view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
EHMT1_chr9_137614005_137841127 | 137716102 | G | GTTGGTGT others(3818): Show |
intron_variant | MODIFIER | HG03490.hp1 HG03492.hp1 |
a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0011a0001c0005t0001g0012 | 2 | 170 | 0.0118 | 3825 | c.86- others(3838): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | chr9 | TogoVar | |||||||
FMN2_chr1_240086883_240480187 | 240185119 | C | CCCCCTTC others(3818): Show |
intron_variant | MODIFIER | HG01081.hp1 | a0071 | a0071c0123 | a0071c0123t0001 | a0071c0123t0001g0077 | 1 | 174 | 0.0058 | 3825 | c.193 others(3844): Show |
FMN2 | ENSG00000155816.21 | transcript | ENST00000319653.14 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SERINC2_chr1_31408213_31439678 | 31431776 | A | AATAGGGT others(3818): Show |
intron_variant | MODIFIER | HG01952.hp1 | a0001 | a0001c0005 | a0001c0005t0002 | a0001c0005t0002g0059 | 1 | 376 | 0.0027 | 3825 | c.101 others(3844): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150585 | T | TACCACAC others(3820): Show |
intron_variant | MODIFIER | HG00140.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0245 | 1 | 294 | 0.0034 | 3827 | c.902 others(3842): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
DOCK1_chr10_126900428_127457516 | 126948274 | T | TTGGTGAT others(3821): Show |
intron_variant | MODIFIER | HG00423.hp1 | a0001 | a0001c0002 | a0001c0002t0008 | a0001c0002t0008g0099 | 1 | 136 | 0.0074 | 3828 | c.47- others(3845): Show |
DOCK1 | ENSG00000150760.13 | transcript | ENST00000623213.2 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
FOXK2_chr17_82514732_82609602 | 82586503 | G | GGGGGAAA others(3821): Show |
intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0134 | 1 | 308 | 0.0033 | 3828 | c.157 others(3845): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
HHAT_chr1_210323902_210681290 | 210653965 | G | GGAATAGT others(3821): Show |
intron_variant | MODIFIER | HG01981.hp2 NA20300.hp2 |
a0001a0003 | a0001c0002a0003c0004 | a0001c0002t0006a0003c0004t0006 | a0001c0002t0006g0042a0003c0004t0006g0136 | 2 | 268 | 0.0075 | 3828 | c.139 others(3849): Show |
HHAT | ENSG00000054392.13 | transcript | ENST00000261458.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150672 | A | ACACCACA others(3821): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0084 | 1 | 294 | 0.0034 | 3828 | c.902 others(3843): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | TogoVar | |||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(3821): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0029 | a0029c0028 | a0029c0028t0001 | a0029c0028t0001g0221 | 1 | 282 | 0.0036 | 3828 | c.299 others(3843): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
SLC38A10_chr17_81239811_81300307 | 81249456 | G | GAGGAGGG others(3821): Show |
intron_variant | MODIFIER | HG03491.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0148 | 1 | 214 | 0.0047 | 3828 | c.206 others(3847): Show |
SLC38A10 | ENSG00000157637.13 | transcript | ENST00000374759.8 | protein_coding | 14/15 | chr17 | TogoVar | |||||||
TAB1_chr22_39394780_39436882 | 39423757 | G | GTAGCATA others(3821): Show |
intron_variant | MODIFIER | NA19066.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0273 | 1 | 312 | 0.0032 | 3828 | c.921 others(3845): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3821): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02280.hp1 HG02723.hp1 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266 | 3 | 268 | 0.0112 | 3828 | c.186 others(3845): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3822): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0009 | a0001c0009t0007 | a0001c0009t0007g0264 | 1 | 268 | 0.0037 | 3829 | c.186 others(3846): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3822): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0132 | 1 | 268 | 0.0037 | 3829 | c.186 others(3846): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(3824): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0028 | a0028c0032 | a0028c0032t0001 | a0028c0032t0001g0235 | 1 | 282 | 0.0036 | 3831 | c.299 others(3846): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
LRRC27_chr10_132327193_132386508 | 132364368 | T | TACACCCA others(3825): Show |
intron_variant | MODIFIER | NA19086.hp2 | a0001 | a0001c0002 | a0001c0002t0020 | a0001c0002t0020g0270 | 1 | 290 | 0.0035 | 3832 | c.129 others(3851): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
UTRN_chr6_144280335_144858034 | 144694251 | T | TGGATTAG others(3825): Show |
intron_variant | MODIFIER | NA19074.hp1 | a0002 | a0002c0005 | a0002c0005t0007 | a0002c0005t0007g0098 | 1 | 128 | 0.0078 | 3832 | c.765 others(3851): Show |
UTRN | ENSG00000152818.20 | transcript | ENST00000367545.8 | protein_coding | 52/74 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
UTRN_chr6_144280335_144858034 | 144694251 | T | TGGATTAG others(3825): Show |
intron_variant | MODIFIER | HG02055.hp1 | a0002 | a0002c0057 | a0002c0057t0012 | a0002c0057t0012g0063 | 1 | 128 | 0.0078 | 3832 | c.765 others(3851): Show |
UTRN | ENSG00000152818.20 | transcript | ENST00000367545.8 | protein_coding | 52/74 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
UTRN_chr6_144280335_144858034 | 144694251 | T | TGGATTAG others(3825): Show |
intron_variant | MODIFIER | NA18954.hp2 | a0002 | a0002c0024 | a0002c0024t0003 | a0002c0024t0003g0097 | 1 | 128 | 0.0078 | 3832 | c.765 others(3851): Show |
UTRN | ENSG00000152818.20 | transcript | ENST00000367545.8 | protein_coding | 52/74 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
IFNAR1_chr21_33319970_33364864 | 33322909 | T | TAATATAT others(3826): Show |
upstream_gene_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 323 | 0.0031 | 3833 | c.-21 others(3844): Show |
IFNAR1 | ENSG00000142166.15 | transcript | ENST00000270139.8 | protein_coding | 2060 | chr21 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(3826): Show |
upstream_gene_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0063 | 1 | 251 | 0.0040 | 3833 | c.-45 others(3842): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
RAB3B_chr1_51902956_51995700 | 51906869 | A | AAGGGAAG others(3826): Show |
downstream_gene_variant | MODIFIER | HG00558.hp1 | a0001 | a0001c0001 | a0001c0001t0045 | a0001c0001t0045g0061 | 1 | 62 | 0.0161 | 3833 | c.*13 others(3846): Show |
RAB3B | ENSG00000169213.7 | transcript | ENST00000371655.4 | protein_coding | 1086 | chr1 | TogoVar | |||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTGGAGAC others(3826): Show |
intron_variant | MODIFIER | HG00642.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0179 | 1 | 268 | 0.0037 | 3833 | c.186 others(3850): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3477303 | G | GTCACCCC others(3827): Show |
intron_variant | MODIFIER | HG02273.hp2 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0165 | 1 | 334 | 0.0030 | 3834 | c.147 others(3851): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
EHMT1_chr9_137614005_137841127 | 137716477 | T | TTGGTGTC others(3827): Show |
intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0117 | 1 | 170 | 0.0059 | 3834 | c.86- others(3847): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
AP2A2_chr11_920870_1017240 | 965240 | C | CGGGAAAT others(3828): Show |
intron_variant | MODIFIER | HG02132.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0108 | 1 | 268 | 0.0037 | 3835 | c.137 others(3852): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
C22orf39_chr22_19435886_19452711 | 19448418 | T | TACCTTAT others(3828): Show |
upstream_gene_variant | MODIFIER | NA18966.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002 | 1 | 420 | 0.0024 | 3835 | c.-73 others(3844): Show |
C22orf39 | ENSG00000242259.9 | transcript | ENST00000399562.9 | protein_coding | 708 | chr22 | TogoVar | |||||||
DOCK1_chr10_126900428_127457516 | 126948184 | A | ATGGTGGT others(3828): Show |
intron_variant | MODIFIER | HG02280.hp2 HG03041.hp1 |
a0001a0003 | a0001c0001a0003c0019 | a0001c0001t0002a0003c0019t0003 | a0001c0001t0002g0128a0003c0019t0003g0051 | 2 | 136 | 0.0147 | 3835 | c.47- others(3852): Show |
DOCK1 | ENSG00000150760.13 | transcript | ENST00000623213.2 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3828): Show |
intron_variant | MODIFIER | NA18957.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0137 | 1 | 268 | 0.0037 | 3835 | c.186 others(3852): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3828): Show |
intron_variant | MODIFIER | HG01070.hp1 HG03704.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0074a0001c0001t0001g0100 | 2 | 268 | 0.0075 | 3835 | c.186 others(3852): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
UFD1_chr22_19444911_19484193 | 19448418 | T | TACCTTAT others(3828): Show |
downstream_gene_variant | MODIFIER | NA18966.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0090 | 1 | 402 | 0.0025 | 3835 | c.*22 others(3846): Show |
UFD1 | ENSG00000070010.19 | transcript | ENST00000263202.15 | protein_coding | 1492 | chr22 | TogoVar | |||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3829): Show |
intron_variant | MODIFIER | NA19057.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 268 | 0.0037 | 3836 | c.186 others(3853): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3829): Show |
