"Illumina Laboratory Services, Illumina"[submitter] AND "SLC46A1"[gene - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 322335	NM_015077.4(SARM1):c.1924-1133C>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GBenign
Select item 892030	NM_015077.4(SARM1):c.1924-1053A>T	SLC46A1, SARM1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322336	NM_015077.4(SARM1):c.1924-1029G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GBenign
Select item 322337	NM_015077.4(SARM1):c.1924-991T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322338	NM_015077.4(SARM1):c.1924-978del	SARM1, SLC46A1	Deletion (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322339	NM_015077.4(SARM1):c.1924-910C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322342	NM_015077.4(SARM1):c.1924-874_1924-873dup	SARM1, SLC46A1	Duplication (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322341	NM_015077.4(SARM1):c.1924-873dup	SARM1, SLC46A1	Duplication (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GBenign
Select item 322340	NM_015077.4(SARM1):c.1924-885G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 888567	NM_015077.4(SARM1):c.1924-833G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GBenign
Select item 888568	NM_015077.4(SARM1):c.1924-667G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322343	NM_015077.4(SARM1):c.1924-572G>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322344	NM_015077.4(SARM1):c.1924-569T>C	SLC46A1, SARM1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322345	NM_015077.4(SARM1):c.1924-565G>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GLikely benign
Select item 888569	NM_015077.4(SARM1):c.1924-433A>C	SLC46A1, SARM1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 890268	NM_015077.4(SARM1):c.1924-407C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 890269	NM_015077.4(SARM1):c.1924-340G>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 890270	NM_015077.4(SARM1):c.1924-320C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 890271	NM_015077.4(SARM1):c.1924-284C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GLikely benign
Select item 322346	NM_015077.4(SARM1):c.1924-279G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GBenign
Select item 890272	NM_015077.4(SARM1):c.1924-234T>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322347	NM_015077.4(SARM1):c.1924-208G>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322348	NM_015077.4(SARM1):c.1924-196C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GBenign
Select item 322349	NM_015077.4(SARM1):c.1924-162T>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322350	NM_015077.4(SARM1):c.1924-38G>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322351	NM_015077.4(SARM1):c.1924-34A>G	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GBenign
Select item 322352	NM_015077.4(SARM1):c.1998G>C (p.Gln666His)	SARM1, SLC46A1 (Q666H)	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322353	NM_015077.4(SARM1):c.2014A>G (p.Met672Val)	SARM1, SLC46A1 (M672V)	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322354	NM_015077.4(SARM1):c.2045+27G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 892076	NM_015077.4(SARM1):c.2089C>G (p.Arg697Gly)	SARM1, SLC46A1 (R697G)	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322355	NM_015077.4(SARM1):c.2143T>C (p.Leu715=)	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322356	NM_015077.4(SARM1):c.2156C>T (p.Ala719Val)	SARM1, SLC46A1 (A719V)	Single nucleotide variant (3 prime UTR variant +1 more)	Congenital defect of folate absorption	GUncertain significance
Select item 322357	NM_015077.4(SARM1):c.*68T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 892077	NM_015077.4(SARM1):c.*91G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322358	NM_015077.4(SARM1):c.*104C>T	SLC46A1, SARM1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 322359	NM_015077.4(SARM1):c.*167T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322360	NM_015077.4(SARM1):c.*235T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 888617	NM_015077.4(SARM1):c.*250T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GLikely benign
Select item 322361	NM_015077.4(SARM1):c.*308G>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 322363	NM_015077.4(SARM1):c.*361C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322362	NM_015077.4(SARM1):c.*361=	SARM1, SLC46A1	Single nucleotide variant (no sequence alteration)	Congenital defect of folate absorption	GBenign
Select item 322364	NM_015077.4(SARM1):c.*402G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 888618	NM_015077.4(SARM1):c.*425C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 890317	NM_015077.4(SARM1):c.*469G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 890318	NM_015077.4(SARM1):c.*502C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322365	NM_015077.4(SARM1):c.*517C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 890319	NM_015077.4(SARM1):c.*518G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GLikely benign
Select item 322366	NM_015077.4(SARM1):c.*527C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 322367	NM_015077.4(SARM1):c.*562C>G	SLC46A1, SARM1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 890320	NM_015077.4(SARM1):c.*624C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 890877	NM_015077.4(SARM1):c.*646C>G	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322368	NM_015077.4(SARM1):c.*709C>G	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322369	NM_015077.4(SARM1):c.*734G>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322370	NM_015077.4(SARM1):c.*812G>A	SLC46A1, SARM1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322371	NM_015077.4(SARM1):c.*857C>G	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322372	NM_015077.4(SARM1):c.*877T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 890878	NM_015077.4(SARM1):c.*884A>G	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322373	NM_015077.4(SARM1):c.*969C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322374	NM_015077.4(SARM1):c.*1097T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 892118	NM_015077.4(SARM1):c.*1108C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322375	NM_015077.4(SARM1):c.*1122A>G	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 892119	NM_015077.4(SARM1):c.*1153T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 322376	NM_015077.4(SARM1):c.*1247C>G	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GLikely benign
Select item 892120	NM_015077.4(SARM1):c.*1343G>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 892121	NM_015077.4(SARM1):c.*1389G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322377	NM_015077.4(SARM1):c.*1389G>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 888671	NM_015077.4(SARM1):c.*1531C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322378	NM_015077.4(SARM1):c.*1539G>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322379	NM_015077.4(SARM1):c.*1575G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322380	NM_015077.4(SARM1):c.*1596T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 322381	NM_015077.4(SARM1):c.*1721T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322382	NM_015077.4(SARM1):c.*1722C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GLikely benign
Select item 322383	NM_015077.4(SARM1):c.*1743A>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 888672	NM_015077.4(SARM1):c.*1849C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322384	NM_015077.4(SARM1):c.*1963G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 322385	NM_015077.4(SARM1):c.*1978G>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GLikely benign
Select item 890375	NM_015077.4(SARM1):c.*1987T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 890376	NM_015077.4(SARM1):c.*2034C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 890377	NM_015077.4(SARM1):c.*2035G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322386	NM_015077.4(SARM1):c.*2038C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GLikely benign
Select item 890378	NM_015077.4(SARM1):c.*2072C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 890379	NM_015077.4(SARM1):c.*2121C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322387	NM_015077.4(SARM1):c.*2127T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 322388	NM_015077.4(SARM1):c.*2150T>C	SLC46A1, SARM1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322389	NM_015077.4(SARM1):c.*2276T>C	LOC130060548, SARM1 +1 more	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322390	NM_015077.4(SARM1):c.*2294C>T	LOC130060548, SARM1 +1 more	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322391	NM_015077.4(SARM1):c.*2308C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322392	NM_015077.4(SARM1):c.*2364T>G	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322393	NM_015077.4(SARM1):c.*2442T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 322394	NM_015077.4(SARM1):c.*2535T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322395	NM_015077.4(SARM1):c.*2585A>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322396	NM_015077.4(SARM1):c.*2641C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 322397	NM_015077.4(SARM1):c.*2678T>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 892167	NM_015077.4(SARM1):c.*2699G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GBenign
Select item 892168	NM_015077.4(SARM1):c.*2894C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 892169	NM_015077.4(SARM1):c.*3019G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 892170	NM_015077.4(SARM1):c.*3073G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322398	NM_015077.4(SARM1):c.*3093T>C	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322399	NM_015077.4(SARM1):c.*3241G>A	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance
Select item 322400	NM_015077.4(SARM1):c.*3280C>T	SARM1, SLC46A1	Single nucleotide variant (3 prime UTR variant)	Congenital defect of folate absorption	GUncertain significance

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