Colon Cancer: Gene >> SNCAIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122451222:122451222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2375C>T
AA Mutation	p.Ala792Val(p.A792V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122423575:122423575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838C>A
AA Mutation	p.Leu280Ile(p.L280I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122423177:122423177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.440A>C
AA Mutation	p.Asp147Ala(p.D147A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122423005:122423005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268G>A
AA Mutation	p.Glu90Lys(p.E90K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122422958:122422958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221G>A
AA Mutation	p.Arg74His(p.R74H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122450676:122450676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1829A>G
AA Mutation	p.Lys610Arg(p.K610R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122422877:122422877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140C>A
AA Mutation	p.Ser47Tyr(p.S47Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122451441:122451441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150746854
CDS Mutation	c.2594G>A
AA Mutation	p.Arg865Gln(p.R865Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261368
Start	122431986:122431986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772706842
CDS Mutation	c.1200C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261368
Start	122450968:122450968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146249796
CDS Mutation	c.2121C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261368
Start	122451400:122451400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762107782
CDS Mutation	c.2553C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261368
Start	122403852:122403852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SNCAIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122451401:122451401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773604913
CDS Mutation	c.2554G>A
AA Mutation	p.Glu852Lys(p.E852K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122432054:122432054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268T>G
AA Mutation	p.Leu423Arg(p.L423R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122440719:122440719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768511867
CDS Mutation	c.1387G>A
AA Mutation	p.Val463Ile(p.V463I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261368
Start	122440634:122440634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1302G>T
AA Mutation	p.Lys434Asn(p.K434N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261368
Start	122422917:122422917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754791570
CDS Mutation	c.180G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261368
Start	122451379:122451379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2532C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261368
Start	122432064:122432064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756418048
CDS Mutation	c.1278C>T
Mutation Classification	Silent
Feature Type	Transcript