Colon Cancer: Gene >> RHCE

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000294413
Start	25375351:25375351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1151C>T
AA Mutation	p.Thr384Ile(p.T384I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294413
Start	25375409:25375409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093C>A
AA Mutation	p.Leu365Ile(p.L365I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294413
Start	25388990:25388990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925G>A
AA Mutation	p.Ala309Thr(p.A309T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294413
Start	25392077:25392077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551C>T
AA Mutation	p.Ala184Val(p.A184V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294413
Start	25420779:25420779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8C>A
AA Mutation	p.Ser3Tyr(p.S3Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294413
Start	25408835:25408835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294413
Start	25375388:25375388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1114T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294413
Start	25392109:25392109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368228913
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294413
Start	25385773:25385773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1011G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294413
Start	25392103:25392103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376509301
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294413
Start	25388992:25388992(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.923delG
AA Mutation	p.Gly308GlufsTer51(p.G308Efs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RHCE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294413
Start	25385792:25385792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992T>C
AA Mutation	p.Ile331Thr(p.I331T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294413
Start	25402694:25402694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.388G>C
AA Mutation	p.Val130Leu(p.V130L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294413
Start	25392103:25392103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376509301
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript