BUB3[gene] and "single gene"[properties] - ClinVar - NCBI

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

Search results

Items: 1 to 100 of 319

<< First< Prev

Page of 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2625368	NM_004725.4(BUB3):c.6C>G (p.Thr2=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1756598	NM_004725.4(BUB3):c.6C>T (p.Thr2=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1761596	NM_004725.4(BUB3):c.7G>A (p.Gly3Ser)	BUB3 (G3S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1747033	NM_004725.4(BUB3):c.11C>G (p.Ser4Cys)	BUB3 (S4C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1776138	NM_004725.4(BUB3):c.15C>T (p.Asn5=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1793647	NM_004725.4(BUB3):c.25C>T (p.Leu9=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1793640	NM_004725.4(BUB3):c.25C>A (p.Leu9Met)	BUB3 (L9M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1727610	NM_004725.4(BUB3):c.30C>T (p.Asn10=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1731027	NM_004725.4(BUB3):c.33G>A (p.Gln11=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1733066	NM_004725.4(BUB3):c.35C>A (p.Pro12Gln)	BUB3 (P12Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496866	NM_004725.4(BUB3):c.36A>C (p.Pro12=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1734056	NM_004725.4(BUB3):c.36A>G (p.Pro12=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2496875	NM_004725.4(BUB3):c.37C>T (p.Pro13Ser)	BUB3 (P13S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1735037	NM_004725.4(BUB3):c.37C>A (p.Pro13Thr)	BUB3 (P13T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2563120	NM_004725.4(BUB3):c.38C>A (p.Pro13His)	BUB3 (P13H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2448131	NM_004725.4(BUB3):c.39C>G (p.Pro13=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1736860	NM_004725.4(BUB3):c.39C>T (p.Pro13=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1737837	NM_004725.4(BUB3):c.40G>A (p.Glu14Lys)	BUB3 (E14K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3224500	NM_004725.4(BUB3):c.41A>G (p.Glu14Gly)	BUB3 (E14G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1742541	NM_004725.4(BUB3):c.46G>A (p.Gly16Ser)	BUB3 (G16S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2625367	NM_004725.4(BUB3):c.47G>T (p.Gly16Val)	BUB3 (G16V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1747942	NM_004725.4(BUB3):c.54C>T (p.Ser18=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1749739	NM_004725.4(BUB3):c.57C>G (p.Ser19=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2496851	NM_004725.4(BUB3):c.136G>C (p.Ala46Pro)	BUB3 (A46P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496827	NM_004725.4(BUB3):c.137C>T (p.Ala46Val)	BUB3 (A46V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1771496	NM_004725.4(BUB3):c.138C>G (p.Ala46=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1771711	NM_004725.4(BUB3):c.139A>G (p.Asn47Asp)	BUB3 (N47D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496881	NM_004725.4(BUB3):c.140A>G (p.Asn47Ser)	BUB3 (N47S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1772218	NM_004725.4(BUB3):c.141C>T (p.Asn47=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3224490	NM_004725.4(BUB3):c.144C>T (p.Ser48=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1772886	NM_004725.4(BUB3):c.144C>G (p.Ser48=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1773116	NM_004725.4(BUB3):c.145A>T (p.Met49Leu)	BUB3 (M49L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1773112	NM_004725.4(BUB3):c.145A>C (p.Met49Leu)	BUB3 (M49L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620102	NM_004725.4(BUB3):c.148C>A (p.Arg50=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1774179	NM_004725.4(BUB3):c.150G>T (p.Arg50=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1774167	NM_004725.4(BUB3):c.150G>A (p.Arg50=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2621410	NM_004725.4(BUB3):c.151C>T (p.Leu51Phe)	BUB3 (L51F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2448141	NM_004725.4(BUB3):c.153C>A (p.Leu51=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1774798	NM_004725.4(BUB3):c.153C>T (p.Leu51=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1774794	NM_004725.4(BUB3):c.153C>G (p.Leu51=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1775481	NM_004725.4(BUB3):c.156G>A (p.Lys52=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3224491	NM_004725.4(BUB3):c.157T>A (p.Tyr53Asn)	BUB3 (Y53N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1775868	NM_004725.4(BUB3):c.158A>G (p.Tyr53Cys)	BUB3 (Y53C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1776802	NM_004725.4(BUB3):c.162G>C (p.Gln54His)	BUB3 (Q54H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1777005	NM_004725.4(BUB3):c.163C>T (p.His55Tyr)	BUB3 (H55Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1777865	NM_004725.4(BUB3):c.167C>G (p.Thr56Ser)	BUB3 (T56S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1778102	NM_004725.4(BUB3):c.168C>T (p.Thr56=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1778097	NM_004725.4(BUB3):c.168C>A (p.Thr56=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1778530	NM_004725.4(BUB3):c.170G>A (p.Gly57Asp)	BUB3 (G57D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496871	NM_004725.4(BUB3):c.171C>T (p.Gly57=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1779164	NM_004725.4(BUB3):c.173C>T (p.Ala58Val)	BUB3 (A58V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1779360	NM_004725.4(BUB3):c.174C>T (p.Ala58=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1779560	NM_004725.4(BUB3):c.175G>C (p.Val59Leu)	BUB3 (V59L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1779938	NM_004725.4(BUB3):c.177C>G (p.Val59=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1780165	NM_004725.4(BUB3):c.178C>G (p.Leu60Val)	BUB3 (L60V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3224492	NM_004725.4(BUB3):c.179T>C (p.Leu60Pro)	BUB3 (L60P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1780562	NM_004725.4(BUB3):c.180G>C (p.Leu60=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1780554	NM_004725.4(BUB3):c.180G>A (p.Leu60=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3224493	NM_004725.4(BUB3):c.181G>C (p.Asp61His)	BUB3 (D61H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402628	NM_004725.4(BUB3):c.185G>T (p.Cys62Phe)	BUB3 (C62F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1781863	NM_004725.4(BUB3):c.187G>A (p.Ala63Thr)	BUB3 (A63T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1782034	NM_004725.4(BUB3):c.188C>A (p.Ala63Asp)	BUB3 (A63D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1782233	NM_004725.4(BUB3):c.189C>G (p.Ala63=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1782489	NM_004725.4(BUB3):c.190T>C (p.Phe64Leu)	BUB3 (F64L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1783180	NM_004725.4(BUB3):c.194A>G (p.Tyr65Cys)	BUB3 (Y65C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1783178	NM_004725.4(BUB3):c.194A>C (p.Tyr65Ser)	BUB3 (Y65S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1783953	NM_004725.4(BUB3):c.198T>C (p.Asp66=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1784869	NM_004725.4(BUB3):c.203C>T (p.Thr68Met)	BUB3 (T68M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1785042	NM_004725.4(BUB3):c.204G>C (p.Thr68=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1785191	NM_004725.4(BUB3):c.205C>T (p.His69Tyr)	BUB3 (H69Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1785712	NM_004725.4(BUB3):c.208G>A (p.Ala70Thr)	BUB3 (A70T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1786046	NM_004725.4(BUB3):c.210C>A (p.Ala70=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1787249	NM_004725.4(BUB3):c.217G>C (p.Gly73Arg)	BUB3 (G73R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1787399	NM_004725.4(BUB3):c.218G>A (p.Gly73Glu)	BUB3 (G73E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561576	NM_004725.4(BUB3):c.220G>A (p.Gly74Arg)	BUB3 (G74R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1787911	NM_004725.4(BUB3):c.221G>C (p.Gly74Ala)	BUB3 (G74A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1788566	NM_004725.4(BUB3):c.225A>C (p.Leu75=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1788769	NM_004725.4(BUB3):c.226G>T (p.Asp76Tyr)	BUB3 (D76Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1789087	NM_004725.4(BUB3):c.228T>C (p.Asp76=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3224494	NM_004725.4(BUB3):c.230A>G (p.His77Arg)	BUB3 (H77R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1790145	NM_004725.4(BUB3):c.235T>C (p.Leu79=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3224495	NM_004725.4(BUB3):c.240A>T (p.Lys80Asn)	BUB3 (K80N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1791305	NM_004725.4(BUB3):c.243G>A (p.Met81Ile)	BUB3 (M81I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1791458	NM_004725.4(BUB3):c.244C>T (p.His82Tyr)	BUB3 (H82Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1791455	NM_004725.4(BUB3):c.244C>A (p.His82Asn)	BUB3 (H82N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1791598	NM_004725.4(BUB3):c.245A>G (p.His82Arg)	BUB3 (H82R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3224496	NM_004725.4(BUB3):c.255C>T (p.Asn85=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1793207	NM_004725.4(BUB3):c.256A>G (p.Thr86Ala)	BUB3 (T86A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496883	NM_004725.4(BUB3):c.258T>C (p.Thr86=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3224497	NM_004725.4(BUB3):c.264A>T (p.Gln88His)	BUB3 (Q88H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135601	NM_004725.4(BUB3):c.264A>C (p.Gln88His)	BUB3 (Q88H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3059802	NM_004725.4(BUB3):c.266-7T>C	BUB3	Single nucleotide variant (intron variant)	BUB3-related disorder	GBenign
Select item 2448138	NM_004725.4(BUB3):c.266A>G (p.Glu89Gly)	BUB3 (E89G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1795157	NM_004725.4(BUB3):c.271C>A (p.Leu91Ile)	BUB3 (L91I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1795428	NM_004725.4(BUB3):c.273T>C (p.Leu91=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2496829	NM_004725.4(BUB3):c.275T>C (p.Val92Ala)	BUB3 (V92A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1795911	NM_004725.4(BUB3):c.277G>T (p.Gly93Trp)	BUB3 (G93W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1796549	NM_004725.4(BUB3):c.282C>A (p.Thr94=)	BUB3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1796696	NM_004725.4(BUB3):c.283C>T (p.His95Tyr)	BUB3 (H95Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1797149	NM_004725.4(BUB3):c.287A>T (p.Asp96Val)	BUB3 (D96V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 4