Colon Cancer: Gene >> SLC22A7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372585
Start	43302376:43302376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776077806
CDS Mutation	c.1238C>T
AA Mutation	p.Thr413Met(p.T413M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372585
Start	43304156:43304156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1504G>T
AA Mutation	p.Ala502Ser(p.A502S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372585
Start	43298629:43298629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.271A>G
AA Mutation	p.Asn91Asp(p.N91D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372585
Start	43301256:43301256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949G>C
AA Mutation	p.Glu317Gln(p.E317Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372585
Start	43301601:43301601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202177785
CDS Mutation	c.970G>A
AA Mutation	p.Ala324Thr(p.A324T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372585
Start	43299662:43299662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539T>C
AA Mutation	p.Val180Ala(p.V180A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372585
Start	43301211:43301211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.904G>A
AA Mutation	p.Ala302Thr(p.A302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372585
Start	43301620:43301620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769610613
CDS Mutation	c.989G>A
AA Mutation	p.Arg330Gln(p.R330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372585
Start	43300047:43300047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.808C>A
AA Mutation	p.Pro270Thr(p.P270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372585
Start	43298410:43298410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.52C>A
AA Mutation	p.Leu18Met(p.L18M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372585
Start	43301600:43301600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372585
Start	43298428:43298428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372585
Start	43302729:43302729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372585
Start	43299639:43299639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372585
Start	43300023:43300023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.784C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372585
Start	43304161:43304161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1509G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372585
Start	43304077:43304077(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1430delG
AA Mutation	p.Gly477AlafsTer67(p.G477Afs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372585
Start	43304146:43304147(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1500dupG
AA Mutation	p.Ile501AspfsTer148(p.I501Dfs*148)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372585
Start	43298730:43298730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372C>A
AA Mutation	p.Phe124Leu(p.F124L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript