ClinVar Miner

List of variants in gene PROS1 reported as likely benign for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 116
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HGVS dbSNP gnomAD frequency
NM_000313.4(PROS1):c.*197C>T rs182088150 0.01026
NM_000313.4(PROS1):c.1032C>T (p.Ile344=) rs78449232 0.00981
NM_000313.4(PROS1):c.1528G>A (p.Val510Met) rs138925964 0.00331
NM_000313.4(PROS1):c.-62T>G rs556711298 0.00328
NM_000313.4(PROS1):c.*992T>G rs538711279 0.00263
NM_000313.4(PROS1):c.*454G>A rs539871594 0.00256
NM_000313.4(PROS1):c.698G>A (p.Arg233Lys) rs41267007 0.00202
NM_000313.4(PROS1):c.*469A>C rs147496684 0.00164
NM_000313.4(PROS1):c.*380A>T rs138546241 0.00133
NM_000313.4(PROS1):c.1248G>A (p.Pro416=) rs148869673 0.00053
NM_000313.4(PROS1):c.1156-19T>C rs534457194 0.00044
NM_000313.4(PROS1):c.1041A>G (p.Ser347=) rs376656035 0.00034
NM_000313.4(PROS1):c.1494T>C (p.Asn498=) rs76877671 0.00033
NC_000003.12:g.93973939G>C rs149028936 0.00031
NM_000313.4(PROS1):c.1815C>T (p.Ala605=) rs758204799 0.00016
NM_000313.4(PROS1):c.585T>C (p.Asn195=) rs372109285 0.00013
NM_000313.4(PROS1):c.503A>G (p.Asn168Ser) rs144430063 0.00008
NM_000313.4(PROS1):c.852T>G (p.Val284=) rs371425622 0.00008
NM_000313.4(PROS1):c.1323+8T>G rs778473220 0.00006
NM_000313.4(PROS1):c.1707C>T (p.Ser569=) rs566166669 0.00005
NM_000313.4(PROS1):c.177C>T (p.Ile59=) rs764115962 0.00005
NM_000313.4(PROS1):c.1020C>T (p.Tyr340=) rs374634410 0.00004
NM_000313.4(PROS1):c.1044G>A (p.Ala348=) rs375245889 0.00003
NM_000313.4(PROS1):c.1446C>T (p.Gly482=) rs535201753 0.00003
NM_000313.4(PROS1):c.1566T>A (p.Val522=) rs753144615 0.00003
NM_000313.4(PROS1):c.727+8G>C rs373359406 0.00003
NM_000313.4(PROS1):c.1629C>T (p.Thr543=) rs773166529 0.00002
NM_000313.4(PROS1):c.444T>C (p.Gly148=) rs1282740437 0.00002
NM_000313.4(PROS1):c.903C>T (p.Tyr301=) rs760392622 0.00002
NM_000313.4(PROS1):c.1156-8A>C rs773586094 0.00001
NM_000313.4(PROS1):c.1752G>A (p.Leu584=) rs772250170 0.00001
NM_000313.4(PROS1):c.1902C>T (p.Ala634=) rs751777823 0.00001
NM_000313.4(PROS1):c.204C>G (p.Ala68=) rs1060504812 0.00001
NM_000313.4(PROS1):c.708C>G (p.Leu236=) rs1231421585 0.00001
NM_000313.4(PROS1):c.1107C>T (p.Ser369=)
NM_000313.4(PROS1):c.1140T>C (p.Asn380=)
NM_000313.4(PROS1):c.1146A>G (p.Leu382=) rs1282696011
NM_000313.4(PROS1):c.1156-10T>G
NM_000313.4(PROS1):c.1156-4G>A
NM_000313.4(PROS1):c.1156-6T>C
NM_000313.4(PROS1):c.119G>T (p.Arg40Leu) rs7614835
NM_000313.4(PROS1):c.1218T>C (p.Asp406=)
NM_000313.4(PROS1):c.1230T>C (p.Pro410=)
NM_000313.4(PROS1):c.1324-4T>G
NM_000313.4(PROS1):c.1324-6del rs762002556
NM_000313.4(PROS1):c.1335T>C (p.Arg445=) rs2107137629
NM_000313.4(PROS1):c.1335T>G (p.Arg445=) rs2107137629
NM_000313.4(PROS1):c.1398T>C (p.Ile466=)
NM_000313.4(PROS1):c.1464T>C (p.Ser488=) rs2107137350
NM_000313.4(PROS1):c.1493-17T>C
NM_000313.4(PROS1):c.1493-9T>C
NM_000313.4(PROS1):c.1500A>G (p.Val500=)
NM_000313.4(PROS1):c.1506T>C (p.Ser502=) rs1254236549
NM_000313.4(PROS1):c.1527T>C (p.Asn509=)
NM_000313.4(PROS1):c.1599G>A (p.Val533=) rs1232149677
NM_000313.4(PROS1):c.1608T>C (p.Ala536=)
NM_000313.4(PROS1):c.1641A>G (p.Ser547=) rs1445245201
NM_000313.4(PROS1):c.1644+18C>A
NM_000313.4(PROS1):c.1645-14G>A
NM_000313.4(PROS1):c.1645-8C>T
NM_000313.4(PROS1):c.1654T>C (p.Leu552=)
NM_000313.4(PROS1):c.183A>G (p.Glu61=) rs536944947
NM_000313.4(PROS1):c.1857G>A (p.Leu619=)
NM_000313.4(PROS1):c.1863C>T (p.Gly621=) rs2107124945
NM_000313.4(PROS1):c.1866T>C (p.Leu622=)
NM_000313.4(PROS1):c.1870+13T>C
NM_000313.4(PROS1):c.1871-18A>G
NM_000313.4(PROS1):c.1878A>G (p.Pro626=)
NM_000313.4(PROS1):c.1938T>A (p.Gly646=)
NM_000313.4(PROS1):c.1938T>C (p.Gly646=) rs1349900185
NM_000313.4(PROS1):c.228G>A (p.Pro76=) rs6121
NM_000313.4(PROS1):c.228G>T (p.Pro76=)
NM_000313.4(PROS1):c.234+11A>G
NM_000313.4(PROS1):c.235-12T>C
NM_000313.4(PROS1):c.235-13T>G
NM_000313.4(PROS1):c.235-16T>C
NM_000313.4(PROS1):c.235-17C>A
NM_000313.4(PROS1):c.240T>C (p.Tyr80=) rs2107197427
NM_000313.4(PROS1):c.259+20A>G
NM_000313.4(PROS1):c.264T>C (p.Cys88=)
NM_000313.4(PROS1):c.294T>C (p.Thr98=)
NM_000313.4(PROS1):c.347-22_347-19del
NM_000313.4(PROS1):c.347-7C>T
NM_000313.4(PROS1):c.36G>A (p.Leu12=)
NM_000313.4(PROS1):c.469+18C>T
NM_000313.4(PROS1):c.469+19G>A
NM_000313.4(PROS1):c.470-10C>T
NM_000313.4(PROS1):c.470-4T>C rs1708668274
NM_000313.4(PROS1):c.480A>G (p.Glu160=)
NM_000313.4(PROS1):c.486A>G (p.Lys162=)
NM_000313.4(PROS1):c.573T>A (p.Val191=)
NM_000313.4(PROS1):c.601+18G>C
NM_000313.4(PROS1):c.606G>C (p.Val202=)
NM_000313.4(PROS1):c.60C>G (p.Pro20=)
NM_000313.4(PROS1):c.60C>T (p.Pro20=) rs1709918178
NM_000313.4(PROS1):c.687C>G (p.Pro229=) rs149129715
NM_000313.4(PROS1):c.687C>T (p.Pro229=)
NM_000313.4(PROS1):c.727+11G>A
NM_000313.4(PROS1):c.727+8G>A rs373359406
NM_000313.4(PROS1):c.728-5C>G
NM_000313.4(PROS1):c.728-8dup rs751417718
NM_000313.4(PROS1):c.76+12A>G
NM_000313.4(PROS1):c.76+19C>T
NM_000313.4(PROS1):c.77-11G>T
NM_000313.4(PROS1):c.77-15G>T
NM_000313.4(PROS1):c.798T>C (p.Tyr266=) rs1447172346
NM_000313.4(PROS1):c.850-12C>G
NM_000313.4(PROS1):c.864C>T (p.Cys288=)
NM_000313.4(PROS1):c.871T>C (p.Leu291=) rs2107155422
NM_000313.4(PROS1):c.909G>A (p.Ala303=) rs537938359
NM_000313.4(PROS1):c.912G>A (p.Glu304=)
NM_000313.4(PROS1):c.965+10C>A
NM_000313.4(PROS1):c.965+10C>G
NM_000313.4(PROS1):c.965+15C>T
NM_000313.4(PROS1):c.966-17C>G
NM_000313.4(PROS1):c.99A>G (p.Ser33=) rs1709035668

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