Colon Cancer: Gene >> MERTK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	112028524:112028524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2660G>A
AA Mutation	p.Gly887Asp(p.G887D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	112003966:112003966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1849G>T
AA Mutation	p.Ala617Ser(p.A617S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111994362:111994362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1408G>A
AA Mutation	p.Gly470Arg(p.G470R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111929312:111929312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254C>A
AA Mutation	p.Ser85Tyr(p.S85Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111997353:111997353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1481C>A
AA Mutation	p.Pro494Gln(p.P494Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	112028382:112028382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2518G>A
AA Mutation	p.Asp840Asn(p.D840N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111994344:111994344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148833587
CDS Mutation	c.1390G>A
AA Mutation	p.Val464Ile(p.V464I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111947552:111947552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769030123
CDS Mutation	c.742G>A
AA Mutation	p.Val248Met(p.V248M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111968170:111968170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34072093
CDS Mutation	c.878G>A
AA Mutation	p.Arg293His(p.R293H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111929204:111929204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146C>A
AA Mutation	p.Pro49Gln(p.P49Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	112021505:112021505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370526555
CDS Mutation	c.2273G>A
AA Mutation	p.Arg758His(p.R758H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295408
Start	111929214:111929214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295408
Start	112021485:112021485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149178674
CDS Mutation	c.2253C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295408
Start	111929406:111929406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775979143
CDS Mutation	c.348A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MERTK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111945022:111945022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.545A>C
AA Mutation	p.Glu182Ala(p.E182A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111929360:111929360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302G>T
AA Mutation	p.Gly101Val(p.G101V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111994288:111994288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202242962
CDS Mutation	c.1334G>A
AA Mutation	p.Arg445Gln(p.R445Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	112028779:112028779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764736804
CDS Mutation	c.2915C>T
AA Mutation	p.Ser972Leu(p.S972L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	111982970:111982970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751150587
CDS Mutation	c.1273G>A
AA Mutation	p.Val425Met(p.V425M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	112001222:112001222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1626T>G
AA Mutation	p.Asp542Glu(p.D542E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295408
Start	112028832:112028832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200644454
CDS Mutation	c.2968G>A
AA Mutation	p.Asp990Asn(p.D990N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295408
Start	111929157:111929157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771189892
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295408
Start	112021462:112021465(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2232_2235delCTCT
AA Mutation	p.Ser745ArgfsTer24(p.S745Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript