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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
BAZ2B_chr2_159313979_159621548 | 159392994 | A | AAAGTATA others(6608): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0008 | a0001c0008t0002 | a0001c0008t0002g0159 | 1 | 205 | 0.0049 | 6615 | c.307 others(6634): Show |
BAZ2B | ENSG00000123636.19 | transcript | ENST00000392783.7 | protein_coding | 20/36 | chr2 | TogoVar | |||||||
CSHL1_chr17_63904608_63916258 | 63915020 | G | GCCTTTAT others(6609): Show |
upstream_gene_variant | MODIFIER | HG02683.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0034 | 1 | 436 | 0.0023 | 6616 | c.-38 others(6627): Show |
CSHL1 | ENSG00000204414.14 | transcript | ENST00000309894.6 | protein_coding | 3763 | chr17 | TogoVar | |||||||
GH1_chr17_63912203_63923839 | 63915020 | G | GCCTTTAT others(6609): Show |
downstream_gene_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 417 | 0.0024 | 6616 | c.*22 others(6627): Show |
GH1 | ENSG00000259384.7 | transcript | ENST00000323322.10 | protein_coding | 2182 | chr17 | TogoVar | |||||||
BAZ2B_chr2_159313979_159621548 | 159392994 | A | AAAGTATA others(6611): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0008 | a0001c0008t0002 | a0001c0008t0002g0179 | 1 | 205 | 0.0049 | 6618 | c.307 others(6637): Show |
BAZ2B | ENSG00000123636.19 | transcript | ENST00000392783.7 | protein_coding | 20/36 | chr2 | TogoVar | |||||||
BAZ2B_chr2_159313979_159621548 | 159392994 | A | AAAGTATA others(6611): Show |
intron_variant | MODIFIER | HG01168.hp2 HG03209.hp2 HG04204.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0007 | a0001c0001t0002a0001c0008t0001a0002c0007t0002 | a0001c0001t0002g0148 a0001c0008t0001g0035 a0001c0008t0001g0061 others(1): Show |
4 | 208 | 0.0192 | 6618 | c.307 others(6637): Show |
BAZ2B | ENSG00000123636.19 | transcript | ENST00000392783.7 | protein_coding | 20/36 | chr2 | TogoVar | |||||||
BAZ2B_chr2_159313979_159621548 | 159392994 | A | AAAGTATA others(6611): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 205 | 0.0049 | 6618 | c.307 others(6637): Show |
BAZ2B | ENSG00000123636.19 | transcript | ENST00000392783.7 | protein_coding | 20/36 | chr2 | TogoVar | |||||||
DOK7_chr4_3458306_3499482 | 3472472 | C | CTAGGTGG others(6611): Show |
intron_variant | MODIFIER | NA18962.hp2 | a0004 | a0004c0004 | a0004c0004t0006 | a0004c0004t0006g0164 | 1 | 368 | 0.0027 | 6618 | c.101 others(6633): Show |
DOK7 | ENSG00000175920.18 | transcript | ENST00000340083.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
BAZ2B_chr2_159313979_159621548 | 159392994 | A | AAAGTATA others(6613): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0002 | a0002c0007 | a0002c0007t0001 | a0002c0007t0001g0045 | 1 | 205 | 0.0049 | 6620 | c.307 others(6639): Show |
BAZ2B | ENSG00000123636.19 | transcript | ENST00000392783.7 | protein_coding | 20/36 | chr2 | TogoVar | |||||||
DOK7_chr4_3458306_3499482 | 3472472 | C | CTAGGTGG others(6614): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0004 | a0004c0004 | a0004c0004t0006 | a0004c0004t0006g0236 | 1 | 368 | 0.0027 | 6621 | c.101 others(6636): Show |
DOK7 | ENSG00000175920.18 | transcript | ENST00000340083.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
DOK7_chr4_3458306_3499482 | 3472472 | C | CTAGGTGG others(6614): Show |
intron_variant | MODIFIER | HG02129.hp1 | a0004 | a0004c0004 | a0004c0004t0006 | a0004c0004t0006g0167 | 1 | 368 | 0.0027 | 6621 | c.101 others(6636): Show |
DOK7 | ENSG00000175920.18 | transcript | ENST00000340083.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
RPH3AL_chr17_207389_357807 | 304161 | G | GGTGGGGA others(6614): Show |
intron_variant | MODIFIER | NA19074.hp2 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0006 | 1 | 102 | 0.0098 | 6621 | c.351 others(6640): Show |
RPH3AL | ENSG00000181031.16 | transcript | ENST00000331302.12 | protein_coding | 5/9 | chr17 | TogoVar | |||||||
DOK7_chr4_3458306_3499482 | 3472472 | C | CTAGGTGG others(6615): Show |
