ClinVar Miner

List of variants in gene MAN2B1 reported by Natera, Inc.

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP
NM_000528.4(MAN2B1):c.1010G>A (p.Arg337Gln) rs1133330
NM_000528.4(MAN2B1):c.1068C>G (p.Pro356=) rs117880912
NM_000528.4(MAN2B1):c.1109+10G>A
NM_000528.4(MAN2B1):c.1158G>A (p.Gln386=) rs112829030
NM_000528.4(MAN2B1):c.1209C>A (p.Arg403=) rs559827776
NM_000528.4(MAN2B1):c.1230G>C (p.Gln410His) rs563097824
NM_000528.4(MAN2B1):c.1398G>T (p.Ala466=) rs774396746
NM_000528.4(MAN2B1):c.1441G>T (p.Ala481Ser) rs34544747
NM_000528.4(MAN2B1):c.1645-3G>A
NM_000528.4(MAN2B1):c.1668C>A (p.Asp556Glu) rs766513928
NM_000528.4(MAN2B1):c.1687G>T (p.Glu563Ter) rs1057516927
NM_000528.4(MAN2B1):c.1779A>G (p.Pro593=) rs146778702
NM_000528.4(MAN2B1):c.1822G>A (p.Glu608Lys) rs145062583
NM_000528.4(MAN2B1):c.1830+1G>C rs80338677
NM_000528.4(MAN2B1):c.1850A>G (p.Asp617Gly) rs370382032
NM_000528.4(MAN2B1):c.2047-4G>A rs768347546
NM_000528.4(MAN2B1):c.2047-5C>T rs200424566
NM_000528.4(MAN2B1):c.2050C>A (p.Pro684Thr)
NM_000528.4(MAN2B1):c.2161G>A (p.Val721Met) rs148134639
NM_000528.4(MAN2B1):c.2248C>T (p.Arg750Trp) rs80338680
NM_000528.4(MAN2B1):c.2260G>A (p.Glu754Lys) rs141212446
NM_000528.4(MAN2B1):c.2267+3G>C rs28639634
NM_000528.4(MAN2B1):c.2267+3dup rs572289342
NM_000528.4(MAN2B1):c.2278C>T (p.Arg760Ter) rs121434331
NM_000528.4(MAN2B1):c.2355+6T>A rs1052970162
NM_000528.4(MAN2B1):c.2355G>A (p.Thr785=) rs1008745697
NM_000528.4(MAN2B1):c.2404A>G (p.Ser802Gly) rs141391488
NM_000528.4(MAN2B1):c.2409C>T (p.Ser803=) rs147850230
NM_000528.4(MAN2B1):c.2426T>C (p.Leu809Pro) rs80338681
NM_000528.4(MAN2B1):c.2437-5C>G rs200695002
NM_000528.4(MAN2B1):c.2622T>C (p.Gly874=)
NM_000528.4(MAN2B1):c.2639A>G (p.Asn880Ser)
NM_000528.4(MAN2B1):c.264C>A (p.Ile88=) rs199592101
NM_000528.4(MAN2B1):c.2670A>G (p.Ser890=) rs199606152
NM_000528.4(MAN2B1):c.26G>A (p.Gly9Glu)
NM_000528.4(MAN2B1):c.2748C>T (p.Arg916=) rs1184081650
NM_000528.4(MAN2B1):c.274A>G (p.Ile92Val)
NM_000528.4(MAN2B1):c.2767G>A (p.Val923Ile) rs755553683
NM_000528.4(MAN2B1):c.2856G>A (p.Gln952=)
NM_000528.4(MAN2B1):c.2865G>C (p.Thr955=) rs148108322
NM_000528.4(MAN2B1):c.2879A>G (p.Gln960Arg)
NM_000528.4(MAN2B1):c.2884C>T (p.Arg962Cys) rs370276057
NM_000528.4(MAN2B1):c.2927C>T (p.Pro976Leu)
NM_000528.4(MAN2B1):c.2973G>A (p.Thr991=) rs148945108
NM_000528.4(MAN2B1):c.2993G>A (p.Arg998His) rs202174515
NM_000528.4(MAN2B1):c.419G>A (p.Arg140Gln) rs139281846
NM_000528.4(MAN2B1):c.439C>T (p.Arg147Cys)
NM_000528.4(MAN2B1):c.455A>G (p.Asn152Ser) rs200164758
NM_000528.4(MAN2B1):c.474C>T (p.Asn158=) rs146331898
NM_000528.4(MAN2B1):c.594C>T (p.Phe198=) rs371341958
NM_000528.4(MAN2B1):c.718C>T (p.Arg240Trp) rs201448121
NM_000528.4(MAN2B1):c.719G>A (p.Arg240Gln) rs11554970
NM_000528.4(MAN2B1):c.743C>T (p.Pro248Leu) rs117843968
NM_000528.4(MAN2B1):c.747C>T (p.Thr249=) rs61737536
NM_000528.4(MAN2B1):c.748G>T (p.Ala250Ser) rs3745650
NM_000528.4(MAN2B1):c.788C>T (p.Pro263Leu) rs746808159
NM_000528.4(MAN2B1):c.789G>A (p.Pro263=) rs149484019
NM_000528.4(MAN2B1):c.81C>T (p.Ala27=) rs1407475487
NM_000528.4(MAN2B1):c.832C>G (p.Leu278Val) rs1054486
NM_000528.4(MAN2B1):c.855C>T (p.Pro285=) rs139218045
NM_000528.4(MAN2B1):c.874C>T (p.Leu292=) rs141077530
NM_000528.4(MAN2B1):c.935C>T (p.Thr312Ile) rs1054487
NM_000528.4(MAN2B1):c.966T>C (p.Tyr322=) rs762918325

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