Project HERA

PALB2 variants

Every PALB2 variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.

61 variants

PALB2 variants

Newest first. Each row opens the full report, criterion by criterion.

61 shown
Variant
Protein change
Classification
PALB2 NM_024675.4:c.886del
NP_078951.2:p.(M296*)
Pathogenic
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PALB2 NM_024675.4:c.829G>A
NP_078951.2:p.(D277N)
Likely Benign
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PALB2 NM_024675.4:c.2945G>T
NP_078951.2:p.(G982V)
VUS
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PALB2 NM_024675.4:c.2970A>T
NP_078951.2:p.(E990D)
VUS
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PALB2 NM_024675.4:c.1096A>G
NP_078951.2:p.(N366D)
VUS
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PALB2 NM_024675.4:c.886dup
NP_078951.2:p.(M296Nfs*7)
Pathogenic
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PALB2 NM_024675.4:c.740C>G
NP_078951.2:p.(T247R)
VUS
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PALB2 NM_024675.4:c.1001A>G
NP_078951.2:p.(Y334C)
VUS
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PALB2 NM_024675.4:c.3044C>T
NP_078951.2:p.(T1015I)
VUS
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PALB2 NM_024675.4:c.1209G>A
NP_078951.2:p.(L403=)
Likely Benign
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PALB2 NM_024675.4:c.1652A>G
NP_078951.2:p.(Y551C)
VUS
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PALB2 NM_024675.4:c.205C>T
NP_078951.2:p.(H69Y)
VUS
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PALB2 NM_024675.4:c.2580G>T
NP_078951.2:p.(E860D)
VUS
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PALB2 NM_024675.4:c.509_510del
NP_078951.2:p.(R170Ifs*14)
Pathogenic
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PALB2 NM_024675.4:c.928A>G
NP_078951.2:p.(S310G)
Likely Benign
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PALB2 NM_024675.4:c.928A>G
NP_078951.2:p.(S310G)
Likely Benign
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PALB2 NM_024675.4:c.1351T>G
NP_078951.2:p.(L451V)
VUS
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PALB2 NM_024675.3:c.721A>G
NP_078951.2:p.(N241D)
Benign
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PALB2 NM_024675.3:c.82T>A
NP_078951.2:p.(Y28N)
VUS
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PALB2 NM_024675.3:c.3049G>A
NP_078951.2:p.(A1017T)
VUS
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PALB2 NM_024675.3:c.1684+1G>A
NP_078951.2:p.?
Pathogenic
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PALB2 NM_024675.4:c.2863dup
NP_078951.2:p.(S955Kfs*2)
Pathogenic
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PALB2 NM_024675.4:c.2469C>G
NP_078951.2:p.(L823=)
Likely Benign
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PALB2 NM_024675.4:c.1578T>C
NP_078951.2:p.(H526=)
Likely Benign
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PALB2 NM_024675.4:c.1960A>G
NP_078951.2:p.(I654V)
VUS
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PALB2 NM_024675.4:c.194C>T
NP_078951.2:p.(P65L)
VUS
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PALB2 NM_024675.4:c.841A>G
NP_078951.2:p.(I281V)
VUS
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PALB2 NM_024675.3:c.871G>A
NP_078951.2:p.(A291T)
VUS
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PALB2 NM_024675.3:c.3549C>A
NP_078951.2:p.(Y1183*)
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PALB2 NM_024675.3:c.3089C>T
NP_078951.2:p.(T1030I)
VUS
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PALB2 NM_024675.4:c.3132A>T
NP_078951.2:p.(Q1044H)
VUS
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PALB2 NM_024675.3:c.338C>T
NP_078951.2:p.(P113L)
VUS
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PALB2 NM_024675.3:c.2734T>G
NP_078951.2:p.(W912G)
VUS
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PALB2 NM_024675.3:c.514_517del
NP_078951.2:p.(S172Gfs*4)
Pathogenic
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PALB2 NM_024675.3:c.7G>T
NP_078951.2:p.(E3*)
Pathogenic
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PALB2 NM_024675.3:c.135G>A
NP_078951.2:p.(K45=)
Likely Benign
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PALB2 NM_024675.3:c.3249G>C
NP_078951.2:p.(E1083D)
Likely Benign
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PALB2 NM_024675.3:c.3054G>C
NP_078951.2:p.(E1018D)
Benign
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PALB2 NM_024675.3:c.3362del
NP_078951.2:p.(G1121Vfs*3)
Likely Pathogenic
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PALB2 NM_024675.3:c.109C>A
NP_078951.2:p.(R37S)
Likely Benign
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PALB2 NM_024675.3:c.49-2A>T
NP_078951.2:p.?
VUS
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PALB2 NM_024675.3:c.682C>T
NP_078951.2:p.(Q228*)
Pathogenic
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PALB2 NM_024675.3:c.2524_2535delinsTCAGA
NP_078951.2:p.(A842Sfs*7)
Pathogenic
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PALB2 NM_024675.4:c.154G>A
NP_078951.2:p.(V52I)
VUS
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PALB2 NM_024675.3:c.2787_2788dup
NP_078951.2:p.(N930Ifs*6)
Pathogenic
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PALB2 NM_024675.3:c.104T>C
NP_078951.2:p.(L35P)
VUS
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PALB2 NM_024675.3:c.2014G>C
NP_078951.2:p.(E672Q)
Benign
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PALB2 NM_024675.3:c.3512del
NP_078951.2:p.(L1171Cfs*20)
Likely Pathogenic
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PALB2 NM_024675.3:c.3113G>A
NP_078951.2:p.(W1038*)
Pathogenic
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PALB2 NM_024675.3:c.2027T>C
NP_078951.2:p.(I676T)
Benign
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PALB2 NM_024675.3:c.532del
NP_078951.2:p.(E178Nfs*15)
Pathogenic
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PALB2 NM_024675.3:c.2831T>A
NP_078951.2:p.(I944N)
VUS
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PALB2 NM_024675.3:c.1794G>A
NP_078951.2:p.(L598=)
Likely Benign
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PALB2 NM_024675.4:c.1058A>T
NP_078951.2:p.(K353I)
VUS
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PALB2 NM_024675.4:c.968C>T
NP_078951.2:p.(A323V)
VUS
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PALB2 NM_024675.4:c.1042C>A
NP_078951.2:p.(Q348K)
VUS
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PALB2 NM_024675.4:c.1432T>C
NP_078951.2:p.(S478P)
VUS
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PALB2 NM_024675.4:c.2234A>G
NP_078951.2:p.(K745R)
Likely Benign
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PALB2 NM_024675.4:c.2631G>C
NP_078951.2:p.(W877C)
VUS
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PALB2 NM_024675.4:c.2329G>A
NP_078951.2:p.(D777N)
VUS
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PALB2 NM_024675.4:c.721A>G
NP_078951.2:p.(N241D)
Benign
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