Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HSPA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000227378
Start	123058377:123058377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1630T>C
AA Mutation	p.Ser544Pro(p.S544P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000227378
Start	123058337:123058337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1670A>C
AA Mutation	p.Lys557Thr(p.K557T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000227378
Start	123059135:123059135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1247G>A
AA Mutation	p.Arg416His(p.R416H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000227378
Start	123058279:123058279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1728A>C
AA Mutation	p.Glu576Asp(p.E576D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227378
Start	123059984:123059984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227378
Start	123059741:123059741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148846437
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227378
Start	123058302:123058303(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1704_1705delGA
AA Mutation	p.Lys569AspfsTer6(p.K569Dfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000227378
Start	123060734:123060734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270G>A
AA Mutation	p.Trp90Ter(p.W90*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000227378
Start	123057810:123057821(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1854_1865delAGGAGGAATGCC
AA Mutation	p.Met621_Gly624del(p.M621_G624del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_lost
Transcription ID	ENST00000227378
Start	123057734:123057734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1941A>T
AA Mutation	p.Ter647TyrextTer5(p.647Yext5)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HSPA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000227378
Start	123059550:123059550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1043A>C
AA Mutation	p.Lys348Thr(p.K348T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000227378
Start	123058460:123058460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547A>G
AA Mutation	p.Glu516Gly(p.E516G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000227378
Start	123059658:123059658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935G>C
AA Mutation	p.Gly312Ala(p.G312A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000227378
Start	123061123:123061123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202T>A
AA Mutation	p.Phe68Ile(p.F68I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript