Colon Cancer: Gene >> PITPNM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67492080:67492080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369506944
CDS Mutation	c.3688C>T
AA Mutation	p.Arg1230Trp(p.R1230W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67502078:67502078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>A
AA Mutation	p.Asp142Asn(p.D142N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67492121:67492121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766305895
CDS Mutation	c.3647C>T
AA Mutation	p.Ala1216Val(p.A1216V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67502334:67502334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201913288
CDS Mutation	c.373G>A
AA Mutation	p.Val125Ile(p.V125I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67495148:67495148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2560G>A
AA Mutation	p.Val854Ile(p.V854I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67499927:67499927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775010489
CDS Mutation	c.1050C>A
AA Mutation	p.Phe350Leu(p.F350L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67492164:67492164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778114702
CDS Mutation	c.3604C>T
AA Mutation	p.Arg1202Cys(p.R1202C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67493550:67493550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3202C>T
AA Mutation	p.Arg1068Trp(p.R1068W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67497392:67497392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560518491
CDS Mutation	c.1985G>A
AA Mutation	p.Arg662Gln(p.R662Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67497934:67497934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1765A>C
AA Mutation	p.Ser589Arg(p.S589R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67492176:67492176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781622887
CDS Mutation	c.3592G>A
AA Mutation	p.Val1198Met(p.V1198M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67502063:67502063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439G>A
AA Mutation	p.Ala147Thr(p.A147T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67493692:67493692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3154G>A
AA Mutation	p.Val1052Ile(p.V1052I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67498752:67498752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328C>A
AA Mutation	p.Pro443His(p.P443H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67495209:67495209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2499G>T
AA Mutation	p.Trp833Cys(p.W833C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356404
Start	67498991:67498991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755765673
CDS Mutation	c.1182C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356404
Start	67498727:67498727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1353G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356404
Start	67498304:67498304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761608912
CDS Mutation	c.1503C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356404
Start	67493509:67493509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769940514
CDS Mutation	c.3243G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356404
Start	67502320:67502320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61757723
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356404
Start	67495185:67495185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2523G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356404
Start	67497634:67497634(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1828delC
AA Mutation	p.Leu610TrpfsTer101(p.L610Wfs*101)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PITPNM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356404
Start	67500401:67500401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Trp(p.R221W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356404
Start	67493009:67493009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753198689
CDS Mutation	c.3396C>T
Mutation Classification	Silent
Feature Type	Transcript