Colon Cancer: Gene >> GATA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8064110:8064110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893G>A
AA Mutation	p.Arg298Gln(p.R298Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8058551:8058551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201023943
CDS Mutation	c.488C>T
AA Mutation	p.Pro163Leu(p.P163L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8055780:8055780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125C>T
AA Mutation	p.Pro42Leu(p.P42L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8064041:8064041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824G>A
AA Mutation	p.Arg275Gln(p.R275Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8064131:8064131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914G>A
AA Mutation	p.Arg305Gln(p.R305Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8064077:8064077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.860G>T
AA Mutation	p.Cys287Phe(p.C287F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8058536:8058536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473C>T
AA Mutation	p.Pro158Leu(p.P158L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8069495:8069495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944C>T
AA Mutation	p.Thr315Met(p.T315M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8073874:8073874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200935603
CDS Mutation	c.1183G>A
AA Mutation	p.Ala395Thr(p.A395T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8055680:8055680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25C>T
AA Mutation	p.Arg9Cys(p.R9C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8055777:8055777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.122A>G
AA Mutation	p.Tyr41Cys(p.Y41C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8058428:8058428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365T>C
AA Mutation	p.Ile122Thr(p.I122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8073953:8073953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771315353
CDS Mutation	c.1262C>T
AA Mutation	p.Pro421Leu(p.P421L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346208
Start	8058507:8058507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346208
Start	8058474:8058474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745734873
CDS Mutation	c.411G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346208
Start	8055802:8055802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346208
Start	8058498:8058498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765392255
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346208
Start	8073912:8073912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144824106
CDS Mutation	c.1221G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346208
Start	8058681:8058681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346208
Start	8058489:8058489(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.431delG
AA Mutation	p.Gly144AlafsTer51(p.G144Afs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346208
Start	8058392:8058392(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.333delC
AA Mutation	p.Trp112GlyfsTer83(p.W112Gfs*83)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346208
Start	8073817:8073817(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1131delA
AA Mutation	p.Val378CysfsTer26(p.V378Cfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346208
Start	8058765:8058765(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776668722
CDS Mutation	c.708delC
AA Mutation	p.Ser237AlafsTer28(p.S237Afs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GATA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8058678:8058678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615G>A
AA Mutation	p.Met205Ile(p.M205I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8058499:8058499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752779081
CDS Mutation	c.436G>A
AA Mutation	p.Ala146Thr(p.A146T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346208
Start	8064131:8064131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914G>A
AA Mutation	p.Arg305Gln(p.R305Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346208
Start	8073885:8073885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1194A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346208
Start	8073939:8073939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1248G>A
Mutation Classification	Silent
Feature Type	Transcript