"Illumina Laboratory Services, Illumina"[submitter] AND "KIFC2"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 362270	NM_001369769.2(KIFC2):c.*377C>A	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GBenign
Select item 362271	NM_001369769.2(KIFC2):c.*398G>A	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 909137	NM_001369769.2(KIFC2):c.*413C>T	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 909138	NM_001369769.2(KIFC2):c.*419C>T	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 909979	NM_001369769.2(KIFC2):c.*426C>T	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 909980	NM_001369769.2(KIFC2):c.*467G>A	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 909981	NM_001369769.2(KIFC2):c.*495G>A	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 909982	NM_001369769.2(KIFC2):c.*527G>T	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 362272	NM_001369769.2(KIFC2):c.*538G>A	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GBenign
Select item 362273	NM_001369769.2(KIFC2):c.612_614del	FOXH1, KIFC2	Deletion (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 909983	NM_001369769.2(KIFC2):c.*616C>T	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GLikely benign
Select item 362274	NM_001369769.2(KIFC2):c.*677G>C	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 909984	NM_001369769.2(KIFC2):c.*761T>C	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 362275	NM_001369769.2(KIFC2):c.*775C>T	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GUncertain significance
Select item 362276	NM_001369769.2(KIFC2):c.*794G>A	FOXH1, KIFC2	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly sequence	GBenign
Select item 988937	GRCh37/hg19 8q24.3(chr8:145033244-146297937)x3	HGH1, MIR1234 +44 more	Copy number gain	not provided	GUncertain significance