Colon Cancer: Gene >> LHX6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373755
Start	122227006:122227006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94G>A
AA Mutation	p.Ala32Thr(p.A32T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373755
Start	122217181:122217181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.482C>T
AA Mutation	p.Ser161Leu(p.S161L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373755
Start	122217241:122217241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Ser141Asn(p.S141N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373755
Start	122217286:122217286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.377G>A
AA Mutation	p.Arg126Gln(p.R126Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373755
Start	122217107:122217107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.556G>A
AA Mutation	p.Asp186Asn(p.D186N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373755
Start	122226976:122226976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124G>A
AA Mutation	p.Ala42Thr(p.A42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373755
Start	122217266:122217266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Trp(p.R133W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373755
Start	122214334:122214334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373755
Start	122226953:122226953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373755
Start	122217108:122217108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373755
Start	122214349:122214349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373755
Start	122217261:122217261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373755
Start	122217246:122217246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756188084
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LHX6

No Mutation Annotation!