ClinVar Miner

List of variants reported as uncertain significance for Usher syndrome type 2 by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_001195263.2(PDZD7):c.878G>A (p.Arg293Gln) rs368026275
NM_007123.5(USH2A):c.586C>T (p.Pro196Ser) rs756041909
NM_032119.4(ADGRV1):c.12128T>C (p.Ile4043Thr) rs375632680
NM_032119.4(ADGRV1):c.12181G>T (p.Val4061Phe) rs200816323
NM_032119.4(ADGRV1):c.12349C>T (p.Arg4117Cys) rs138908576
NM_032119.4(ADGRV1):c.12704A>G (p.Tyr4235Cys) rs200644004
NM_032119.4(ADGRV1):c.12982G>A (p.Glu4328Lys) rs182452385
NM_032119.4(ADGRV1):c.13358A>G (p.His4453Arg) rs200212083
NM_032119.4(ADGRV1):c.13382A>G (p.His4461Arg) rs182698253
NM_032119.4(ADGRV1):c.14303C>T (p.Ser4768Leu) rs200130204
NM_032119.4(ADGRV1):c.14719G>T (p.Val4907Phe) rs373391623
NM_032119.4(ADGRV1):c.15169C>T (p.Pro5057Ser) rs183633457
NM_032119.4(ADGRV1):c.16331C>A (p.Thr5444Lys) rs370906851
NM_032119.4(ADGRV1):c.17758C>A (p.Leu5920Ile) rs202110635
NM_032119.4(ADGRV1):c.3509A>G (p.Tyr1170Cys) rs188772875
NM_032119.4(ADGRV1):c.3775T>A (p.Ser1259Thr) rs376900429
NM_032119.4(ADGRV1):c.3974C>T (p.Thr1325Met) rs756414393
NM_032119.4(ADGRV1):c.4487A>G (p.Tyr1496Cys) rs376401006
NM_032119.4(ADGRV1):c.5576A>G (p.His1859Arg) rs200974394
NM_032119.4(ADGRV1):c.7571T>A (p.Val2524Glu) rs191036195
NM_032119.4(ADGRV1):c.7873C>T (p.Arg2625Cys) rs201583659
NM_032119.4(ADGRV1):c.8110A>T (p.Ile2704Phe) rs376318779
NM_032119.4(ADGRV1):c.8369A>G (p.Tyr2790Cys) rs751129081
NM_032119.4(ADGRV1):c.9635T>C (p.Ile3212Thr) rs199833843
NM_032119.4(ADGRV1):c.9643G>A (p.Glu3215Lys) rs199499672
NM_206933.3(USH2A):c.14914C>T (p.Arg4972Cys) rs766759858
NM_206933.3(USH2A):c.2414G>C (p.Gly805Ala) rs587783023
NM_206933.3(USH2A):c.4070C>T (p.Thr1357Met) rs201190539
NM_206933.3(USH2A):c.5666A>G (p.Asp1889Gly) rs775803174
NM_206933.3(USH2A):c.6670G>T (p.Gly2224Cys) rs149553844
NM_206933.4(USH2A):c.10564A>G (p.Arg3522Gly) rs147374057
NM_206933.4(USH2A):c.10904C>A (p.Thr3635Asn) rs727505166
NM_206933.4(USH2A):c.14191G>A (p.Gly4731Arg) rs148674752
NM_206933.4(USH2A):c.4378G>A (p.Gly1460Arg) rs139311927
NM_206933.4(USH2A):c.5858C>G (p.Ala1953Gly) rs41302239
NM_206933.4(USH2A):c.6730G>A (p.Val2244Met) rs550772689
NM_206933.4(USH2A):c.9842G>T (p.Cys3281Phe) rs727504654

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