Colon Cancer: Gene >> HSPA12A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116675197:116675197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1612G>A
AA Mutation	p.Gly538Arg(p.G538R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116679590:116679590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199C>T
AA Mutation	p.Pro400Leu(p.P400L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116674987:116674987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374935080
CDS Mutation	c.1822G>A
AA Mutation	p.Asp608Asn(p.D608N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116698680:116698680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501A>C
AA Mutation	p.Glu167Asp(p.E167D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116675208:116675208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781852527
CDS Mutation	c.1601C>T
AA Mutation	p.Pro534Leu(p.P534L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116675179:116675179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782115853
CDS Mutation	c.1630C>T
AA Mutation	p.Arg544Cys(p.R544C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116676486:116676486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303T>C
AA Mutation	p.Trp435Arg(p.W435R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116676428:116676428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782777572
CDS Mutation	c.1361C>T
AA Mutation	p.Pro454Leu(p.P454L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116675214:116675214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782629136
CDS Mutation	c.1595G>A
AA Mutation	p.Arg532Gln(p.R532Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116707219:116707219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107T>C
AA Mutation	p.Leu36Pro(p.L36P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116701011:116701011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.373C>A
AA Mutation	p.Leu125Met(p.L125M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369209
Start	116692408:116692408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367814906
CDS Mutation	c.606G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369209
Start	116675210:116675210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41284378
CDS Mutation	c.1599G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369209
Start	116675201:116675201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1608C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369209
Start	116675012:116675012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367596673
CDS Mutation	c.1797C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369209
Start	116679538:116679538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201032256
CDS Mutation	c.1251C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369209
Start	116681804:116681804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.909C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369209
Start	116675387:116675387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1422C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369209
Start	116674861:116674861(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1948delG
AA Mutation	p.Asp650ThrfsTer11(p.D650Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369209
Start	116679705:116679705(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1084delA
AA Mutation	p.Ile362TyrfsTer21(p.I362Yfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369209
Start	116676433:116676433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1356delT
AA Mutation	p.Phe452LeufsTer88(p.F452Lfs*88)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HSPA12A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116674935:116674935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555217651
CDS Mutation	c.1874G>A
AA Mutation	p.Arg625His(p.R625H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116705221:116705221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184G>A
AA Mutation	p.Asp62Asn(p.D62N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369209
Start	116679636:116679636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1153G>T
AA Mutation	p.Ala385Ser(p.A385S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369209
Start	116701042:116701042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374384405
CDS Mutation	c.342C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369209
Start	116681840:116681840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.873C>A
Mutation Classification	Silent
Feature Type	Transcript