ClinVar Miner

List of variants in gene FLVCR1 reported as likely benign for not provided

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Gene type:
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Total variants: 43
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HGVS dbSNP
NM_014053.4(FLVCR1):c.1017C>T (p.Ile339=)
NM_014053.4(FLVCR1):c.1168T>C (p.Leu390=)
NM_014053.4(FLVCR1):c.1197-4T>G
NM_014053.4(FLVCR1):c.1258T>C (p.Leu420=)
NM_014053.4(FLVCR1):c.1284G>A (p.Val428=)
NM_014053.4(FLVCR1):c.1307+14G>T
NM_014053.4(FLVCR1):c.1414-11T>C
NM_014053.4(FLVCR1):c.1419T>C (p.Phe473=)
NM_014053.4(FLVCR1):c.1467T>C (p.Gly489=)
NM_014053.4(FLVCR1):c.1521A>G (p.Leu507=) rs74607124
NM_014053.4(FLVCR1):c.1525+12C>T
NM_014053.4(FLVCR1):c.1594-10G>T
NM_014053.4(FLVCR1):c.1624C>T (p.Pro542Ser) rs141575859
NM_014053.4(FLVCR1):c.1626A>G (p.Pro542=) rs888869006
NM_014053.4(FLVCR1):c.1632G>A (p.Thr544=)
NM_014053.4(FLVCR1):c.1657T>G (p.Ser553Ala) rs149887215
NM_014053.4(FLVCR1):c.177C>T (p.Ala59=)
NM_014053.4(FLVCR1):c.198G>T (p.Gly66=)
NM_014053.4(FLVCR1):c.201T>C (p.Pro67=)
NM_014053.4(FLVCR1):c.216C>A (p.Ala72=) rs1398603103
NM_014053.4(FLVCR1):c.279C>A (p.Ala93=)
NM_014053.4(FLVCR1):c.279C>T (p.Ala93=)
NM_014053.4(FLVCR1):c.294G>T (p.Leu98=) rs376377158
NM_014053.4(FLVCR1):c.303G>C (p.Thr101=) rs1189185318
NM_014053.4(FLVCR1):c.306G>A (p.Ala102=)
NM_014053.4(FLVCR1):c.346C>T (p.Leu116=)
NM_014053.4(FLVCR1):c.366C>T (p.Ala122=)
NM_014053.4(FLVCR1):c.372G>A (p.Gln124=)
NM_014053.4(FLVCR1):c.42C>T (p.Pro14=) rs886045923
NM_014053.4(FLVCR1):c.525C>T (p.Leu175=) rs755329362
NM_014053.4(FLVCR1):c.532C>T (p.Leu178=)
NM_014053.4(FLVCR1):c.663C>T (p.Pro221=)
NM_014053.4(FLVCR1):c.690G>A (p.Gly230=) rs1352757781
NM_014053.4(FLVCR1):c.69C>T (p.Leu23=) rs374379789
NM_014053.4(FLVCR1):c.6G>A (p.Ala2=)
NM_014053.4(FLVCR1):c.738+10G>A
NM_014053.4(FLVCR1):c.75G>A (p.Leu25=)
NM_014053.4(FLVCR1):c.768A>G (p.Pro256=) rs774690148
NM_014053.4(FLVCR1):c.884-20C>T
NM_014053.4(FLVCR1):c.906T>C (p.Tyr302=)
NM_014053.4(FLVCR1):c.952G>A (p.Glu318Lys) rs41297444
NM_014053.4(FLVCR1):c.981C>T (p.Asn327=) rs886045928
NM_014053.4(FLVCR1):c.996T>C (p.Ile332=) rs755552497

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