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Variants
search result for
Homo sapiens
(View Results for all Objects and Ontologies)
6
records found for search term
Ddx3y
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RGD ID
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Variant Type
Name
Trait
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156434993
CV2403257
deletion
NM_004660.5(
DDX3Y
):c.1609+1del
Non-obstructive azoospermia [RCV003127207]
likely pathogenic
Y
12916633
12916633
Human
2
name
408378687
CV3500960
single nucleotide variant
NM_004660.5(
DDX3Y
):c.948C>T (p.His316=)
not provided [RCV004722610]
likely benign
Y
12915156
12915156
Human
name
156434989
CV2403254
duplication
NM_004660.5(
DDX3Y
):c.428dup (p.Glu145fs)
Non-obstructive azoospermia [RCV003127204]
likely pathogenic
Y
12912872
12912873
Human
2
name
405255876
CV3208392
single nucleotide variant
NM_004660.5(
DDX3Y
):c.1116C>T (p.Gly372=)
DDX3Y
-related disorder [RCV003939496]
likely benign
Y
12915726
12915726
Human
name , trait , alternate_id
156434991
CV2403256
duplication
NM_004660.5(
DDX3Y
):c.1272dup (p.Lys425Ter)
Non-obstructive azoospermia [RCV003127206]
likely pathogenic
Y
12915989
12915990
Human
2
name
156434990
CV2403255
deletion
NM_004660.5(
DDX3Y
):c.1230_1231del (p.Asn412fs)
Non-obstructive azoospermia [RCV003127205]
likely pathogenic
Y
12915948
12915949
Human
2
name