ClinVar Miner

List of variants in gene PRKCG reported by Athena Diagnostics Inc

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Gene type:
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Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_002739.5(PRKCG):c.72C>T (p.Ala24=) rs2547362 0.89099
NM_002739.5(PRKCG):c.567T>C (p.Asn189=) rs3745406 0.35855
NM_002739.5(PRKCG):c.285C>T (p.Asp95=) rs17854523 0.03329
NM_002739.5(PRKCG):c.1404C>G (p.Leu468=) rs35079513 0.02248
NM_002739.5(PRKCG):c.1722C>T (p.Tyr574=) rs34616316 0.00781
NM_002739.5(PRKCG):c.642G>A (p.Thr214=) rs77550964 0.00099
NM_002739.5(PRKCG):c.1524C>A (p.Pro508=) rs115736276 0.00076
NM_002739.5(PRKCG):c.1836C>T (p.Gly612=) rs56211557 0.00059
NM_002739.5(PRKCG):c.638G>A (p.Arg213Gln) rs115832790 0.00056
NM_002739.5(PRKCG):c.714C>T (p.Arg238=) rs367543210 0.00031
NM_002739.5(PRKCG):c.1281+9G>C rs370400523 0.00024
NM_002739.5(PRKCG):c.1747G>A (p.Val583Met) rs143513754 0.00014
NM_002739.5(PRKCG):c.1738C>T (p.Arg580Trp) rs149266855 0.00009
NM_002739.5(PRKCG):c.1871G>A (p.Arg624Gln) rs146367309 0.00007
NM_002739.5(PRKCG):c.2075T>G (p.Val692Gly) rs78437096 0.00007
NM_002739.5(PRKCG):c.530-6G>A rs375941615 0.00006
NM_002739.5(PRKCG):c.397+10C>G rs759781185 0.00005
NM_002739.5(PRKCG):c.1529C>A (p.Thr510Lys) rs749199519 0.00004
NM_002739.5(PRKCG):c.866C>A (p.Pro289Gln) rs376704133 0.00003
NM_002739.5(PRKCG):c.1899C>T (p.Pro633=) rs367543219 0.00002
NM_002739.5(PRKCG):c.522C>T (p.His174=) rs200879722 0.00002
NM_002739.5(PRKCG):c.613C>T (p.Arg205Trp) rs367543208 0.00002
NM_002739.5(PRKCG):c.1764+1G>T rs1406338491 0.00001
NM_002739.5(PRKCG):c.412G>A (p.Val138Met) rs1192424800 0.00001
NM_002739.5(PRKCG):c.745C>T (p.Arg249Trp) rs1180121813 0.00001
NM_002739.5(PRKCG):c.974C>T (p.Pro325Leu) rs145197557 0.00001
NM_002739.5(PRKCG):c.1055G>A (p.Ser352Asn) rs762206157
NM_002739.5(PRKCG):c.1081A>C (p.Ser361Arg) rs121918517
NM_002739.5(PRKCG):c.1081A>G (p.Ser361Gly) rs121918517
NM_002739.5(PRKCG):c.114C>T (p.Phe38=)
NM_002739.5(PRKCG):c.1192G>T (p.Val398Leu) rs1165667637
NM_002739.5(PRKCG):c.1195G>C (p.Glu399Gln) rs2068734193
NM_002739.5(PRKCG):c.1225G>C (p.Gly409Arg) rs1207949925
NM_002739.5(PRKCG):c.1290G>A (p.Leu430=)
NM_002739.5(PRKCG):c.1349G>A (p.Gly450Asp) rs2123016083
NM_002739.5(PRKCG):c.143T>C (p.Phe48Ser)
NM_002739.5(PRKCG):c.1553C>T (p.Thr518Ile) rs2068757477
NM_002739.5(PRKCG):c.1668T>G (p.Asp556Glu) rs1599954407
NM_002739.5(PRKCG):c.1706A>G (p.Glu569Gly) rs1461447265
NM_002739.5(PRKCG):c.1764+1G>A rs1406338491
NM_002739.5(PRKCG):c.1985T>C (p.Leu662Pro) rs1555808814
NM_002739.5(PRKCG):c.2004del (p.Asp669fs) rs1375924761
NM_002739.5(PRKCG):c.208_231del (p.Ser70_Cys77del) rs1599938583
NM_002739.5(PRKCG):c.221A>G (p.His74Arg) rs1568749767
NM_002739.5(PRKCG):c.229T>C (p.Cys77Arg) rs386134160
NM_002739.5(PRKCG):c.230G>A (p.Cys77Tyr) rs1599938631
NM_002739.5(PRKCG):c.254G>T (p.Cys85Phe) rs1599938680
NM_002739.5(PRKCG):c.356C>T (p.Ser119Phe) rs386134163
NM_002739.5(PRKCG):c.362T>C (p.Leu121Pro) rs1568752907
NM_002739.5(PRKCG):c.362_379dup (p.Leu121_His126dup) rs2068657289
NM_002739.5(PRKCG):c.367G>C (p.Gly123Arg) rs386134164
NM_002739.5(PRKCG):c.380A>G (p.Gln127Arg) rs121918515
NM_002739.5(PRKCG):c.382G>C (p.Gly128Arg) rs1568752939
NM_002739.5(PRKCG):c.392G>A (p.Cys131Tyr) rs386134167
NM_002739.5(PRKCG):c.401_402delinsTT (p.Cys134Phe) rs2068659442
NM_002739.5(PRKCG):c.413T>A (p.Val138Glu) rs386134168
NM_002739.5(PRKCG):c.415C>A (p.His139Asn) rs1555807019
NM_002739.5(PRKCG):c.425G>A (p.Cys142Tyr)
NM_002739.5(PRKCG):c.448T>C (p.Cys150Arg) rs1599943341
NM_002739.5(PRKCG):c.466G>A (p.Glu156Lys) rs1304701232
NM_002739.5(PRKCG):c.475G>A (p.Gly159Arg) rs866406014
NM_002739.5(PRKCG):c.476G>A (p.Gly159Glu) rs1599943390
NM_002739.5(PRKCG):c.479G>T (p.Arg160Leu) rs1555807032
NM_002739.5(PRKCG):c.495C>G (p.Ile165Met) rs1252158483
NM_002739.5(PRKCG):c.68G>A (p.Gly23Glu) rs1599937005
NM_002739.5(PRKCG):c.707T>C (p.Val236Ala) rs1599945617
NM_002739.5(PRKCG):c.70_72delinsCCT (p.Ala24Pro)
NM_002739.5(PRKCG):c.713G>A (p.Arg238His)
NM_002739.5(PRKCG):c.811G>A (p.Val271Met) rs375466358
NM_002739.5(PRKCG):c.866C>T (p.Pro289Leu) rs376704133
NM_002739.5(PRKCG):c.881A>T (p.Asp294Val)
NM_002739.5(PRKCG):c.8G>A (p.Gly3Asp)
NM_002739.5(PRKCG):c.99C>G (p.Val33=)

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