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Links from Gene

Items: 61

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SUPV3L1
(R369Q +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(Y90F +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SUPV3L1
(I326V +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SUPV3L1
(R29H)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
SUPV3L1
(G151S +1 more)
Single nucleotide variant
(missense variant +3 more)
not specified
GLikely benign
SUPV3L1
(F3L +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SUPV3L1
Single nucleotide variant
(synonymous variant +1 more)
not specified
GLikely benign
SUPV3L1
(E621G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(G581S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(N541S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(D322G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(R315Q +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(D502N +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(K284R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(R478C +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(S467G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130003975, SUPV3L1
(A6S)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
SUPV3L1
(G54A)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
RRP12, RTKN2
+332 more
Copy number gain
not provided
GPathogenic
SUPV3L1
(N251S +3 more)
Single nucleotide variant
(missense variant +1 more)
EBV-positive nodal T- and NK-cell lymphoma
GLikely benign
SUPV3L1
Single nucleotide variant
(5 prime UTR variant +2 more)
not provided
GLikely benign
SUPV3L1
(L527V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(S354G +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
AGAP5, CRTAC1
+682 more
Copy number gain
Distal trisomy 10q
GPathogenic
ABRAXAS2, CHCHD1
+673 more
Copy number loss
Distal 10q deletion syndrome
GPathogenic
SUPV3L1
(E160Q +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(N415S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(R234Q +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(S569L +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130003975, SUPV3L1
(R5G)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
SUPV3L1
(F161I +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SUPV3L1
(Y214C +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(R590H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(I38V +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SUPV3L1
(A103E +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SUPV3L1
(G73S)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
SUPV3L1
(A399E +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(T205A +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(P66L)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
SUPV3L1
(R49C +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SUPV3L1
(I296V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(G340D +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(N129T)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
SUPV3L1
(K57R)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
SUPV3L1
(S43A)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
SUPV3L1
(N124D +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SUPV3L1
(T151R +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SUPV3L1
(R262W +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SUPV3L1
(V362I +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADAMTS14, ADK
+91 more
Copy number loss
not specified
GPathogenic
ATOH7, CCAR1
+24 more
Deletion
not provided
GPathogenic
ACTA2, ADAMTS14
+168 more
Copy number gain
not provided
GPathogenic
COX15, CPEB3
+569 more
Copy number loss
Poly (ADP-Ribose) polymerase inhibitor response
Gdrug response
INA, INPP5A
+721 more
Copy number gain
See cases
GPathogenic
A1CF, ABCC2
+721 more
Copy number gain
See cases
GPathogenic
A1CF, ABCC2
+722 more
Copy number gain
See cases
GPathogenic
LOC129390180, LOC129390181
+1008 more
Copy number gain
See cases
GPathogenic
HERC4, HK1
+514 more
Copy number loss
See cases
GPathogenic
LOC130004125, LOC130004126
+580 more
Copy number gain
See cases
GPathogenic
A1CF, ADAMTS14
+902 more
Copy number gain
See cases
GPathogenic
LOC129390190, LOC129390191
+610 more
Copy number loss
See cases
GPathogenic
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