Colon Cancer: Gene >> HSPA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161525455:161525455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797G>A
AA Mutation	p.Arg266His(p.R266H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161526475:161526475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781574993
CDS Mutation	c.1817G>A
AA Mutation	p.Arg606His(p.R606H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161526315:161526315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1657G>T
AA Mutation	p.Gly553Cys(p.G553C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161524922:161524922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264C>A
AA Mutation	p.Asp88Glu(p.D88E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161525146:161525146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488C>T
AA Mutation	p.Ala163Val(p.A163V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161525088:161525088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>A
AA Mutation	p.Ala144Thr(p.A144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161525247:161525247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139552185
CDS Mutation	c.589G>A
AA Mutation	p.Val197Met(p.V197M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161526052:161526052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773522375
CDS Mutation	c.1394G>A
AA Mutation	p.Gly465Asp(p.G465D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161526281:161526281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1623A>C
AA Mutation	p.Lys541Asn(p.K541N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309758
Start	161526368:161526368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1710C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309758
Start	161525528:161525528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759271260
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309758
Start	161525159:161525159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370008079
CDS Mutation	c.501G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309758
Start	161525426:161525426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309758
Start	161525663:161525663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375914735
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309758
Start	161525675:161525675(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1022delG
AA Mutation	p.Gly341AlafsTer21(p.G341Afs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000309758
Start	161526246:161526246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1588G>T
AA Mutation	p.Glu530Ter(p.E530*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309758
Start	161526547:161526548(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1894dupG
AA Mutation	p.Asp632GlyfsTer9(p.D632Gfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HSPA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161526354:161526354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750741969
CDS Mutation	c.1696G>A
AA Mutation	p.Glu566Lys(p.E566K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161524756:161524756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98A>G
AA Mutation	p.Asn33Ser(p.N33S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309758
Start	161525120:161525120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462C>A
AA Mutation	p.Asp154Glu(p.D154E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript