Colon Cancer: Gene >> GPSM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000440944
Start	136338703:136338703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.967G>A
AA Mutation	p.Ala323Thr(p.A323T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000440944
Start	136337913:136337913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770A>G
AA Mutation	p.Asn257Ser(p.N257S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000440944
Start	136356513:136356513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782663989
CDS Mutation	c.1784C>T
AA Mutation	p.Pro595Leu(p.P595L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000440944
Start	136356382:136356382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782116136
CDS Mutation	c.1653C>A
AA Mutation	p.Phe551Leu(p.F551L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000440944
Start	136348709:136348709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220A>T
AA Mutation	p.Lys407Met(p.K407M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000440944
Start	136358138:136358138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1946G>A
AA Mutation	p.Arg649Gln(p.R649Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440944
Start	136348731:136348731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440944
Start	136337875:136337875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440944
Start	136356520:136356520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782204453
CDS Mutation	c.1791C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440944
Start	136355703:136355703(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1472delC
AA Mutation	p.Pro491ArgfsTer12(p.P491Rfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GPSM1

No Mutation Annotation!