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Links from Gene

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RASGRP1
(L383I)
Single nucleotide variant
(missense variant)
Immunodeficiency 64
GUncertain significance
LOC130056800, RASGRP1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
RASGRP1
(K686N +1 more)
Single nucleotide variant
(missense variant +1 more)
Immunodeficiency 64
GUncertain significance
LOC130056800, RASGRP1
(R12G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130056800, RASGRP1
Deletion
(intron variant)
not provided
GLikely benign
LOC130056800, RASGRP1
(R12W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RASGRP1
(P462L)
Single nucleotide variant
(missense variant +1 more)
Immunodeficiency 64
GUncertain significance
RASGRP1
Deletion
(intron variant)
Schizophrenia
GUncertain significance
LOC130056800, RASGRP1
(M1I)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
RASGRP1
(A400D)
Single nucleotide variant
(missense variant)
Immunodeficiency 64
GUncertain significance
RASGRP1
Single nucleotide variant
(splice acceptor variant)
Immunodeficiency 64
GPathogenic
LOC130056800, RASGRP1
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
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