intron_variant | MODIFIER | HG02165.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0163 | 1 | 368 | 0.0027 | 6622 | c.101 others(6637): Show |
DOK7 | ENSG00000175920.18 | transcript | ENST00000340083.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
DOK7_chr4_3458306_3499482 | 3472472 | C | CTAGGTGG others(6615): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0004 | a0004c0007 | a0004c0007t0022 | a0004c0007t0022g0238 | 1 | 368 | 0.0027 | 6622 | c.101 others(6637): Show |
DOK7 | ENSG00000175920.18 | transcript | ENST00000340083.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
DOK7_chr4_3458306_3499482 | 3472472 | C | CTAGGTGG others(6616): Show |
intron_variant | MODIFIER | HG00597.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0241 | 1 | 368 | 0.0027 | 6623 | c.101 others(6638): Show |
DOK7 | ENSG00000175920.18 | transcript | ENST00000340083.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
RPH3AL_chr17_207389_357807 | 356432 | C | CCACACTT others(6618): Show |
upstream_gene_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0061 | 1 | 113 | 0.0088 | 6625 | c.-39 others(6636): Show |
RPH3AL | ENSG00000181031.16 | transcript | ENST00000331302.12 | protein_coding | 3626 | chr17 | TogoVar | |||||||
FOXK2_chr17_82514732_82609602 | 82586547 | G | GCCGGGGG others(6623): Show |
intron_variant | MODIFIER | HG01258.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0082 | 1 | 277 | 0.0036 | 6630 | c.157 others(6647): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
CLPTM1L_chr5_1312752_1350099 | 1333699 | A | TGAGGATA others(6624): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0158 | 1 | 299 | 0.0033 | 6631 | c.891 others(6646): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
ZFPM1_chr16_88448280_88542031 | 88501629 | G | GTGCGTGG others(6626): Show |
intron_variant | MODIFIER | HG02738.hp1 | a0008 | a0008c0041 | a0008c0041t0050 | a0008c0041t0050g0155 | 1 | 290 | 0.0034 | 6633 | c.268 others(6652): Show |
ZFPM1 | ENSG00000179588.9 | transcript | ENST00000319555.8 | protein_coding | 3/9 | chr16 | TogoVar | |||||||
EHMT1_chr9_137614005_137841127 | 137716460 | T | TGGGGGAG others(6631): Show |
intron_variant | MODIFIER | NA19079.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0033 | 1 | 129 | 0.0078 | 6638 | c.86- others(6651): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
ZFPM1_chr16_88448280_88542031 | 88501580 | G | GTGGGTGC others(6632): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0002 | a0002c0011 | a0002c0011t0007 | a0002c0011t0007g0015 | 1 | 248 | 0.0040 | 6639 | c.268 others(6658): Show |
ZFPM1 | ENSG00000179588.9 | transcript | ENST00000319555.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABR_chr17_998519_1184981 | 1065227 | C | TTGTTATG others(6639): Show |
intron_variant | MODIFIER | HG02071.hp1 HG02135.hp1 HG02135.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0007a0001c0001t0033 | a0001c0001t0006g0055 a0001c0001t0007g0334 a0001c0001t0033g0265 |
3 | 213 | 0.0141 | 6646 | c.118 others(6665): Show |
ABR | ENSG00000159842.16 | transcript | ENST00000302538.10 | protein_coding | 10/22 | chr17 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693738 | T | TCCACCAC others(6648): Show |
downstream_gene_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 292 | 0.0034 | 6655 | c.*67 others(6666): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4908 | chr20 | TogoVar | |||||||
FOXK2_chr17_82514732_82609602 | 82586502 | G | TGGGGGAA others(6657): Show |
intron_variant | MODIFIER | NA19074.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 | 1 | 284 | 0.0035 | 6664 | c.157 others(6681): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | chr17 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(6661): Show |
intron_variant | MODIFIER | HG02602.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0084 | 1 | 55 | 0.0182 | 6668 | c.891 others(6683): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
FOXK2_chr17_82514732_82609602 | 82586551 | A | AGGGGAAA others(6661): Show |
intron_variant | MODIFIER | HG00639.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0167 | 1 | 172 | 0.0058 | 6668 | c.157 others(6685): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
LRRC27_chr10_132327193_132386508 | 132364375 | A | ACGCTTAC others(6666): Show |
intron_variant | MODIFIER | HG03017.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0218 | 1 | 259 | 0.0039 | 6673 | c.129 others(6692): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
SERINC2_chr1_31408213_31439678 | 31432102 | C | CAGGGTGG others(6671): Show |
intron_variant | MODIFIER | NA19005.hp1 | a0002 | a0002c0002 | a0002c0002t0006 | a0002c0002t0006g0306 | 1 | 182 | 0.0055 | 6678 | c.101 others(6695): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
DCLK1_chr13_35763652_36136382 | 35958284 | G | GCTATAAC others(6672): Show |
intron_variant | MODIFIER | HG01433.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0062 | 1 | 83 | 0.0120 | 6679 | c.724 others(6698): Show |
DCLK1 | ENSG00000133083.15 | transcript | ENST00000360631.8 | protein_coding | 3/16 | chr13 | TogoVar | |||||||
LRRC27_chr10_132327193_132386508 | 132364472 | T | TACACCCA others(6677): Show |
intron_variant | MODIFIER | NA19010.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0196 | 1 | 216 | 0.0046 | 6684 | c.129 others(6701): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
CACNA1C_chr12_2047987_2702950 | 2256047 | C | CTTTACAA others(6683): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0002 | a0002c0013 | a0002c0013t0016 | a0002c0013t0016g0017 | 1 | 2 | 0.5000 | 6690 | c.477 others(6711): Show |
CACNA1C | ENSG00000151067.23 | transcript | ENST00000399603.6 | protein_coding | 3/46 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
EHMT1_chr9_137614005_137841127 | 137716460 | T | TGGGGGAG others(6684): Show |
intron_variant | MODIFIER | HG02293.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0019 | 1 | 129 | 0.0078 | 6691 | c.86- others(6704): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
ABR_chr17_998519_1184981 | 1065276 | C | TGTGAACT others(6687): Show |
intron_variant | MODIFIER | HG00642.hp2 HG01070.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | 318 | 0.0063 | 6694 | c.118 others(6713): Show |
ABR | ENSG00000159842.16 | transcript | ENST00000302538.10 | protein_coding | 10/22 | chr17 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(6694): Show |
intron_variant | MODIFIER | HG02083.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0145 | 1 | 55 | 0.0182 | 6701 | c.891 others(6716): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
DDX60_chr4_168211294_168323752 | 168243865 | T | TAACAATA others(6697): Show |
intron_variant | MODIFIER | HG01168.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0224 | 1 | 263 | 0.0038 | 6704 | c.416 others(6723): Show |
DDX60 | ENSG00000137628.18 | transcript | ENST00000393743.8 | protein_coding | 30/37 | chr4 | TogoVar | |||||||
LRRC27_chr10_132327193_132386508 | 132364519 | G | GCACTTAC others(6697): Show |
intron_variant | MODIFIER | NA19009.hp1 | a0001 | a0001c0002 | a0001c0002t0019 | a0001c0002t0019g0237 | 1 | 207 | 0.0048 | 6704 | c.129 others(6721): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
DDX60_chr4_168211294_168323752 | 168243865 | T | TAACAATA others(6698): Show |
intron_variant | MODIFIER | HG01169.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0225 | 1 | 263 | 0.0038 | 6705 | c.416 others(6724): Show |
DDX60 | ENSG00000137628.18 | transcript | ENST00000393743.8 | protein_coding | 30/37 | chr4 | TogoVar | |||||||
HTR2C_chrX_114579086_114915061 | 114644568 | T | TTATAATC others(6698): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0036 | 1 | 173 | 0.0058 | 6705 | c.-80 others(6724): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
DDX60_chr4_168211294_168323752 | 168243865 | T | TAACAATA others(6699): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0229 | 1 | 263 | 0.0038 | 6706 | c.416 others(6725): Show |
DDX60 | ENSG00000137628.18 | transcript | ENST00000393743.8 | protein_coding | 30/37 | chr4 | TogoVar | |||||||
HTR2C_chrX_114579086_114915061 | 114644568 | T | TTATAATC others(6700): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0037 | 1 | 173 | 0.0058 | 6707 | c.-80 others(6726): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
DDX60_chr4_168211294_168323752 | 168243865 | T | TAACAATA others(6701): Show |
intron_variant | MODIFIER | HG04228.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0242 | 1 | 263 | 0.0038 | 6708 | c.416 others(6727): Show |
DDX60 | ENSG00000137628.18 | transcript | ENST00000393743.8 | protein_coding | 30/37 | chr4 | TogoVar | |||||||
FAM120B_chr6_170301758_170412067 | 170398553 | A | AAAGGTAG others(6710): Show |
intron_variant | MODIFIER | HG03710.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0198 | 1 | 273 | 0.0037 | 6717 | c.269 others(6736): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
CACNA1C_chr12_2047987_2702950 | 2256047 | C | CTTTACAA others(6713): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0032 | a0001c0032t0031 | a0001c0032t0031g0103 | 1 | 2 | 0.5000 | 6720 | c.477 others(6741): Show |
CACNA1C | ENSG00000151067.23 | transcript | ENST00000399603.6 | protein_coding | 3/46 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CACNA1C_chr12_2047987_2702950 | 2256047 | C | CTTTACAA others(6713): Show |
intron_variant | MODIFIER | HG02970.hp2 HG03540.hp2 |
a0001a0002 | a0001c0003a0002c0013 | a0001c0003t0001a0002c0013t0035 | a0001c0003t0001g0009 a0002c0013t0035g0019 |
2 | 3 | 0.6667 | 6720 | c.477 others(6741): Show |
CACNA1C | ENSG00000151067.23 | transcript | ENST00000399603.6 | protein_coding | 3/46 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NAALADL2_chr3_174854334_175815548 | 175382586 | G | GATTTTAA others(6715): Show |
intron_variant | MODIFIER | HG02451.hp2 | a0013 | a0013c0023 | a0013c0023t0001 | a0013c0023t0001g0037 | 1 | 43 | 0.0233 | 6722 | c.109 others(6743): Show |
NAALADL2 | ENSG00000177694.16 | transcript | ENST00000454872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
FOXK2_chr17_82514732_82609602 | 82586500 | C | CGGGGGGG others(6716): Show |
intron_variant | MODIFIER | NA19081.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0300 | 1 | 229 | 0.0044 | 6723 | c.157 others(6740): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
FOXK2_chr17_82514732_82609602 | 82586503 | G | GGGGGAAA others(6717): Show |
intron_variant | MODIFIER | HG00140.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0193 | 1 | 234 | 0.0043 | 6724 | c.157 others(6741): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
PRIM2_chr6_57312630_57651850 | 57444882 | T | TGGGGTGG others(6717): Show |
intron_variant | MODIFIER | HG01358.hp1 | a0002 | a0002c0004 | a0002c0004t0004 | a0002c0004t0004g0007 | 1 | 296 | 0.0034 | 6724 | c.694 others(6743): Show |
PRIM2 | ENSG00000146143.19 | transcript | ENST00000615550.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
NAALADL2_chr3_174854334_175815548 | 175382586 | G | GATTTTAA others(6718): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0020 | 1 | 43 | 0.0233 | 6725 | c.109 others(6746): Show |
NAALADL2 | ENSG00000177694.16 | transcript | ENST00000454872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
NAALADL2_chr3_174854334_175815548 | 175382586 | G | GATTTTAA others(6718): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0012 | a0012c0017 | a0012c0017t0006 | a0012c0017t0006g0025 | 1 | 43 | 0.0233 | 6725 | c.109 others(6746): Show |
NAALADL2 | ENSG00000177694.16 | transcript | ENST00000454872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
NAALADL2_chr3_174854334_175815548 | 175382586 | G | GATTTTAA others(6718): Show |
intron_variant | MODIFIER | HG00639.hp2 | a0005 | a0005c0006 | a0005c0006t0015 | a0005c0006t0015g0013 | 1 | 43 | 0.0233 | 6725 | c.109 others(6746): Show |
NAALADL2 | ENSG00000177694.16 | transcript | ENST00000454872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |