C44E4.1
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193319501snpG/T0.01980.0975088missenseC44E4.1, ?WS195I:4612920TTCGGATCACTGACA[G/T]CATTCGTTCCACCAT172068
rs193319502snpC/T0.02030240.0986865intron-variantC44E4.1WS195I:4621720GAACTGCAGGACCAA[C/T]CAGCGATTTGCTCCG172068
rs193573661snpA/Cutr-variant-3-prime?WS195I:4610166TTGATTAAATATTTT[A/C]TTTATTAAAAACTCT172068
rs193573662snpC/Tintron-variant?, C44E4.1WS195I:4611882GCGGTAATTCTAAAA[C/T]TCGGTGCTTTCAAAT172068
rs193573663snpA/Tintron-variantC44E4.1WS195I:4616594CAAAAAAATGAAAAA[A/T]TTTTTTTTGAGGTCT172068
rs193573664snpA/Tintron-variantC44E4.1WS195I:4616647ATTGGCCGATATTGT[A/T]CGTCGGAAAATAAAT172068
rs193573665snpA/Tintron-variantC44E4.1WS195I:4618124CAAAATTTTCTTAAA[A/T]TTCCAATTTAATTAA172068
rs193573666snpC/TmissenseC44E4.1WS195I:4620224TCAATCGGAATAGTT[C/T]CAGCGATTTTCGCGA172068
rs193573667snpA/Gintron-variantC44E4.1WS195I:4622777TGCATTGTGGCAACT[A/G]AAAATTCGAAATTAT172068
rs353105373snpA/Gintron-variantC44E4.1WS195I:4616781ATTTTCAACTTTTTG[A/G]TCCAAAATAATTTTC172068
rs353107631snpC/Tintron-variantC44E4.1WS195I:4621814TGGCTTAATCTATCT[C/T]GATTTTTCAATATTT172068
rs353131990in-del-/Aintron-variantC44E4.1WS195I:4616154CGCCTGAAAATTTCG[-/A]AAAAAAAAAATTTCA172068
rs353141771in-del-/Tintron-variantC44E4.1WS195I:4621264GAAATTTTTCAATTG[-/T]TTTTTTTTTTCAATT172068
rs353145121in-del-/Tintron-variantC44E4.1WS195I:4621409TGCTAAACGTTGCGA[-/T]TTTTTTTTGATTTTC172068
rs353150911snpC/Tintron-variantC44E4.1WS195I:4619472TTTTAAAAAGTTTTT[C/T]AGACAAAAAAATTCT172068
rs353163584snpA/Tintron-variant?, C44E4.1WS195I:4613037AACTAGAAAAAGTTT[A/T]AAATTTTGGGTTTTA172068