Colon Cancer: Gene >> SNPH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381873
Start	1296379:1296379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8T>A
AA Mutation	p.Met3Lys(p.M3K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381873
Start	1304965:1304965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396G>T
AA Mutation	p.Gln132His(p.Q132H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381873
Start	1305129:1305129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560C>T
AA Mutation	p.Ala187Val(p.A187V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381873
Start	1297167:1297167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771345502
CDS Mutation	c.73G>A
AA Mutation	p.Val25Met(p.V25M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381873
Start	1305504:1305504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373195415
CDS Mutation	c.935G>A
AA Mutation	p.Arg312His(p.R312H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381873
Start	1305249:1305249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191018281
CDS Mutation	c.680G>A
AA Mutation	p.Arg227His(p.R227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381873
Start	1305485:1305485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916G>T
AA Mutation	p.Ala306Ser(p.A306S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381873
Start	1300613:1300613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.210G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381873
Start	1305004:1305004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SNPH

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381873
Start	1305523:1305523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.954C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381873
Start	1305088:1305088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757349234
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript