List of variants in gene CUBN reported as benign for Imerslund-Gräsbeck syndrome

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 73

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HGVS	dbSNP
NM_001081.3(CUBN):c.10039G>A (p.Gly3347Arg)	rs146027947
NM_001081.3(CUBN):c.1003G>A (p.Ala335Thr)	rs57335729
NM_001081.3(CUBN):c.10119C>A (p.Val3373=)	rs139596037
NM_001081.3(CUBN):c.10245C>T (p.Tyr3415=)	rs147730705
NM_001081.3(CUBN):c.10265C>T (p.Thr3422Ile)	rs1801230
NM_001081.3(CUBN):c.10267G>A (p.Val3423Ile)	rs145872906
NM_001081.3(CUBN):c.10383C>T (p.Ser3461=)	rs141937843
NM_001081.3(CUBN):c.10759G>A (p.Gly3587Arg)	rs201484266
NM_001081.3(CUBN):c.1794C>T (p.Tyr598=)	rs140184467
NM_001081.3(CUBN):c.196G>A (p.Gly66Arg)	rs12259370
NM_001081.3(CUBN):c.2182T>C (p.Phe728Leu)	rs147752521
NM_001081.3(CUBN):c.2188C>T (p.His730Tyr)	rs7905349
NM_001081.3(CUBN):c.2445C>T (p.Val815=)	rs116350428
NM_001081.3(CUBN):c.2571C>T (p.Asn857=)	rs17432826
NM_001081.3(CUBN):c.2756A>G (p.His919Arg)	rs148869805
NM_001081.3(CUBN):c.2791+130G>A	rs4747297
NM_001081.3(CUBN):c.2791+6A>C	rs78549445
NM_001081.3(CUBN):c.3252A>G (p.Gln1084=)	rs142560894
NM_001081.3(CUBN):c.3522C>T (p.Gly1174=)	rs1873469
NM_001081.3(CUBN):c.3752G>C (p.Ser1251Thr)	rs115048360
NM_001081.3(CUBN):c.4872C>T (p.Ile1624=)	rs114958584
NM_001081.3(CUBN):c.5098G>A (p.Asp1700Asn)	rs116114483
NM_001081.3(CUBN):c.516C>T (p.Asn172=)	rs576450214
NM_001081.3(CUBN):c.5304C>T (p.Ile1768=)	rs61841454
NM_001081.3(CUBN):c.5518G>A (p.Gly1840Ser)	rs2271462
NM_001081.3(CUBN):c.5680A>G (p.Ile1894Val)	rs76789390
NM_001081.3(CUBN):c.5803A>G (p.Ser1935Gly)	rs41289305
NM_001081.3(CUBN):c.6089G>A (p.Arg2030Gln)	rs143400113
NM_001081.3(CUBN):c.6225G>A (p.Ser2075=)	rs75737363
NM_001081.3(CUBN):c.6276C>T (p.Cys2092=)	rs146319349
NM_001081.3(CUBN):c.6788T>G (p.Phe2263Cys)	rs2271460
NM_001081.3(CUBN):c.6924A>T (p.Ser2308=)	rs115303408
NM_001081.3(CUBN):c.6938A>T (p.Tyr2313Phe)	rs140806389
NM_001081.3(CUBN):c.6997A>G (p.Ile2333Val)	rs149507036
NM_001081.3(CUBN):c.7346T>C (p.Met2449Thr)	rs41301097
NM_001081.3(CUBN):c.7365T>A (p.Asp2455Glu)	rs117128556
NM_001081.3(CUBN):c.758T>C (p.Phe253Ser)	rs1801222
NM_001081.3(CUBN):c.7724C>G (p.Pro2575Arg)	rs3740168
NM_001081.3(CUBN):c.7868A>C (p.Glu2623Ala)	rs115449747
NM_001081.3(CUBN):c.8139C>A (p.Thr2713=)	rs147742103
NM_001081.3(CUBN):c.8671G>A (p.Val2891Ile)	rs150488625
NM_001081.3(CUBN):c.8741C>T (p.Ala2914Val)	rs45551835
NM_001081.3(CUBN):c.8902G>C (p.Glu2968Gln)	rs45569534
NM_001081.3(CUBN):c.8905+137T>A	rs780847
NM_001081.3(CUBN):c.8921C>T (p.Thr2974Met)	rs374477671
NM_001081.3(CUBN):c.8950A>G (p.Ile2984Val)	rs1801239
NM_001081.3(CUBN):c.8968G>A (p.Val2990Ile)	rs115888073
NM_001081.3(CUBN):c.910G>A (p.Glu304Lys)	rs78201384
NM_001081.3(CUBN):c.9340G>A (p.Gly3114Ser)	rs117035284
NM_001081.3(CUBN):c.9491C>G (p.Ser3164Trp)	rs57163243
NM_001081.3(CUBN):c.9565A>G (p.Ile3189Val)	rs111265129
NM_001081.3(CUBN):c.963C>T (p.Pro321=)	rs150309054
NM_001081.3(CUBN):c.9986C>T (p.Ser3329Leu)	rs74431427
NM_001081.4(CUBN):c.10656C>T (p.Asn3552=)	rs1801232
NM_001081.4(CUBN):c.1470G>A (p.Pro490=)	rs143255616
NM_001081.4(CUBN):c.1947+9T>A	rs376950340
NM_001081.4(CUBN):c.2103A>G (p.Thr701=)	rs143693723
NM_001081.4(CUBN):c.2791+9_2791+16del	rs375796983
NM_001081.4(CUBN):c.2792-6C>G	rs185269080
NM_001081.4(CUBN):c.3292G>T (p.Ala1098Ser)	rs146593010
NM_001081.4(CUBN):c.3546G>A (p.Pro1182=)	rs369417721
NM_001081.4(CUBN):c.4200C>T (p.Gly1400=)	rs150663813
NM_001081.4(CUBN):c.4470C>T (p.Thr1490=)	rs768720429
NM_001081.4(CUBN):c.4671T>G (p.Leu1557=)	rs151197305
NM_001081.4(CUBN):c.5011A>C (p.Arg1671=)	rs144472791
NM_001081.4(CUBN):c.6039C>T (p.Pro2013=)	rs149569558
NM_001081.4(CUBN):c.6469A>G (p.Asn2157Asp)	rs144360241
NM_001081.4(CUBN):c.657G>A (p.Gly219=)	rs142553474
NM_001081.4(CUBN):c.9125A>G (p.Asn3042Ser)	rs142581908
NM_001081.4(CUBN):c.9204C>T (p.Ile3068=)	rs117755237
NM_001081.4(CUBN):c.9206C>T (p.Thr3069Ile)	rs117400821
NM_001081.4(CUBN):c.9207C>A (p.Thr3069=)	rs117936668
NM_001081.4(CUBN):c.9987G>A (p.Ser3329=)	rs80308930

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