603Asp(p.N603D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101371678:101371678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264A>C
AA Mutation	p.Glu88Asp(p.E88D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101356059:101356059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs128621202
CDS Mutation	c.1559G>A
AA Mutation	p.Arg520Gln(p.R520Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101358411:101358411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001A>G
AA Mutation	p.Tyr334Cys(p.Y334C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101374624:101374624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152G>A
AA Mutation	p.Ser51Asn(p.S51N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101375278:101375278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368549990
CDS Mutation	c.7G>A
AA Mutation	p.Ala3Thr(p.A3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308731
Start	101353284:101353284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1818T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308731
Start	101356855:101356855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1278C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308731
Start	101356232:101356232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1386C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308731
Start	101349952:101349952(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1913delC
AA Mutation	p.Ala638GlufsTer11(p.A638Efs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BTK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101353918:101353918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1702G>T
AA Mutation	p.Val568Phe(p.V568F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308731
Start	101358417:101358417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995G>A
AA Mutation	p.Arg332His(p.R332H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308731
Start	101353302:101353302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1800A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308731
Start	101374593:101374593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183C>A
Mutation Classification	Silent
Feature Type	Transcript