ClinVar Miner

List of variants in gene CRX studied for not provided

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Gene type:
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Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_000554.6(CRX):c.253-213G>C rs8100405 0.47359
NM_000554.6(CRX):c.253-282G>A rs60934372 0.43795
NM_000554.6(CRX):c.253-235C>T rs59440203 0.43708
NM_000554.6(CRX):c.253-242C>T rs59657689 0.43702
NM_000554.6(CRX):c.101-200T>C rs3745752 0.34347
NM_000554.6(CRX):c.252+203T>A rs12985683 0.32944
NM_000554.6(CRX):c.100+12C>T rs62128766 0.14108
NM_000554.6(CRX):c.-35-150T>C rs4801737 0.12303
NM_000554.6(CRX):c.-35-120A>G rs3760817 0.03727
NM_000554.6(CRX):c.472G>A (p.Ala158Thr) rs61748445 0.02598
NM_000554.6(CRX):c.101-12A>G rs73941294 0.01428
NM_000554.6(CRX):c.365G>A (p.Gly122Asp) rs61748441 0.00614
NM_000554.6(CRX):c.724G>A (p.Val242Met) rs61748459 0.00521
NM_000554.6(CRX):c.196G>A (p.Val66Ile) rs61748438 0.00231
NM_000554.6(CRX):c.253-15G>A rs145805694 0.00187
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.549G>A (p.Gly183=) rs61748451 0.00020
NM_000554.6(CRX):c.332A>G (p.Gln111Arg) rs760741667 0.00004
NM_000554.6(CRX):c.335C>T (p.Ala112Val) rs61748439 0.00004
NM_000554.6(CRX):c.568C>T (p.Pro190Ser) rs151169551 0.00004
NM_000554.6(CRX):c.818C>T (p.Thr273Met) rs281865203 0.00004
NM_000554.6(CRX):c.166G>A (p.Ala56Thr) rs61748437 0.00002
NM_000554.6(CRX):c.206G>A (p.Arg69His) rs775073228 0.00002
NM_000554.6(CRX):c.268C>T (p.Arg90Trp) rs104894673 0.00002
NM_000554.6(CRX):c.487T>C (p.Trp163Arg) rs779912365 0.00002
NM_000554.6(CRX):c.118C>T (p.Arg40Trp) rs749738655 0.00001
NM_000554.6(CRX):c.121C>T (p.Arg41Trp) rs104894672 0.00001
NM_000554.6(CRX):c.122G>A (p.Arg41Gln) rs61748436 0.00001
NM_000554.6(CRX):c.128G>A (p.Arg43His) rs771736389 0.00001
NM_000554.6(CRX):c.269G>A (p.Arg90Gln) rs1209634994 0.00001
NM_000554.6(CRX):c.*308AAG[2] rs398059782
NM_000554.6(CRX):c.-29T>A rs1568624071
NM_000554.6(CRX):c.100+2T>C rs281865198
NM_000554.6(CRX):c.100+3_100+5delinsTTA rs1064796109
NM_000554.6(CRX):c.100+97G>A rs62128767
NM_000554.6(CRX):c.101-13C>G rs281865199
NM_000554.6(CRX):c.101-147A>G rs2123739726
NM_000554.6(CRX):c.101-3del rs727503894
NM_000554.6(CRX):c.101-65A>T rs281865200
NM_000554.6(CRX):c.164dup (p.Ala56fs) rs1555801777
NM_000554.6(CRX):c.238G>A (p.Glu80Lys) rs62654391
NM_000554.6(CRX):c.239A>C (p.Glu80Ala) rs104894671
NM_000554.6(CRX):c.24dup (p.Pro9fs) rs62636512
NM_000554.6(CRX):c.253-18T>A rs281865201
NM_000554.6(CRX):c.263A>G (p.Lys88Arg) rs1001151383
NM_000554.6(CRX):c.274G>A (p.Ala92Thr) rs786205521
NM_000554.6(CRX):c.327G>A (p.Gly109=) rs1029300491
NM_000554.6(CRX):c.351dup (p.Lys118fs) rs61748440
NM_000554.6(CRX):c.380C>A (p.Pro127His) rs1968163788
NM_000554.6(CRX):c.403C>A (p.Pro135Thr) rs572439956
NM_000554.6(CRX):c.404del (p.Pro135fs) rs1064797246
NM_000554.6(CRX):c.436_447del (p.Leu146_Pro149del) rs281865202
NM_000554.6(CRX):c.445_467del (p.Pro149fs)
NM_000554.6(CRX):c.447dup (p.Ser150fs) rs61748444
NM_000554.6(CRX):c.448del (p.Ser150fs) rs886044121
NM_000554.6(CRX):c.501dup (p.Glu168fs) rs1968166700
NM_000554.6(CRX):c.503_504del (p.Glu168fs) rs61748446
NM_000554.6(CRX):c.505del (p.Ser169fs) rs61748447
NM_000554.6(CRX):c.520del (p.Ala174fs) rs281865515
NM_000554.6(CRX):c.529del (p.Ala177fs) rs61748449
NM_000554.6(CRX):c.531T>C (p.Ala177=)
NM_000554.6(CRX):c.541del (p.Ala181fs) rs61748450
NM_000554.6(CRX):c.570C>A (p.Pro190=) rs1599991852
NM_000554.6(CRX):c.571del (p.Tyr191fs) rs61748452
NM_000554.6(CRX):c.585dup (p.Ala196fs) rs61748453
NM_000554.6(CRX):c.587_590del (p.Ala196fs) rs61748454
NM_000554.6(CRX):c.615del (p.Ser206fs) rs281865516
NM_000554.6(CRX):c.650del (p.Gly217fs) rs281865517
NM_000554.6(CRX):c.663C>A (p.Tyr221Ter) rs1064797247
NM_000554.6(CRX):c.695del (p.Pro232fs) rs786205630
NM_000554.6(CRX):c.709del (p.Leu237fs) rs281865518
NM_000554.6(CRX):c.723C>T (p.Ser241=) rs770257260
NM_000554.6(CRX):c.733T>C (p.Ser245Pro) rs1555802042
NM_000554.6(CRX):c.734C>A (p.Ser245Tyr) rs2123743557
NM_000554.6(CRX):c.753del (p.Ser252fs) rs61749660
NM_000554.6(CRX):c.789del (p.Val264fs) rs281865519
NM_000554.6(CRX):c.856_865delinsGATCCC (p.Leu286fs) rs1555802058
NM_000554.6(CRX):c.879C>G (p.Ala293=)

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