Colon Cancer: Gene >> SLAMF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302035
Start	160637410:160637410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196A>C
AA Mutation	p.Met66Leu(p.M66L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302035
Start	160637524:160637524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82C>T
AA Mutation	p.Arg28Cys(p.R28C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302035
Start	160637338:160637338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117250272
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Cys(p.R90C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302035
Start	160637367:160637367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239C>T
AA Mutation	p.Ser80Phe(p.S80F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302035
Start	160637245:160637245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.361A>T
AA Mutation	p.Thr121Ser(p.T121S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302035
Start	160624129:160624129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757A>G
AA Mutation	p.Ile253Val(p.I253V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302035
Start	160634641:160634641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199624846
CDS Mutation	c.672G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302035
Start	160646877:160646877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147176135
CDS Mutation	c.69C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302035
Start	160634806:160634806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302035
Start	160637284:160637284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302035
Start	160637216:160637216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLAMF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302035
Start	160612495:160612495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950C>A
AA Mutation	p.Ser317Tyr(p.S317Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302035
Start	160637449:160637449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.157A>C
AA Mutation	p.Asn53His(p.N53H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302035
Start	160637323:160637323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Cys(p.R95C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript