regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CFL2_chr14_34704113_34719593 | 34704350 | T | TCTATTCC others(3158): Show |
downstream_gene_variant | MODIFIER | HG03669.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0005 | 1 | 431 | 0.0023 | 3165 | c.*85 others(3176): Show |
CFL2 | ENSG00000165410.15 | transcript | ENST00000298159.11 | protein_coding | 4762 | chr14 | TogoVar | ||||||
CFL2_chr14_34704113_34719593 | 34704350 | T | TCTATTCC others(3158): Show |
downstream_gene_variant | MODIFIER | HG00544.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0005 | 1 | 431 | 0.0023 | 3165 | c.*85 others(3176): Show |
CFL2 | ENSG00000165410.15 | transcript | ENST00000298159.11 | protein_coding | 4762 | chr14 | TogoVar | ||||||
CFL2_chr14_34704113_34719593 | 34704350 | T | TCTATTCC others(3158): Show |
downstream_gene_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0003 | 1 | 431 | 0.0023 | 3165 | c.*85 others(3176): Show |
CFL2 | ENSG00000165410.15 | transcript | ENST00000298159.11 | protein_coding | 4762 | chr14 | TogoVar | ||||||
CFL2_chr14_34704113_34719593 | 34704350 | T | TCTATTCC others(3158): Show |
downstream_gene_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0005 | 1 | 431 | 0.0023 | 3165 | c.*85 others(3176): Show |
CFL2 | ENSG00000165410.15 | transcript | ENST00000298159.11 | protein_coding | 4762 | chr14 | TogoVar | ||||||
DIP2B_chr12_50499985_50753657 | 50604179 | A | ACTCTGAA others(3158): Show |
intron_variant | MODIFIER | NA18952.hp2 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0039 | 1 | 284 | 0.0035 | 3165 | c.101 others(3184): Show |
DIP2B | ENSG00000066084.13 | transcript | ENST00000301180.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
LAMA5_chr20_62304065_62372312 | 62318240 | G | GGAAGGGG others(3158): Show |
intron_variant | MODIFIER | NA18970.hp1 | a0044 | a0044c0095 | a0044c0095t0001 | a0044c0095t0001g0163 | 1 | 186 | 0.0054 | 3165 | c.723 others(3182): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 53/79 | chr20 | TogoVar | ||||||
MED16_chr19_862963_898187 | 871891 | C | CGGGGAGA others(3158): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0031 | 1 | 56 | 0.0179 | 3165 | c.209 others(3180): Show |
MED16 | ENSG00000175221.16 | transcript | ENST00000325464.6 | protein_coding | 12/15 | chr19 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21097957 | T | TAAATGTT others(3158): Show |
intron_variant | MODIFIER | HG01361.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0110 | 1 | 132 | 0.0076 | 3165 | c.55+ others(3182): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
TUBA4B_chr2_219248243_219277197 | 219270701 | C | CCCGTCCC others(3158): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0197 | 1 | 350 | 0.0029 | 3165 | c.192 others(3180): Show |
TUBA4B | ENSG00000243910.9 | transcript | ENST00000490341.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ZNF461_chr19_36631618_36671837 | 36661642 | T | TAAGATGA others(3158): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0127 | 1 | 354 | 0.0028 | 3165 | c.9+3 others(3178): Show |
ZNF461 | ENSG00000197808.14 | transcript | ENST00000588268.6 | protein_coding | 2/5 | chr19 | TogoVar | ||||||
ANO2_chr12_5557655_5950259 | 5932398 | A | ATAGACTA others(3159): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 162 | 0.0062 | 3166 | c.23- others(3181): Show |
ANO2 | ENSG00000047617.18 | transcript | ENST00000682330.1 | protein_coding | 1/24 | chr12 | TogoVar | ||||||
CFL2_chr14_34704113_34719593 | 34704350 | T | TCTATTCC others(3159): Show |
downstream_gene_variant | MODIFIER | HG00597.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0003 | 1 | 431 | 0.0023 | 3166 | c.*85 others(3177): Show |
CFL2 | ENSG00000165410.15 | transcript | ENST00000298159.11 | protein_coding | 4762 | chr14 | TogoVar | ||||||
CRIP2_chr14_105469821_105485162 | 105477719 | G | GGGGAAGC others(3159): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0052 | 1 | 316 | 0.0032 | 3166 | c.44- others(3179): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
DOCK2_chr5_169632275_170088382 | 169949675 | T | TCAATGTG others(3159): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0009 | a0001c0009t0002 | a0001c0009t0002g0173 | 1 | 184 | 0.0054 | 3166 | c.280 others(3187): Show |
DOCK2 | ENSG00000134516.20 | transcript | ENST00000520908.7 | protein_coding | 27/51 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
INSYN2B_chr5_169856303_169985495 | 169949675 | T | TCAATGTG others(3159): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0002 | a0002c0002 | a0002c0002t0008 | a0002c0002t0008g0303 | 1 | 318 | 0.0031 | 3166 | c.-91 others(3187): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | TogoVar | ||||||
SLC35F3_chr1_233899676_234329511 | 234207442 | T | TCCTTCTT others(3159): Show |
intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048 | 1 | 158 | 0.0063 | 3166 | c.284 others(3185): Show |
SLC35F3 | ENSG00000183780.13 | transcript | ENST00000366618.8 | protein_coding | 2/7 | chr1 | TogoVar | ||||||
ZNF718_chr4_119501_169162 | 152956 | G | GTACTTTG others(3159): Show |
intron_variant | MODIFIER | HG03688.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0034 | 1 | 330 | 0.0030 | 3166 | c.227 others(3183): Show |
ZNF718 | ENSG00000250312.8 | transcript | ENST00000510175.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
CACNA1H_chr16_1148106_1226768 | 1185865 | G | GGTCGGCG others(3160): Show |
intron_variant | MODIFIER | HG00438.hp1 | a0002 | a0002c0014 | a0002c0014t0008 | a0002c0014t0008g0267 | 1 | 338 | 0.0030 | 3167 | c.300 others(3184): Show |
CACNA1H | ENSG00000196557.14 | transcript | ENST00000348261.11 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CFL2_chr14_34704113_34719593 | 34704350 | T | TCTATTCC others(3160): Show |
downstream_gene_variant | MODIFIER | NA18985.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0015 | 1 | 431 | 0.0023 | 3167 | c.*85 others(3178): Show |
CFL2 | ENSG00000165410.15 | transcript | ENST00000298159.11 | protein_coding | 4762 | chr14 | TogoVar | ||||||
CFL2_chr14_34704113_34719593 | 34704350 | T | TCTATTCC others(3160): Show |
downstream_gene_variant | MODIFIER | HG01433.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0063 | 1 | 431 | 0.0023 | 3167 | c.*85 others(3178): Show |
CFL2 | ENSG00000165410.15 | transcript | ENST00000298159.11 | protein_coding | 4762 | chr14 | TogoVar | ||||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3160): Show |
intron_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0001 | a0001c0001t0056 | a0001c0001t0056g0258 | 1 | 264 | 0.0038 | 3167 | c.400 others(3186): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
INSYN2B_chr5_169856303_169985495 | 169949675 | T | TCAATGTG others(3160): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0263 | 1 | 318 | 0.0031 | 3167 | c.-91 others(3188): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154180619 | A | ACATTTTT others(3161): Show |
intron_variant | MODIFIER | HG00140.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0150 | 1 | 283 | 0.0035 | 3168 | c.148 others(3187): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | TogoVar | ||||||
ATP10A_chr15_25673712_25868327 | 25758208 | C | CCACCTGC others(3161): Show |
intron_variant | MODIFIER | NA19000.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0126 | 1 | 300 | 0.0033 | 3168 | c.655 others(3187): Show |
ATP10A | ENSG00000206190.13 | transcript | ENST00000555815.7 | protein_coding | 2/20 | chr15 | TogoVar | ||||||
FMN2_chr1_240086883_240480187 | 240185119 | C | CCCCTTCT others(3161): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0007 | a0007c0099 | a0007c0099t0001 | a0007c0099t0001g0163 | 1 | 174 | 0.0058 | 3168 | c.193 others(3187): Show |
FMN2 | ENSG00000155816.21 | transcript | ENST00000319653.14 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21097957 | T | TAAATGTT others(3161): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0001c0012others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(6): Show | a0001c0001t0001g0085a0001c0001t0005g0076a0001c0001t0009g0001others(6): Show | 9 | 132 | 0.0682 | 3168 | c.55+ others(3185): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21097957 | T | TAAATGTT others(3161): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02976.hp1 HG03516.hp1 |
a0001a0002 | a0001c0001a0002c0003a0002c0008 | a0001c0001t0014a0002c0003t0003a0002c0008t0015 | a0001c0001t0014g0033a0002c0003t0003g0107a0002c0008t0015g0129 | 3 | 132 | 0.0227 | 3168 | c.55+ others(3185): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21097957 | T | TAAATGTT others(3161): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0001 | a0001c0001t0038 | a0001c0001t0038g0053 | 1 | 132 | 0.0076 | 3168 | c.55+ others(3185): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21097957 | T | TAAATGTT others(3161): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(50): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0014others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0040others(50): Show | 53 | 132 | 0.4015 | 3168 | c.55+ others(3185): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21097957 | T | TAAATGTT others(3161): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032 | 1 | 132 | 0.0076 | 3168 | c.55+ others(3185): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21097957 | T | TAAATGTT others(3161): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0003 | a0003c0005 | a0003c0005t0005 | a0003c0005t0005g0105 | 1 | 132 | 0.0076 | 3168 | c.55+ others(3185): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21097957 | T | TAAATGTT others(3161): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0002 | a0002c0002 | a0002c0002t0010 | a0002c0002t0010g0092 | 1 | 132 | 0.0076 | 3168 | c.55+ others(3185): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
SERINC2_chr1_31408213_31439678 | 31431778 | T | TAGGGTGG others(3161): Show |
intron_variant | MODIFIER | NA19066.hp2 | a0002 | a0002c0006 | a0002c0006t0008 | a0002c0006t0008g0227 | 1 | 376 | 0.0027 | 3168 | c.101 others(3187): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
TUBA4B_chr2_219248243_219277197 | 219270701 | C | CCCGTCCC others(3161): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0005 | a0005c0005 | a0005c0005t0001 | a0005c0005t0001g0228 | 1 | 350 | 0.0029 | 3168 | c.192 others(3183): Show |
TUBA4B | ENSG00000243910.9 | transcript | ENST00000490341.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236714689 | T | TACCACTG others(3162): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0048 | 1 | 344 | 0.0029 | 3169 | c.127 others(3186): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
SNRNP35_chr12_123453139_123471936 | 123453143 | T | TAAAAATA others(3162): Show |
upstream_gene_variant | MODIFIER | HG00323.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0023 | 1 | 186 | 0.0054 | 3169 | c.-50 others(3180): Show |
SNRNP35 | ENSG00000184209.15 | transcript | ENST00000526639.3 | protein_coding | 4995 | chr12 | TogoVar | ||||||
VCX3B_chrX_8459830_8471510 | 8466927 | A | AGGTGGTG others(3162): Show |
downstream_gene_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0042 | 1 | 271 | 0.0037 | 3169 | c.*54 others(3178): Show |
VCX3B | ENSG00000205642.11 | transcript | ENST00000381032.6 | protein_coding | 418 | chrX | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154180619 | A | ACATTTTT others(3163): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0015a0001c0001t0030 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | 283 | 0.0141 | 3170 | c.148 others(3189): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154180619 | A | ACATTTTT others(3163): Show |
intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(70): Show |
a0001a0002a0006others(3): Show | a0001c0001a0002c0002a0002c0003others(6): Show | a0001c0001t0007a0001c0001t0017a0002c0002t0003others(18): Show | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(70): Show | 73 | 283 | 0.2580 | 3170 | c.148 others(3189): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154180619 | A | ACATTTTT others(3163): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0005 | a0005c0008 | a0005c0008t0014 | a0005c0008t0014g0122 | 1 | 283 | 0.0035 | 3170 | c.148 others(3189): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154180619 | A | ACATTTTT others(3163): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0133 | 1 | 283 | 0.0035 | 3170 | c.148 others(3189): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154180619 | A | ACATTTTT others(3163): Show |
intron_variant | MODIFIER | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
a0002 | a0002c0002a0002c0003 | a0002c0002t0051a0002c0003t0018a0002c0003t0044others(2): Show | a0002c0002t0051g0033a0002c0003t0018g0092a0002c0003t0044g0094others(2): Show | 5 | 283 | 0.0177 | 3170 | c.148 others(3189): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | TogoVar | ||||||
EHMT1_chr9_137614005_137841127 | 137716360 | T | TGTGGTGG others(3163): Show |
intron_variant | MODIFIER | HG01516.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107 | 1 | 170 | 0.0059 | 3170 | c.86- others(3183): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3163): Show |
intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0012 | a0001c0012t0001 | a0001c0012t0001g0027 | 1 | 264 | 0.0038 | 3170 | c.400 others(3189): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3163): Show |
intron_variant | MODIFIER | NA19056.hp2 | a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0174 | 1 | 264 | 0.0038 | 3170 | c.400 others(3189): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3163): Show |
intron_variant | MODIFIER | NA18612.hp1 NA18612.hp2 |
a0001a0009 | a0001c0001a0009c0024 | a0001c0001t0001a0009c0024t0003 | a0001c0001t0001g0225a0009c0024t0003g0110 | 2 | 264 | 0.0076 | 3170 | c.400 others(3189): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
HHAT_chr1_210323902_210681290 | 210653965 | G | GGAATAGT others(3163): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0213 | 1 | 268 | 0.0037 | 3170 | c.139 others(3191): Show |
HHAT | ENSG00000054392.13 | transcript | ENST00000261458.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF9_chr1_149047186_149108551 | 149060900 | C | AACACACA others(3163): Show |
intron_variant | MODIFIER | NA19091.hp1 | a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0078 | 1 | 344 | 0.0029 | 3170 | c.230 others(3187): Show |
NBPF9 | ENSG00000269713.9 | transcript | ENST00000698832.1 | protein_coding | 23/29 | chr1 | TogoVar | ||||||
PTGR1_chr9_111557567_111604647 | 111578316 | T | TTATTTCT others(3163): Show |
intron_variant | MODIFIER | NA19082.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0264 | 1 | 408 | 0.0025 | 3170 | c.651 others(3185): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | TogoVar | ||||||
SLC35F3_chr1_233899676_234329511 | 234207442 | T | TCCTTCTT others(3163): Show |
intron_variant | MODIFIER | HG01516.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0103 | 1 | 158 | 0.0063 | 3170 | c.284 others(3189): Show |
SLC35F3 | ENSG00000183780.13 | transcript | ENST00000366618.8 | protein_coding | 2/7 | chr1 | TogoVar |