view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | 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 | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
GALNT9_chr12_132191372_132334589 | 132242108 | C | CCACACAC others(5734): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 | 1 | 162 | 0.0062 | 5741 | c.107 others(5760): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | |||||||
ATP9B_chr18_79064394_79383283 | 79200703 | T | TGTCAGAG others(5736): Show |
intron_variant | MODIFIER | HG02738.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0120 | 1 | 76 | 0.0132 | 5743 | c.955 others(5760): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
GALNT9_chr12_132191372_132334589 | 132241973 | A | ACACACAC others(5739): Show |
intron_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 | 1 | 87 | 0.0115 | 5746 | c.107 others(5765): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | |||||||
TAOK1_chr17_29385363_29556903 | 29487254 | A | AAAAAAAA others(5739): Show |
intron_variant | MODIFIER | HG01515.hp2 | a0001 | a0001c0003 | a0001c0003t0008 | a0001c0003t0008g0009 | 1 | 324 | 0.0031 | 5746 | c.656 others(5763): Show |
TAOK1 | ENSG00000160551.12 | transcript | ENST00000261716.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RPH3AL_chr17_207389_357807 | 315058 | A | ACTGTAGT others(5740): Show |
intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0059 | 1 | 104 | 0.0096 | 5747 | c.351 others(5764): Show |
RPH3AL | ENSG00000181031.16 | transcript | ENST00000331302.12 | protein_coding | 5/9 | chr17 | TogoVar | |||||||
ABR_chr17_998519_1184981 | 1065223 | A | ACTGTTAT others(5742): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0001 | a0001c0001t0066 | a0001c0001t0066g0090 | 1 | 300 | 0.0033 | 5749 | c.118 others(5768): Show |
ABR | ENSG00000159842.16 | transcript | ENST00000302538.10 | protein_coding | 10/22 | chr17 | TogoVar | |||||||
PTP4A3_chr8_141387021_141437454 | 141415694 | G | GGGGTAGG others(5744): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0282 | 1 | 322 | 0.0031 | 5751 | c.-85 others(5770): Show |
PTP4A3 | ENSG00000184489.13 | transcript | ENST00000521578.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
OR2T1_chr1_248398048_248413020 | 248404195 | C | CGTGTGTG others(5745): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0068 | 1 | 3 | 0.3333 | 5752 | c.-34 others(5767): Show |
OR2T1 | ENSG00000175143.5 | transcript | ENST00000642005.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
FOXK2_chr17_82514732_82609602 | 82586404 | G | GGGGGAAA others(5746): Show |
intron_variant | MODIFIER | NA20905.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0119 | 1 | 276 | 0.0036 | 5753 | c.157 others(5770): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(5749): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0021 | a0021c0039 | a0021c0039t0001 | a0021c0039t0001g0185 | 1 | 34 | 0.0294 | 5756 | c.299 others(5771): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(5756): Show |
intron_variant | MODIFIER | NA19081.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096 | 1 | 55 | 0.0182 | 5763 | c.891 others(5778): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(5756): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0215 | 1 | 62 | 0.0161 | 5763 | c.286 others(5780): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(5759): Show |
intron_variant | MODIFIER | HG01975.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0164 | 1 | 55 | 0.0182 | 5766 | c.891 others(5781): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(5759): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 | 1 | 55 | 0.0182 | 5766 | c.891 others(5781): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
YBEY_chr21_46281342_46302751 | 46294693 | G | GTCAGCCA others(5761): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0204 | 1 | 198 | 0.0051 | 5768 | c.340 others(5785): Show |
YBEY | ENSG00000182362.14 | transcript | ENST00000397701.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
SERINC2_chr1_31408213_31439678 | 31432174 | T | TAGGGTGG others(5762): Show |
intron_variant | MODIFIER | HG01943.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0308 | 1 | 228 | 0.0044 | 5769 | c.101 others(5786): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
YBEY_chr21_46281342_46302751 | 46294532 | G | GGGACTCA others(5762): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033 | 1 | 397 | 0.0025 | 5769 | c.340 others(5786): Show |
YBEY | ENSG00000182362.14 | transcript | ENST00000397701.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
FOXK2_chr17_82514732_82609602 | 82586449 | C | CAGTGGGG others(5765): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033 | 1 | 244 | 0.0041 | 5772 | c.157 others(5789): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | chr17 | TogoVar | |||||||
GALNT9_chr12_132191372_132334589 | 132243309 | A | ATTACACA others(5767): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0018 | a0001c0018t0001 | a0001c0018t0001g0047 | 1 | 175 | 0.0057 | 5774 | c.107 others(5793): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | |||||||
ACTN2_chr1_236681499_236769631 | 236714890 | T | TACCACTG others(5769): Show |
intron_variant | MODIFIER | HG01361.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0263 | 1 | 241 | 0.0041 | 5776 | c.127 others(5793): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236714890 | T | TACCACTG others(5769): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0230 | 1 | 241 | 0.0041 | 5776 | c.127 others(5793): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(5775): Show |
upstream_gene_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0146 | 1 | 8 | 0.1250 | 5782 | c.-45 others(5791): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(5775): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0139 | 1 | 62 | 0.0161 | 5782 | c.286 others(5799): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CLPTM1L_chr5_1312752_1350099 | 1333251 | C | CGGATGAG others(5776): Show |
intron_variant | MODIFIER | HG02738.hp1 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0199 | 1 | 302 | 0.0033 | 5783 | c.891 others(5800): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
CFAP20DC_chr3_58737008_59055025 | 58815696 | G | GAAGGACA others(5778): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0127 | 1 | 198 | 0.0051 | 5785 | c.217 others(5804): Show |
CFAP20DC | ENSG00000163689.21 | transcript | ENST00000482387.7 | protein_coding | 14/16 | chr3 | TogoVar | |||||||
CFAP20DC_chr3_58737008_59055025 | 58819255 | T | TTCAAAAG others(5778): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0123 | 1 | 201 | 0.0050 | 5785 | c.217 others(5806): Show |
CFAP20DC | ENSG00000163689.21 | transcript | ENST00000482387.7 | protein_coding | 14/16 | chr3 | TogoVar | |||||||
CFAP20DC_chr3_58737008_59055025 | 58819372 | C | TAACAAAA others(5778): Show |
intron_variant | MODIFIER | HG01934.hp1 HG03139.hp2 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0129 |
3 | 202 | 0.0149 | 5785 | c.217 others(5806): Show |
CFAP20DC | ENSG00000163689.21 | transcript | ENST00000482387.7 | protein_coding | 14/16 | chr3 | TogoVar | |||||||
DOCK1_chr10_126900428_127457516 | 126948419 | A | ATGGTGGT others(5779): Show |
intron_variant | MODIFIER | HG02738.hp1 | a0002 | a0002c0017 | a0002c0017t0002 | a0002c0017t0002g0136 | 1 | 3 | 0.3333 | 5786 | c.47- others(5803): Show |
DOCK1 | ENSG00000150760.13 | transcript | ENST00000623213.2 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
LRRC27_chr10_132327193_132386508 | 132364513 | A | ACGCCCAC others(5781): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 | 1 | 263 | 0.0038 | 5788 | c.129 others(5805): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
PTP4A3_chr8_141387021_141437454 | 141415691 | A | AGAGGGGT others(5782): Show |
intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0286 | 1 | 8 | 0.1250 | 5789 | c.-85 others(5808): Show |
PTP4A3 | ENSG00000184489.13 | transcript | ENST00000521578.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(5784): Show |
upstream_gene_variant | MODIFIER | HG02273.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 | 1 | 8 | 0.1250 | 5791 | c.-45 others(5800): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
SIGIRR_chr11_400716_419999 | 412442 | G | GGTGGGGG others(5784): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0109 | 1 | 239 | 0.0042 | 5791 | c.-15 others(5810): Show |
SIGIRR | ENSG00000185187.13 | transcript | ENST00000431843.7 | protein_coding | 1/9 | chr11 | TogoVar | |||||||
FAM120B_chr6_170301758_170412067 | 170377914 | C | CGCCCGGG others(5788): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0146 | 1 | 152 | 0.0066 | 5795 | c.228 others(5816): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
FAM120B_chr6_170301758_170412067 | 170377914 | C | CGCCCGGG others(5788): Show |
intron_variant | MODIFIER | HG01070.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0138 | 1 | 152 | 0.0066 | 5795 | c.228 others(5816): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
FAM120B_chr6_170301758_170412067 | 170377914 | C | CGCCCGGG others(5788): Show |
intron_variant | MODIFIER | HG03669.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0129 | 1 | 152 | 0.0066 | 5795 | c.228 others(5816): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
FAM120B_chr6_170301758_170412067 | 170377914 | C | CGCCCGGG others(5788): Show |
intron_variant | MODIFIER | HG00099.hp2 HG03710.hp2 |
a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0007 | 2 | 153 | 0.0131 | 5795 | c.228 others(5816): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
FAM120B_chr6_170301758_170412067 | 170377914 | C | CGCCCGGG others(5788): Show |
intron_variant | MODIFIER | HG01256.hp1 HG01361.hp1 |
a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0127 a0002c0003t0002g0130 |
2 | 153 | 0.0131 | 5795 | c.228 others(5816): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
RTEL1_chr20_63653312_63701245 | 63693645 | T | TCCCCTCC others(5788): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 | 1 | 46 | 0.0217 | 5795 | c.299 others(5812): Show |
RTEL1 | ENSG00000258366.12 | transcript | ENST00000360203.11 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
SERINC2_chr1_31408213_31439678 | 31431776 | A | AATAGGGT others(5789): Show |
intron_variant | MODIFIER | HG02080.hp2 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0163 | 1 | 259 | 0.0039 | 5796 | c.101 others(5815): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119359860 | T | TAAAAATC others(5790): Show |
intron_variant | MODIFIER | HG02698.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0275 | 1 | 307 | 0.0033 | 5797 | c.101 others(5814): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(5794): Show |
intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0074 | 1 | 34 | 0.0294 | 5801 | c.299 others(5816): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119359860 | T | TAAAAATC others(5796): Show |
intron_variant | MODIFIER | HG03831.hp2 | a0001 | a0001c0004 | a0001c0004t0010 | a0001c0004t0010g0274 | 1 | 307 | 0.0033 | 5803 | c.101 others(5820): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
EHMT1_chr9_137614005_137841127 | 137716460 | T | TGGGGGAG others(5796): Show |
intron_variant | MODIFIER | NA19070.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0027 | 1 | 129 | 0.0078 | 5803 | c.86- others(5814): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
IFNAR1_chr21_33319970_33364864 | 33322912 | T | TATATGTA others(5797): Show |
upstream_gene_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0090 | 1 | 271 | 0.0037 | 5804 | c.-21 others(5815): Show |
IFNAR1 | ENSG00000142166.15 | transcript | ENST00000270139.8 | protein_coding | 2057 | chr21 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311780 | G | GTGCCCCA others(5798): Show |
intron_variant | MODIFIER | HG00323.hp2 HG01123.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | 318 | 0.0063 | 5805 | c.327 others(5822): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311780 | G | GTGCCCCA others(5798): Show |
intron_variant | MODIFIER | HG00323.hp1 HG01074.hp1 HG02027.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0016others(1): Show | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0144 others(5): Show |
8 | 324 | 0.0247 | 5805 | c.327 others(5822): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311780 | G | GTGCCCCA others(5798): Show |
intron_variant | MODIFIER | NA19010.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0108 | 1 | 317 | 0.0032 | 5805 | c.327 others(5822): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311780 | G | GTGCCCCA others(5798): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0154 | 1 | 317 | 0.0032 | 5805 | c.327 others(5822): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311780 | G | GTGCCCCA others(5798): Show |
intron_variant | MODIFIER | HG01109.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0156 | 1 | 317 | 0.0032 | 5805 | c.327 others(5822): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311780 | G | GTGCCCCA others(5798): Show |
intron_variant | MODIFIER | HG01106.hp2 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0155 | 1 | 317 | 0.0032 | 5805 | c.327 others(5822): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar |