Colon Cancer: Gene >> CARD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371732
Start	136370637:136370637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.692C>T
AA Mutation	p.Thr231Met(p.T231M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371732
Start	136369757:136369757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1070G>A
AA Mutation	p.Arg357Gln(p.R357Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371732
Start	136371444:136371444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>A
AA Mutation	p.Leu68Met(p.L68M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371732
Start	136367761:136367761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540891739
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382His(p.R382H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371732
Start	136364396:136364396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1517G>A
AA Mutation	p.Arg506His(p.R506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371732
Start	136370362:136370362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883C>A
AA Mutation	p.Gln295Lys(p.Q295K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000371732
Start	136369874:136369874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.953G>T
AA Mutation	p.Cys318Phe(p.C318F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371732
Start	136370873:136370873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772249417
CDS Mutation	c.595G>A
AA Mutation	p.Ala199Thr(p.A199T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371732
Start	136371382:136371382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753481864
CDS Mutation	c.264G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371732
Start	136372007:136372007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371732
Start	136371066:136371066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CARD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371732
Start	136367662:136367662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147340708
CDS Mutation	c.1244G>A
AA Mutation	p.Arg415Gln(p.R415Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript