Colon Cancer: Gene >> HSPA1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31811737:31811737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236A>C
AA Mutation	p.Lys79Thr(p.K79T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31810106:31810106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746297288
CDS Mutation	c.1867G>A
AA Mutation	p.Gly623Arg(p.G623R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31811189:31811189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142416335
CDS Mutation	c.784G>A
AA Mutation	p.Val262Met(p.V262M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31810231:31810231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371717441
CDS Mutation	c.1742C>T
AA Mutation	p.Ser581Leu(p.S581L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31811360:31811360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613G>T
AA Mutation	p.Gly205Cys(p.G205C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31811008:31811008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768126334
CDS Mutation	c.965C>T
AA Mutation	p.Ala322Val(p.A322V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31810111:31810111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1862C>T
AA Mutation	p.Ala621Val(p.A621V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31810689:31810689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1284G>T
AA Mutation	p.Gln428His(p.Q428H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31810618:31810618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1355C>T
AA Mutation	p.Thr452Ile(p.T452I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31811279:31811279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.694G>T
AA Mutation	p.Gly232Trp(p.G232W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31810526:31810526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1447G>T
AA Mutation	p.Asp483Tyr(p.D483Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31811258:31811258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715C>G
AA Mutation	p.Leu239Val(p.L239V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31811621:31811621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352C>T
AA Mutation	p.Pro118Ser(p.P118S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31810493:31810493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1480G>A
AA Mutation	p.Asp494Asn(p.D494N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31811879:31811879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745365008
CDS Mutation	c.94G>A
AA Mutation	p.Ala32Thr(p.A32T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375654
Start	31811232:31811232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375654
Start	31810752:31810752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2075799
CDS Mutation	c.1221G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375654
Start	31811604:31811604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375654
Start	31811682:31811682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375654
Start	31811925:31811925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000375654
Start	31810340:31810340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1633G>T
AA Mutation	p.Glu545Ter(p.E545*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HSPA1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375654
Start	31811186:31811186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.787A>G
AA Mutation	p.Arg263Gly(p.R263G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript