ClinVar for Gene (Select 84033) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3341621	NM_001386125.1(OBSCN):c.3074G>A (p.Ser1025Asn)	OBSCN (S1025N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3302100	NM_001386125.1(OBSCN):c.7241G>A (p.Gly2414Asp)	OBSCN (G2414D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302099	NM_001386125.1(OBSCN):c.19868T>G (p.Leu6623Arg)	OBSCN (L5666R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302098	NM_001386125.1(OBSCN):c.25949C>T (p.Ala8650Val)	OBSCN (A7693V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302097	NM_001386125.1(OBSCN):c.21650G>T (p.Gly7217Val)	OBSCN (G7217V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302096	NM_001386125.1(OBSCN):c.20384G>A (p.Arg6795His)	OBSCN (R5838H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302095	NM_001386125.1(OBSCN):c.1829C>A (p.Ala610Asp)	OBSCN (A610D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302094	NM_001386125.1(OBSCN):c.18004C>T (p.Pro6002Ser)	OBSCN (P5045S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302093	NM_001386125.1(OBSCN):c.11358C>G (p.Ile3786Met)	OBSCN (I3786M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302092	NM_001386125.1(OBSCN):c.11728T>G (p.Trp3910Gly)	OBSCN (W3910G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302091	NM_001386125.1(OBSCN):c.389G>A (p.Arg130His)	OBSCN, OBSCN-AS1 (R130H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302090	NM_001386125.1(OBSCN):c.9739G>C (p.Ala3247Pro)	OBSCN (A3247P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302089	NM_001386125.1(OBSCN):c.26750A>G (p.Lys8917Arg)	OBSCN (K7960R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302088	NM_001386125.1(OBSCN):c.1420C>T (p.Arg474Cys)	OBSCN (R474C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302087	NM_001386125.1(OBSCN):c.14965G>T (p.Ala4989Ser)	OBSCN (A4032S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302086	NM_001386125.1(OBSCN):c.25995G>C (p.Lys8665Asn)	OBSCN (K8665N +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302085	NM_001386125.1(OBSCN):c.7598G>A (p.Arg2533Gln)	OBSCN (R2158Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302084	NM_001386125.1(OBSCN):c.18760G>C (p.Asp6254His)	OBSCN (D5297H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302083	NM_001386125.1(OBSCN):c.10646G>C (p.Ser3549Thr)	OBSCN (S3120T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302082	NM_001386125.1(OBSCN):c.23854A>G (p.Ile7952Val)	OBSCN (I6995V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302081	NM_001386125.1(OBSCN):c.26020T>C (p.Tyr8674His)	OBSCN (Y8674H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302080	NM_001386125.1(OBSCN):c.25958G>A (p.Arg8653Gln)	OBSCN (R7696Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302079	NM_001386125.1(OBSCN):c.19916G>A (p.Gly6639Glu)	OBSCN (G6639E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302078	NM_001386125.1(OBSCN):c.24986A>G (p.Glu8329Gly)	OBSCN (E7372G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302076	NM_001386125.1(OBSCN):c.26633G>A (p.Cys8878Tyr)	LOC129932715, OBSCN (C8876Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302075	NM_001386125.1(OBSCN):c.15524G>A (p.Arg5175Gln)	OBSCN (R5175Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302074	NM_001386125.1(OBSCN):c.18852C>G (p.Asp6284Glu)	OBSCN (D5327E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302073	NM_001386125.1(OBSCN):c.11002C>G (p.Leu3668Val)	OBSCN (L3668V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302072	NM_001386125.1(OBSCN):c.18043A>C (p.Ile6015Leu)	OBSCN (I5058L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302071	NM_001386125.1(OBSCN):c.12346G>C (p.Val4116Leu)	OBSCN (V3687L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302070	NM_001386125.1(OBSCN):c.1204T>C (p.Tyr402His)	OBSCN, OBSCN-AS1 (Y402H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3302069	NM_001386125.1(OBSCN):c.10526C>A (p.Ala3509Glu)	OBSCN (A3509E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302068	NM_001386125.1(OBSCN):c.25184A>T (p.Lys8395Met)	OBSCN (K8395M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302067	NM_001386125.1(OBSCN):c.15124G>C (p.Ala5042Pro)	OBSCN (A4085P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302066	NM_001386125.1(OBSCN):c.21533-2501A>G	OBSCN (R6395G)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3302065	NM_001386125.1(OBSCN):c.17434G>A (p.Val5812Met)	OBSCN (V5812M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302064	NM_001386125.1(OBSCN):c.10844G>A (p.Arg3615Gln)	OBSCN (R3615Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302063	NM_001386125.1(OBSCN):c.26591C>T (p.Ala8864Val)	OBSCN (A8864V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302062	NM_001386125.1(OBSCN):c.2134G>A (p.Ala712Thr)	OBSCN (A712T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302061	NM_001386125.1(OBSCN):c.15626T>C (p.Ile5209Thr)	OBSCN (I4252T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302060	NM_001386125.1(OBSCN):c.23638G>A (p.Val7880Met)	OBSCN (V6923M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302059	NM_001386125.1(OBSCN):c.3227A>G (p.Lys1076Arg)	OBSCN (K984R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302058	NM_001386125.1(OBSCN):c.17056G>A (p.Glu5686Lys)	OBSCN (E4729K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302057	NM_001386125.1(OBSCN):c.10219G>A (p.Glu3407Lys)	OBSCN (E2978K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302056	NM_001386125.1(OBSCN):c.10793C>T (p.Ala3598Val)	OBSCN (A3169V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302055	NM_001386125.1(OBSCN):c.21574C>G (p.Leu7192Val)	OBSCN (L6235V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302054	NM_001386125.1(OBSCN):c.11999A>G (p.Lys4000Arg)	OBSCN (K3571R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302053	NM_001386125.1(OBSCN):c.8846G>A (p.Gly2949Asp)	OBSCN (G2520D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302052	NM_001386125.1(OBSCN):c.21455C>T (p.Ala7152Val)	OBSCN (A7152V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302051	NM_001386125.1(OBSCN):c.26033A>G (p.Lys8678Arg)	OBSCN (K7721R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302050	NM_001386125.1(OBSCN):c.20603C>T (p.Ala6868Val)	LOC112577546, OBSCN (A6868V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302049	NM_001386125.1(OBSCN):c.18593A>G (p.Tyr6198Cys)	OBSCN (Y6198C +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302048	NM_001386125.1(OBSCN):c.25018G>A (p.Val8340Met)	OBSCN (V7383M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302047	NM_001386125.1(OBSCN):c.24457T>C (p.Phe8153Leu)	OBSCN (F7196L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302046	NM_001386125.1(OBSCN):c.24488A>G (p.Gln8163Arg)	OBSCN (Q7206R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302045	NM_001386125.1(OBSCN):c.8123C>T (p.Ser2708Leu)	OBSCN (S2708L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302044	NM_001386125.1(OBSCN):c.26091C>G (p.His8697Gln)	OBSCN (H7740Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302043	NM_001386125.1(OBSCN):c.21185A>G (p.Gln7062Arg)	OBSCN (Q6105R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302042	NM_001386125.1(OBSCN):c.14729G>A (p.Arg4910His)	OBSCN (R3953H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302041	NM_001386125.1(OBSCN):c.2516A>G (p.His839Arg)	OBSCN (H839R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302040	NM_001386125.1(OBSCN):c.21533-1975C>T	OBSCN (S6570F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302039	NM_001386125.1(OBSCN):c.23614C>T (p.Arg7872Cys)	OBSCN (R6915C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302038	NM_001386125.1(OBSCN):c.25724G>A (p.Arg8575Gln)	OBSCN (R7618Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302037	NM_001386125.1(OBSCN):c.17251C>T (p.Arg5751Cys)	OBSCN (R5751C +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302036	NM_001386125.1(OBSCN):c.25115G>A (p.Arg8372His)	OBSCN (R7415H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302035	NM_001386125.1(OBSCN):c.2113G>A (p.Ala705Thr)	OBSCN (A705T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302034	NM_001386125.1(OBSCN):c.16352G>A (p.Arg5451His)	OBSCN (R5451H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302033	NM_001386125.1(OBSCN):c.22730A>C (p.Gln7577Pro)	OBSCN (Q7577P +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302032	NM_001386125.1(OBSCN):c.9173C>T (p.Ala3058Val)	OBSCN (A2629V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302031	NM_001386125.1(OBSCN):c.15061C>T (p.Arg5021Cys)	OBSCN (R4064C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302030	NM_001386125.1(OBSCN):c.21533-2339C>G	OBSCN (L6449V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302029	NM_001386125.1(OBSCN):c.11450C>T (p.Ala3817Val)	OBSCN (A3817V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302028	NM_001386125.1(OBSCN):c.20544G>T (p.Gln6848His)	OBSCN (Q6848H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302027	NM_001386125.1(OBSCN):c.25579G>A (p.Ala8527Thr)	OBSCN (A7570T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302026	NM_001386125.1(OBSCN):c.17672A>C (p.Asp5891Ala)	OBSCN (D5891A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302025	NM_001386125.1(OBSCN):c.8602C>T (p.Arg2868Trp)	OBSCN (R2439W +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302024	NM_001386125.1(OBSCN):c.2012G>A (p.Arg671Gln)	OBSCN (R671Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3302023	NM_001386125.1(OBSCN):c.8957A>G (p.Glu2986Gly)	OBSCN (E2557G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302022	NM_001386125.1(OBSCN):c.6849G>C (p.Val2283=)	OBSCN	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3302021	NM_001386125.1(OBSCN):c.534C>T (p.Asp178=)	OBSCN, OBSCN-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3302020	NM_001386125.1(OBSCN):c.20318A>G (p.Asp6773Gly)	OBSCN (D6773G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302019	NM_001386125.1(OBSCN):c.12618G>A (p.Val4206=)	OBSCN	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3302018	NM_001386125.1(OBSCN):c.20637G>A (p.Val6879=)	LOC112577546, OBSCN	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3302017	NM_001386125.1(OBSCN):c.17627G>A (p.Cys5876Tyr)	OBSCN (C4919Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302015	NM_001386125.1(OBSCN):c.15364C>T (p.Leu5122=)	OBSCN	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3302014	NM_001386125.1(OBSCN):c.16762G>C (p.Glu5588Gln)	OBSCN (E4631Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302013	NM_001386125.1(OBSCN):c.16029C>A (p.Ala5343=)	OBSCN	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3302012	NM_001386125.1(OBSCN):c.16418G>A (p.Arg5473Gln)	OBSCN (R4516Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302011	NM_001386125.1(OBSCN):c.20083G>A (p.Ala6695Thr)	OBSCN (A5738T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302010	NM_001386125.1(OBSCN):c.10498A>C (p.Lys3500Gln)	OBSCN (K3500Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302009	NM_001386125.1(OBSCN):c.3675G>A (p.Leu1225=)	OBSCN	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3302008	NM_001386125.1(OBSCN):c.19995C>G (p.Phe6665Leu)	OBSCN (F5708L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302007	NM_001386125.1(OBSCN):c.10556G>T (p.Arg3519Leu)	OBSCN (R3519L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302006	NM_001386125.1(OBSCN):c.2089G>A (p.Val697Ile)	OBSCN (V697I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302005	NM_001386125.1(OBSCN):c.21533-2971C>A	OBSCN (T6238N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302004	NM_001386125.1(OBSCN):c.16822G>T (p.Ala5608Ser)	OBSCN (A5608S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302003	NM_001386125.1(OBSCN):c.1563A>G (p.Val521=)	OBSCN	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3302002	NM_001386125.1(OBSCN):c.17247G>T (p.Leu5749=)	OBSCN	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3302001	NM_001386125.1(OBSCN):c.9564G>A (p.Leu3188=)	OBSCN	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3302000	NM_001386125.1(OBSCN):c.20810G>A (p.Arg6937His)	OBSCN (R6937H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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