CES2[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 726481	NM_003869.6(CES2):c.-188C>G	CES2 (T2S)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2206363	NM_003869.6(CES2):c.-143G>A	CES2 (S17N)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2256775	NM_001365405.1(CES2):c.-107C>T	CES2	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2610550	NM_001365405.1(CES2):c.-95G>A	CES2	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2309840	NM_001365405.1(CES2):c.-65C>T	CES2	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3143233	NM_001365405.1(CES2):c.-56C>T	CES2	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3143236	NM_001365405.1(CES2):c.-16G>T	CES2	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3266360	NM_001365405.1(CES2):c.19C>T (p.Arg7Cys)	CES2 (R7C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2646607	NM_001365405.1(CES2):c.51T>C (p.Leu17=)	CES2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3266361	NM_001365405.1(CES2):c.68G>A (p.Arg23Gln)	CES2 (R23Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3143237	NM_001365405.1(CES2):c.139C>T (p.His47Tyr)	CES2 (H47Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282208	NM_001365405.1(CES2):c.230A>C (p.Glu77Ala)	CES2 (E77A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3266362	NM_001365405.1(CES2):c.284G>A (p.Cys95Tyr)	CES2 (C95Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404659	NM_001365405.1(CES2):c.395C>T (p.Ala132Val)	CES2 (A132V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318005	NM_001365405.1(CES2):c.421C>G (p.Pro141Ala)	CES2 (P48A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2646608	NM_001365405.1(CES2):c.441C>T (p.His147=)	CES2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2209488	NM_001365405.1(CES2):c.451C>T (p.Leu151Phe)	CES2 (L151F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486724	NM_001365405.1(CES2):c.599A>G (p.Asp200Gly)	CES2 (D200G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207530	NM_001365405.1(CES2):c.637G>C (p.Ala213Pro)	CES2 (A120P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3143238	NM_001365405.1(CES2):c.662G>A (p.Arg221His)	CES2 (R128H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457041	NM_001365405.1(CES2):c.695C>T (p.Thr232Met)	CES2 (T139M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3143239	NM_001365405.1(CES2):c.766G>A (p.Val256Met)	CES2 (V256M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3143240	NM_001365405.1(CES2):c.805G>T (p.Val269Phe)	CES2 (V176F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569815	NM_001365405.1(CES2):c.806T>C (p.Val269Ala)	CES2 (V269A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3143234	NM_001365405.1(CES2):c.1288C>T (p.Arg430Trp)	CES2 (R337W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303813	NM_001365405.1(CES2):c.1339A>G (p.Asn447Asp)	CES2 (N354D +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2303814	NM_001365405.1(CES2):c.1340A>T (p.Asn447Ile)	CES2 (N447I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612451	NM_001365405.1(CES2):c.1463T>A (p.Met488Lys)	CES2 (M379K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3143235	NM_001365405.1(CES2):c.1534G>A (p.Asp512Asn)	CES2 (D512N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3266363	NM_001365405.1(CES2):c.1669A>G (p.Thr557Ala)	CES2 (T448A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 30