Project HERA
PALB2 variants
Every PALB2 variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
PALB2 variants
Newest first. Each row opens the full report, criterion by criterion.
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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