Colon Cancer: Gene >> SIRPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356025
Start	1915404:1915404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772467858
CDS Mutation	c.385C>T
AA Mutation	p.Pro129Ser(p.P129S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356025
Start	1915419:1915419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400T>C
AA Mutation	p.Phe134Leu(p.F134L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356025
Start	1915393:1915393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767136065
CDS Mutation	c.374G>A
AA Mutation	p.Arg125Gln(p.R125Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356025
Start	1921671:1921671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.713A>G
AA Mutation	p.Asp238Gly(p.D238G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356025
Start	1924860:1924860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184G>A
AA Mutation	p.Arg395Gln(p.R395Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356025
Start	1922356:1922356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798G>T
AA Mutation	p.Glu266Asp(p.E266D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356025
Start	1937492:1937492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566700469
CDS Mutation	c.1439G>A
AA Mutation	p.Arg480Gln(p.R480Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356025
Start	1921436:1921436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478G>A
AA Mutation	p.Ala160Thr(p.A160T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356025
Start	1915188:1915188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776144552
CDS Mutation	c.169G>A
AA Mutation	p.Ala57Thr(p.A57T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356025
Start	1921621:1921621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754015483
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356025
Start	1922434:1922434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775792515
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356025
Start	1922395:1922395(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.841delC
AA Mutation	p.Gln281ArgfsTer5(p.Q281Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SIRPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356025
Start	1924829:1924829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1153G>A
AA Mutation	p.Ala385Thr(p.A385T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript