Mutation

Primary Site >> Stomach Cancer

Gene >> LEPR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65636994:65636994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3477G>T
AA Mutation	p.Lys1159Asn(p.K1159N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65608866:65608866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748855258
CDS Mutation	c.1717C>T
AA Mutation	p.Arg573Cys(p.R573C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65636476:65636476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776269726
CDS Mutation	c.2959G>A
AA Mutation	p.Ala987Thr(p.A987T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65636212:65636212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2695T>G
AA Mutation	p.Phe899Val(p.F899V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65636819:65636819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267598694
CDS Mutation	c.3302C>T
AA Mutation	p.Ser1101Leu(p.S1101L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65619997:65619997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2465C>A
AA Mutation	p.Pro822Gln(p.P822Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65636213:65636213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2696T>C
AA Mutation	p.Phe899Ser(p.F899S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65619940:65619940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2408C>A
AA Mutation	p.Pro803His(p.P803H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65617976:65617976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2225A>T
AA Mutation	p.Gln742Leu(p.Q742L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65616035:65616035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2023A>T
AA Mutation	p.Ser675Cys(p.S675C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65636430:65636430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2913G>T
AA Mutation	p.Glu971Asp(p.E971D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000349533
Start	65601436:65601436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039A>G
AA Mutation	p.Asn347Asp(p.N347D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349533
Start	65610257:65610257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1956T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349533
Start	65636244:65636244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2727T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349533
Start	65565571:65565571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349533
Start	65636445:65636445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138826362
CDS Mutation	c.2928C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349533
Start	65616058:65616058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192825082
CDS Mutation	c.2046C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349533
Start	65622936:65622936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748857078
CDS Mutation	c.2628G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349533
Start	65636928:65636928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3411T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000349533
Start	65636877:65636877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3360C>A
AA Mutation	p.Cys1120Ter(p.C1120*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349533
Start	65636776:65636777(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3268_3269dupAG
AA Mutation	p.Ser1090ArgfsTer6(p.S1090Rfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript