Colon Cancer: Gene >> NIM1K

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326035
Start	43245984:43245984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770268418
CDS Mutation	c.209G>A
AA Mutation	p.Arg70Gln(p.R70Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326035
Start	43245902:43245902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768600358
CDS Mutation	c.127C>T
AA Mutation	p.Arg43Cys(p.R43C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326035
Start	43280533:43280533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115G>A
AA Mutation	p.Arg372Gln(p.R372Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326035
Start	43245837:43245837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144641529
CDS Mutation	c.62G>A
AA Mutation	p.Arg21Gln(p.R21Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326035
Start	43277252:43277252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488G>T
AA Mutation	p.Ser163Ile(p.S163I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326035
Start	43277203:43277203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439C>T
AA Mutation	p.His147Tyr(p.H147Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000326035
Start	43280723:43280723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305T>G
AA Mutation	p.Ile435Met(p.I435M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000326035
Start	43245986:43245986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211A>T
AA Mutation	p.Ile71Leu(p.I71L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326035
Start	43280609:43280609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326035
Start	43280720:43280720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1302G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326035
Start	43245919:43245919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370653085
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326035
Start	43280057:43280057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326035
Start	43280366:43280366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267600643
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326035
Start	43280297:43280297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000326035
Start	43280475:43280475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057G>T
AA Mutation	p.Glu353Ter(p.E353*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000326035
Start	43280016:43280016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598G>T
AA Mutation	p.Glu200Ter(p.E200*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NIM1K

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326035
Start	43245999:43245999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140198619
CDS Mutation	c.224G>A
AA Mutation	p.Arg75Gln(p.R75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000326035
Start	43246004:43246004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Ter(p.R77*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000326035
Start	43277125:43277125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>T
AA Mutation	p.Glu121Ter(p.E121*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript