ClinVar Miner

List of variants in gene SLC34A1 studied for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 18
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NM_003052.5(SLC34A1):c.1006+1G>A rs200095793
NM_003052.5(SLC34A1):c.1006T>G (p.Cys336Gly) rs876661338
NM_003052.5(SLC34A1):c.1204G>C (p.Gly402Arg) rs376131751
NM_003052.5(SLC34A1):c.142_143delinsTT (p.Ala48Phe) rs121918610
NM_003052.5(SLC34A1):c.1708C>A (p.Pro570Thr)
NM_003052.5(SLC34A1):c.1724C>T (p.Thr575Ile) rs201331677
NM_003052.5(SLC34A1):c.272_292del (p.Val91_Ala97del) rs876661296
NM_003052.5(SLC34A1):c.398C>T (p.Ala133Val) rs148976897
NM_003052.5(SLC34A1):c.439G>A (p.Val147Met) rs121918611
NM_003052.5(SLC34A1):c.458G>C (p.Gly153Ala) rs769409705
NM_003052.5(SLC34A1):c.458G>T (p.Gly153Val) rs769409705
NM_003052.5(SLC34A1):c.460_480dup (p.Ile154_Val160dup) rs1554095263
NM_003052.5(SLC34A1):c.536T>C (p.Leu179Pro) rs142772770
NM_003052.5(SLC34A1):c.604G>A (p.Val202Met) rs146919762
NM_003052.5(SLC34A1):c.644+1G>A rs201304511
NM_003052.5(SLC34A1):c.654G>A (p.Ala218=) rs150592440
NM_003052.5(SLC34A1):c.713A>C (p.Glu238Ala) rs1554095500
NM_003052.5(SLC34A1):c.934C>T (p.Gln312Ter) rs1554095568

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