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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SMOC2_chr6_168436184_168672992 | 168560941 | TGGAGGAG others(1397): Show |
T | intron_variant | MODIFIER | NA18971.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0105 | 1 | 180 | 0.0056 | -1404 | c.637 others(19): Show |
SMOC2 | ENSG00000112562.20 | transcript | ENST00000356284.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
SMOC2_chr6_168436184_168672992 | 168561014 | GCCCTGAG others(1397): Show |
G | intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0038 | 1 | 180 | 0.0056 | -1404 | c.637 others(19): Show |
SMOC2 | ENSG00000112562.20 | transcript | ENST00000356284.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
SNTG2_chr2_945849_1372613 | 1106794 | GAGTGGAC others(1397): Show |
G | intron_variant | MODIFIER | HG01496.hp2 HG01975.hp1 HG02976.hp2 others(3): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0003a0003c0008others(1): Show | a0001c0001t0001a0002c0003t0001a0003c0008t0001others(1): Show | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0067others(3): Show | 6 | 190 | 0.0316 | -1404 | c.325 others(17): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
EVI5_chr1_92503696_92790108 | 92719086 | ATGGATTC others(1396): Show |
A | intron_variant | MODIFIER | HG02145.hp2 HG02486.hp1 |
a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0053a0001c0001t0023g0054 | 2 | 168 | 0.0119 | -1403 | c.150 others(19): Show |
EVI5 | ENSG00000067208.17 | transcript | ENST00000684568.2 | protein_coding | 2/19 | chr1 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132148890 | ACCTCGGT others(1396): Show |
A | intron_variant | MODIFIER | NA19010.hp1 NA19083.hp2 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0093a0002c0002t0001g0097 | 2 | 294 | 0.0068 | -1403 | c.901 others(14): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NOC4L_chr12_132139457_132157468 | 132149045 | ACTCACAC others(1396): Show |
A | intron_variant | MODIFIER | HG03239.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0242 | 1 | 294 | 0.0034 | -1403 | c.901 others(15): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ADARB2_chr10_1172313_1742525 | 1188991 | CTCCAGGA others(1394): Show |
C | intron_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0002 | a0002c0002t0053 | a0002c0002t0053g0106 | 1 | 106 | 0.0094 | -1401 | c.186 others(19): Show |
ADARB2 | ENSG00000185736.16 | transcript | ENST00000381312.6 | protein_coding | 8/9 | chr10 | TogoVar | ||||||
BBOF1_chr14_74014349_74071092 | 74051137 | GGGAGGCT others(1394): Show |
G | intron_variant | MODIFIER | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
a0004 | a0004c0007 | a0004c0007t0003 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | 386 | 0.0078 | -1401 | c.128 others(18): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
CALD1_chr7_134774634_134975729 | 134857231 | CGATCTCG others(1394): Show |
C | intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0089 | 1 | 262 | 0.0038 | -1401 | c.-41 others(18): Show |
CALD1 | ENSG00000122786.20 | transcript | ENST00000361675.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
D2HGDH_chr2_241729630_241773811 | 241765457 | TGGGGAGA others(1394): Show |
T | intron_variant | MODIFIER | NA18969.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0113 | 1 | 412 | 0.0024 | -1401 | c.130 others(18): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
FNBP4_chr11_47711494_47772341 | 47740285 | TGCGCCTG others(1394): Show |
T | intron_variant | MODIFIER | HG02257.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0036a0001c0001t0001g0067a0001c0001t0001g0219others(2): Show | 5 | 350 | 0.0143 | -1401 | c.145 others(19): Show |
FNBP4 | ENSG00000109920.13 | transcript | ENST00000263773.10 | protein_coding | 8/16 | chr11 | TogoVar | ||||||
HIF3A_chr19_46292042_46348433 | 46314067 | TTGGGCTG others(1394): Show |
T | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(104): Show |
a0001a0002a0009others(1): Show | a0001c0001a0002c0002a0002c0004others(4): Show | a0001c0001t0008a0001c0001t0013a0001c0001t0027others(22): Show | a0001c0001t0008g0158a0001c0001t0008g0159a0001c0001t0013g0005others(103): Show | 107 | 418 | 0.2560 | -1401 | c.102 others(19): Show |
HIF3A | ENSG00000124440.16 | transcript | ENST00000377670.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
IL3RA_chrX_1331785_1387689 | 1371818 | CCTCCAGC others(1394): Show |
C | intron_variant | MODIFIER | HG03927.hp1 NA18943.hp1 |
a0001a0013 | a0001c0001a0013c0016 | a0001c0001t0001a0013c0016t0004 | a0001c0001t0001g0010a0013c0016t0004g0054 | 2 | 115 | 0.0174 | -1401 | c.874 others(17): Show |
IL3RA | ENSG00000185291.12 | transcript | ENST00000331035.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
IL3RA_chrX_1331785_1387689 | 1373093 | AGAGGAGA others(1394): Show |
A | intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0080 | 1 | 115 | 0.0087 | -1401 | c.875 others(17): Show |
IL3RA | ENSG00000185291.12 | transcript | ENST00000331035.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
LINGO2_chr9_27932617_29218601 | 28846388 | TTTTGCCA others(1394): Show |
T | intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0025 | a0001c0001t0025g0055 | 1 | 62 | 0.0161 | -1401 | c.-39 others(23): Show |
LINGO2 | ENSG00000174482.11 | transcript | ENST00000698399.1 | protein_coding | 2/6 | chr9 | TogoVar | ||||||
ASMT_chrX_1610059_1648081 | 1638675 | GTCCATCC others(1393): Show |
G | intron_variant | MODIFIER | HG01975.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0062 | 1 | 223 | 0.0045 | -1400 | c.910 others(17): Show |
ASMT | ENSG00000196433.13 | transcript | ENST00000381241.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ASMT_chrX_1610059_1648081 | 1638726 | TGATGGGG others(1393): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG01975.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0040a0001c0001t0001g0128 | 2 | 223 | 0.0090 | -1400 | c.910 others(17): Show |
ASMT | ENSG00000196433.13 | transcript | ENST00000381241.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ASMT_chrX_1610059_1648081 | 1639466 | ATGATGGG others(1393): Show |
A | intron_variant | MODIFIER | HG01070.hp2 HG02257.hp1 HG03486.hp1 others(4): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0016 | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(1): Show | a0001c0001t0001g0012a0001c0001t0001g0014a0002c0002t0001g0122others(4): Show | 7 | 223 | 0.0314 | -1400 | c.910 others(17): Show |
ASMT | ENSG00000196433.13 | transcript | ENST00000381241.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ASMT_chrX_1610059_1648081 | 1639498 | GTCCATCC others(1393): Show |
G | intron_variant | MODIFIER | HG00597.hp2 HG00741.hp2 HG01175.hp1 others(11): Show |
a0001a0002a0007 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0003t0001a0002c0002t0001others(1): Show | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0021others(11): Show | 14 | 223 | 0.0628 | -1400 | c.910 others(17): Show |
ASMT | ENSG00000196433.13 | transcript | ENST00000381241.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ASMT_chrX_1610059_1648081 | 1639553 | GGGGACAG others(1393): Show |
G | intron_variant | MODIFIER | NA18954.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0151 | 1 | 223 | 0.0045 | -1400 | c.910 others(17): Show |
ASMT | ENSG00000196433.13 | transcript | ENST00000381241.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
CYP4F11_chr19_15907377_15939529 | 15932529 | AGAATGAG others(1393): Show |
A | intron_variant | MODIFIER | NA18965.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0235 | 1 | 386 | 0.0026 | -1400 | c.198 others(16): Show |
CYP4F11 | ENSG00000171903.17 | transcript | ENST00000402119.9 | protein_coding | 1/11 | chr19 | TogoVar | ||||||
D2HGDH_chr2_241729630_241773811 | 241765305 | CTTGGGGA others(1393): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0026a0001c0027others(8): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0016others(18): Show | a0001c0001t0002g0010a0001c0001t0002g0030a0001c0001t0002g0033others(77): Show | 83 | 412 | 0.2015 | -1400 | c.130 others(18): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAD1L1_chr7_1810795_2237945 | 1990776 | CGAGCACC others(1393): Show |
C | intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0207 | 1 | 264 | 0.0038 | -1400 | c.141 others(20): Show |
MAD1L1 | ENSG00000002822.16 | transcript | ENST00000265854.12 | protein_coding | 14/18 | chr7 | TogoVar | ||||||
ANKRD30B_chr18_14743172_14859667 | 14856087 | CGGGCAGA others(1392): Show |
C | downstream_gene_variant | MODIFIER | HG03453.hp2 | a0013 | a0013c0017 | a0013c0017t0001 | a0013c0017t0001g0009 | 1 | 316 | 0.0032 | -1399 | c.*19 others(11): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1421 | chr18 | TogoVar | ||||||
ASMT_chrX_1610059_1648081 | 1637186 | GTCCTGTG others(1392): Show |
G | intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0022 | 1 | 223 | 0.0045 | -1399 | c.910 others(16): Show |
ASMT | ENSG00000196433.13 | transcript | ENST00000381241.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ASMT_chrX_1610059_1648081 | 1637201 | TCCATCCT others(1392): Show |
T | intron_variant | MODIFIER | HG02886.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0009 | 1 | 223 | 0.0045 | -1399 | c.910 others(16): Show |
ASMT | ENSG00000196433.13 | transcript | ENST00000381241.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
C2CD6_chr2_201482421_201624178 | 201508948 | TGCGAAAT others(1392): Show |
T | intron_variant | MODIFIER | HG02486.hp2 HG02615.hp2 HG02922.hp2 others(4): Show |
a0001a0002a0006others(1): Show | a0001c0001a0002c0007a0006c0009others(2): Show | a0001c0001t0001a0002c0007t0001a0006c0009t0001others(2): Show | a0001c0001t0001g0102a0002c0007t0001g0060a0006c0009t0001g0019others(4): Show | 7 | 270 | 0.0259 | -1399 | c.150 others(21): Show |
C2CD6 | ENSG00000155754.15 | transcript | ENST00000439140.6 | protein_coding | 13/15 | chr2 | TogoVar | ||||||
EXOC3_chr5_438176_472290 | 467405 | CCTCCTGG others(1392): Show |
C | downstream_gene_variant | MODIFIER | HG02132.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 | 1 | 418 | 0.0024 | -1399 | c.*50 others(10): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 116 | chr5 | TogoVar | ||||||
SLC9A3_chr5_465456_529449 | 467405 | CCTCCTGG others(1392): Show |
C | downstream_gene_variant | MODIFIER | HG02132.hp1 | a0001 | a0001c0001 | a0001c0001t0031 | a0001c0001t0031g0198 | 1 | 218 | 0.0046 | -1399 | c.*45 others(11): Show |
SLC9A3 | ENSG00000066230.12 | transcript | ENST00000264938.8 | protein_coding | 3050 | chr5 | TogoVar | ||||||
ASMT_chrX_1610059_1648081 | 1639397 | GTGTCCCA others(1391): Show |
G | intron_variant | MODIFIER | HG01516.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0199 | 1 | 223 | 0.0045 | -1398 | c.910 others(17): Show |
ASMT | ENSG00000196433.13 | transcript | ENST00000381241.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
HRNR_chr1_152207076_152229193 | 152218701 | GCTAGATC others(1391): Show |
G | disruptive_inframe_deletion | MODERATE | HG02145.hp2 | a0001 | a0001c0180 | a0001c0180t0001 | a0001c0180t0001g0071 | 1 | 418 | 0.0024 | -1398 | c.153 others(9): Show |
p.Ala others(13): Show |
HRNR | ENSG00000197915.7 | transcript | ENST00000368801.4 | protein_coding | 3/3 | 3003/9629 | 1530/8553 | 510/2850 | chr1 | TogoVar | ||
ARK2C_chr18_46329018_46468140 | 46397555 | TGAGGGTG others(1390): Show |
T | intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050 | 1 | 260 | 0.0039 | -1397 | c.62- others(17): Show |
ARK2C | ENSG00000141622.14 | transcript | ENST00000269439.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
DENND5B_chr12_31377226_31596136 | 31501293 | GCCATATG others(1390): Show |
G | intron_variant | MODIFIER | HG04228.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0255 | 1 | 308 | 0.0033 | -1397 | c.128 others(17): Show |
DENND5B | ENSG00000170456.16 | transcript | ENST00000389082.10 | protein_coding | 1/20 | chr12 | TogoVar | ||||||
P3H2_chr3_189951728_190125897 | 190121973 | ACCCAGCT others(1390): Show |
A | upstream_gene_variant | MODIFIER | HG02280.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(2): Show | a0001c0001t0001g0097a0001c0001t0003g0099a0001c0001t0007g0098others(3): Show | 6 | 304 | 0.0197 | -1397 | c.-26 others(11): Show |
P3H2 | ENSG00000090530.10 | transcript | ENST00000319332.10 | protein_coding | 1077 | chr3 | TogoVar | ||||||
PATJ_chr1_61737480_62168915 | 62157260 | GTTGCAGT others(1390): Show |
G | intron_variant | MODIFIER | HG00280.hp2 HG00642.hp2 HG01074.hp1 others(10): Show |
a0002a0003a0004others(6): Show | a0002c0049a0002c0106a0003c0003others(8): Show | a0002c0049t0004a0002c0106t0012a0003c0003t0004others(9): Show | a0002c0049t0004g0029a0002c0106t0012g0104a0003c0003t0004g0093others(10): Show | 13 | 158 | 0.0823 | -1397 | c.550 others(19): Show |
PATJ | ENSG00000132849.22 | transcript | ENST00000642238.2 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
TACC2_chr10_121984163_122259542 | 122121073 | TAATCCAC others(1390): Show |
T | intron_variant | MODIFIER | NA18980.hp2 | a0002 | a0002c0008 | a0002c0008t0003 | a0002c0008t0003g0082 | 1 | 306 | 0.0033 | -1397 | c.557 others(21): Show |
TACC2 | ENSG00000138162.19 | transcript | ENST00000369005.6 | protein_coding | 5/22 | chr10 | TogoVar | ||||||
TOR1AIP2_chr1_179834976_179882803 | 179837278 | GTCGCGCA others(1390): Show |
G | downstream_gene_variant | MODIFIER | HG01069.hp1 | a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0050 | 1 | 280 | 0.0036 | -1397 | c.*73 others(11): Show |
TOR1AIP2 | ENSG00000169905.13 | transcript | ENST00000609928.6 | protein_coding | 2697 | chr1 | TogoVar | ||||||
DLGAP2_chr8_732628_1713476 | 991175 | ACCCCCTG others(1389): Show |
A | intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0039 | 1 | 40 | 0.0250 | -1396 | c.73+ others(17): Show |
DLGAP2 | ENSG00000198010.13 | transcript | ENST00000637795.2 | protein_coding | 2/14 | chr8 | TogoVar | ||||||
IL3RA_chrX_1331785_1387689 | 1372307 | GGGAGAAT others(1389): Show |
G | intron_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0014 | 1 | 115 | 0.0087 | -1396 | c.875 others(17): Show |
IL3RA | ENSG00000185291.12 | transcript | ENST00000331035.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
THSD4_chr15_71110471_71788383 | 71589230 | TAAAGGAC others(1389): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(13): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(11): Show | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 16 | 116 | 0.1379 | -1396 | c.115 others(21): Show |
THSD4 | ENSG00000187720.15 | transcript | ENST00000261862.8 | protein_coding | 7/17 | chr15 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240977411 | TCTCTGGG others(1388): Show |
T | intron_variant | MODIFIER | HG03490.hp2 HG03492.hp1 HG03704.hp2 |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002 | a0002c0002t0001g0057a0002c0002t0002g0301a0002c0002t0002g0302 | 3 | 350 | 0.0086 | -1395 | c.440 others(19): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NRK_chrX_105817539_105963610 | 105887094 | ATTAAAAT others(1388): Show |
A | exon_loss_variant others(4): Show |
HIGH | HG01981.hp1 | a0011 | a0011c0006 | a0011c0006t0001 | a0011c0006t0001g0117 | 1 | 219 | 0.0046 | -1395 | c.253 others(15): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
GPC5_chr13_91393621_92872237 | 92592217 | GAGAATGG others(1387): Show |
G | intron_variant | MODIFIER | HG03486.hp1 | a0005 | a0005c0005 | a0005c0005t0002 | a0005c0005t0002g0035 | 1 | 42 | 0.0238 | -1394 | c.156 others(23): Show |
GPC5 | ENSG00000179399.16 | transcript | ENST00000377067.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
PPP1R9A_chr7_94902594_95301400 | 95071032 | ATCAAACT others(1386): Show |
A | intron_variant | MODIFIER | HG02523.hp1 | a0002 | a0002c0001 | a0002c0001t0004 | a0002c0001t0004g0140 | 1 | 290 | 0.0035 | -1393 | c.139 others(21): Show |
PPP1R9A | ENSG00000158528.12 | transcript | ENST00000433360.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
SPDYE3_chr7_100302702_100327196 | 100312496 | CAAAAAAA others(1386): Show |
C | exon_loss_variant others(4): Show |
HIGH | NA18953.hp2 | a0006 | a0006c0022 | a0006c0022t0005 | a0006c0022t0005g0043 | 1 | 344 | 0.0029 | -1393 | c.763 others(15): Show |
SPDYE3 | ENSG00000214300.7 | transcript | ENST00000332397.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
SPDYE3_chr7_100302702_100327196 | 100312524 | GAAAAAAG others(1386): Show |
G | exon_loss_variant others(4): Show |
HIGH | HG02723.hp1 NA19240.hp1 |
a0002 | a0002c0005 | a0002c0005t0004 | a0002c0005t0004g0045 | 2 | 344 | 0.0058 | -1393 | c.764 others(15): Show |
SPDYE3 | ENSG00000214300.7 | transcript | ENST00000332397.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
DOC2B_chr17_137789_186650 | 166829 | CATGGTCT others(1385): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(43): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(8): Show | a0001c0001t0001g0167a0001c0001t0001g0254a0001c0001t0002g0005others(39): Show | 46 | 339 | 0.1357 | -1392 | c.454 others(17): Show |
DOC2B | ENSG00000272636.5 | transcript | ENST00000613549.3 | protein_coding | 2/8 | chr17 | TogoVar | ||||||
SPDYE3_chr7_100302702_100327196 | 100313165 | ACGTAGGT others(1385): Show |
A | exon_loss_variant others(4): Show |
HIGH | HG01891.hp1 HG03453.hp2 |
a0002 | a0002c0006 | a0002c0006t0010 | a0002c0006t0010g0041 | 2 | 344 | 0.0058 | -1392 | c.982 others(14): Show |
SPDYE3 | ENSG00000214300.7 | transcript | ENST00000332397.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
SPDYE3_chr7_100302702_100327196 | 100313637 | GATTGCTT others(1385): Show |
G | exon_loss_variant others(4): Show |
HIGH | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
a0002a0003 | a0002c0004a0002c0006a0003c0012 | a0002c0004t0002a0002c0004t0005a0002c0004t0014others(2): Show | a0002c0004t0002g0008a0002c0004t0002g0044a0002c0004t0002g0185others(13): Show | 21 | 344 | 0.0611 | -1392 | c.982 others(16): Show |
SPDYE3 | ENSG00000214300.7 | transcript | ENST00000332397.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
C3orf20_chr3_14670141_14778036 | 14768046 | CCTGTAAC others(1383): Show |
C | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0121 | 1 | 380 | 0.0026 | -1390 | c.249 others(19): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |