ClinVar Miner

List of variants reported as uncertain significance for colorectal cancer, susceptibility to, 1 by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_024642.5(GALNT12):c.1339G>A (p.Gly447Arg) rs376441206 0.00029
NM_024642.5(GALNT12):c.776T>C (p.Val259Ala) rs147356342 0.00026
NM_024642.5(GALNT12):c.329G>A (p.Arg110His) rs374994372 0.00014
NM_024642.5(GALNT12):c.5G>T (p.Trp2Leu) rs898798901 0.00014
NM_024642.5(GALNT12):c.890G>A (p.Arg297Gln) rs751386354 0.00010
NM_024642.5(GALNT12):c.715G>C (p.Glu239Gln) rs777144221 0.00008
NM_024642.5(GALNT12):c.608A>G (p.Asn203Ser) rs375844934 0.00007
NM_024642.5(GALNT12):c.784T>C (p.Trp262Arg) rs373792075 0.00007
NM_024642.5(GALNT12):c.1216C>A (p.Pro406Thr) rs769837927 0.00003
NM_024642.5(GALNT12):c.1672A>G (p.Ser558Gly) rs759843363 0.00003
NM_024642.5(GALNT12):c.1145G>A (p.Arg382His) rs868590153 0.00002
NM_024642.5(GALNT12):c.1277A>G (p.Lys426Arg) rs753534837 0.00002
NM_024642.5(GALNT12):c.1655G>A (p.Arg552Lys) rs1285871027 0.00001
NM_024642.5(GALNT12):c.550A>C (p.Lys184Gln) rs1835864602 0.00001
NM_024642.5(GALNT12):c.609C>A (p.Asn203Lys) rs370024536 0.00001
NM_024642.5(GALNT12):c.758T>C (p.Val253Ala) rs1316883841 0.00001
NM_024642.5(GALNT12):c.802C>G (p.Leu268Val) rs772466597 0.00001
NM_024642.5(GALNT12):c.1017C>A (p.Asn339Lys) rs756614355
NM_024642.5(GALNT12):c.104C>G (p.Ser35Trp)
NM_024642.5(GALNT12):c.1052G>T (p.Gly351Val)
NM_024642.5(GALNT12):c.1265G>T (p.Cys422Phe) rs755796376
NM_024642.5(GALNT12):c.139G>T (p.Ala47Ser)
NM_024642.5(GALNT12):c.140C>A (p.Ala47Asp) rs1304764723
NM_024642.5(GALNT12):c.1463T>G (p.Phe488Cys)
NM_024642.5(GALNT12):c.154C>A (p.Pro52Thr)
NM_024642.5(GALNT12):c.1594A>T (p.Ile532Phe)
NM_024642.5(GALNT12):c.166_174dup (p.Pro56_Pro58dup) rs1379414621
NM_024642.5(GALNT12):c.1A>C (p.Met1Leu) rs1259048855
NM_024642.5(GALNT12):c.329G>T (p.Arg110Leu) rs374994372
NM_024642.5(GALNT12):c.344GCC[1] (p.Arg116del) rs866699148
NM_024642.5(GALNT12):c.361T>G (p.Trp121Gly)
NM_024642.5(GALNT12):c.430T>C (p.Phe144Leu)
NM_024642.5(GALNT12):c.5G>C (p.Trp2Ser) rs898798901
NM_024642.5(GALNT12):c.629G>C (p.Arg210Pro) rs780705882
NM_024642.5(GALNT12):c.759G>A (p.Val253=)

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