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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NVL_chr1_224222345_224335172 | 224260513 | T | TCCAAAGT others(611): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143 | 1 | 284 | 0.0035 | 618 | c.218 others(637): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | TogoVar | ||||||
NXN_chr17_794310_984776 | 841443 | T | TCCCCCCG others(611): Show |
intron_variant | MODIFIER | HG01433.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0161 | 1 | 242 | 0.0041 | 618 | c.361 others(637): Show |
NXN | ENSG00000167693.17 | transcript | ENST00000336868.8 | protein_coding | 1/7 | chr17 | TogoVar | ||||||
NXN_chr17_794310_984776 | 841591 | A | AGCAGGTC others(611): Show |
intron_variant | MODIFIER | NA19000.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0123 | 1 | 242 | 0.0041 | 618 | c.361 others(637): Show |
NXN | ENSG00000167693.17 | transcript | ENST00000336868.8 | protein_coding | 1/7 | chr17 | TogoVar | ||||||
P2RX1_chr17_3891592_3921465 | 3899245 | G | GCCAGGCT others(611): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0143 | 1 | 378 | 0.0027 | 618 | c.876 others(633): Show |
P2RX1 | ENSG00000108405.4 | transcript | ENST00000225538.4 | protein_coding | 8/11 | chr17 | TogoVar | ||||||
PAX1_chr20_21700664_21723481 | 21721646 | T | TATGTATT others(611): Show |
downstream_gene_variant | MODIFIER | HG03942.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0001 | 1 | 400 | 0.0025 | 618 | c.*70 others(629): Show |
PAX1 | ENSG00000125813.15 | transcript | ENST00000613128.5 | protein_coding | 3166 | chr20 | TogoVar | ||||||
PCNT_chr21_46319156_46450769 | 46404022 | G | GTGTGTGT others(611): Show |
intron_variant | MODIFIER | HG02647.hp1 HG02895.hp2 HG02965.hp1 others(5): Show |
a0004 | a0004c0004 | a0004c0004t0001a0004c0004t0006 | a0004c0004t0001g0090a0004c0004t0001g0098a0004c0004t0001g0099others(5): Show | 8 | 332 | 0.0241 | 618 | c.511 others(637): Show |
PCNT | ENSG00000160299.19 | transcript | ENST00000359568.10 | protein_coding | 27/46 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
PGAP6_chr16_365788_386978 | 370341 | A | ACCCCCCC others(611): Show |
downstream_gene_variant | MODIFIER | NA18988.hp1 | a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0177 | 1 | 376 | 0.0027 | 618 | c.*16 others(629): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 446 | chr16 | TogoVar | ||||||
PRR22_chr19_5777960_5789746 | 5787180 | C | CGGTGGTG others(611): Show |
upstream_gene_variant | MODIFIER | HG01515.hp1 | a0012 | a0012c0015 | a0012c0015t0001 | a0012c0015t0001g0033 | 1 | 382 | 0.0026 | 618 | c.-25 others(629): Show |
PRR22 | ENSG00000212123.4 | transcript | ENST00000419421.3 | protein_coding | 2435 | chr19 | TogoVar | ||||||
PTPN4_chr2_119754922_119989899 | 119843893 | A | ACCTCCCG others(611): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0002 | a0002c0002 | a0002c0002t0016 | a0002c0002t0016g0242 | 1 | 252 | 0.0040 | 618 | c.139 others(637): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PTPN4_chr2_119754922_119989899 | 119843893 | A | ACCTCCCG others(611): Show |
intron_variant | MODIFIER | HG01070.hp1 HG01255.hp2 HG01257.hp1 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007a0001c0001t0014others(5): Show | a0001c0001t0002g0167a0001c0001t0002g0176a0001c0001t0002g0178others(16): Show | 19 | 252 | 0.0754 | 618 | c.139 others(637): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PTPN4_chr2_119754922_119989899 | 119843893 | A | ACCTCCCG others(611): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0153 | 1 | 252 | 0.0040 | 618 | c.139 others(637): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PTPN4_chr2_119754922_119989899 | 119843893 | A | ACCTCCCG others(611): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0159 | 1 | 252 | 0.0040 | 618 | c.139 others(637): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PTPN4_chr2_119754922_119989899 | 119843893 | A | ACCTCCCG others(611): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0232 | 1 | 252 | 0.0040 | 618 | c.139 others(637): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PTPN4_chr2_119754922_119989899 | 119843893 | A | ACCTCCCG others(611): Show |
intron_variant | MODIFIER | HG01358.hp2 HG01928.hp2 HG01981.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0019 | a0001c0001t0002g0175a0001c0001t0002g0230a0001c0001t0019g0207 | 3 | 252 | 0.0119 | 618 | c.139 others(637): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PTPN4_chr2_119754922_119989899 | 119843893 | A | ACCTCCCG others(611): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0163 | 1 | 252 | 0.0040 | 618 | c.139 others(637): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PTPRT_chr20_42067756_43194906 | 43095827 | A | ACCCTCCT others(611): Show |
intron_variant | MODIFIER | HG00738.hp2 HG02647.hp2 |
a0001 | a0001c0003a0001c0025 | a0001c0003t0018a0001c0025t0015 | a0001c0003t0018g0046a0001c0025t0015g0028 | 2 | 62 | 0.0323 | 618 | c.88+ others(635): Show |
PTPRT | ENSG00000196090.14 | transcript | ENST00000373187.6 | protein_coding | 1/30 | chr20 | TogoVar | ||||||
RAB11FIP3_chr16_420649_528011 | 492419 | G | GGCCCTCC others(611): Show |
intron_variant | MODIFIER | HG00558.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0192 | 1 | 295 | 0.0034 | 618 | c.126 others(637): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
RASA3_chr13_113972783_114137623 | 114099624 | C | CCCCCCGT others(611): Show |
intron_variant | MODIFIER | HG01943.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0059 | 1 | 67 | 0.0149 | 618 | c.56- others(635): Show |
RASA3 | ENSG00000185989.11 | transcript | ENST00000334062.8 | protein_coding | 1/23 | chr13 | TogoVar | ||||||
RFC1_chr4_39282456_39371362 | 39348424 | A | AAAAAGAA others(611): Show |
intron_variant | MODIFIER | HG02738.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0245 | 1 | 276 | 0.0036 | 618 | c.132 others(635): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | TogoVar | ||||||
ROBO1_chr3_78592239_79772998 | 79709674 | T | TTTTTTTT others(611): Show |
intron_variant | MODIFIER | HG03041.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0025 | 1 | 44 | 0.0227 | 618 | c.-51 others(637): Show |
ROBO1 | ENSG00000169855.21 | transcript | ENST00000464233.6 | protein_coding | 1/30 | chr3 | TogoVar | ||||||
ROBO1_chr3_78592239_79772998 | 79709674 | T | TTTTTTTT others(611): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0002 | a0001c0002t0013 | a0001c0002t0013g0008 | 1 | 44 | 0.0227 | 618 | c.-51 others(637): Show |
ROBO1 | ENSG00000169855.21 | transcript | ENST00000464233.6 | protein_coding | 1/30 | chr3 | TogoVar | ||||||
RUNX1_chr21_34782801_35054302 | 34931569 | A | ATGTATAC others(611): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0046 | 1 | 170 | 0.0059 | 618 | c.59- others(635): Show |
RUNX1 | ENSG00000159216.19 | transcript | ENST00000675419.1 | protein_coding | 2/8 | chr21 | TogoVar | ||||||
SCTR_chr2_119434843_119529483 | 119444768 | T | TATATACA others(611): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0004 | a0001c0004t0004 | a0001c0004t0004g0070 | 1 | 290 | 0.0035 | 618 | c.114 others(637): Show |
SCTR | ENSG00000080293.10 | transcript | ENST00000019103.8 | protein_coding | 11/12 | chr2 | TogoVar | ||||||
SEPTIN9_chr17_77276499_77505593 | 77356670 | C | CCCCCTCC others(611): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0002 | a0002c0004 | a0002c0004t0022 | a0002c0004t0022g0040 | 1 | 150 | 0.0067 | 618 | c.77- others(635): Show |
SEPTIN9 | ENSG00000184640.20 | transcript | ENST00000427177.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
SEPTIN9_chr17_77314518_77505593 | 77356670 | C | CCCCCTCC others(611): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0002 | a0002c0005 | a0002c0005t0011 | a0002c0005t0011g0135 | 1 | 158 | 0.0063 | 618 | c.22+ others(635): Show |
SEPTIN9 | ENSG00000184640.20 | transcript | ENST00000329047.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
SPAAR_chr9_35904490_35916686 | 35914229 | G | GGTGAGTG others(611): Show |
downstream_gene_variant | MODIFIER | HG02165.hp1 NA18955.hp2 NA19010.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 3 | 420 | 0.0071 | 618 | c.*35 others(629): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2544 | chr9 | TogoVar | ||||||
SPAAR_chr9_35904490_35916686 | 35914229 | G | GGTGAGTG others(611): Show |
downstream_gene_variant | MODIFIER | HG01943.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 420 | 0.0024 | 618 | c.*35 others(629): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2544 | chr9 | TogoVar | ||||||
SPAAR_chr9_35904490_35916686 | 35914229 | G | GGTGAGTG others(611): Show |
downstream_gene_variant | MODIFIER | HG02155.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 420 | 0.0024 | 618 | c.*35 others(629): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2544 | chr9 | TogoVar | ||||||
SPIRE2_chr16_89823475_89876319 | 89843760 | C | CGTGATCT others(611): Show |
intron_variant | MODIFIER | HG00140.hp1 HG01070.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069a0001c0001t0001g0086 | 2 | 356 | 0.0056 | 618 | c.245 others(635): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
TBC1D22A_chr22_46757650_47180693 | 46860456 | C | CATAGAGG others(611): Show |
intron_variant | MODIFIER | HG02486.hp2 HG03516.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0005a0002c0003t0009 | a0001c0001t0005g0002a0002c0003t0009g0034 | 2 | 112 | 0.0179 | 618 | c.638 others(637): Show |
TBC1D22A | ENSG00000054611.14 | transcript | ENST00000337137.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
TCF3_chr19_1604292_1657615 | 1628085 | G | GGGGGTGA others(611): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0095 | 1 | 352 | 0.0028 | 618 | c.299 others(633): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | TogoVar | ||||||
TCF3_chr19_1604292_1657615 | 1628878 | A | AGGCGGGA others(611): Show |
intron_variant | MODIFIER | HG00544.hp2 | a0014 | a0014c0020 | a0014c0020t0034 | a0014c0020t0034g0316 | 1 | 352 | 0.0028 | 618 | c.299 others(635): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | TogoVar | ||||||
TGM2_chr20_38122385_38170270 | 38124011 | T | TATAAAAT others(611): Show |
downstream_gene_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0131 | 1 | 360 | 0.0028 | 618 | c.*62 others(629): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3373 | chr20 | TogoVar | ||||||
TLL2_chr10_96359608_96518926 | 96415729 | G | GTCTCTCT others(611): Show |
intron_variant | MODIFIER | HG02622.hp2 NA18954.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0004a0001c0003t0003 | a0001c0002t0004g0047a0001c0003t0003g0080 | 2 | 256 | 0.0078 | 618 | c.924 others(635): Show |
TLL2 | ENSG00000095587.9 | transcript | ENST00000357947.4 | protein_coding | 7/20 | chr10 | TogoVar | ||||||
TMEM120B_chr12_121707752_121787068 | 121748187 | G | GCTGGGGT others(611): Show |
intron_variant | MODIFIER | HG03710.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0210 | 1 | 314 | 0.0032 | 618 | c.189 others(633): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM178B_chr7_141069064_141485380 | 141337158 | T | TCACCACC others(611): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0042 | 1 | 80 | 0.0125 | 618 | c.497 others(639): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
TMPRSS9_chr19_2355265_2431261 | 2418721 | T | TCCTTCCC others(611): Show |
intron_variant | MODIFIER | HG03041.hp2 | a0014 | a0014c0026 | a0014c0026t0002 | a0014c0026t0002g0102 | 1 | 114 | 0.0088 | 618 | c.215 others(635): Show |
TMPRSS9 | ENSG00000178297.15 | transcript | ENST00000696167.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
TNFSF13B_chr13_108264718_108313478 | 108278578 | C | CTCCTCCT others(611): Show |
intron_variant | MODIFIER | HG02451.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | 384 | 0.0052 | 618 | c.424 others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
TNFSF13B_chr13_108264718_108313478 | 108278578 | C | CTCCTCCT others(611): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0096others(133): Show | 147 | 384 | 0.3828 | 618 | c.424 others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
TNFSF13B_chr13_108264718_108313478 | 108278578 | C | CTCCTCCT others(611): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0187 | 1 | 384 | 0.0026 | 618 | c.424 others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
TNFSF13B_chr13_108264718_108313478 | 108278578 | C | CTCCTCCT others(611): Show |
intron_variant | MODIFIER | NA18953.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0194 | 1 | 384 | 0.0026 | 618 | c.424 others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
TNFSF13B_chr13_108264718_108313478 | 108278578 | C | CTCCTCCT others(611): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 2 | 384 | 0.0052 | 618 | c.424 others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
TNFSF13B_chr13_108264718_108313478 | 108278578 | C | CTCCTCCT others(611): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0275 | 1 | 384 | 0.0026 | 618 | c.424 others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
TNFSF13B_chr13_108264718_108313478 | 108278578 | C | CTCCTCCT others(611): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0002g0150others(11): Show | 14 | 384 | 0.0365 | 618 | c.424 others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
TNFSF13B_chr13_108264718_108313478 | 108278578 | C | CTCCTCCT others(611): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0220 | 1 | 384 | 0.0026 | 618 | c.424 others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
TNFSF13B_chr13_108264718_108313478 | 108278578 | C | CTCCTCCT others(611): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0001 | a0001c0001t0020 | a0001c0001t0020g0286 | 1 | 384 | 0.0026 | 618 | c.424 others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
TTC16_chr9_127711079_127736590 | 127720831 | T | TTCCCCCT others(611): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0130 | 1 | 334 | 0.0030 | 618 | c.657 others(633): Show |
TTC16 | ENSG00000167094.16 | transcript | ENST00000373289.4 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
TWIST2_chr2_238843085_238915534 | 238870577 | A | ACACCCCA others(611): Show |
intron_variant | MODIFIER | NA18939.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 | 1 | 338 | 0.0030 | 618 | c.*35 others(637): Show |
TWIST2 | ENSG00000233608.5 | transcript | ENST00000612363.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
VCX3B_chrX_8459830_8471510 | 8466642 | A | AGGGAGGA others(611): Show |
downstream_gene_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 | 1 | 271 | 0.0037 | 618 | c.*25 others(627): Show |
VCX3B | ENSG00000205642.11 | transcript | ENST00000381032.6 | protein_coding | 133 | chrX | TogoVar | ||||||
VGLL4_chr3_11551069_11648915 | 11605172 | G | GCCCACCC others(611): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0002 | a0001c0002t0019 | a0001c0002t0019g0241 | 1 | 388 | 0.0026 | 618 | c.83- others(633): Show |
VGLL4 | ENSG00000144560.16 | transcript | ENST00000430365.7 | protein_coding | 1/4 | chr3 | TogoVar |