ClinVar Miner

List of variants in gene PRKAR1A studied for not specified

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_002734.5(PRKAR1A):c.87G>A (p.Ala29=) rs3730349 0.01815
NM_002734.5(PRKAR1A):c.204G>A (p.Leu68=) rs74863634 0.00405
NM_002734.5(PRKAR1A):c.1029C>T (p.Gly343=) rs1803241 0.00265
NM_002734.5(PRKAR1A):c.221G>A (p.Arg74His) rs200069356 0.00036
NM_002734.5(PRKAR1A):c.-49G>T rs1024932138 0.00032
NM_002734.5(PRKAR1A):c.489T>C (p.Thr163=) rs143672551 0.00021
NM_002734.5(PRKAR1A):c.330G>A (p.Ala110=) rs371834376 0.00016
NM_002734.5(PRKAR1A):c.483A>G (p.Gly161=) rs141518491 0.00011
NM_002734.5(PRKAR1A):c.103A>G (p.Ile35Val) rs377513504 0.00009
NM_002734.5(PRKAR1A):c.798G>A (p.Thr266=) rs201774040 0.00006
NM_002734.5(PRKAR1A):c.552C>G (p.Val184=) rs751501857 0.00005
NM_002734.5(PRKAR1A):c.178-8T>G rs771192586 0.00004
NM_002734.5(PRKAR1A):c.546G>A (p.Thr182=) rs117639566 0.00004
NM_002734.5(PRKAR1A):c.984A>G (p.Ala328=) rs1161181036 0.00004
NM_002734.5(PRKAR1A):c.19G>A (p.Ala7Thr) rs369210646 0.00003
NM_002734.5(PRKAR1A):c.378C>T (p.Ala126=) rs199974368 0.00003
NM_002734.5(PRKAR1A):c.477C>T (p.Ile159=) rs372389205 0.00003
NM_002734.5(PRKAR1A):c.522C>T (p.Phe174=) rs148109898 0.00003
NM_002734.5(PRKAR1A):c.756A>C (p.Lys252Asn) rs1242606073 0.00003
NM_002734.5(PRKAR1A):c.1134A>G (p.Ser378=) rs1001156045 0.00002
NM_002734.5(PRKAR1A):c.329C>T (p.Ala110Val) rs1194755479 0.00002
NM_002734.5(PRKAR1A):c.60C>G (p.Leu20=) rs372451862 0.00002
NM_002734.5(PRKAR1A):c.675C>A (p.Gly225=) rs150244650 0.00002
NM_002734.5(PRKAR1A):c.727C>A (p.Arg243=) rs770136522 0.00002
NM_002734.5(PRKAR1A):c.25A>C (p.Ser9Arg) rs778468626 0.00001
NM_002734.5(PRKAR1A):c.27T>G (p.Ser9Arg) rs745391692 0.00001
NM_002734.5(PRKAR1A):c.289C>A (p.Arg97=) rs1555813217 0.00001
NM_002734.5(PRKAR1A):c.303C>T (p.Ser101=) rs1294747986 0.00001
NM_002734.5(PRKAR1A):c.306T>C (p.Ala102=) rs757511127 0.00001
NM_002734.5(PRKAR1A):c.51A>T (p.Glu17Asp) rs771518581 0.00001
NM_002734.5(PRKAR1A):c.545C>T (p.Thr182Met) rs199801675 0.00001
NM_002734.5(PRKAR1A):c.549+10A>C rs751413552 0.00001
NM_002734.5(PRKAR1A):c.63C>T (p.Tyr21=) rs777110464 0.00001
NM_002734.5(PRKAR1A):c.790C>T (p.Arg264Cys) rs2085877268 0.00001
NM_002734.5(PRKAR1A):c.810A>G (p.Ala270=) rs778165219 0.00001
NM_002734.5(PRKAR1A):c.813G>A (p.Leu271=) rs1325106678 0.00001
NM_002734.5(PRKAR1A):c.891+6G>T rs1222751049 0.00001
NM_002734.5(PRKAR1A):c.974-6C>A rs745570426 0.00001
NC_000017.10:g.(?_66508519)_(66529573_?)dup
NM_002734.5(PRKAR1A):c.-7+14G>C rs1555811117
NM_002734.5(PRKAR1A):c.1051G>A (p.Asp351Asn)
NM_002734.5(PRKAR1A):c.1110C>A (p.Ile370=) rs62638722
NM_002734.5(PRKAR1A):c.1133C>A (p.Ser378Ter)
NM_002734.5(PRKAR1A):c.1133C>T (p.Ser378Leu) rs1568703465
NM_002734.5(PRKAR1A):c.25A>G (p.Ser9Gly) rs778468626
NM_002734.5(PRKAR1A):c.349-5dup rs3841514
NM_002734.5(PRKAR1A):c.387C>G (p.Ala129=) rs1411849784
NM_002734.5(PRKAR1A):c.440+15T>C rs78183210
NM_002734.5(PRKAR1A):c.441-5del rs777677808
NM_002734.5(PRKAR1A):c.441-6T>C rs1340450132
NM_002734.5(PRKAR1A):c.465G>A (p.Ser155=) rs746705941
NM_002734.5(PRKAR1A):c.47G>A (p.Arg16Gln) rs2085401218
NM_002734.5(PRKAR1A):c.489T>G (p.Thr163=) rs143672551
NM_002734.5(PRKAR1A):c.530T>C (p.Ile177Thr) rs587778626
NM_002734.5(PRKAR1A):c.550-6C>T rs1555814031
NM_002734.5(PRKAR1A):c.770-9G>T rs562094333
NM_002734.5(PRKAR1A):c.791G>A (p.Arg264His) rs1303569195
NM_002734.5(PRKAR1A):c.917G>A (p.Arg306Gln) rs1568702564
NM_002734.5(PRKAR1A):c.981T>C (p.Ile327=) rs2085937729

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