intron_variant | MODIFIER | HG02572.hp2 HG02630.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0014 | a0001c0001t0003g0188a0001c0001t0014g0018 | 2 | 268 | 0.0075 | 3836 | c.186 others(3853): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3829): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(37): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(6): Show | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(37): Show | 40 | 268 | 0.1493 | 3836 | c.186 others(3853): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3829): Show |
intron_variant | MODIFIER | HG01081.hp1 HG01123.hp1 HG01261.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0003g0104others(2): Show | 5 | 268 | 0.0187 | 3836 | c.186 others(3853): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTGGAGAC others(3829): Show |
intron_variant | MODIFIER | NA18954.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0158 | 1 | 268 | 0.0037 | 3836 | c.186 others(3853): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3830): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(37): Show |
a0001a0003 | a0001c0001a0001c0003a0003c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(6): Show | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0037others(37): Show | 40 | 268 | 0.1493 | 3837 | c.186 others(3854): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3830): Show |
intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0071 | 1 | 268 | 0.0037 | 3837 | c.186 others(3854): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3830): Show |
intron_variant | MODIFIER | HG00140.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0015 | 1 | 268 | 0.0037 | 3837 | c.186 others(3854): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3830): Show |
intron_variant | MODIFIER | HG00741.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0109 | 1 | 268 | 0.0037 | 3837 | c.186 others(3854): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3830): Show |
intron_variant | MODIFIER | HG01256.hp2 HG01258.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | 268 | 0.0075 | 3837 | c.186 others(3854): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTGGAGAC others(3830): Show |
intron_variant | MODIFIER | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(19): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0002c0002t0010 | a0001c0001t0004g0011a0001c0001t0004g0027a0001c0001t0004g0038others(19): Show | 22 | 268 | 0.0821 | 3837 | c.186 others(3854): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTGGAGAC others(3830): Show |
intron_variant | MODIFIER | HG02027.hp1 NA18995.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0019 | a0001c0001t0004g0180a0001c0001t0019g0157 | 2 | 268 | 0.0075 | 3837 | c.186 others(3854): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTGGAGAC others(3830): Show |
intron_variant | MODIFIER | NA18943.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0181 | 1 | 268 | 0.0037 | 3837 | c.186 others(3854): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTGGAGAC others(3830): Show |
intron_variant | MODIFIER | HG01361.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0007 | 1 | 268 | 0.0037 | 3837 | c.186 others(3854): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
FBXL14_chr12_1560993_1599581 | 1574377 | G | GGTGTGGA others(3831): Show |
intron_variant | MODIFIER | NA18991.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0322 | 1 | 418 | 0.0024 | 3838 | c.119 others(3857): Show |
FBXL14 | ENSG00000171823.7 | transcript | ENST00000339235.4 | protein_coding | 1/1 | chr12 | TogoVar | |||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3831): Show |
intron_variant | MODIFIER | NA19012.hp1 | a0005 | a0005c0008 | a0005c0008t0001 | a0005c0008t0001g0242 | 1 | 268 | 0.0037 | 3838 | c.186 others(3855): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3831): Show |
intron_variant | MODIFIER | HG00544.hp2 HG01099.hp2 HG03139.hp1 others(10): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(2): Show | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0073others(10): Show | 13 | 268 | 0.0485 | 3838 | c.186 others(3855): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3831): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0130a0001c0001t0013g0131a0001c0001t0013g0152 | 3 | 268 | 0.0112 | 3838 | c.186 others(3855): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TBCE_chr1_235362427_235457443 | 235409824 | T | TTCGAGAC others(3831): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01169.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | 268 | 0.0075 | 3838 | c.186 others(3855): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |