Colon Cancer: Gene >> SPARCL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87499538:87499538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37A>G
AA Mutation	p.Thr13Ala(p.T13A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87491676:87491676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233G>T
AA Mutation	p.Glu411Asp(p.E411D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87494995:87494995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188965626
CDS Mutation	c.187G>A
AA Mutation	p.Asp63Asn(p.D63N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87494271:87494271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529A>G
AA Mutation	p.Arg177Gly(p.R177G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87493921:87493921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.879G>C
AA Mutation	p.Trp293Cys(p.W293C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87494369:87494369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431G>A
AA Mutation	p.Gly144Asp(p.G144D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87495070:87495070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746899306
CDS Mutation	c.112G>A
AA Mutation	p.Asp38Asn(p.D38N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87493788:87493788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1012G>A
AA Mutation	p.Asp338Asn(p.D338N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87494057:87494057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743A>G
AA Mutation	p.Asp248Gly(p.D248G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87479506:87479506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1890C>A
AA Mutation	p.Phe630Leu(p.F630L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87494381:87494381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419T>G
AA Mutation	p.Phe140Cys(p.F140C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87490365:87490365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1439C>T
AA Mutation	p.Ala480Val(p.A480V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87480510:87480510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1679T>G
AA Mutation	p.Ile560Ser(p.I560S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87493916:87493916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884G>T
AA Mutation	p.Ser295Ile(p.S295I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282470
Start	87494996:87494996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766671889
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282470
Start	87493756:87493756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770599706
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282470
Start	87499555:87499555(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.20delT
AA Mutation	p.Phe7SerfsTer29(p.F7Sfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SPARCL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87493955:87493955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200319615
CDS Mutation	c.845C>T
AA Mutation	p.Ser282Leu(p.S282L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282470
Start	87490370:87490370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434C>T
Mutation Classification	Silent
Feature Type	Transcript