Colon Cancer: Gene >> SPRED1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299084
Start	38322383:38322383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749378713
CDS Mutation	c.350G>A
AA Mutation	p.Arg117Gln(p.R117Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299084
Start	38299450:38299450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.110G>A
AA Mutation	p.Ser37Asn(p.S37N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299084
Start	38299501:38299501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161G>A
AA Mutation	p.Gly54Asp(p.G54D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299084
Start	38299393:38299393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758855467
CDS Mutation	c.53G>A
AA Mutation	p.Arg18Gln(p.R18Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299084
Start	38351199:38351199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.870A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299084
Start	38351295:38351295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299084
Start	38339780:38339780(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.471delT
AA Mutation	p.Gln158SerfsTer16(p.Q158Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299084
Start	38322262:38322262(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.234delA
AA Mutation	p.Asp79ThrfsTer42(p.D79Tfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299084
Start	38322324:38322324(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.291delG
AA Mutation	p.Lys98SerfsTer23(p.K98Sfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000299084
Start	38339743:38339743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>T
AA Mutation	p.Glu144Ter(p.E144*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SPRED1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299084
Start	38299411:38299411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71G>A
AA Mutation	p.Arg24Gln(p.R24Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299084
Start	38351274:38351274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945T>C
Mutation Classification	Silent
Feature Type	Transcript