Colon Cancer: Gene >> SPIDR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47673828:47673828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1572T>G
AA Mutation	p.Cys524Trp(p.C524W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47729007:47729007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2510T>A
AA Mutation	p.Leu837Gln(p.L837Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47293933:47293933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.428T>C
AA Mutation	p.Phe143Ser(p.F143S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47599012:47599012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777715546
CDS Mutation	c.1360C>T
AA Mutation	p.Arg454Cys(p.R454C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47407901:47407901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.817G>C
AA Mutation	p.Glu273Gln(p.E273Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47396578:47396578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782244112
CDS Mutation	c.728C>G
AA Mutation	p.Ala243Gly(p.A243G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47440517:47440517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072G>T
AA Mutation	p.Asp358Tyr(p.D358Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47595879:47595879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1166T>C
AA Mutation	p.Val389Ala(p.V389A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47713587:47713587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374494194
CDS Mutation	c.2287A>G
AA Mutation	p.Met763Val(p.M763V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47673866:47673866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746475893
CDS Mutation	c.1610C>T
AA Mutation	p.Ser537Leu(p.S537L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000297423
Start	47713491:47713491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766801688
CDS Mutation	c.2191C>T
AA Mutation	p.Arg731Trp(p.R731W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297423
Start	47728936:47728936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767477984
CDS Mutation	c.2439C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SPIDR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47407917:47407917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.833C>A
AA Mutation	p.Ser278Tyr(p.S278Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297423
Start	47673847:47673847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1591C>T
AA Mutation	p.His531Tyr(p.H531Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript