ClinVar Miner

List of variants in gene CRX reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_000554.6(CRX):c.28C>G (p.His10Asp) rs139340178 0.00060
NM_000554.6(CRX):c.597C>T (p.Ser199=) rs61748455 0.00033
NM_000554.6(CRX):c.425A>G (p.Tyr142Cys) rs61748442 0.00032
NM_000554.6(CRX):c.22G>C (p.Gly8Arg) rs146240568 0.00023
NM_000554.6(CRX):c.309G>A (p.Gln103=) rs138242846 0.00023
NM_000554.6(CRX):c.549G>A (p.Gly183=) rs61748451 0.00020
NM_000554.6(CRX):c.537G>A (p.Leu179=) rs753262074 0.00012
NM_000554.6(CRX):c.765C>T (p.Gly255=) rs145913500 0.00012
NM_000554.6(CRX):c.564C>T (p.Ser188=) rs148622001 0.00009
NM_000554.6(CRX):c.100+8C>T rs375411321 0.00007
NM_000554.6(CRX):c.159G>A (p.Glu53=) rs767773596 0.00007
NM_000554.6(CRX):c.253-11T>C rs199991284 0.00007
NM_000554.6(CRX):c.311A>G (p.Gln104Arg) rs769592519 0.00006
NM_000554.6(CRX):c.101-6C>T rs781316943 0.00005
NM_000554.6(CRX):c.369G>A (p.Thr123=) rs368752695 0.00005
NM_000554.6(CRX):c.552G>A (p.Pro184=) rs779118593 0.00005
NM_000554.6(CRX):c.606C>T (p.Cys202=) rs764877352 0.00005
NM_000554.6(CRX):c.774T>C (p.Tyr258=) rs767273026 0.00005
NM_000554.6(CRX):c.42C>T (p.Asn14=) rs774344094 0.00004
NM_000554.6(CRX):c.585C>T (p.Tyr195=) rs373497612 0.00004
NM_000554.6(CRX):c.648C>T (p.Ser216=) rs772398140 0.00004
NM_000554.6(CRX):c.720C>G (p.Pro240=) rs748655180 0.00004
NM_000554.6(CRX):c.789C>T (p.Pro263=) rs550083287 0.00004
NM_000554.6(CRX):c.9G>A (p.Ala3=) rs140766502 0.00004
NM_000554.6(CRX):c.100+13G>A rs770361425 0.00003
NM_000554.6(CRX):c.21G>A (p.Pro7=) rs772745666 0.00002
NM_000554.6(CRX):c.252+8G>C rs773348946 0.00002
NM_000554.6(CRX):c.253-16C>T rs372605680 0.00002
NM_000554.6(CRX):c.594C>T (p.Ala198=) rs1186532132 0.00002
NM_000554.6(CRX):c.747C>G (p.Ser249=) rs748748807 0.00002
NM_000554.6(CRX):c.195C>T (p.Asp65=) rs757731373 0.00001
NM_000554.6(CRX):c.273G>A (p.Arg91=) rs1254989456 0.00001
NM_000554.6(CRX):c.363G>A (p.Ala121=) rs141888455 0.00001
NM_000554.6(CRX):c.367A>G (p.Thr123Ala) rs755554804 0.00001
NM_000554.6(CRX):c.696G>A (p.Pro232=) rs1466177047 0.00001
NM_000554.6(CRX):c.726G>A (p.Val242=) rs371406142 0.00001
NM_000554.6(CRX):c.846C>A (p.Pro282=) rs1172429450 0.00001
NM_000554.6(CRX):c.101-10C>T
NM_000554.6(CRX):c.109A>C (p.Arg37=)
NM_000554.6(CRX):c.123G>A (p.Arg41=) rs181068147
NM_000554.6(CRX):c.129C>T (p.Arg43=) rs775065439
NM_000554.6(CRX):c.138C>T (p.Phe46=)
NM_000554.6(CRX):c.151C>T (p.Leu51=)
NM_000554.6(CRX):c.165G>A (p.Glu55=)
NM_000554.6(CRX):c.177C>T (p.Ala59=)
NM_000554.6(CRX):c.198C>T (p.Val66=)
NM_000554.6(CRX):c.213G>A (p.Glu71=)
NM_000554.6(CRX):c.216G>A (p.Val72=) rs2123739992
NM_000554.6(CRX):c.240G>A (p.Glu80=)
NM_000554.6(CRX):c.252+18_252+24del rs2123740025
NM_000554.6(CRX):c.270G>C (p.Arg90=)
NM_000554.6(CRX):c.339G>A (p.Lys113=) rs761978269
NM_000554.6(CRX):c.342C>T (p.Ala114=)
NM_000554.6(CRX):c.345G>A (p.Arg115=) rs1968162928
NM_000554.6(CRX):c.360G>A (p.Lys120=)
NM_000554.6(CRX):c.372C>A (p.Ser124=) rs755797220
NM_000554.6(CRX):c.390T>C (p.Asp130=)
NM_000554.6(CRX):c.406C>T (p.Leu136=)
NM_000554.6(CRX):c.408G>C (p.Leu136=)
NM_000554.6(CRX):c.441C>A (p.Pro147=)
NM_000554.6(CRX):c.441C>T (p.Pro147=) rs147422878
NM_000554.6(CRX):c.462C>T (p.Thr154=) rs2123743108
NM_000554.6(CRX):c.522G>A (p.Ala174=) rs376827106
NM_000554.6(CRX):c.52C>T (p.Leu18=)
NM_000554.6(CRX):c.534G>C (p.Gly178=)
NM_000554.6(CRX):c.543C>A (p.Ala181=)
NM_000554.6(CRX):c.555T>A (p.Ser185=)
NM_000554.6(CRX):c.570C>A (p.Pro190=) rs1599991852
NM_000554.6(CRX):c.60C>T (p.Gly20=)
NM_000554.6(CRX):c.633G>A (p.Pro211=)
NM_000554.6(CRX):c.678G>A (p.Val226=)
NM_000554.6(CRX):c.690G>T (p.Gly230=) rs936709261
NM_000554.6(CRX):c.717C>A (p.Gly239=) rs886054546
NM_000554.6(CRX):c.723C>T (p.Ser241=) rs770257260
NM_000554.6(CRX):c.777C>T (p.Gly259=)
NM_000554.6(CRX):c.786C>T (p.Ser262=)
NM_000554.6(CRX):c.81C>T (p.His27=) rs2123738329
NM_000554.6(CRX):c.852C>T (p.Asp284=) rs771721958
NM_000554.6(CRX):c.856C>T (p.Leu286=) rs2123743743
NM_000554.6(CRX):c.876T>C (p.Ser292=) rs2123743757
NM_000554.6(CRX):c.894C>A (p.Ile298=)

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