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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:
PRLR
& Disease:
MFAB
, 6 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
88996
PRLR
c.508A>C
p.Ile170Leu (p.I170L)
NM_000949.7
M
SNV
P
1
+
2
PRLR
c.508A>C
p.Ile170Leu (p.I170L)
NM_001204318.1
SNV
P
1
+
2
PRLR
c.508A>C
p.Ile170Leu (p.I170L)
NM_001204317.1
SNV
P
1
+
2
PRLR
c.508A>C
p.Ile170Leu (p.I170L)
NM_001204316.1
SNV
P
1
+
2
PRLR
c.508A>C
p.Ile170Leu (p.I170L)
NM_001204315.1
SNV
P
1
+
2
PRLR
c.205A>C
p.Ile69Leu (p.I69L)
NM_001204314.2
SNV
P
1
+
2
6 Results, 20 per Page
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