Colon Cancer: Gene >> SATB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18416083:18416083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439G>A
AA Mutation	p.Asp147Asn(p.D147N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18394707:18394707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961C>A
AA Mutation	p.Leu321Met(p.L321M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18394664:18394664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004G>T
AA Mutation	p.Arg335Ile(p.R335I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18394613:18394613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055C>T
AA Mutation	p.Pro352Leu(p.P352L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18378189:18378189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1556T>G
AA Mutation	p.Val519Gly(p.V519G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18349323:18349323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2139G>C
AA Mutation	p.Glu713Asp(p.E713D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18378191:18378191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554G>T
AA Mutation	p.Lys518Asn(p.K518N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18416040:18416040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482A>G
AA Mutation	p.Tyr161Cys(p.Y161C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338745
Start	18394570:18394570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1098G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338745
Start	18352052:18352052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1719G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338745
Start	18394810:18394810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201064692
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338745
Start	18349656:18349656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1806G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338745
Start	18349585:18349585(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1877delC
AA Mutation	p.Pro626HisfsTer81(p.P626Hfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000338745
Start	18349538:18349538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752755275
CDS Mutation	c.1924C>T
AA Mutation	p.Arg642Ter(p.R642*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000338745
Start	18349520:18349520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1942C>T
AA Mutation	p.Arg648Ter(p.R648*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000338745
Start	18420811:18420811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157C>T
AA Mutation	p.Gln53Ter(p.Q53*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SATB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18349512:18349512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1950A>C
AA Mutation	p.Lys650Asn(p.K650N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18397188:18397188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.742G>T
AA Mutation	p.Asp248Tyr(p.D248Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338745
Start	18394698:18394698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.970G>C
AA Mutation	p.Ala324Pro(p.A324P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338745
Start	18349605:18349605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1857G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000338745
Start	18397227:18397227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703G>T
AA Mutation	p.Glu235Ter(p.E235*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript