ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_000528.4(MAN2B1):c.1109+10G>A
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.1645-3G>A
NM_000528.4(MAN2B1):c.1668C>A (p.Asp556Glu) rs766513928
NM_000528.4(MAN2B1):c.1779A>G (p.Pro593=) rs146778702
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.2355+6T>A rs1052970162
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.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.2879A>G (p.Gln960Arg)
NM_000528.4(MAN2B1):c.2927C>T (p.Pro976Leu)
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.718C>T (p.Arg240Trp) rs201448121
NM_000528.4(MAN2B1):c.81C>T (p.Ala27=) rs1407475487
NM_000528.4(MAN2B1):c.855C>T (p.Pro285=) rs139218045

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