Colon Cancer: Gene >> TRMT10A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273962
Start	99549101:99549101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007C>T
AA Mutation	p.Ser336Phe(p.S336F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273962
Start	99558126:99558126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>A
AA Mutation	p.Arg91Ser(p.R91S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273962
Start	99549344:99549344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764T>G
AA Mutation	p.Ile255Ser(p.I255S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273962
Start	99558075:99558075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322A>G
AA Mutation	p.Ser108Gly(p.S108G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273962
Start	99559157:99559157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775920482
CDS Mutation	c.182G>A
AA Mutation	p.Arg61His(p.R61H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000273962
Start	99549269:99549269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839C>T
AA Mutation	p.Pro280Leu(p.P280L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273962
Start	99559249:99559249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273962
Start	99558193:99558193(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.204delA
AA Mutation	p.Lys68AsnfsTer7(p.K68Nfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000273962
Start	99549138:99549138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.970C>T
AA Mutation	p.Gln324Ter(p.Q324*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000273962
Start	99558120:99558120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277C>T
AA Mutation	p.Arg93Ter(p.R93*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRMT10A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273962
Start	99556180:99556180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.461T>A
AA Mutation	p.Met154Lys(p.M154K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273962
Start	99559301:99559301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.38C>A
AA Mutation	p.Ser13Tyr(p.S13Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript