Colon Cancer: Gene >> CYP24A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216862
Start	54157470:54157470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200955146
CDS Mutation	c.1352C>T
AA Mutation	p.Ala451Val(p.A451V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216862
Start	54173440:54173440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755653308
CDS Mutation	c.140C>T
AA Mutation	p.Thr47Ile(p.T47I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216862
Start	54157453:54157453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112596218
CDS Mutation	c.1369G>A
AA Mutation	p.Val457Ile(p.V457I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216862
Start	54158159:54158159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571886397
CDS Mutation	c.1163C>T
AA Mutation	p.Thr388Met(p.T388M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216862
Start	54164492:54164492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804G>T
AA Mutation	p.Trp268Cys(p.W268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216862
Start	54171582:54171582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538A>G
AA Mutation	p.Asn180Asp(p.N180D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000216862
Start	54169597:54169597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635T>G
AA Mutation	p.Phe212Cys(p.F212C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000216862
Start	54171628:54171628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492G>C
AA Mutation	p.Lys164Asn(p.K164N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000216862
Start	54157195:54157195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116065115
CDS Mutation	c.1529C>T
AA Mutation	p.Ala510Val(p.A510V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216862
Start	54157194:54157194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150155645
CDS Mutation	c.1530G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216862
Start	54173448:54173448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYP24A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216862
Start	54158995:54158995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1119T>G
AA Mutation	p.Asn373Lys(p.N373K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216862
Start	54164522:54164522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216862
Start	54173340:54173340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.240G>A
Mutation Classification	Silent
Feature Type	Transcript