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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
Amyotrophic Lateral Sclerosis 1
USH2A c.8559-2A>G
Cystic Fibrosis
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Mutation Direct
Effortless mutation search and display tool
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Search criteria:
Gene:
FLRT3
& Disease:
HH21
, 16 results
Search
Reset
ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
50862
FLRT3
c.290A>G
p.Glu97Gly (p.E97G)
NM_198391.3
M
SNV
VUS
1
+
3
FLRT3
c.290A>G
p.Glu97Gly (p.E97G)
NM_013281.4
SNV
VUS
1
+
3
1226971
FLRT3
c.1257C>T
p.Thr419= (p.T419=)
NM_198391.3
M
SNV
B
1
+
2
1029224
FLRT3
c.1255A>T
p.Thr419Ser (p.T419S)
NM_198391.3
M
SNV
VUS
1
+
2
1226971
FLRT3
c.1257C>T
p.Thr419= (p.T419=)
NM_013281.4
SNV
B
1
+
2
1029224
FLRT3
c.1255A>T
p.Thr419Ser (p.T419S)
NM_013281.4
SNV
VUS
1
+
2
50863
FLRT3
c.431G>T
p.Ser144Ile (p.S144I)
NM_198391.3
M
SNV
VUS
1
+
1
50864
FLRT3
c.205C>A
p.Gln69Lys (p.Q69K)
NM_198391.3
M
SNV
VUS
1
+
1
50865
FLRT3
c.1016A>G
p.Lys339Arg (p.K339R)
NM_198391.3
M
SNV
P
1
+
1
2441519
FLRT3
c.1727C>T
p.Ala576Val (p.A576V)
NM_198391.3
M
SNV
VUS
1
+
1
1710063
FLRT3
c.999G>A
p.Met333Ile (p.M333I)
NM_198391.3
M
SNV
VUS
1
+
1
50863
FLRT3
c.431G>T
p.Ser144Ile (p.S144I)
NM_013281.4
SNV
VUS
1
+
1
50864
FLRT3
c.205C>A
p.Gln69Lys (p.Q69K)
NM_013281.4
SNV
VUS
1
+
1
50865
FLRT3
c.1016A>G
p.Lys339Arg (p.K339R)
NM_013281.4
SNV
P
1
+
1
2441519
FLRT3
c.1727C>T
p.Ala576Val (p.A576V)
NM_013281.4
SNV
VUS
1
+
1
1710063
FLRT3
c.999G>A
p.Met333Ile (p.M333I)
NM_013281.4
SNV
VUS
1
+
1
16 Results, 20 per Page
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