Colon Cancer: Gene >> ACSBG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78179628:78179628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748664490
CDS Mutation	c.1406G>A
AA Mutation	p.Arg469His(p.R469H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78182770:78182770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679C>T
AA Mutation	p.Pro227Ser(p.P227S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78234404:78234404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98T>A
AA Mutation	p.Ile33Asn(p.I33N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78178659:78178659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370057969
CDS Mutation	c.1657C>T
AA Mutation	p.Arg553Cys(p.R553C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78234374:78234374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128C>A
AA Mutation	p.Thr43Asn(p.T43N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78178622:78178622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1694G>A
AA Mutation	p.Arg565His(p.R565H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78174438:78174438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554607936
CDS Mutation	c.1789G>A
AA Mutation	p.Ala597Thr(p.A597T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78234494:78234494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138685512
CDS Mutation	c.8G>A
AA Mutation	p.Arg3His(p.R3H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000258873
Start	78174386:78174386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1841A>G
AA Mutation	p.Lys614Arg(p.K614R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78180915:78180915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751633265
CDS Mutation	c.1093C>T
AA Mutation	p.Arg365Trp(p.R365W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78182099:78182099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941C>T
AA Mutation	p.Pro314Leu(p.P314L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258873
Start	78193970:78193970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779049682
CDS Mutation	c.504G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258873
Start	78174469:78174469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375037443
CDS Mutation	c.1758C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000258873
Start	78234387:78234387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115G>T
AA Mutation	p.Glu39Ter(p.E39*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258873
Start	78171448:78171449(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2170dupA
AA Mutation	p.Met724AsnfsTer59(p.M724Nfs*59)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ACSBG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78193534:78193534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750963555
CDS Mutation	c.635C>T
AA Mutation	p.Thr212Met(p.T212M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258873
Start	78182781:78182781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668G>C
AA Mutation	p.Trp223Ser(p.W223S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258873
Start	78179699:78179699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1335T>C
Mutation Classification	Silent
Feature Type	Transcript