Colon Cancer: Gene >> HDAC7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000427332
Start	47791702:47791702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1700T>A
AA Mutation	p.Leu567His(p.L567H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000427332
Start	47788146:47788146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747647941
CDS Mutation	c.2137G>A
AA Mutation	p.Gly713Ser(p.G713S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000427332
Start	47798855:47798855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371297447
CDS Mutation	c.71G>A
AA Mutation	p.Arg24His(p.R24H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000427332
Start	47798817:47798817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109C>A
AA Mutation	p.Leu37Met(p.L37M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000427332
Start	47797392:47797392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.452G>A
AA Mutation	p.Arg151His(p.R151H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000427332
Start	47796233:47796233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652G>A
AA Mutation	p.Gly218Ser(p.G218S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000427332
Start	47785865:47785865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2476C>A
AA Mutation	p.Gln826Lys(p.Q826K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000427332
Start	47797419:47797419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425G>A
AA Mutation	p.Ser142Asn(p.S142N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427332
Start	47798200:47798200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.252G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427332
Start	47791961:47791961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200152997
CDS Mutation	c.1605C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427332
Start	47796273:47796273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148220732
CDS Mutation	c.612G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427332
Start	47798596:47798596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427332
Start	47786697:47786697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778316682
CDS Mutation	c.2343C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000427332
Start	47787744:47787744(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2304delC
AA Mutation	p.Met769TrpfsTer12(p.M769Wfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000427332
Start	47788128:47788130(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2153_2155delTCT
AA Mutation	p.Phe718del(p.F718del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HDAC7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000427332
Start	47795324:47795324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027C>T
AA Mutation	p.Arg343Trp(p.R343W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000427332
Start	47787744:47787744(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2304delC
AA Mutation	p.Met769TrpfsTer12(p.M769Wfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript