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Variants
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6
records found for search term
Rpl36al
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RGD ID
Symbol
Variant Type
Name
Trait
Clinical Significance
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597709427
CV3594219
single nucleotide variant
NM_001001.5(
RPL36AL
):c.8A>T (p.Asn3Ile)
not specified [RCV004860838]
uncertain significance
14
49619097
49619097
Human
name
156334655
CV2230952
single nucleotide variant
NM_001001.5(
RPL36AL
):c.61C>T (p.His21Tyr)
not specified [RCV004092413]
uncertain significance
14
49619044
49619044
Human
name
405738108
CV3320137
single nucleotide variant
NM_001001.5(
RPL36AL
):c.95C>A (p.Ser32Tyr)
not specified [RCV004451958]
uncertain significance
14
49619010
49619010
Human
name
407487666
CV3476111
single nucleotide variant
NM_001001.5(
RPL36AL
):c.29C>T (p.Thr10Ile)
not specified [RCV004665728]
uncertain significance
14
49619076
49619076
Human
name
407487662
CV3476110
single nucleotide variant
NM_001001.5(
RPL36AL
):c.136A>G (p.Ser46Gly)
not specified [RCV004665727]
uncertain significance
14
49618969
49618969
Human
name
597786182
CV3594217
single nucleotide variant
NM_001001.5(
RPL36AL
):c.127C>T (p.Arg43Trp)
not specified [RCV004854827]
uncertain significance
14
49618978
49618978
Human
name