Item | Value |
---|---|
geneid | 80267 |
ensemblid | ENSG00000116406.20 |
hgncid | 16787 |
symbol | EDEM3 |
name | ER degradation enhancing alpha-mannosidase like protein 3 |
refseq_nuc | NM_025191.4 |
refseq_prot | NP_079467.3 |
ensembl_nuc | ENST00000318130.13 |
ensembl_prot | ENSP00000318147.7 |
mane_status | MANE Select |
chr | chr1 |
start | 184690237 |
end | 184754858 |
strand | - |
ver | v1.2 |
region | chr1:184690237-184754858 |
region5000 | chr1:184685237-184759858 |
regionname0 | EDEM3_chr1_184690237_184754858 |
regionname5000 | EDEM3_chr1_184685237_184759858 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 932 | 211 | 83 | 37 | 73 | 6 | 10 | 53 | EDEM3_chr1_184685237_184759858 | EDEM3 | MSEAG others(927): Show |
chr1 | 184685237 | 184759858 |
a0002 | 0/0 | 932 | 102 | 3 | 17 | 66 | 6 | 10 | 50 | EDEM3_chr1_184685237_184759858 | EDEM3 | MSEAG others(927): Show |
chr1 | 184685237 | 184759858 |
a0003 | 0/0 | 932 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | EDEM3_chr1_184685237_184759858 | EDEM3 | MSEVG others(927): Show |
chr1 | 184685237 | 184759858 |
a0004 | 0/0 | 932 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | EDEM3_chr1_184685237_184759858 | EDEM3 | MSEAG others(927): Show |
chr1 | 184685237 | 184759858 |
a0005 | 0/0 | 932 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | MSEAG others(927): Show |
chr1 | 184685237 | 184759858 |
a0006 | 0/0 | 932 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | MSEAG others(927): Show |
chr1 | 184685237 | 184759858 |
a0007 | 0/0 | 932 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | MSEAG others(927): Show |
chr1 | 184685237 | 184759858 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2796 | 102 | 12 | 19 | 54 | 5 | 10 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0001c0003 | 0/0 | 2796 | 83 | 56 | 12 | 15 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0001c0004 | 0/0 | 2796 | 23 | 12 | 6 | 4 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0001c0008 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0001c0010 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0001c0013 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0002c0002 | 0/0 | 2796 | 101 | 3 | 17 | 65 | 6 | 10 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0002c0011 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0003c0005 | 0/0 | 2796 | 4 | 0 | 0 | 4 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0004c0006 | 0/0 | 2796 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0005c0007 | 0/0 | 2796 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0006c0012 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 | ||
a0007c0009 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | ATGAG others(2791): Show |
chr1 | 184685237 | 184759858 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 6837 | 90 | 12 | 18 | 44 | 5 | 9 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0001t0007 | 0/0 | 6837 | 5 | 0 | 0 | 5 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0001t0026 | 0/0 | 6838 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0001t0028 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0001t0029 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0001t0031 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0001t0032 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0001t0033 | 0/0 | 6838 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0001t0039 | 0/0 | 6837 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0001 | 0/0 | 6837 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0003 | 0/0 | 6838 | 41 | 28 | 7 | 6 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0005 | 0/0 | 6837 | 11 | 0 | 2 | 9 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0006 | 0/0 | 6838 | 7 | 7 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0009 | 0/0 | 6838 | 6 | 5 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0010 | 0/0 | 6837 | 4 | 4 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0011 | 0/0 | 6838 | 4 | 3 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0017 | 0/0 | 6838 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0018 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0019 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0027 | 0/0 | 6839 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6834): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0030 | 0/0 | 6837 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0034 | 0/0 | 6838 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0035 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0003t0038 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0004t0004 | 0/0 | 6837 | 17 | 7 | 6 | 3 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0004t0013 | 0/0 | 6837 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0004t0023 | 0/0 | 6837 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0004t0025 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0004t0036 | 0/0 | 6837 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0001c0008t0020 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0010t0006 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0001c0013t0040 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0002c0002t0002 | 0/0 | 6838 | 82 | 2 | 11 | 57 | 3 | 9 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0002c0002t0004 | 0/0 | 6837 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0002c0002t0008 | 0/0 | 6838 | 6 | 1 | 3 | 0 | 1 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0002c0002t0012 | 0/0 | 6838 | 3 | 0 | 2 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0002c0002t0015 | 0/0 | 6838 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0002c0002t0016 | 0/0 | 6838 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0002c0002t0021 | 0/0 | 6838 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0002c0002t0022 | 0/0 | 6838 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0002c0002t0037 | 0/0 | 6838 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0002c0011t0002 | 0/0 | 6838 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0003c0005t0001 | 0/0 | 6837 | 4 | 0 | 0 | 4 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0004c0006t0014 | 0/0 | 6845 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6840): Show |
chr1 | 184685237 | 184759858 |
a0005c0007t0007 | 0/0 | 6837 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
a0006c0012t0006 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6833): Show |
chr1 | 184685237 | 184759858 |
a0007c0009t0024 | 0/0 | 6837 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | GCTCC others(6832): Show |
chr1 | 184685237 | 184759858 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0007g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0007g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0026g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0028g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0029g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0031g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0032g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0033g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0001t0039g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0009g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0009g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0010g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0011g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0017g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0017g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0018g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0019g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0027g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0030g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0034g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0035g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0003t0038g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0013g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0023g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0025g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0004t0036g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0008t0020g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0010t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0001c0013t0040g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0001 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0008g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0008g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0008g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0008g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0008g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0012g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0012g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0012g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0015g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0016g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0016g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0021g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0022g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0002t0037g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0002c0011t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0003c0005t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0003c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0003c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0004c0006t0014g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0004c0006t0014g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0004c0006t0014g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0005c0007t0007g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0006c0012t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
a0007c0009t0024g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0004 | t0004 | g0269 | EUR | GBR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00140 | hp2 | a0002 | c0002 | t0008 | g0235 | EUR | GBR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0251 | EUR | FIN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00323 | hp1 | a0002 | c0002 | t0022 | g0231 | EUR | FIN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00423 | hp2 | a0001 | c0003 | t0005 | g0032 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00544 | hp1 | a0001 | c0001 | t0007 | g0101 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00609 | hp2 | a0001 | c0001 | t0007 | g0131 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00621 | hp2 | a0004 | c0006 | t0014 | g0282 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00639 | hp1 | a0001 | c0004 | t0004 | g0266 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00642 | hp1 | a0001 | c0001 | t0039 | g0286 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00642 | hp2 | a0002 | c0002 | t0008 | g0212 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00673 | hp1 | a0001 | c0001 | t0026 | g0158 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00733 | hp1 | a0002 | c0002 | t0008 | g0233 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0193 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00738 | hp2 | a0001 | c0003 | t0003 | g0008 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG00741 | hp2 | a0001 | c0004 | t0004 | g0272 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01069 | hp1 | a0001 | c0004 | t0004 | g0276 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01069 | hp2 | a0001 | c0003 | t0003 | g0073 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01070 | hp1 | a0001 | c0003 | t0005 | g0036 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01071 | hp1 | a0001 | c0004 | t0004 | g0275 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01071 | hp2 | a0001 | c0003 | t0005 | g0037 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01081 | hp2 | a0001 | c0004 | t0004 | g0265 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01099 | hp2 | a0001 | c0003 | t0009 | g0086 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01106 | hp2 | a0001 | c0004 | t0004 | g0271 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01109 | hp2 | a0001 | c0003 | t0003 | g0044 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01168 | hp2 | a0001 | c0003 | t0003 | g0083 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01192 | hp2 | a0001 | c0003 | t0011 | g0047 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01243 | hp1 | a0001 | c0003 | t0003 | g0084 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01243 | hp2 | a0001 | c0003 | t0034 | g0117 | AMR | PUR | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01346 | hp2 | a0002 | c0002 | t0008 | g0248 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01361 | hp2 | a0002 | c0002 | t0012 | g0208 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0250 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0222 | AMR | CLM | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0190 | EUR | IBS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0236 | EUR | IBS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01884 | hp1 | a0001 | c0003 | t0003 | g0009 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01884 | hp2 | a0001 | c0003 | t0011 | g0045 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01891 | hp1 | a0001 | c0004 | t0004 | g0024 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01891 | hp2 | a0001 | c0003 | t0035 | g0279 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01975 | hp2 | a0001 | c0003 | t0003 | g0074 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01978 | hp2 | a0002 | c0002 | t0037 | g0247 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0220 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG01981 | hp2 | a0001 | c0003 | t0003 | g0008 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02040 | hp1 | a0001 | c0003 | t0005 | g0027 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02055 | hp2 | a0001 | c0003 | t0018 | g0026 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02056 | hp1 | a0001 | c0003 | t0003 | g0049 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02056 | hp2 | a0002 | c0002 | t0004 | g0245 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02074 | hp2 | a0002 | c0002 | t0004 | g0232 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02132 | hp1 | a0001 | c0003 | t0005 | g0029 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02135 | hp1 | a0001 | c0003 | t0003 | g0081 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | KHV | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02145 | hp1 | a0001 | c0003 | t0010 | g0259 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02155 | hp1 | a0002 | c0011 | t0002 | g0209 | EAS | CDX | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | CDX | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0194 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02257 | hp2 | a0001 | c0003 | t0003 | g0069 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02258 | hp1 | a0001 | c0003 | t0009 | g0002 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02258 | hp2 | a0001 | c0010 | t0006 | g0277 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02293 | hp2 | a0002 | c0002 | t0012 | g0199 | AMR | PEL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02451 | hp1 | a0006 | c0012 | t0006 | g0155 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02451 | hp2 | a0001 | c0003 | t0038 | g0056 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0246 | SAS | PJL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02615 | hp1 | a0001 | c0004 | t0023 | g0189 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02615 | hp2 | a0001 | c0003 | t0003 | g0055 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02622 | hp1 | a0001 | c0003 | t0003 | g0064 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02622 | hp2 | a0001 | c0003 | t0006 | g0150 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02630 | hp1 | a0001 | c0003 | t0030 | g0151 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02630 | hp2 | a0001 | c0003 | t0006 | g0120 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0080 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02647 | hp2 | a0001 | c0003 | t0003 | g0052 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02717 | hp1 | a0001 | c0003 | t0003 | g0007 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02717 | hp2 | a0001 | c0003 | t0011 | g0048 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02723 | hp1 | a0001 | c0003 | t0003 | g0070 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02809 | hp2 | a0001 | c0004 | t0004 | g0274 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02818 | hp1 | a0001 | c0003 | t0003 | g0076 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02895 | hp1 | a0001 | c0003 | t0003 | g0062 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02895 | hp2 | a0001 | c0003 | t0010 | g0257 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02896 | hp1 | a0001 | c0003 | t0006 | g0152 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02897 | hp1 | a0001 | c0003 | t0006 | g0153 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02897 | hp2 | a0001 | c0003 | t0010 | g0256 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02922 | hp1 | a0001 | c0003 | t0003 | g0061 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02922 | hp2 | a0001 | c0003 | t0003 | g0051 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02965 | hp2 | a0001 | c0003 | t0009 | g0002 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02970 | hp1 | a0001 | c0003 | t0003 | g0067 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02976 | hp1 | a0001 | c0003 | t0019 | g0088 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02976 | hp2 | a0001 | c0003 | t0017 | g0144 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03041 | hp1 | a0001 | c0003 | t0003 | g0054 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03041 | hp2 | a0001 | c0003 | t0011 | g0046 | AFR | GWD | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03098 | hp1 | a0001 | c0004 | t0036 | g0041 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03098 | hp2 | a0001 | c0004 | t0004 | g0267 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03139 | hp1 | a0001 | c0003 | t0009 | g0002 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03139 | hp2 | a0001 | c0013 | t0040 | g0287 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03195 | hp1 | a0001 | c0003 | t0009 | g0089 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03195 | hp2 | a0001 | c0004 | t0004 | g0262 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03209 | hp1 | a0001 | c0003 | t0010 | g0258 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03209 | hp2 | a0001 | c0003 | t0003 | g0065 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03225 | hp1 | a0001 | c0003 | t0003 | g0059 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03225 | hp2 | a0001 | c0003 | t0003 | g0058 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0241 | SAS | PJL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03453 | hp2 | a0001 | c0003 | t0006 | g0149 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03486 | hp1 | a0001 | c0003 | t0003 | g0068 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03516 | hp1 | a0001 | c0003 | t0003 | g0071 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03516 | hp2 | a0001 | c0004 | t0013 | g0040 | AFR | ESN | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0053 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03579 | hp2 | a0001 | c0003 | t0003 | g0007 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03654 | hp2 | a0002 | c0002 | t0008 | g0228 | SAS | PJL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0253 | SAS | STU | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0187 | SAS | PJL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0230 | SAS | PJL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0244 | SAS | BEB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0243 | SAS | STU | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG04115 | hp2 | a0001 | c0001 | t0033 | g0278 | SAS | STU | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0242 | SAS | STU | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18522 | hp1 | a0001 | c0003 | t0003 | g0063 | AFR | YRI | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18522 | hp2 | a0001 | c0008 | t0020 | g0066 | AFR | YRI | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18612 | hp1 | a0005 | c0007 | t0007 | g0012 | EAS | CHB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | CHB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18747 | hp1 | a0001 | c0003 | t0003 | g0075 | EAS | CHB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18906 | hp1 | a0001 | c0003 | t0003 | g0060 | AFR | YRI | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18906 | hp2 | a0001 | c0003 | t0009 | g0090 | AFR | YRI | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18940 | hp2 | a0003 | c0005 | t0001 | g0285 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18943 | hp1 | a0001 | c0003 | t0003 | g0082 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18950 | hp1 | a0001 | c0001 | t0007 | g0109 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18952 | hp1 | a0001 | c0001 | t0029 | g0108 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18954 | hp1 | a0001 | c0003 | t0005 | g0033 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18956 | hp2 | a0001 | c0003 | t0003 | g0077 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18957 | hp2 | a0002 | c0002 | t0021 | g0218 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18961 | hp2 | a0001 | c0004 | t0025 | g0273 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18963 | hp2 | a0001 | c0004 | t0004 | g0264 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18964 | hp2 | a0002 | c0002 | t0016 | g0229 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18966 | hp1 | a0001 | c0001 | t0032 | g0097 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18971 | hp1 | a0001 | c0003 | t0005 | g0031 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18971 | hp2 | a0002 | c0002 | t0015 | g0017 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18975 | hp1 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18983 | hp1 | a0004 | c0006 | t0014 | g0283 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18986 | hp2 | a0001 | c0001 | t0028 | g0146 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18995 | hp1 | a0003 | c0005 | t0001 | g0025 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19001 | hp2 | a0004 | c0006 | t0014 | g0281 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19005 | hp1 | a0001 | c0003 | t0005 | g0035 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19007 | hp1 | a0002 | c0002 | t0015 | g0017 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19009 | hp1 | a0001 | c0001 | t0031 | g0176 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19030 | hp1 | a0001 | c0004 | t0004 | g0024 | AFR | LWK | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19030 | hp2 | a0001 | c0003 | t0006 | g0154 | AFR | LWK | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19043 | hp1 | a0001 | c0003 | t0027 | g0087 | AFR | LWK | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19043 | hp2 | a0001 | c0004 | t0004 | g0261 | AFR | LWK | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19056 | hp2 | a0001 | c0003 | t0005 | g0028 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19063 | hp2 | a0001 | c0003 | t0005 | g0030 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19068 | hp1 | a0001 | c0004 | t0004 | g0270 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19072 | hp1 | a0001 | c0001 | t0007 | g0096 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19074 | hp1 | a0003 | c0005 | t0001 | g0025 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19074 | hp2 | a0002 | c0002 | t0016 | g0223 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19081 | hp2 | a0001 | c0003 | t0003 | g0078 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19082 | hp1 | a0002 | c0002 | t0004 | g0255 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19082 | hp2 | a0001 | c0003 | t0005 | g0034 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19085 | hp2 | a0005 | c0007 | t0007 | g0012 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19091 | hp2 | a0003 | c0005 | t0001 | g0284 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19240 | hp1 | a0001 | c0003 | t0017 | g0192 | AFR | YRI | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA19240 | hp2 | a0001 | c0003 | t0003 | g0079 | AFR | YRI | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ASW | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA20129 | hp2 | a0001 | c0003 | t0003 | g0009 | AFR | ASW | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA20752 | hp2 | a0002 | c0002 | t0012 | g0207 | EUR | TSI | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | GIH | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | GIH | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02109 | hp1 | a0001 | c0003 | t0003 | g0057 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02109 | hp2 | a0001 | c0004 | t0013 | g0042 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02559 | hp1 | a0001 | c0003 | t0003 | g0072 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG02559 | hp2 | a0001 | c0003 | t0006 | g0085 | AFR | ACB | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03471 | hp1 | a0001 | c0004 | t0013 | g0043 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG03471 | hp2 | a0001 | c0003 | t0003 | g0050 | AFR | MSL | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG06807 | hp1 | a0002 | c0002 | t0008 | g0195 | AFR | USA | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
HG06807 | hp2 | a0001 | c0004 | t0004 | g0260 | AFR | USA | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18955 | hp1 | a0001 | c0004 | t0004 | g0263 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0221 | AFR | USA | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | USA | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
NA21309 | hp2 | a0007 | c0009 | t0024 | g0268 | AFR | LWK | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0174 | REF | REF | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0123 | REF | REF | EDEM3_chr1_184685237_184759858 | EDEM3 | chr1 | 184685237 | 184759858 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:184694154 | C | A | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2708G>T | p.Trp903Leu | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2920/6837 | 2708/2799 | 903/932 | chr1 | 184694154 | |||
chr1:184694403 | A | C | 1 | a0002 | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
missense_variant | MODERATE | c.2459T>G | p.Ile820Ser | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2671/6837 | 2459/2799 | 820/932 | chr1 | 184694403 | |||
chr1:184721290 | G | A | 1 | a0006 | 1 | HG02451.hp1 | missense_variant&splice_region_variant | MODERATE | c.950C>T | p.Thr317Ile | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/20 | 1162/6837 | 950/2799 | 317/932 | chr1 | 184721290 | |||
chr1:184734595 | T | C | 1 | a0005 | 2 | NA18612.hp1 NA19085.hp2 |
missense_variant | MODERATE | c.394A>G | p.Arg132Gly | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/20 | 606/6837 | 394/2799 | 132/932 | chr1 | 184734595 | |||
chr1:184754587 | T | G | 1 | a0004 | 3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
missense_variant | MODERATE | c.60A>C | p.Arg20Ser | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/20 | 272/6837 | 60/2799 | 20/932 | chr1 | 184754587 | |||
chr1:184754636 | G | A | 1 | a0003 | 4 | NA18940.hp2 NA18995.hp1 NA19074.hp1 others(1): Show |
missense_variant | MODERATE | c.11C>T | p.Ala4Val | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/20 | 223/6837 | 11/2799 | 4/932 | chr1 | 184754636 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:184694447 | T | C | 4 | a0001c0004 a0002c0002 a0002c0011 others(1): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
synonymous_variant | LOW | c.2415A>G | p.Gln805Gln | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2627/6837 | 2415/2799 | 805/932 | chr1 | 184694447 | |||
chr1:184702824 | T | C | 1 | a0004c0006 | 3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
synonymous_variant | LOW | c.2376A>G | p.Lys792Lys | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/20 | 2588/6837 | 2376/2799 | 792/932 | chr1 | 184702824 | |||
chr1:184706680 | G | A | 2 | a0002c0002 a0002c0011 |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
synonymous_variant | LOW | c.2166C>T | p.Asn722Asn | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/20 | 2378/6837 | 2166/2799 | 722/932 | chr1 | 184706680 | |||
chr1:184708321 | T | C | 1 | a0001c0010 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.1869A>G | p.Glu623Glu | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/20 | 2081/6837 | 1869/2799 | 623/932 | chr1 | 184708321 | |||
chr1:184708330 | G | A | 10 | a0001c0003 a0001c0004 a0001c0008 others(7): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
synonymous_variant | LOW | c.1860C>T | p.Ile620Ile | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/20 | 2072/6837 | 1860/2799 | 620/932 | chr1 | 184708330 | |||
chr1:184710517 | G | A | 1 | a0002c0011 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.1722C>T | p.Pro574Pro | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/20 | 1934/6837 | 1722/2799 | 574/932 | chr1 | 184710517 | |||
chr1:184711839 | A | G | 1 | a0001c0008 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1575T>C | p.Asp525Asp | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 15/20 | 1787/6837 | 1575/2799 | 525/932 | chr1 | 184711839 | |||
chr1:184732885 | G | A | 1 | a0001c0013 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.564C>T | p.Tyr188Tyr | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/20 | 776/6837 | 564/2799 | 188/932 | chr1 | 184732885 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:184690264 | A | T | 1 | a0004c0006t0014 | 3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3799T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 3799 | chr1 | 184690264 | ||||||
chr1:184690350 | G | A | 1 | a0001c0004t0023 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3713C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 3713 | chr1 | 184690350 | ||||||
chr1:184690393 | C | T | 1 | a0002c0002t0016 | 2 | NA18964.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3670G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 3670 | chr1 | 184690393 | ||||||
chr1:184690411 | T | TA | 29 | a0001c0001t0033 a0001c0003t0003 a0001c0003t0005 others(26): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*3651dupT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 3651 | chr1 | 184690411 | ||||||
chr1:184690454 | A | C | 1 | a0001c0001t0031 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3609T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 3609 | chr1 | 184690454 | ||||||
chr1:184690466 | T | C | 4 | a0001c0001t0007 a0001c0001t0028 a0001c0001t0029 others(1): Show |
9 | HG00544.hp1 HG00609.hp2 NA18612.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3597A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 3597 | chr1 | 184690466 | ||||||
chr1:184690572 | G | T | 1 | a0001c0003t0034 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3491C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 3491 | chr1 | 184690572 | ||||||
chr1:184690801 | G | GT | 5 | a0001c0003t0006 a0001c0003t0011 a0001c0003t0034 others(2): Show |
14 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3261dupA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 3261 | chr1 | 184690801 | ||||||
chr1:184690976 | TA | T | 17 | a0001c0004t0004 a0001c0004t0013 a0001c0004t0023 others(14): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*3086delT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 3086 | chr1 | 184690976 | ||||||
chr1:184691071 | T | A | 28 | a0001c0001t0033 a0001c0003t0003 a0001c0003t0005 others(25): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*2992A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2992 | chr1 | 184691071 | ||||||
chr1:184691082 | A | G | 1 | a0001c0003t0030 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2981T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2981 | chr1 | 184691082 | ||||||
chr1:184691103 | G | A | 1 | a0001c0001t0032 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2960C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2960 | chr1 | 184691103 | ||||||
chr1:184691217 | T | C | 1 | a0001c0003t0011 | 4 | HG01192.hp2 HG01884.hp2 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2846A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2846 | chr1 | 184691217 | ||||||
chr1:184691315 | C | T | 1 | a0001c0001t0029 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2748G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2748 | chr1 | 184691315 | ||||||
chr1:184691419 | C | CCTTA | 1 | a0004c0006t0014 | 3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2643_*2644insTAAG | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2643 | chr1 | 184691419 | ||||||
chr1:184691545 | C | T | 1 | a0004c0006t0014 | 3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2518G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2518 | chr1 | 184691545 | ||||||
chr1:184691633 | A | C | 1 | a0001c0001t0028 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2430T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2430 | chr1 | 184691633 | ||||||
chr1:184691721 | T | C | 1 | a0002c0002t0022 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2342A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2342 | chr1 | 184691721 | ||||||
chr1:184691744 | C | T | 1 | a0002c0002t0015 | 2 | NA18971.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2319G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2319 | chr1 | 184691744 | ||||||
chr1:184691833 | T | A | 1 | a0001c0003t0018 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2230A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2230 | chr1 | 184691833 | ||||||
chr1:184691862 | A | G | 1 | a0001c0001t0033 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2201T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 2201 | chr1 | 184691862 | ||||||
chr1:184692247 | T | C | 1 | a0007c0009t0024 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1816A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1816 | chr1 | 184692247 | ||||||
chr1:184692462 | A | G | 1 | a0002c0002t0021 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1601T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1601 | chr1 | 184692462 | ||||||
chr1:184692508 | G | A | 34 | a0001c0001t0033 a0001c0003t0003 a0001c0003t0005 others(31): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*1555C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1555 | chr1 | 184692508 | ||||||
chr1:184692546 | C | G | 1 | a0004c0006t0014 | 3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1517G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1517 | chr1 | 184692546 | ||||||
chr1:184692639 | G | T | 2 | a0001c0003t0009 a0001c0003t0019 |
7 | HG01099.hp2 HG02258.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1424C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1424 | chr1 | 184692639 | ||||||
chr1:184692771 | T | TACA | 1 | a0004c0006t0014 | 3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1289_*1291dupTGT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1291 | chr1 | 184692771 | ||||||
chr1:184692787 | C | CG | 1 | a0004c0006t0014 | 3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1275_*1276insC | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1275 | chr1 | 184692787 | ||||||
chr1:184692797 | A | AG | 1 | a0002c0002t0012 | 3 | HG01361.hp2 HG02293.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1265_*1266insC | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1265 | chr1 | 184692797 | ||||||
chr1:184692798 | A | AG | 10 | a0001c0001t0026 a0001c0003t0027 a0002c0002t0002 others(7): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1264dupC | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1264 | chr1 | 184692798 | ||||||
chr1:184692798 | A | G | 1 | a0002c0002t0012 | 3 | HG01361.hp2 HG02293.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1265T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1265 | chr1 | 184692798 | ||||||
chr1:184692923 | C | A | 1 | a0001c0003t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1140G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1140 | chr1 | 184692923 | ||||||
chr1:184692929 | C | T | 1 | a0002c0002t0008 | 6 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1134G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1134 | chr1 | 184692929 | ||||||
chr1:184692999 | G | A | 1 | a0001c0004t0025 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1064C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1064 | chr1 | 184692999 | ||||||
chr1:184693047 | C | T | 18 | a0001c0004t0004 a0001c0004t0013 a0001c0004t0023 others(15): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1016G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 1016 | chr1 | 184693047 | ||||||
chr1:184693186 | G | A | 2 | a0001c0004t0013 a0001c0004t0036 |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*877C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 877 | chr1 | 184693186 | ||||||
chr1:184693300 | C | T | 1 | a0004c0006t0014 | 3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*763G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 763 | chr1 | 184693300 | ||||||
chr1:184693317 | C | A | 1 | a0002c0002t0037 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*746G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 746 | chr1 | 184693317 | ||||||
chr1:184693412 | G | A | 1 | a0001c0008t0020 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*651C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 651 | chr1 | 184693412 | ||||||
chr1:184693467 | GA | G | 1 | a0001c0003t0005 | 11 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*595delT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 595 | chr1 | 184693467 | ||||||
chr1:184693525 | A | G | 4 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0038 others(1): Show |
54 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*538T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 538 | chr1 | 184693525 | ||||||
chr1:184693707 | A | C | 1 | a0001c0003t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*356T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 356 | chr1 | 184693707 | ||||||
chr1:184693721 | T | G | 1 | a0001c0004t0013 | 3 | HG02109.hp2 HG03471.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*342A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 342 | chr1 | 184693721 | ||||||
chr1:184693766 | C | A | 1 | a0001c0003t0038 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*297G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 297 | chr1 | 184693766 | ||||||
chr1:184693918 | C | T | 1 | a0001c0003t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 145 | chr1 | 184693918 | ||||||
chr1:184693925 | T | G | 1 | a0004c0006t0014 | 3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*138A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 20/20 | 138 | chr1 | 184693925 | ||||||
chr1:184754660 | C | G | 1 | a0001c0003t0005 | 11 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/20 | 14 | chr1 | 184754660 | ||||||
chr1:184754778 | C | A | 1 | a0001c0001t0039 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-132G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/20 | 132 | chr1 | 184754778 | ||||||
chr1:184754791 | C | T | 2 | a0001c0003t0018 a0001c0013t0040 |
2 | HG02055.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-145G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/20 | 145 | chr1 | 184754791 | ||||||
chr1:184754840 | G | A | 1 | a0001c0013t0040 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-194C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/20 | 194 | chr1 | 184754840 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:184694509 | TA | T | 106 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(103): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.2390-38delT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184694509 | |||||||
chr1:184694764 | C | T | 116 | a0001c0003t0006g0085 a0001c0003t0006g0120 a0001c0003t0006g0149 others(113): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2390-292G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184694764 | |||||||
chr1:184694868 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-396A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184694868 | |||||||
chr1:184695009 | C | T | 1 | a0002c0002t0002g0236 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2390-537G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695009 | |||||||
chr1:184695173 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-701G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695173 | |||||||
chr1:184695320 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2390-848A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695320 | |||||||
chr1:184695360 | G | T | 1 | a0002c0002t0002g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2390-888C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695360 | |||||||
chr1:184695392 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-920C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695392 | |||||||
chr1:184695420 | G | A | 1 | a0002c0002t0002g0280 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2390-948C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695420 | |||||||
chr1:184695454 | T | C | 2 | a0002c0002t0008g0195 a0002c0002t0008g0248 |
2 | HG01346.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2390-982A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695454 | |||||||
chr1:184695466 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-994G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695466 | |||||||
chr1:184695507 | T | G | 7 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0111 others(4): Show |
8 | HG00597.hp2 HG00621.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2390-1035A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695507 | |||||||
chr1:184695519 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-1047A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695519 | |||||||
chr1:184695673 | C | T | 4 | a0001c0001t0007g0096 a0001c0001t0007g0143 a0001c0001t0028g0146 others(1): Show |
5 | NA18612.hp1 NA18975.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.2390-1201G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695673 | |||||||
chr1:184695878 | G | C | 7 | a0001c0003t0009g0002 a0001c0003t0009g0086 a0001c0003t0009g0089 others(4): Show |
9 | HG01099.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2390-1406C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695878 | |||||||
chr1:184695879 | G | A | 1 | a0001c0003t0027g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2390-1407C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184695879 | |||||||
chr1:184696111 | C | T | 1 | a0001c0008t0020g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2390-1639G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696111 | |||||||
chr1:184696194 | T | G | 6 | a0001c0003t0009g0002 a0001c0003t0009g0086 a0001c0003t0009g0089 others(3): Show |
8 | HG01099.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2390-1722A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696194 | |||||||
chr1:184696363 | AT | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0164 |
3 | NA18951.hp2 NA19001.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2390-1892delA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696363 | |||||||
chr1:184696400 | A | G | 2 | a0001c0004t0023g0189 a0001c0013t0040g0287 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2390-1928T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696400 | |||||||
chr1:184696412 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2390-1940G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696412 | |||||||
chr1:184696459 | C | A | 111 | a0001c0001t0033g0278 a0001c0003t0017g0144 a0001c0003t0017g0192 others(108): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2390-1987G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696459 | |||||||
chr1:184696459 | C | T | 5 | a0001c0001t0007g0096 a0001c0001t0007g0101 a0001c0001t0007g0143 others(2): Show |
6 | HG00544.hp1 NA18612.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2390-1987G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696459 | |||||||
chr1:184696494 | C | T | 2 | a0001c0001t0007g0109 a0001c0001t0007g0131 |
2 | HG00609.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.2390-2022G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696494 | |||||||
chr1:184696575 | T | G | 1 | a0001c0001t0039g0286 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2390-2103A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696575 | |||||||
chr1:184696582 | TC | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-2111delG | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696582 | |||||||
chr1:184696813 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0180 |
2 | NA18959.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2390-2341C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184696813 | |||||||
chr1:184697042 | A | G | 1 | a0002c0002t0002g0227 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2390-2570T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697042 | |||||||
chr1:184697080 | C | T | 5 | a0002c0002t0002g0186 a0002c0002t0002g0206 a0002c0002t0002g0226 others(2): Show |
5 | HG02056.hp2 HG02135.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.2390-2608G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697080 | |||||||
chr1:184697194 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-2722C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697194 | |||||||
chr1:184697250 | G | A | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2390-2778C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697250 | |||||||
chr1:184697337 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-2865A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697337 | |||||||
chr1:184697360 | A | T | 136 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(133): Show |
161 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.2390-2888T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697360 | |||||||
chr1:184697498 | G | C | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2390-3026C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697498 | |||||||
chr1:184697532 | G | A | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2390-3060C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697532 | |||||||
chr1:184697574 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2390-3102A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697574 | |||||||
chr1:184697644 | A | G | 1 | a0002c0002t0002g0023 | 2 | HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2390-3172T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697644 | |||||||
chr1:184697687 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-3215T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697687 | |||||||
chr1:184697886 | T | TTG | 12 | a0001c0003t0005g0027 a0001c0003t0005g0028 a0001c0003t0005g0029 others(9): Show |
12 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2390-3416_2390-341 others(6): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697886 | |||||||
chr1:184697998 | CACAA | C | 15 | a0001c0003t0003g0008 a0001c0003t0003g0009 a0001c0003t0003g0049 others(12): Show |
17 | HG00738.hp2 HG01168.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2390-3530_2390-352 others(8): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184697998 | |||||||
chr1:184698136 | T | C | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2390-3664A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698136 | |||||||
chr1:184698204 | G | A | 8 | a0001c0003t0006g0085 a0001c0003t0006g0120 a0001c0003t0006g0149 others(5): Show |
8 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2390-3732C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698204 | |||||||
chr1:184698237 | C | A | 160 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(157): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2390-3765G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698237 | |||||||
chr1:184698255 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-3783G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698255 | |||||||
chr1:184698272 | T | C | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2390-3800A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698272 | |||||||
chr1:184698345 | T | C | 51 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(48): Show |
54 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.2390-3873A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698345 | |||||||
chr1:184698417 | A | G | 51 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(48): Show |
54 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.2390-3945T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698417 | |||||||
chr1:184698420 | G | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2390-3948C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698420 | |||||||
chr1:184698474 | A | G | 187 | a0001c0001t0033g0278 a0001c0003t0003g0007 a0001c0003t0003g0008 others(184): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.2390-4002T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698474 | |||||||
chr1:184698597 | T | C | 20 | a0001c0003t0017g0144 a0001c0003t0017g0192 a0001c0004t0004g0024 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.2390-4125A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698597 | |||||||
chr1:184698666 | T | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+4145A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698666 | |||||||
chr1:184698762 | T | A | 51 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(48): Show |
54 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.2389+4049A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698762 | |||||||
chr1:184698790 | CAG | C | 4 | a0001c0001t0001g0124 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG00733.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2389+4019_2389+402 others(6): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698790 | |||||||
chr1:184698960 | A | G | 1 | a0001c0003t0006g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2389+3851T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698960 | |||||||
chr1:184698974 | T | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+3837A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184698974 | |||||||
chr1:184699018 | G | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+3793C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699018 | |||||||
chr1:184699088 | T | C | 1 | a0001c0003t0018g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2389+3723A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699088 | |||||||
chr1:184699124 | A | G | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2389+3687T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699124 | |||||||
chr1:184699125 | T | C | 51 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(48): Show |
54 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.2389+3686A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699125 | |||||||
chr1:184699179 | CCATT | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+3628_2389+363 others(8): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699179 | |||||||
chr1:184699317 | C | A | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2389+3494G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699317 | |||||||
chr1:184699388 | A | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+3423T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699388 | |||||||
chr1:184699397 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+3414A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699397 | |||||||
chr1:184699401 | G | A | 7 | a0001c0003t0009g0002 a0001c0003t0009g0086 a0001c0003t0009g0089 others(4): Show |
9 | HG01099.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2389+3410C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699401 | |||||||
chr1:184699445 | A | C | 2 | a0001c0003t0003g0062 a0001c0003t0003g0073 |
2 | HG01069.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2389+3366T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699445 | |||||||
chr1:184699494 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0166 a0001c0001t0001g0167 others(4): Show |
7 | HG01928.hp2 HG02273.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.2389+3317C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699494 | |||||||
chr1:184699640 | G | A | 1 | a0002c0002t0002g0239 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2389+3171C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699640 | |||||||
chr1:184699689 | T | G | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2389+3122A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699689 | |||||||
chr1:184699766 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+3045A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699766 | |||||||
chr1:184699837 | A | C | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2389+2974T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699837 | |||||||
chr1:184699852 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+2959T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699852 | |||||||
chr1:184699872 | G | A | 2 | a0001c0003t0003g0083 a0001c0003t0003g0084 |
2 | HG01168.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.2389+2939C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699872 | |||||||
chr1:184699972 | C | G | 24 | a0001c0003t0017g0144 a0001c0003t0017g0192 a0001c0004t0004g0024 others(21): Show |
25 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2389+2839G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699972 | |||||||
chr1:184699984 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2389+2827A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184699984 | |||||||
chr1:184700206 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+2605T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700206 | |||||||
chr1:184700337 | C | T | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2389+2474G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700337 | |||||||
chr1:184700494 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0094 |
3 | HG02165.hp1 NA18964.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2389+2317C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700494 | |||||||
chr1:184700563 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2389+2248C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700563 | |||||||
chr1:184700573 | T | C | 2 | a0001c0003t0003g0007 a0001c0003t0003g0055 |
3 | HG02615.hp2 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2389+2238A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700573 | |||||||
chr1:184700669 | A | T | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2389+2142T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700669 | |||||||
chr1:184700693 | G | A | 3 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 |
3 | HG02109.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2389+2118C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700693 | |||||||
chr1:184700787 | T | C | 1 | a0002c0002t0002g0230 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2389+2024A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700787 | |||||||
chr1:184700809 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+2002G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700809 | |||||||
chr1:184700920 | A | C | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.2389+1891T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700920 | |||||||
chr1:184700998 | T | G | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2389+1813A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184700998 | |||||||
chr1:184701033 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+1778C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184701033 | |||||||
chr1:184701710 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+1101C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184701710 | |||||||
chr1:184701895 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0145 |
3 | HG02055.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2389+916G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184701895 | |||||||
chr1:184702211 | C | G | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2389+600G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184702211 | |||||||
chr1:184702259 | T | G | 1 | a0001c0001t0001g0157 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2389+552A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184702259 | |||||||
chr1:184702287 | T | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2389+524A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184702287 | |||||||
chr1:184702447 | C | A | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2389+364G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184702447 | |||||||
chr1:184702455 | A | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2389+356T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184702455 | |||||||
chr1:184702775 | C | A | 24 | a0001c0003t0017g0144 a0001c0003t0017g0192 a0001c0004t0004g0024 others(21): Show |
25 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2389+36G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 19/19 | chr1 | 184702775 | |||||||
chr1:184703009 | T | C | 1 | a0002c0002t0002g0204 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2204-13A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184703009 | |||||||
chr1:184703045 | A | G | 51 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(48): Show |
54 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.2204-49T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184703045 | |||||||
chr1:184703081 | T | C | 1 | a0001c0003t0005g0030 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2204-85A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184703081 | |||||||
chr1:184703139 | T | C | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2204-143A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184703139 | |||||||
chr1:184703181 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2204-185A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184703181 | |||||||
chr1:184703184 | C | T | 8 | a0001c0003t0006g0085 a0001c0003t0006g0120 a0001c0003t0006g0149 others(5): Show |
8 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2204-188G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184703184 | |||||||
chr1:184703628 | T | G | 1 | a0002c0002t0002g0224 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2204-632A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184703628 | |||||||
chr1:184703629 | TTTACTGA others(14): Show |
T | 1 | a0002c0002t0002g0224 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2204-654_2204-634d others(23): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184703629 | |||||||
chr1:184703640 | C | T | 8 | a0002c0002t0002g0001 a0002c0002t0002g0018 a0002c0002t0002g0215 others(5): Show |
8 | HG00323.hp1 NA18612.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.2204-644G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184703640 | |||||||
chr1:184704058 | T | C | 2 | a0001c0003t0003g0083 a0001c0003t0003g0084 |
2 | HG01168.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.2204-1062A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704058 | |||||||
chr1:184704183 | G | A | 16 | a0001c0003t0017g0144 a0001c0003t0017g0192 a0001c0004t0004g0024 others(13): Show |
17 | HG00140.hp1 HG00741.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.2204-1187C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704183 | |||||||
chr1:184704190 | T | A | 1 | a0001c0001t0007g0109 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2204-1194A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704190 | |||||||
chr1:184704472 | G | A | 2 | a0001c0004t0004g0269 a0001c0004t0004g0272 |
2 | HG00140.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.2204-1476C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704472 | |||||||
chr1:184704597 | C | G | 20 | a0001c0003t0017g0144 a0001c0003t0017g0192 a0001c0004t0004g0024 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.2204-1601G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704597 | |||||||
chr1:184704649 | C | CA | 31 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0100 others(28): Show |
32 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.2204-1654dupT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | C | CAA | 76 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0145 others(73): Show |
96 | HG00140.hp2 HG00438.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.2204-1655_2204-165 others(6): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | C | CAAA | 39 | a0001c0001t0007g0096 a0001c0003t0003g0007 a0001c0003t0003g0051 others(36): Show |
43 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.2204-1656_2204-165 others(7): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | C | CAAAA | 14 | a0001c0003t0003g0009 a0001c0003t0003g0050 a0001c0003t0003g0052 others(11): Show |
15 | HG00280.hp2 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.2204-1657_2204-165 others(8): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | C | CAAAAA | 6 | a0001c0003t0003g0044 a0001c0003t0003g0076 a0001c0003t0003g0080 others(3): Show |
6 | HG01109.hp2 HG02132.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2204-1658_2204-165 others(9): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | C | CAAAAAAA | 7 | a0001c0003t0017g0192 a0001c0004t0004g0262 a0001c0004t0004g0263 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.2204-1660_2204-165 others(11): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | C | CAAAAAAA others(1): Show |
7 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0264 others(4): Show |
8 | HG00639.hp1 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.2204-1661_2204-165 others(12): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | C | CAAAAAAA others(7): Show |
1 | a0007c0009t0024g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2204-1667_2204-165 others(18): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | CA | C | 11 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0136 others(8): Show |
13 | HG00733.hp2 HG01099.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2204-1654delT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | CAAAAAAA others(1): Show |
C | 15 | a0001c0001t0001g0107 a0001c0003t0006g0085 a0001c0003t0006g0120 others(12): Show |
15 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2204-1661_2204-165 others(12): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | CAAAAAAA others(4): Show |
C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2204-1664_2204-165 others(15): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704649 | CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0003g0081 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2204-1665_2204-165 others(16): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704649 | |||||||
chr1:184704751 | T | A | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2204-1755A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704751 | |||||||
chr1:184704763 | A | G | 2 | a0002c0002t0002g0186 a0002c0002t0004g0245 |
2 | HG02056.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.2204-1767T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704763 | |||||||
chr1:184704769 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2204-1773A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704769 | |||||||
chr1:184704833 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2203+1810T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704833 | |||||||
chr1:184704844 | G | A | 1 | a0001c0003t0019g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2203+1799C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704844 | |||||||
chr1:184704852 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2203+1791C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704852 | |||||||
chr1:184704908 | AT | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2203+1734delA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704908 | |||||||
chr1:184704909 | T | A | 14 | a0001c0001t0007g0096 a0001c0001t0007g0101 a0001c0001t0007g0109 others(11): Show |
17 | HG00544.hp1 HG00609.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.2203+1734A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184704909 | |||||||
chr1:184705110 | T | C | 1 | a0001c0003t0003g0082 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2203+1533A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705110 | |||||||
chr1:184705116 | A | ATCATGAG others(3): Show |
1 | a0001c0001t0001g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2203+1517_2203+152 others(14): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705116 | |||||||
chr1:184705225 | T | A | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2203+1418A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705225 | |||||||
chr1:184705275 | A | C | 160 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(157): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2203+1368T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705275 | |||||||
chr1:184705452 | T | G | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2203+1191A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705452 | |||||||
chr1:184705497 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2203+1146A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705497 | |||||||
chr1:184705611 | T | C | 1 | a0002c0002t0002g0239 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2203+1032A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705611 | |||||||
chr1:184705692 | C | T | 49 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(46): Show |
52 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.2203+951G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705692 | |||||||
chr1:184705783 | A | C | 1 | a0002c0002t0002g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2203+860T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705783 | |||||||
chr1:184705855 | C | A | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2203+788G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705855 | |||||||
chr1:184705871 | T | G | 51 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(48): Show |
54 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.2203+772A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705871 | |||||||
chr1:184705923 | T | C | 1 | a0006c0012t0006g0155 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2203+720A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705923 | |||||||
chr1:184705940 | A | G | 14 | a0001c0003t0006g0085 a0001c0003t0006g0120 a0001c0003t0006g0149 others(11): Show |
14 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2203+703T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705940 | |||||||
chr1:184705955 | A | C | 1 | a0002c0002t0002g0280 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2203+688T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184705955 | |||||||
chr1:184706139 | TA | T | 52 | a0001c0001t0001g0105 a0001c0003t0003g0007 a0001c0003t0003g0008 others(49): Show |
55 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.2203+503delT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184706139 | |||||||
chr1:184706151 | A | C | 169 | a0001c0001t0033g0278 a0001c0003t0003g0007 a0001c0003t0003g0008 others(166): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2203+492T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184706151 | |||||||
chr1:184706274 | T | C | 1 | a0001c0003t0018g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2203+369A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184706274 | |||||||
chr1:184706366 | T | A | 9 | a0001c0003t0003g0057 a0001c0003t0003g0058 a0001c0003t0003g0063 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2203+277A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184706366 | |||||||
chr1:184706385 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2203+258A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184706385 | |||||||
chr1:184706496 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2203+147T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 18/19 | chr1 | 184706496 | |||||||
chr1:184706871 | C | T | 2 | a0002c0002t0002g0186 a0002c0002t0004g0245 |
2 | HG02056.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.2038-63G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184706871 | |||||||
chr1:184706892 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2038-84T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184706892 | |||||||
chr1:184707125 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2038-317G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707125 | |||||||
chr1:184707150 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2038-342C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707150 | |||||||
chr1:184707362 | G | A | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2038-554C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707362 | |||||||
chr1:184707525 | T | C | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2037+628A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707525 | |||||||
chr1:184707583 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2037+570A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707583 | |||||||
chr1:184707619 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2037+534T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707619 | |||||||
chr1:184707676 | G | A | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2037+477C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707676 | |||||||
chr1:184707683 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0094 |
3 | HG02165.hp1 NA18964.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2037+470G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707683 | |||||||
chr1:184707688 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0127 |
2 | HG01361.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2037+465A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707688 | |||||||
chr1:184707702 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2037+451C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707702 | |||||||
chr1:184707871 | A | C | 2 | a0004c0006t0014g0281 a0004c0006t0014g0282 |
2 | HG00621.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2037+282T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 17/19 | chr1 | 184707871 | |||||||
chr1:184708362 | T | C | 10 | a0001c0003t0003g0044 a0001c0003t0003g0050 a0001c0003t0003g0051 others(7): Show |
10 | HG01109.hp2 HG01192.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1846-18A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184708362 | |||||||
chr1:184708405 | T | A | 11 | a0001c0003t0005g0027 a0001c0003t0005g0028 a0001c0003t0005g0029 others(8): Show |
11 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1846-61A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184708405 | |||||||
chr1:184708407 | T | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1846-63A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184708407 | |||||||
chr1:184708541 | C | T | 4 | a0001c0004t0023g0189 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG02615.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1846-197G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184708541 | |||||||
chr1:184708542 | G | GT | 9 | a0001c0003t0005g0027 a0001c0003t0005g0028 a0001c0003t0005g0029 others(6): Show |
9 | HG00423.hp2 HG02040.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1846-199dupA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184708542 | |||||||
chr1:184708769 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1846-425T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184708769 | |||||||
chr1:184708904 | T | C | 3 | a0002c0002t0008g0195 a0002c0002t0008g0235 a0002c0002t0008g0248 |
3 | HG00140.hp2 HG01346.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1846-560A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184708904 | |||||||
chr1:184708962 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1846-618C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184708962 | |||||||
chr1:184709138 | G | A | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1846-794C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184709138 | |||||||
chr1:184709156 | G | A | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1846-812C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184709156 | |||||||
chr1:184709237 | A | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1846-893T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184709237 | |||||||
chr1:184709359 | G | A | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1846-1015C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184709359 | |||||||
chr1:184709393 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1845+1001A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184709393 | |||||||
chr1:184709459 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1845+935A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184709459 | |||||||
chr1:184709777 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1845+617A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184709777 | |||||||
chr1:184709885 | A | G | 187 | a0001c0001t0033g0278 a0001c0003t0003g0007 a0001c0003t0003g0008 others(184): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1845+509T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184709885 | |||||||
chr1:184709890 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1845+504A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184709890 | |||||||
chr1:184709959 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1845+435G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184709959 | |||||||
chr1:184710068 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1845+326A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184710068 | |||||||
chr1:184710100 | G | A | 20 | a0001c0003t0017g0144 a0001c0003t0017g0192 a0001c0004t0004g0024 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1845+294C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184710100 | |||||||
chr1:184710120 | GAA | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1845+272_1845+273d others(4): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184710120 | |||||||
chr1:184710149 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1845+245T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184710149 | |||||||
chr1:184710287 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1845+107C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 16/19 | chr1 | 184710287 | |||||||
chr1:184710677 | A | G | 1 | a0001c0003t0011g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1692-130T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 15/19 | chr1 | 184710677 | |||||||
chr1:184711132 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1692-585G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 15/19 | chr1 | 184711132 | |||||||
chr1:184711160 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1691+563C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 15/19 | chr1 | 184711160 | |||||||
chr1:184711198 | A | C | 5 | a0001c0004t0004g0263 a0001c0004t0004g0264 a0001c0004t0004g0270 others(2): Show |
5 | HG01106.hp2 NA18955.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.1691+525T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 15/19 | chr1 | 184711198 | |||||||
chr1:184711440 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1691+283A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 15/19 | chr1 | 184711440 | |||||||
chr1:184711480 | C | T | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1691+243G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 15/19 | chr1 | 184711480 | |||||||
chr1:184711508 | A | C | 1 | a0001c0003t0034g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1691+215T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 15/19 | chr1 | 184711508 | |||||||
chr1:184711532 | A | T | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1691+191T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 15/19 | chr1 | 184711532 | |||||||
chr1:184711636 | T | C | 6 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(3): Show |
7 | HG01891.hp1 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1691+87A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 15/19 | chr1 | 184711636 | |||||||
chr1:184711947 | A | G | 189 | a0001c0001t0033g0278 a0001c0003t0001g0140 a0001c0003t0003g0007 others(186): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1537-70T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 14/19 | chr1 | 184711947 | |||||||
chr1:184711979 | T | G | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1537-102A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 14/19 | chr1 | 184711979 | |||||||
chr1:184712014 | T | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0125 others(1): Show |
4 | HG01099.hp1 HG01496.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537-137A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 14/19 | chr1 | 184712014 | |||||||
chr1:184712264 | T | C | 1 | a0001c0004t0004g0269 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1536+169A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 14/19 | chr1 | 184712264 | |||||||
chr1:184712401 | A | C | 1 | a0004c0006t0014g0282 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1536+32T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 14/19 | chr1 | 184712401 | |||||||
chr1:184712668 | T | C | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1371-70A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184712668 | |||||||
chr1:184712789 | A | C | 1 | a0002c0002t0002g0187 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1371-191T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184712789 | |||||||
chr1:184712899 | A | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1371-301T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184712899 | |||||||
chr1:184712997 | G | A | 1 | a0001c0003t0034g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1371-399C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184712997 | |||||||
chr1:184713245 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1371-647A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184713245 | |||||||
chr1:184713461 | T | C | 1 | a0001c0003t0027g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1371-863A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184713461 | |||||||
chr1:184713496 | T | C | 4 | a0001c0003t0003g0075 a0001c0003t0003g0077 a0001c0003t0003g0078 others(1): Show |
4 | NA18747.hp1 NA18943.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1371-898A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184713496 | |||||||
chr1:184713578 | GT | G | 5 | a0001c0003t0003g0007 a0001c0003t0003g0055 a0001c0003t0003g0070 others(2): Show |
6 | HG02559.hp1 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1371-981delA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184713578 | |||||||
chr1:184713811 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1371-1213A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184713811 | |||||||
chr1:184713941 | A | G | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1371-1343T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184713941 | |||||||
chr1:184714377 | G | A | 1 | a0001c0001t0007g0101 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1371-1779C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184714377 | |||||||
chr1:184714416 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1371-1818T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184714416 | |||||||
chr1:184714800 | TA | T | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370+2087delT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184714800 | |||||||
chr1:184715109 | C | G | 14 | a0001c0001t0001g0015 a0001c0001t0001g0121 a0001c0001t0001g0132 others(11): Show |
15 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1370+1779G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184715109 | |||||||
chr1:184715140 | T | TC | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370+1747_1370+174 others(5): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184715140 | |||||||
chr1:184715141 | G | A | 1 | a0002c0002t0021g0218 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1370+1747C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184715141 | |||||||
chr1:184715205 | T | C | 1 | a0001c0003t0003g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1370+1683A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184715205 | |||||||
chr1:184715282 | A | G | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1370+1606T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184715282 | |||||||
chr1:184715596 | A | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1370+1292T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184715596 | |||||||
chr1:184715949 | G | C | 8 | a0001c0003t0006g0085 a0001c0003t0006g0120 a0001c0003t0006g0149 others(5): Show |
8 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1370+939C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184715949 | |||||||
chr1:184716063 | G | A | 185 | a0001c0001t0033g0278 a0001c0003t0003g0007 a0001c0003t0003g0008 others(182): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1370+825C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184716063 | |||||||
chr1:184716223 | G | C | 2 | a0001c0003t0003g0060 a0001c0003t0003g0061 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1370+665C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184716223 | |||||||
chr1:184716672 | G | A | 1 | a0002c0002t0002g0238 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1370+216C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184716672 | |||||||
chr1:184716809 | T | C | 14 | a0001c0003t0003g0007 a0001c0003t0003g0055 a0001c0003t0003g0057 others(11): Show |
15 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1370+79A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 13/19 | chr1 | 184716809 | |||||||
chr1:184717699 | T | C | 1 | a0002c0002t0002g0217 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1162-76A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184717699 | |||||||
chr1:184717984 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1162-361A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184717984 | |||||||
chr1:184718117 | T | C | 2 | a0002c0002t0002g0019 a0002c0002t0002g0236 |
3 | HG00741.hp1 HG01109.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1162-494A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718117 | |||||||
chr1:184718228 | A | T | 7 | a0001c0003t0009g0002 a0001c0003t0009g0086 a0001c0003t0009g0089 others(4): Show |
9 | HG01099.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1162-605T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718228 | |||||||
chr1:184718311 | A | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1162-688T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718311 | |||||||
chr1:184718338 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1162-715A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718338 | |||||||
chr1:184718387 | C | T | 1 | a0001c0004t0004g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1162-764G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718387 | |||||||
chr1:184718442 | C | T | 107 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(104): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1161+720G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718442 | |||||||
chr1:184718575 | T | G | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1161+587A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718575 | |||||||
chr1:184718581 | C | T | 187 | a0001c0001t0033g0278 a0001c0003t0001g0140 a0001c0003t0003g0007 others(184): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1161+581G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718581 | |||||||
chr1:184718680 | G | A | 2 | a0001c0003t0010g0256 a0001c0003t0010g0257 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1161+482C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718680 | |||||||
chr1:184718757 | A | G | 1 | a0001c0001t0028g0146 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1161+405T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718757 | |||||||
chr1:184718945 | A | G | 1 | a0002c0002t0016g0223 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1161+217T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184718945 | |||||||
chr1:184719103 | C | T | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1161+59G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 11/19 | chr1 | 184719103 | |||||||
chr1:184719327 | T | C | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-82A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 10/19 | chr1 | 184719327 | |||||||
chr1:184719379 | C | G | 8 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0205 others(5): Show |
12 | HG01106.hp1 HG01257.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1077+64G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 10/19 | chr1 | 184719379 | |||||||
chr1:184719802 | T | C | 11 | a0001c0003t0005g0027 a0001c0003t0005g0028 a0001c0003t0005g0029 others(8): Show |
11 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.952-234A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184719802 | |||||||
chr1:184719975 | G | A | 1 | a0007c0009t0024g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.952-407C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184719975 | |||||||
chr1:184720029 | C | T | 1 | a0002c0002t0002g0220 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.952-461G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720029 | |||||||
chr1:184720269 | AT | A | 20 | a0001c0003t0003g0007 a0001c0003t0003g0055 a0001c0003t0003g0057 others(17): Show |
21 | HG00621.hp2 HG01069.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.952-702delA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720269 | |||||||
chr1:184720503 | CCCATACT others(111): Show |
C | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.951+668_951+785del | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720503 | |||||||
chr1:184720508 | A | C | 1 | a0001c0004t0004g0271 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.951+781T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720508 | |||||||
chr1:184720509 | C | CTTTTTTT others(6): Show |
13 | a0001c0004t0004g0260 a0001c0004t0004g0261 a0001c0004t0004g0262 others(10): Show |
13 | HG00140.hp1 HG00639.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.951+767_951+779dup others(13): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720509 | |||||||
chr1:184720509 | C | CTTTTTTT others(7): Show |
4 | a0001c0004t0004g0024 a0001c0004t0004g0272 a0001c0004t0004g0275 others(1): Show |
5 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+766_951+779dup others(14): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720509 | |||||||
chr1:184720509 | C | CTTTTTTT others(12): Show |
1 | a0001c0004t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.951+779_951+780ins others(19): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720509 | |||||||
chr1:184720509 | C | CTTTTTTT others(13): Show |
3 | a0001c0001t0033g0278 a0001c0003t0018g0026 a0001c0003t0035g0279 |
3 | HG01891.hp2 HG02055.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.951+779_951+780ins others(20): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720509 | |||||||
chr1:184720509 | C | CTTTTTTT others(14): Show |
2 | a0001c0003t0009g0089 a0001c0003t0019g0088 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.951+779_951+780ins others(21): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720509 | |||||||
chr1:184720509 | C | CTTTTTTT others(15): Show |
1 | a0001c0003t0009g0002 | 3 | HG02258.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.951+779_951+780ins others(22): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720509 | |||||||
chr1:184720509 | C | CTTTTTTT others(16): Show |
2 | a0001c0003t0009g0086 a0001c0003t0009g0090 |
2 | HG01099.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.951+779_951+780ins others(23): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720509 | |||||||
chr1:184720509 | CT | C | 76 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(73): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.951+779delA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720509 | |||||||
chr1:184720606 | T | C | 17 | a0001c0003t0003g0007 a0001c0003t0003g0055 a0001c0003t0003g0057 others(14): Show |
18 | HG01069.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.951+683A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720606 | |||||||
chr1:184720689 | G | A | 22 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(19): Show |
23 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.951+600C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720689 | |||||||
chr1:184720836 | A | G | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.951+453T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720836 | |||||||
chr1:184720844 | T | G | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.951+445A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720844 | |||||||
chr1:184720898 | T | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.951+391A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184720898 | |||||||
chr1:184721209 | G | A | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.951+80C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 9/19 | chr1 | 184721209 | |||||||
chr1:184721439 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.854-53A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184721439 | |||||||
chr1:184721568 | T | G | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.854-182A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184721568 | |||||||
chr1:184721632 | G | A | 10 | a0001c0003t0003g0008 a0001c0003t0003g0049 a0001c0003t0003g0074 others(7): Show |
11 | HG00738.hp2 HG01168.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.854-246C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184721632 | |||||||
chr1:184721752 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.854-366A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184721752 | |||||||
chr1:184721870 | G | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.854-484C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184721870 | |||||||
chr1:184721873 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.854-487A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184721873 | |||||||
chr1:184721879 | C | T | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.854-493G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184721879 | |||||||
chr1:184721985 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.854-599C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184721985 | |||||||
chr1:184721994 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.854-608G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184721994 | |||||||
chr1:184722200 | T | C | 49 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(46): Show |
52 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.854-814A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184722200 | |||||||
chr1:184722370 | T | C | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.854-984A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184722370 | |||||||
chr1:184722490 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.854-1104T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184722490 | |||||||
chr1:184722637 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.853+1114G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184722637 | |||||||
chr1:184722672 | T | C | 1 | a0001c0003t0027g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.853+1079A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184722672 | |||||||
chr1:184722723 | TTTTA | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.853+1024_853+1027d others(6): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184722723 | |||||||
chr1:184722779 | C | T | 2 | a0001c0003t0018g0026 a0001c0003t0027g0087 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.853+972G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184722779 | |||||||
chr1:184722849 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.853+902A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184722849 | |||||||
chr1:184722987 | T | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.853+764A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184722987 | |||||||
chr1:184723003 | T | C | 1 | a0001c0004t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.853+748A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184723003 | |||||||
chr1:184723251 | C | T | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.853+500G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184723251 | |||||||
chr1:184723413 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.853+338C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184723413 | |||||||
chr1:184723444 | A | G | 1 | a0002c0002t0002g0249 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.853+307T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184723444 | |||||||
chr1:184723492 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.853+259T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 8/19 | chr1 | 184723492 | |||||||
chr1:184723865 | T | A | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.748-9A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184723865 | |||||||
chr1:184723865 | T | TA | 229 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(226): Show |
263 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.748-10dupT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184723865 | |||||||
chr1:184723865 | T | TAA | 29 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0139 others(26): Show |
32 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.748-11_748-10dupTT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184723865 | |||||||
chr1:184724021 | C | T | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.748-165G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724021 | |||||||
chr1:184724043 | C | A | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.748-187G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724043 | |||||||
chr1:184724044 | A | C | 1 | a0001c0001t0033g0278 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.748-188T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724044 | |||||||
chr1:184724072 | T | C | 1 | a0001c0003t0034g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.748-216A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724072 | |||||||
chr1:184724153 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.748-297A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724153 | |||||||
chr1:184724202 | C | G | 3 | a0001c0004t0004g0260 a0001c0004t0004g0274 a0007c0009t0024g0268 |
3 | HG02809.hp2 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.748-346G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724202 | |||||||
chr1:184724441 | G | T | 22 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(19): Show |
23 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.748-585C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724441 | |||||||
chr1:184724513 | G | A | 15 | a0001c0003t0003g0008 a0001c0003t0003g0009 a0001c0003t0003g0049 others(12): Show |
17 | HG00738.hp2 HG01168.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.748-657C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724513 | |||||||
chr1:184724634 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.748-778G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724634 | |||||||
chr1:184724727 | T | G | 2 | a0001c0003t0003g0077 a0001c0003t0003g0078 |
2 | NA18956.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.748-871A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724727 | |||||||
chr1:184724785 | T | C | 1 | a0003c0005t0001g0284 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.748-929A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724785 | |||||||
chr1:184724792 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.748-936G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724792 | |||||||
chr1:184724831 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.748-975T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724831 | |||||||
chr1:184724932 | A | G | 14 | a0001c0003t0003g0007 a0001c0003t0003g0055 a0001c0003t0003g0057 others(11): Show |
15 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.748-1076T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724932 | |||||||
chr1:184724933 | G | A | 2 | a0001c0003t0001g0140 a0001c0003t0030g0151 |
2 | HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.748-1077C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184724933 | |||||||
chr1:184725023 | C | T | 27 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0092 others(24): Show |
29 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.748-1167G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725023 | |||||||
chr1:184725058 | T | C | 1 | a0001c0003t0030g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.747+1197A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725058 | |||||||
chr1:184725100 | G | A | 4 | a0001c0003t0010g0256 a0001c0003t0010g0257 a0001c0003t0010g0258 others(1): Show |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+1155C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725100 | |||||||
chr1:184725120 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.747+1135T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725120 | |||||||
chr1:184725154 | C | T | 1 | a0001c0003t0009g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.747+1101G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725154 | |||||||
chr1:184725290 | G | GCAT | 6 | a0001c0003t0003g0044 a0001c0003t0003g0050 a0001c0003t0003g0051 others(3): Show |
6 | HG01109.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.747+962_747+964dup others(3): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725290 | |||||||
chr1:184725317 | T | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.747+938A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725317 | |||||||
chr1:184725449 | C | A | 185 | a0001c0001t0033g0278 a0001c0003t0003g0007 a0001c0003t0003g0008 others(182): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.747+806G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725449 | |||||||
chr1:184725532 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.747+723A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725532 | |||||||
chr1:184725549 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.747+706T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725549 | |||||||
chr1:184725552 | T | G | 1 | a0003c0005t0001g0285 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.747+703A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725552 | |||||||
chr1:184725696 | A | C | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.747+559T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725696 | |||||||
chr1:184725749 | C | T | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+506G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725749 | |||||||
chr1:184725868 | TAGA | T | 4 | a0001c0003t0010g0256 a0001c0003t0010g0257 a0001c0003t0010g0258 others(1): Show |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+384_747+386del others(3): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184725868 | |||||||
chr1:184726024 | C | T | 1 | a0004c0006t0014g0281 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.747+231G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184726024 | |||||||
chr1:184726093 | C | G | 1 | a0001c0003t0003g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.747+162G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184726093 | |||||||
chr1:184726114 | A | C | 11 | a0001c0003t0005g0027 a0001c0003t0005g0028 a0001c0003t0005g0029 others(8): Show |
11 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.747+141T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184726114 | |||||||
chr1:184726221 | A | G | 1 | a0001c0003t0003g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.747+34T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184726221 | |||||||
chr1:184726233 | T | G | 1 | a0002c0002t0002g0241 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.747+22A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 7/19 | chr1 | 184726233 | |||||||
chr1:184726437 | C | T | 187 | a0001c0001t0033g0278 a0001c0003t0001g0140 a0001c0003t0003g0007 others(184): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.613-48G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184726437 | |||||||
chr1:184726461 | A | T | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.613-72T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184726461 | |||||||
chr1:184726693 | A | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.613-304T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184726693 | |||||||
chr1:184726860 | T | G | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.613-471A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184726860 | |||||||
chr1:184726862 | T | C | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.613-473A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184726862 | |||||||
chr1:184726898 | C | T | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.613-509G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184726898 | |||||||
chr1:184726899 | G | A | 1 | a0001c0003t0018g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.613-510C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184726899 | |||||||
chr1:184726900 | G | A | 1 | a0002c0002t0004g0255 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.613-511C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184726900 | |||||||
chr1:184727112 | C | T | 5 | a0002c0002t0002g0200 a0002c0002t0002g0210 a0002c0002t0002g0219 others(2): Show |
5 | NA18957.hp2 NA18982.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.613-723G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184727112 | |||||||
chr1:184727217 | G | A | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.613-828C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184727217 | |||||||
chr1:184727492 | T | C | 1 | a0001c0003t0005g0035 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.613-1103A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184727492 | |||||||
chr1:184727568 | G | A | 1 | a0001c0003t0018g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.613-1179C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184727568 | |||||||
chr1:184727651 | G | C | 1 | a0002c0002t0002g0244 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.613-1262C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184727651 | |||||||
chr1:184727731 | T | G | 1 | a0001c0003t0034g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.613-1342A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184727731 | |||||||
chr1:184728180 | G | C | 20 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0004t0004g0024 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.613-1791C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184728180 | |||||||
chr1:184728196 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.613-1807A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184728196 | |||||||
chr1:184728213 | T | C | 1 | a0001c0004t0004g0266 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.613-1824A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184728213 | |||||||
chr1:184728457 | A | G | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.613-2068T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184728457 | |||||||
chr1:184728492 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0175 |
3 | HG01192.hp1 HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.613-2103G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184728492 | |||||||
chr1:184728603 | CT | C | 7 | a0001c0001t0001g0147 a0001c0001t0007g0096 a0001c0003t0010g0256 others(4): Show |
7 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.613-2215delA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184728603 | |||||||
chr1:184728617 | T | A | 7 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(4): Show |
7 | HG00621.hp2 HG02109.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.613-2228A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184728617 | |||||||
chr1:184728850 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.613-2461G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184728850 | |||||||
chr1:184728957 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18944.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.613-2568T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184728957 | |||||||
chr1:184728997 | A | G | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.613-2608T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184728997 | |||||||
chr1:184729039 | C | T | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.613-2650G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729039 | |||||||
chr1:184729212 | C | A | 34 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(31): Show |
37 | HG00738.hp2 HG01069.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.613-2823G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729212 | |||||||
chr1:184729277 | C | T | 4 | a0001c0004t0004g0265 a0001c0004t0004g0266 a0001c0004t0004g0275 others(1): Show |
4 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-2888G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729277 | |||||||
chr1:184729418 | A | T | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.613-3029T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729418 | |||||||
chr1:184729421 | T | A | 11 | a0001c0003t0005g0027 a0001c0003t0005g0028 a0001c0003t0005g0029 others(8): Show |
11 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.613-3032A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729421 | |||||||
chr1:184729429 | G | A | 3 | a0001c0003t0003g0059 a0001c0003t0003g0079 a0001c0003t0003g0080 |
3 | HG02647.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.613-3040C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729429 | |||||||
chr1:184729490 | G | C | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.613-3101C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729490 | |||||||
chr1:184729548 | C | T | 3 | a0001c0003t0011g0046 a0001c0003t0011g0047 a0001c0003t0011g0048 |
3 | HG01192.hp2 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.613-3159G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729548 | |||||||
chr1:184729576 | A | C | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.613-3187T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729576 | |||||||
chr1:184729614 | A | G | 1 | a0001c0010t0006g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.612+3223T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729614 | |||||||
chr1:184729682 | A | G | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.612+3155T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729682 | |||||||
chr1:184729712 | C | T | 3 | a0001c0003t0010g0256 a0001c0003t0010g0257 a0001c0003t0010g0259 |
3 | HG02145.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.612+3125G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729712 | |||||||
chr1:184729736 | T | A | 3 | a0001c0003t0003g0070 a0001c0003t0003g0071 a0001c0003t0003g0072 |
3 | HG02559.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.612+3101A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729736 | |||||||
chr1:184729806 | G | A | 4 | a0001c0003t0009g0002 a0001c0003t0009g0086 a0001c0003t0009g0089 others(1): Show |
6 | HG01099.hp2 HG02258.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+3031C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729806 | |||||||
chr1:184729820 | CTGTTT | C | 7 | a0001c0003t0009g0002 a0001c0003t0009g0086 a0001c0003t0009g0089 others(4): Show |
9 | HG01099.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.612+3012_612+3016d others(7): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729820 | |||||||
chr1:184729898 | A | G | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.612+2939T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729898 | |||||||
chr1:184729903 | T | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.612+2934A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184729903 | |||||||
chr1:184730055 | A | G | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.612+2782T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184730055 | |||||||
chr1:184730314 | G | A | 2 | a0001c0003t0017g0144 a0001c0003t0017g0192 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.612+2523C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184730314 | |||||||
chr1:184730356 | AG | A | 8 | a0001c0003t0006g0085 a0001c0003t0006g0149 a0001c0003t0006g0150 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+2480delC | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184730356 | |||||||
chr1:184730585 | AAAAC | A | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+2248_612+2251d others(6): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184730585 | |||||||
chr1:184730603 | AAAAG | A | 5 | a0001c0004t0004g0263 a0001c0004t0004g0264 a0001c0004t0004g0270 others(2): Show |
5 | HG01106.hp2 NA18955.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.612+2230_612+2233d others(6): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184730603 | |||||||
chr1:184730828 | G | A | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+2009C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184730828 | |||||||
chr1:184730852 | A | C | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.612+1985T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184730852 | |||||||
chr1:184731033 | T | C | 5 | a0001c0003t0009g0002 a0001c0003t0009g0086 a0001c0003t0009g0089 others(2): Show |
7 | HG01099.hp2 HG02258.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+1804A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731033 | |||||||
chr1:184731131 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.612+1706G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731131 | |||||||
chr1:184731541 | C | T | 3 | a0002c0002t0002g0215 a0002c0002t0002g0216 a0002c0002t0002g0217 |
3 | NA18947.hp1 NA18951.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.612+1296G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731541 | |||||||
chr1:184731553 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.612+1284A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731553 | |||||||
chr1:184731598 | A | G | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0161 others(2): Show |
5 | NA18951.hp2 NA19001.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.612+1239T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731598 | |||||||
chr1:184731679 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.612+1158A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731679 | |||||||
chr1:184731769 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.612+1068G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731769 | |||||||
chr1:184731785 | T | A | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+1052A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731785 | |||||||
chr1:184731873 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.612+964A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731873 | |||||||
chr1:184731903 | G | A | 1 | a0001c0004t0004g0272 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.612+934C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731903 | |||||||
chr1:184731943 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.612+894C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184731943 | |||||||
chr1:184732011 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.612+826G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732011 | |||||||
chr1:184732180 | CA | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.612+656delT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732180 | |||||||
chr1:184732181 | A | C | 148 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(145): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.612+656T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732181 | |||||||
chr1:184732181 | A | T | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.612+656T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732181 | |||||||
chr1:184732182 | C | A | 45 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(42): Show |
48 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.612+655G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732182 | |||||||
chr1:184732184 | A | C | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+653T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732184 | |||||||
chr1:184732244 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0119 others(1): Show |
5 | HG01257.hp2 HG01346.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.612+593C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732244 | |||||||
chr1:184732279 | TAG | T | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.612+556_612+557del others(2): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732279 | |||||||
chr1:184732314 | G | C | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.612+523C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732314 | |||||||
chr1:184732323 | G | T | 2 | a0002c0002t0002g0242 a0002c0002t0002g0246 |
2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.612+514C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732323 | |||||||
chr1:184732337 | TAGGG | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.612+496_612+499del others(4): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732337 | |||||||
chr1:184732458 | A | G | 17 | a0001c0003t0003g0007 a0001c0003t0003g0055 a0001c0003t0003g0057 others(14): Show |
18 | HG01069.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.612+379T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732458 | |||||||
chr1:184732470 | T | C | 1 | a0002c0002t0002g0210 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.612+367A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732470 | |||||||
chr1:184732480 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.612+357A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732480 | |||||||
chr1:184732780 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.612+57T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732780 | |||||||
chr1:184732792 | A | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.612+45T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 6/19 | chr1 | 184732792 | |||||||
chr1:184733067 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.459-77A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184733067 | |||||||
chr1:184733198 | T | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.459-208A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184733198 | |||||||
chr1:184733231 | C | T | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.459-241G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184733231 | |||||||
chr1:184733333 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.459-343G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184733333 | |||||||
chr1:184733420 | T | C | 1 | a0002c0002t0002g0211 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.459-430A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184733420 | |||||||
chr1:184733622 | T | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.459-632A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184733622 | |||||||
chr1:184734125 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.458+406A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184734125 | |||||||
chr1:184734215 | TC | T | 79 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(76): Show |
101 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.458+315delG | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184734215 | |||||||
chr1:184734220 | G | A | 17 | a0001c0003t0003g0008 a0001c0003t0003g0009 a0001c0003t0003g0049 others(14): Show |
19 | HG00738.hp2 HG01168.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.458+311C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184734220 | |||||||
chr1:184734383 | C | T | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.458+148G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184734383 | |||||||
chr1:184734400 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0094 |
3 | HG02165.hp1 NA18964.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.458+131G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184734400 | |||||||
chr1:184734422 | T | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.458+109A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 5/19 | chr1 | 184734422 | |||||||
chr1:184734860 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.346-217G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184734860 | |||||||
chr1:184734900 | T | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.346-257A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184734900 | |||||||
chr1:184735399 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.346-756T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184735399 | |||||||
chr1:184735615 | A | G | 9 | a0001c0003t0003g0057 a0001c0003t0003g0058 a0001c0003t0003g0063 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.346-972T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184735615 | |||||||
chr1:184735749 | T | C | 22 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(19): Show |
23 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.346-1106A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184735749 | |||||||
chr1:184735798 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.346-1155A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184735798 | |||||||
chr1:184735890 | A | G | 1 | a0001c0003t0017g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.345+1135T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184735890 | |||||||
chr1:184736040 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.345+985C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736040 | |||||||
chr1:184736110 | C | A | 1 | a0002c0002t0002g0241 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.345+915G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736110 | |||||||
chr1:184736128 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.345+897A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736128 | |||||||
chr1:184736216 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.345+809A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736216 | |||||||
chr1:184736245 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.345+780C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736245 | |||||||
chr1:184736303 | C | T | 152 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(149): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.345+722G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736303 | |||||||
chr1:184736532 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.345+493A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736532 | |||||||
chr1:184736558 | T | C | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+467A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736558 | |||||||
chr1:184736606 | T | C | 11 | a0001c0003t0005g0027 a0001c0003t0005g0028 a0001c0003t0005g0029 others(8): Show |
11 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.345+419A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736606 | |||||||
chr1:184736615 | G | A | 6 | a0001c0003t0009g0002 a0001c0003t0009g0086 a0001c0003t0009g0089 others(3): Show |
8 | HG01099.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.345+410C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736615 | |||||||
chr1:184736668 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.345+357G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736668 | |||||||
chr1:184736686 | G | A | 1 | a0001c0004t0025g0273 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.345+339C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736686 | |||||||
chr1:184736749 | A | G | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.345+276T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736749 | |||||||
chr1:184736796 | C | T | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.345+229G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736796 | |||||||
chr1:184736990 | A | G | 1 | a0002c0002t0002g0250 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.345+35T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 4/19 | chr1 | 184736990 | |||||||
chr1:184737078 | GT | G | 183 | a0001c0001t0033g0278 a0001c0003t0003g0007 a0001c0003t0003g0008 others(180): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.306-15delA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 3/19 | chr1 | 184737078 | |||||||
chr1:184737172 | G | A | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.306-108C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 3/19 | chr1 | 184737172 | |||||||
chr1:184737272 | T | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.306-208A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 3/19 | chr1 | 184737272 | |||||||
chr1:184737751 | C | A | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-40G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184737751 | |||||||
chr1:184737918 | A | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.205-207T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184737918 | |||||||
chr1:184738104 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-393G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738104 | |||||||
chr1:184738123 | T | G | 2 | a0002c0002t0002g0242 a0002c0002t0002g0246 |
2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.205-412A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738123 | |||||||
chr1:184738131 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-420G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738131 | |||||||
chr1:184738219 | T | C | 161 | a0001c0001t0033g0278 a0001c0003t0003g0007 a0001c0003t0003g0008 others(158): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.205-508A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738219 | |||||||
chr1:184738428 | CTGA | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-720_205-718del others(3): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738428 | |||||||
chr1:184738438 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.205-727A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738438 | |||||||
chr1:184738476 | A | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-765T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738476 | |||||||
chr1:184738496 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.205-785T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738496 | |||||||
chr1:184738573 | G | A | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-862C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738573 | |||||||
chr1:184738649 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-938A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738649 | |||||||
chr1:184738696 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-985G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738696 | |||||||
chr1:184738714 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.205-1003A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738714 | |||||||
chr1:184738746 | T | C | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-1035A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738746 | |||||||
chr1:184738920 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0119 others(1): Show |
5 | HG01257.hp2 HG01346.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-1209A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738920 | |||||||
chr1:184738940 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-1229T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738940 | |||||||
chr1:184738994 | TG | T | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-1284delC | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184738994 | |||||||
chr1:184739002 | A | G | 1 | a0001c0003t0003g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.205-1291T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184739002 | |||||||
chr1:184739103 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-1392A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184739103 | |||||||
chr1:184739140 | T | C | 151 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(148): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.205-1429A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184739140 | |||||||
chr1:184739141 | G | A | 2 | a0002c0002t0002g0198 a0002c0002t0002g0254 |
2 | NA18940.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.205-1430C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184739141 | |||||||
chr1:184739304 | C | CTT | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-1594_205-1593i others(4): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184739304 | |||||||
chr1:184739484 | A | C | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.205-1773T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184739484 | |||||||
chr1:184739493 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-1782A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184739493 | |||||||
chr1:184739582 | T | A | 1 | a0001c0003t0003g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.205-1871A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184739582 | |||||||
chr1:184739980 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-2269A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184739980 | |||||||
chr1:184740043 | C | T | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-2332G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740043 | |||||||
chr1:184740064 | G | A | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.205-2353C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740064 | |||||||
chr1:184740127 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-2416T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740127 | |||||||
chr1:184740144 | T | C | 45 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(42): Show |
48 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.205-2433A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740144 | |||||||
chr1:184740252 | T | C | 1 | a0001c0003t0027g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-2541A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740252 | |||||||
chr1:184740297 | G | T | 2 | a0001c0003t0003g0062 a0001c0003t0003g0073 |
2 | HG01069.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.205-2586C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740297 | |||||||
chr1:184740369 | T | C | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-2658A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740369 | |||||||
chr1:184740387 | A | G | 1 | a0001c0001t0007g0131 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.205-2676T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740387 | |||||||
chr1:184740430 | G | A | 116 | a0001c0001t0033g0278 a0001c0003t0009g0002 a0001c0003t0009g0086 others(113): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.205-2719C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740430 | |||||||
chr1:184740532 | T | C | 10 | a0001c0003t0003g0044 a0001c0003t0003g0050 a0001c0003t0003g0051 others(7): Show |
10 | HG01109.hp2 HG01192.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.205-2821A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740532 | |||||||
chr1:184740597 | C | T | 1 | a0001c0003t0018g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.205-2886G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740597 | |||||||
chr1:184740598 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-2887C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740598 | |||||||
chr1:184740601 | C | T | 1 | a0002c0002t0002g0214 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.205-2890G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740601 | |||||||
chr1:184740614 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-2903T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740614 | |||||||
chr1:184740781 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.205-3070C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740781 | |||||||
chr1:184740833 | C | T | 1 | a0001c0003t0019g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.205-3122G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740833 | |||||||
chr1:184740870 | T | A | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.205-3159A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740870 | |||||||
chr1:184740922 | A | G | 2 | a0001c0003t0005g0028 a0001c0003t0005g0032 |
2 | HG00423.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.205-3211T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184740922 | |||||||
chr1:184741044 | G | A | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.205-3333C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741044 | |||||||
chr1:184741057 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-3346T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741057 | |||||||
chr1:184741270 | G | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-3559C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741270 | |||||||
chr1:184741313 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-3602A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741313 | |||||||
chr1:184741345 | G | A | 1 | a0001c0003t0027g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-3634C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741345 | |||||||
chr1:184741348 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.205-3637C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741348 | |||||||
chr1:184741407 | A | C | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-3696T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741407 | |||||||
chr1:184741409 | T | A | 2 | a0002c0002t0002g0006 a0002c0002t0002g0249 |
4 | NA18963.hp1 NA18966.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-3698A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741409 | |||||||
chr1:184741439 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-3728A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741439 | |||||||
chr1:184741454 | A | G | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.205-3743T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741454 | |||||||
chr1:184741492 | A | G | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.205-3781T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741492 | |||||||
chr1:184741583 | T | C | 3 | a0001c0003t0011g0046 a0001c0003t0011g0047 a0001c0003t0011g0048 |
3 | HG01192.hp2 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.205-3872A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741583 | |||||||
chr1:184741625 | G | A | 1 | a0001c0003t0018g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.205-3914C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741625 | |||||||
chr1:184741639 | G | A | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-3928C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741639 | |||||||
chr1:184741697 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.205-3986G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741697 | |||||||
chr1:184741733 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-4022A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741733 | |||||||
chr1:184741762 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-4051G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741762 | |||||||
chr1:184741847 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.205-4136C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741847 | |||||||
chr1:184741916 | C | T | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.205-4205G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741916 | |||||||
chr1:184741998 | C | T | 11 | a0001c0003t0005g0027 a0001c0003t0005g0028 a0001c0003t0005g0029 others(8): Show |
11 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.205-4287G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184741998 | |||||||
chr1:184742078 | A | T | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-4367T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742078 | |||||||
chr1:184742204 | G | A | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.205-4493C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742204 | |||||||
chr1:184742249 | T | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.205-4538A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742249 | |||||||
chr1:184742365 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-4654T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742365 | |||||||
chr1:184742414 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.205-4703G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742414 | |||||||
chr1:184742475 | T | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-4764A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742475 | |||||||
chr1:184742551 | T | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.205-4840A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742551 | |||||||
chr1:184742619 | C | T | 1 | a0002c0002t0012g0199 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.205-4908G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742619 | |||||||
chr1:184742683 | C | T | 1 | a0001c0003t0011g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.205-4972G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742683 | |||||||
chr1:184742814 | C | T | 1 | a0001c0004t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.205-5103G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742814 | |||||||
chr1:184742838 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-5127A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742838 | |||||||
chr1:184742855 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-5144T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742855 | |||||||
chr1:184742999 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-5288A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184742999 | |||||||
chr1:184743094 | T | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18944.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.205-5383A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743094 | |||||||
chr1:184743111 | C | T | 1 | a0002c0002t0002g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.205-5400G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743111 | |||||||
chr1:184743227 | A | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-5516T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743227 | |||||||
chr1:184743276 | T | C | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.205-5565A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743276 | |||||||
chr1:184743351 | C | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.205-5640G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743351 | |||||||
chr1:184743381 | T | C | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-5670A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743381 | |||||||
chr1:184743474 | A | AAAAAT | 4 | a0001c0001t0007g0096 a0001c0001t0007g0143 a0001c0001t0028g0146 others(1): Show |
5 | NA18612.hp1 NA18975.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-5768_205-5764d others(7): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743474 | |||||||
chr1:184743474 | AAAAAT | A | 7 | a0001c0003t0009g0002 a0001c0003t0009g0086 a0001c0003t0009g0089 others(4): Show |
9 | HG01099.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.205-5768_205-5764d others(7): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743474 | |||||||
chr1:184743814 | T | G | 11 | a0001c0003t0005g0027 a0001c0003t0005g0028 a0001c0003t0005g0029 others(8): Show |
11 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+5733A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743814 | |||||||
chr1:184743832 | G | A | 2 | a0001c0004t0004g0260 a0001c0004t0004g0274 |
2 | HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.204+5715C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743832 | |||||||
chr1:184743928 | A | T | 1 | a0002c0002t0008g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.204+5619T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184743928 | |||||||
chr1:184744020 | C | A | 1 | a0001c0003t0001g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.204+5527G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744020 | |||||||
chr1:184744085 | A | AC | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+5461_204+5462i others(3): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744085 | |||||||
chr1:184744109 | T | C | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.204+5438A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744109 | |||||||
chr1:184744248 | AAATATAT others(6): Show |
A | 1 | a0001c0003t0003g0063 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204+5286_204+5298d others(15): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744248 | |||||||
chr1:184744249 | A | AAT | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(43): Show |
53 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.204+5296_204+5297d others(4): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | A | AATAT | 12 | a0001c0001t0001g0011 a0001c0001t0001g0099 a0001c0001t0001g0100 others(9): Show |
13 | HG00544.hp1 HG00597.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.204+5294_204+5297d others(6): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | A | AATATAT | 10 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0157 others(7): Show |
10 | HG00673.hp1 HG01978.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+5292_204+5297d others(8): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | A | AATATATA others(1): Show |
4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0156 others(1): Show |
4 | HG02165.hp1 NA18982.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+5290_204+5297d others(10): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | AAT | A | 23 | a0001c0001t0001g0010 a0001c0001t0001g0132 a0001c0001t0001g0133 others(20): Show |
26 | HG00323.hp2 HG00609.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.204+5296_204+5297d others(4): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | AATAT | A | 15 | a0001c0001t0001g0139 a0001c0001t0001g0164 a0001c0001t0001g0172 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.204+5294_204+5297d others(6): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | AATATAT | A | 5 | a0001c0003t0005g0032 a0001c0003t0005g0033 a0001c0003t0005g0034 others(2): Show |
5 | HG00423.hp2 HG02055.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+5292_204+5297d others(8): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | AATATATA others(1): Show |
A | 13 | a0001c0003t0003g0057 a0001c0003t0003g0065 a0001c0003t0006g0150 others(10): Show |
14 | HG01346.hp2 HG02083.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.204+5290_204+5297d others(10): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | AATATATA others(3): Show |
A | 24 | a0001c0003t0003g0061 a0001c0003t0006g0085 a0001c0003t0006g0152 others(21): Show |
28 | HG00280.hp2 HG00673.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.204+5288_204+5297d others(12): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | AATATATA others(5): Show |
A | 53 | a0001c0003t0003g0070 a0001c0003t0003g0071 a0001c0003t0003g0072 others(50): Show |
70 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.204+5286_204+5297d others(14): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | AATATATA others(7): Show |
A | 9 | a0001c0001t0001g0092 a0001c0003t0003g0007 a0001c0003t0003g0055 others(6): Show |
10 | HG01358.hp1 HG01978.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.204+5284_204+5297d others(16): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | AATATATA others(9): Show |
A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.204+5282_204+5297d others(18): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | AATATATA others(11): Show |
A | 4 | a0001c0001t0001g0145 a0001c0001t0007g0143 a0001c0003t0017g0144 others(1): Show |
4 | HG02055.hp1 HG02976.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+5280_204+5297d others(20): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744249 | AATATATA others(17): Show |
A | 21 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(18): Show |
22 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.204+5274_204+5297d others(26): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744249 | |||||||
chr1:184744286 | A | G | 1 | a0002c0002t0002g0193 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.204+5261T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744286 | |||||||
chr1:184744501 | T | C | 1 | a0002c0002t0002g0020 | 2 | NA18950.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.204+5046A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744501 | |||||||
chr1:184744847 | T | A | 2 | a0001c0003t0005g0036 a0001c0003t0005g0037 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.204+4700A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744847 | |||||||
chr1:184744929 | G | A | 4 | a0001c0013t0040g0287 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG03139.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+4618C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744929 | |||||||
chr1:184744961 | C | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+4586G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744961 | |||||||
chr1:184744961 | C | T | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.204+4586G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184744961 | |||||||
chr1:184745000 | T | G | 1 | a0001c0001t0001g0038 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.204+4547A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184745000 | |||||||
chr1:184745328 | A | G | 1 | a0001c0003t0003g0074 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.204+4219T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184745328 | |||||||
chr1:184745352 | C | A | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.204+4195G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184745352 | |||||||
chr1:184745407 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+4140G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184745407 | |||||||
chr1:184745523 | T | C | 1 | a0001c0001t0028g0146 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.204+4024A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184745523 | |||||||
chr1:184745597 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.204+3950C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184745597 | |||||||
chr1:184745615 | A | G | 1 | a0001c0003t0003g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.204+3932T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184745615 | |||||||
chr1:184745705 | G | GT | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+3841dupA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184745705 | |||||||
chr1:184745757 | A | C | 2 | a0001c0003t0003g0062 a0001c0003t0003g0073 |
2 | HG01069.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.204+3790T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184745757 | |||||||
chr1:184745801 | T | C | 2 | a0002c0002t0002g0021 a0002c0002t0002g0022 |
4 | NA18954.hp2 NA18960.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+3746A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184745801 | |||||||
chr1:184746139 | T | C | 2 | a0001c0001t0001g0148 a0001c0003t0003g0072 |
2 | HG00323.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.204+3408A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746139 | |||||||
chr1:184746215 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+3332A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746215 | |||||||
chr1:184746283 | A | G | 109 | a0001c0001t0033g0278 a0001c0003t0035g0279 a0001c0004t0004g0024 others(106): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.204+3264T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746283 | |||||||
chr1:184746333 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+3214A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746333 | |||||||
chr1:184746358 | G | T | 4 | a0001c0004t0004g0265 a0001c0004t0004g0266 a0001c0004t0004g0275 others(1): Show |
4 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+3189C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746358 | |||||||
chr1:184746449 | T | C | 17 | a0001c0003t0003g0008 a0001c0003t0003g0009 a0001c0003t0003g0049 others(14): Show |
19 | HG00738.hp2 HG01168.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.204+3098A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746449 | |||||||
chr1:184746456 | C | T | 1 | a0001c0004t0004g0264 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.204+3091G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746456 | |||||||
chr1:184746757 | G | A | 4 | a0001c0003t0010g0256 a0001c0003t0010g0257 a0001c0003t0010g0258 others(1): Show |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+2790C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746757 | |||||||
chr1:184746862 | G | A | 1 | a0001c0001t0039g0286 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.204+2685C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746862 | |||||||
chr1:184746884 | T | A | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+2663A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746884 | |||||||
chr1:184746891 | A | G | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.204+2656T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746891 | |||||||
chr1:184746895 | T | C | 2 | a0002c0002t0002g0250 a0002c0002t0002g0251 |
2 | HG00280.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.204+2652A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184746895 | |||||||
chr1:184747020 | C | CA | 94 | a0001c0001t0033g0278 a0001c0003t0003g0007 a0001c0003t0003g0055 others(91): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.204+2526dupT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747020 | |||||||
chr1:184747020 | C | CAA | 6 | a0001c0003t0003g0069 a0002c0002t0002g0186 a0002c0002t0002g0243 others(3): Show |
6 | HG02056.hp2 HG02135.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+2525_204+2526d others(4): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747020 | |||||||
chr1:184747020 | CA | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0183 others(11): Show |
17 | HG01099.hp2 HG01346.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.204+2526delT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747020 | |||||||
chr1:184747101 | G | A | 8 | a0001c0003t0006g0085 a0001c0003t0006g0149 a0001c0003t0006g0150 others(5): Show |
8 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+2446C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747101 | |||||||
chr1:184747168 | T | TA | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.204+2378dupT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747168 | |||||||
chr1:184747283 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+2264C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747283 | |||||||
chr1:184747323 | T | C | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.204+2224A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747323 | |||||||
chr1:184747426 | G | T | 109 | a0001c0001t0033g0278 a0001c0003t0035g0279 a0001c0004t0004g0024 others(106): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.204+2121C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747426 | |||||||
chr1:184747500 | G | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+2047C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747500 | |||||||
chr1:184747566 | T | C | 1 | a0002c0002t0002g0187 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.204+1981A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747566 | |||||||
chr1:184747683 | A | T | 1 | a0002c0002t0037g0247 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.204+1864T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747683 | |||||||
chr1:184747845 | T | C | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.204+1702A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747845 | |||||||
chr1:184747986 | C | T | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.204+1561G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184747986 | |||||||
chr1:184748009 | C | T | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.204+1538G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748009 | |||||||
chr1:184748119 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+1428T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748119 | |||||||
chr1:184748169 | G | A | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+1378C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748169 | |||||||
chr1:184748194 | C | A | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+1353G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748194 | |||||||
chr1:184748303 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.204+1244G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748303 | |||||||
chr1:184748356 | A | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+1191T>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748356 | |||||||
chr1:184748389 | G | A | 2 | a0002c0002t0002g0190 a0002c0002t0037g0247 |
2 | HG01515.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.204+1158C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748389 | |||||||
chr1:184748444 | G | A | 1 | a0002c0002t0002g0022 | 2 | NA18954.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.204+1103C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748444 | |||||||
chr1:184748448 | CA | C | 114 | a0001c0001t0001g0091 a0001c0001t0033g0278 a0001c0003t0009g0002 others(111): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.204+1098delT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748448 | |||||||
chr1:184748545 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+1002C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748545 | |||||||
chr1:184748580 | A | C | 1 | a0001c0003t0003g0057 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.204+967T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748580 | |||||||
chr1:184748631 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.204+916C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748631 | |||||||
chr1:184748680 | T | C | 5 | a0001c0003t0003g0007 a0001c0003t0003g0055 a0001c0003t0003g0070 others(2): Show |
6 | HG02559.hp1 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+867A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748680 | |||||||
chr1:184748682 | T | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0156 a0001c0001t0001g0157 others(8): Show |
12 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+865A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748682 | |||||||
chr1:184748806 | A | G | 1 | a0001c0003t0038g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.204+741T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748806 | |||||||
chr1:184748828 | C | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+719G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748828 | |||||||
chr1:184748921 | T | G | 9 | a0001c0001t0001g0039 a0001c0001t0001g0166 a0001c0001t0001g0167 others(6): Show |
9 | HG01928.hp2 HG02273.hp2 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.204+626A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748921 | |||||||
chr1:184748982 | C | G | 34 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(31): Show |
37 | HG00738.hp2 HG01069.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.204+565G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184748982 | |||||||
chr1:184749154 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.204+393T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184749154 | |||||||
chr1:184749323 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.204+224A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184749323 | |||||||
chr1:184749419 | G | C | 1 | a0001c0003t0003g0082 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.204+128C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184749419 | |||||||
chr1:184749467 | G | A | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.204+80C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 2/19 | chr1 | 184749467 | |||||||
chr1:184749616 | G | GA | 12 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(9): Show |
12 | HG01192.hp2 HG01978.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.159-25dupT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184749616 | |||||||
chr1:184749616 | GA | G | 11 | a0001c0001t0033g0278 a0001c0003t0003g0007 a0001c0003t0003g0055 others(8): Show |
14 | HG01069.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.159-25delT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184749616 | |||||||
chr1:184749616 | GAAA | G | 96 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(93): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.159-27_159-25delTT others(1): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184749616 | |||||||
chr1:184749674 | C | A | 1 | a0001c0003t0003g0073 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.159-82G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184749674 | |||||||
chr1:184749804 | T | C | 2 | a0002c0002t0002g0250 a0002c0002t0002g0251 |
2 | HG00280.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.159-212A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184749804 | |||||||
chr1:184750043 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.159-451T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750043 | |||||||
chr1:184750050 | T | C | 2 | a0001c0001t0001g0181 a0003c0005t0001g0025 |
3 | HG00597.hp2 NA18995.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.159-458A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750050 | |||||||
chr1:184750069 | C | T | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.159-477G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750069 | |||||||
chr1:184750222 | T | A | 2 | a0001c0003t0003g0083 a0001c0003t0003g0084 |
2 | HG01168.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.159-630A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750222 | |||||||
chr1:184750230 | C | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.159-638G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750230 | |||||||
chr1:184750294 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.159-702A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750294 | |||||||
chr1:184750295 | C | A | 2 | a0002c0002t0002g0021 a0002c0002t0002g0022 |
4 | NA18954.hp2 NA18960.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-703G>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750295 | |||||||
chr1:184750385 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.159-793C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750385 | |||||||
chr1:184750490 | C | G | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.159-898G>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750490 | |||||||
chr1:184750518 | C | CTTTTTT | 69 | a0001c0001t0033g0278 a0001c0003t0003g0007 a0001c0003t0003g0008 others(66): Show |
73 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.159-932_159-927dup others(6): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750518 | |||||||
chr1:184750518 | C | CTTTTTTT | 80 | a0001c0004t0004g0024 a0001c0004t0004g0261 a0001c0004t0004g0262 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.159-933_159-927dup others(7): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750518 | |||||||
chr1:184750561 | A | G | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.159-969T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750561 | |||||||
chr1:184750582 | A | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.159-990T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750582 | |||||||
chr1:184750616 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.159-1024C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750616 | |||||||
chr1:184750715 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.159-1123C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750715 | |||||||
chr1:184750748 | T | C | 149 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(146): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.159-1156A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750748 | |||||||
chr1:184750748 | T | G | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.159-1156A>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184750748 | |||||||
chr1:184751032 | A | G | 6 | a0001c0003t0003g0044 a0001c0003t0003g0050 a0001c0003t0003g0051 others(3): Show |
6 | HG01109.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-1440T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751032 | |||||||
chr1:184751034 | A | G | 1 | a0002c0002t0008g0195 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.159-1442T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751034 | |||||||
chr1:184751091 | ACATTTCA others(27): Show |
A | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.159-1533_159-1500d others(36): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751091 | |||||||
chr1:184751127 | T | TAG | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.159-1536_159-1535i others(4): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751127 | |||||||
chr1:184751157 | CAT | C | 4 | a0001c0010t0006g0277 a0004c0006t0014g0281 a0004c0006t0014g0282 others(1): Show |
4 | HG00621.hp2 HG02258.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-1567_159-1566d others(4): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751157 | |||||||
chr1:184751235 | G | GA | 17 | a0001c0003t0003g0008 a0001c0003t0003g0009 a0001c0003t0003g0049 others(14): Show |
19 | HG00621.hp2 HG00738.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.159-1644dupT | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751235 | |||||||
chr1:184751381 | G | T | 1 | a0001c0003t0018g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.159-1789C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751381 | |||||||
chr1:184751575 | T | TCTGA | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.159-1984_159-1983i others(6): Show |
EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751575 | |||||||
chr1:184751753 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.159-2161C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751753 | |||||||
chr1:184751788 | T | C | 1 | a0001c0010t0006g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.159-2196A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751788 | |||||||
chr1:184751879 | G | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.159-2287C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751879 | |||||||
chr1:184751958 | G | A | 1 | a0002c0002t0004g0255 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.159-2366C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184751958 | |||||||
chr1:184752260 | G | A | 77 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(74): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.158+2229C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752260 | |||||||
chr1:184752264 | A | G | 45 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(42): Show |
48 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.158+2225T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752264 | |||||||
chr1:184752274 | A | G | 6 | a0001c0003t0003g0044 a0001c0003t0003g0050 a0001c0003t0003g0051 others(3): Show |
6 | HG01109.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+2215T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752274 | |||||||
chr1:184752371 | A | G | 1 | a0001c0003t0003g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.158+2118T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752371 | |||||||
chr1:184752376 | T | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.158+2113A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752376 | |||||||
chr1:184752753 | T | C | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.158+1736A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752753 | |||||||
chr1:184752764 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.158+1725C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752764 | |||||||
chr1:184752773 | TG | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.158+1715delC | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752773 | |||||||
chr1:184752860 | T | C | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.158+1629A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752860 | |||||||
chr1:184752912 | T | C | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.158+1577A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752912 | |||||||
chr1:184752932 | C | T | 1 | a0002c0002t0002g0191 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.158+1557G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752932 | |||||||
chr1:184752983 | G | A | 1 | a0001c0004t0023g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.158+1506C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752983 | |||||||
chr1:184752996 | A | G | 1 | a0002c0002t0002g0190 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.158+1493T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184752996 | |||||||
chr1:184753021 | T | C | 1 | a0001c0013t0040g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.158+1468A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184753021 | |||||||
chr1:184753201 | AT | A | 6 | a0001c0001t0033g0278 a0001c0003t0010g0256 a0001c0003t0010g0257 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+1287delA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184753201 | |||||||
chr1:184753218 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.158+1271A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184753218 | |||||||
chr1:184753387 | A | C | 1 | a0001c0004t0004g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.158+1102T>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184753387 | |||||||
chr1:184753407 | CT | C | 86 | a0001c0003t0010g0256 a0001c0003t0010g0257 a0001c0003t0010g0258 others(83): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.158+1081delA | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184753407 | |||||||
chr1:184753452 | G | T | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+1037C>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184753452 | |||||||
chr1:184753485 | A | G | 4 | a0001c0003t0011g0045 a0001c0003t0011g0046 a0001c0003t0011g0047 others(1): Show |
4 | HG01192.hp2 HG01884.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+1004T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184753485 | |||||||
chr1:184753870 | T | A | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.158+619A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184753870 | |||||||
chr1:184753987 | A | G | 1 | a0001c0003t0003g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.158+502T>C | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184753987 | |||||||
chr1:184754001 | T | C | 18 | a0001c0004t0004g0024 a0001c0004t0004g0260 a0001c0004t0004g0261 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.158+488A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754001 | |||||||
chr1:184754047 | G | C | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+442C>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754047 | |||||||
chr1:184754194 | GC | G | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+294delG | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754194 | |||||||
chr1:184754203 | T | C | 1 | a0001c0010t0006g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.158+286A>G | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754203 | |||||||
chr1:184754211 | C | T | 4 | a0001c0004t0013g0040 a0001c0004t0013g0042 a0001c0004t0013g0043 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+278G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754211 | |||||||
chr1:184754298 | C | T | 3 | a0004c0006t0014g0281 a0004c0006t0014g0282 a0004c0006t0014g0283 |
3 | HG00621.hp2 NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.158+191G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754298 | |||||||
chr1:184754319 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.158+170G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754319 | |||||||
chr1:184754341 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.158+148G>A | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754341 | |||||||
chr1:184754345 | G | A | 2 | a0001c0001t0033g0278 a0001c0003t0035g0279 |
2 | HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.158+144C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754345 | |||||||
chr1:184754360 | G | A | 1 | a0002c0002t0002g0280 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.158+129C>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754360 | |||||||
chr1:184754381 | T | A | 1 | a0001c0003t0018g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.158+108A>T | EDEM3 | ENSG00000116406.20 | transcript | ENST00000318130.13 | protein_coding | 1/19 | chr1 | 184754381 |