Colon Cancer: Gene >> SPHK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245222
Start	48628854:48628854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753977026
CDS Mutation	c.1046G>A
AA Mutation	p.Arg349His(p.R349H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245222
Start	48629357:48629357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549G>A
AA Mutation	p.Asp517Asn(p.D517N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000245222
Start	48628247:48628247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842C>T
AA Mutation	p.Ala281Val(p.A281V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000245222
Start	48626245:48626245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394A>G
AA Mutation	p.Thr132Ala(p.T132A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000245222
Start	48629373:48629373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1565C>T
AA Mutation	p.Pro522Leu(p.P522L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245222
Start	48625974:48625974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245222
Start	48628054:48628054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768473899
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245222
Start	48629602:48629602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1794G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245222
Start	48628003:48628003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245222
Start	48629277:48629277(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1473delC
AA Mutation	p.Val492Ter(p.V492*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SPHK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245222
Start	48629391:48629391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1583C>T
AA Mutation	p.Pro528Leu(p.P528L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript