Colon Cancer: Gene >> SIPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65641352:65641352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431G>T
AA Mutation	p.Gly144Val(p.G144V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65646309:65646309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1352G>A
AA Mutation	p.Arg451His(p.R451H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65646589:65646589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1555G>A
AA Mutation	p.Gly519Ser(p.G519S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65642348:65642348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778A>G
AA Mutation	p.Ser260Gly(p.S260G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65642363:65642363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374792529
CDS Mutation	c.793G>A
AA Mutation	p.Val265Met(p.V265M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65650639:65650639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3053C>T
AA Mutation	p.Ala1018Val(p.A1018V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65649832:65649832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2713C>T
AA Mutation	p.Arg905Cys(p.R905C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65642328:65642328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758G>A
AA Mutation	p.Ser253Asn(p.S253N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65650425:65650425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2928G>T
AA Mutation	p.Glu976Asp(p.E976D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394224
Start	65649262:65649262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2307G>T
AA Mutation	p.Arg769Ser(p.R769S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65650662:65650662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371548442
CDS Mutation	c.3076C>T
AA Mutation	p.Arg1026Cys(p.R1026C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65644991:65644991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021C>T
AA Mutation	p.Arg341Trp(p.R341W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394224
Start	65641080:65641080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394224
Start	65642558:65642558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394224
Start	65645086:65645086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394224
Start	65649780:65649780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2661C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394224
Start	65649283:65649283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764068625
CDS Mutation	c.2328G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394224
Start	65649309:65649309(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2359delG
AA Mutation	p.Ala787ProfsTer12(p.A787Pfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SIPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65649956:65649956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371556373
CDS Mutation	c.2753C>T
AA Mutation	p.Ser918Leu(p.S918L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394224
Start	65649962:65649962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148088934
CDS Mutation	c.2759C>T
AA Mutation	p.Ala920Val(p.A920V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript