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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
LAMA5_chr20_62304065_62372312 | 62349805 | T | TGGCGGTG others(722): Show |
intron_variant | MODIFIER | HG01175.hp2 | a0039 | a0039c0096 | a0039c0096t0002 | a0039c0096t0002g0088 | 1 | 136 | 0.0074 | 729 | c.956 others(746): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 6/79 | chr20 | TogoVar | |||||||
LHPP_chr10_124456823_124619141 | 124610989 | C | CGGGTGAG others(722): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0187 | 1 | 37 | 0.0270 | 729 | c.717 others(746): Show |
LHPP | ENSG00000107902.14 | transcript | ENST00000368842.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
MICAL3_chr22_17782649_18029561 | 17876951 | G | GTTAGGGA others(722): Show |
intron_variant | MODIFIER | HG02523.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 | 1 | 265 | 0.0038 | 729 | c.224 others(748): Show |
MICAL3 | ENSG00000243156.9 | transcript | ENST00000441493.7 | protein_coding | 16/31 | chr22 | TogoVar | |||||||
MICAL3_chr22_17782649_18029561 | 17877288 | T | TGGAGGTT others(722): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0004 | a0004c0007 | a0004c0007t0005 | a0004c0007t0005g0204 | 1 | 226 | 0.0044 | 729 | c.224 others(748): Show |
MICAL3 | ENSG00000243156.9 | transcript | ENST00000441493.7 | protein_coding | 16/31 | chr22 | TogoVar | |||||||
MICAL3_chr22_17782649_18029561 | 17877441 | G | GGGAGGTT others(722): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0083 | 1 | 264 | 0.0038 | 729 | c.224 others(748): Show |
MICAL3 | ENSG00000243156.9 | transcript | ENST00000441493.7 | protein_coding | 16/31 | chr22 | TogoVar | |||||||
NEU4_chr2_241804193_241822413 | 241807935 | T | TCCCCCCT others(722): Show |
upstream_gene_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0055 | 1 | 296 | 0.0034 | 729 | c.-13 others(740): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 1257 | chr2 | TogoVar | |||||||
NKAIN2_chr6_123798865_124830640 | 124687566 | T | TATATTCC others(722): Show |
intron_variant | MODIFIER | HG02602.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0043 | 1 | 35 | 0.0286 | 729 | c.474 others(748): Show |
NKAIN2 | ENSG00000188580.16 | transcript | ENST00000368417.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
NXN_chr17_794310_984776 | 841624 | G | GGGCGAGC others(722): Show |
intron_variant | MODIFIER | HG04199.hp2 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0002 | 1 | 222 | 0.0045 | 729 | c.361 others(748): Show |
NXN | ENSG00000167693.17 | transcript | ENST00000336868.8 | protein_coding | 1/7 | chr17 | TogoVar | |||||||
NXN_chr17_794310_984776 | 948839 | C | CCCCGCGG others(722): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0005 | a0001c0005t0005 | a0001c0005t0005g0080 | 1 | 228 | 0.0044 | 729 | c.360 others(748): Show |
NXN | ENSG00000167693.17 | transcript | ENST00000336868.8 | protein_coding | 1/7 | chr17 | TogoVar | |||||||
PCDH15_chr10_53797771_54806231 | 54332334 | A | ATATTATT others(722): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 1 | 90 | 0.0111 | 729 | c.595 others(746): Show |
PCDH15 | ENSG00000150275.20 | transcript | ENST00000644397.2 | protein_coding | 6/37 | chr10 | TogoVar | |||||||
PCDH15_chr10_53816099_54806231 | 54332334 | A | ATATTATT others(722): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 1 | 84 | 0.0119 | 729 | c.595 others(746): Show |
PCDH15 | ENSG00000150275.20 | transcript | ENST00000320301.11 | protein_coding | 6/32 | chr10 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984158 | T | TAACCACC others(722): Show |
intron_variant | MODIFIER | HG02723.hp2 HG03130.hp1 |
a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0165 a0001c0004t0005g0166 |
2 | 294 | 0.0068 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0220 | 1 | 70 | 0.0143 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG02717.hp2 HG03041.hp1 HG03486.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0017 | a0001c0001t0001a0001c0001t0004a0001c0002t0006others(1): Show | a0001c0001t0001g0032 a0001c0001t0001g0107 a0001c0001t0004g0176 others(2): Show |
5 | 74 | 0.0676 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01934.hp2 HG02109.hp2 |
a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0004 a0001c0002t0009g0005 |
2 | 71 | 0.0282 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01106.hp2 HG04228.hp2 |
a0002 | a0002c0003 | a0002c0003t0012 | a0002c0003t0012g0221 a0002c0003t0012g0222 |
2 | 71 | 0.0282 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG02572.hp2 NA19240.hp2 |
a0001 | a0001c0002 | a0001c0002t0006a0001c0002t0016 | a0001c0002t0006g0237 a0001c0002t0016g0003 |
2 | 71 | 0.0282 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0223 | 1 | 70 | 0.0143 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02486.hp2 HG02622.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0016a0001c0002t0008a0001c0002t0009others(1): Show | a0001c0001t0016g0020 a0001c0002t0008g0021 a0001c0002t0009g0022 others(1): Show |
4 | 73 | 0.0548 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00597.hp1 HG02523.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0034 | a0001c0001t0001g0214 a0001c0001t0002g0185 a0001c0001t0002g0193 others(2): Show |
5 | 74 | 0.0676 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG02970.hp1 HG04228.hp1 |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0037a0002c0007t0009 | a0001c0001t0037g0066 a0002c0007t0009g0001 |
2 | 71 | 0.0282 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | NA18980.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0085 | 1 | 70 | 0.0143 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01255.hp2 HG02602.hp2 HG03927.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(1): Show | a0001c0001t0001g0200 a0001c0001t0002g0201 a0001c0001t0008g0024 others(1): Show |
4 | 73 | 0.0548 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG00423.hp2 HG01099.hp2 HG01167.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0041 a0001c0001t0001g0262 a0001c0001t0001g0263 others(9): Show |
12 | 81 | 0.1481 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0002 | a0001c0002t0036 | a0001c0002t0036g0241 | 1 | 70 | 0.0143 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0002 | a0002c0003 | a0002c0003t0011 | a0002c0003t0011g0238 | 1 | 70 | 0.0143 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | NA18944.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0197 | 1 | 70 | 0.0143 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0002 | a0002c0007 | a0002c0007t0005 | a0002c0007t0005g0235 | 1 | 70 | 0.0143 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | |||||||
PLCB1_chr20_8127266_8889900 | 8662119 | T | TAATTATA others(722): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0018 | a0001c0018t0017 | a0001c0018t0017g0018 | 1 | 25 | 0.0400 | 729 | c.862 others(746): Show |
PLCB1 | ENSG00000182621.19 | transcript | ENST00000338037.11 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
PLEKHG4B_chr5_87168_194966 | 141104 | C | CCCCCTGC others(722): Show |
intron_variant | MODIFIER | HG04204.hp2 | a0004 | a0004c0006 | a0004c0006t0093 | a0004c0006t0093g0049 | 1 | 24 | 0.0417 | 729 | c.147 others(746): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2124224 | C | CGGCTATA others(722): Show |
intron_variant | MODIFIER | NA18967.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069 | 1 | 117 | 0.0085 | 729 | c.335 others(748): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PWWP2B_chr10_132392200_132422859 | 132392564 | G | GTGATGAT others(722): Show |
upstream_gene_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0210 | 1 | 199 | 0.0050 | 729 | c.-46 others(740): Show |
PWWP2B | ENSG00000171813.14 | transcript | ENST00000305233.6 | protein_coding | 4635 | chr10 | TogoVar | |||||||
ROBO2_chr3_77035099_77654964 | 77323064 | T | TATATTAT others(722): Show |
intron_variant | MODIFIER | NA18959.hp2 NA19077.hp2 |
a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0037 a0001c0001t0010g0144 |
2 | 131 | 0.0153 | 729 | c.389 others(750): Show |
ROBO2 | ENSG00000185008.19 | transcript | ENST00000696593.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
SAMD11_chr1_918923_949574 | 934241 | G | GGCTGCGT others(722): Show |
intron_variant | MODIFIER | HG00323.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0112 | 1 | 419 | 0.0024 | 729 | c.843 others(746): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SAMD11_chr1_918923_949574 | 934377 | G | GGGCGGCT others(722): Show |
intron_variant | MODIFIER | HG01346.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0201 | 1 | 332 | 0.0030 | 729 | c.843 others(746): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SERINC2_chr1_31408213_31439678 | 31431777 | A | ATAGGGTG others(722): Show |
intron_variant | MODIFIER | NA19004.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0263 | 1 | 337 | 0.0030 | 729 | c.101 others(748): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SERINC2_chr1_31408213_31439678 | 31431949 | T | TAGAGTGG others(722): Show |
intron_variant | MODIFIER | HG01943.hp2 | a0001 | a0001c0005 | a0001c0005t0002 | a0001c0005t0002g0363 | 1 | 334 | 0.0030 | 729 | c.101 others(748): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SLC12A7_chr5_1045384_1117063 | 1098348 | C | CAGCCCCC others(722): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0014 | 1 | 111 | 0.0090 | 729 | c.125 others(746): Show |
SLC12A7 | ENSG00000113504.21 | transcript | ENST00000264930.10 | protein_coding | 1/23 | chr5 | TogoVar | |||||||
SLC37A3_chr7_140328752_140403530 | 140387809 | A | AAATATAA others(722): Show |
intron_variant | MODIFIER | HG01255.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0173 | 1 | 132 | 0.0076 | 729 | c.-70 others(746): Show |
SLC37A3 | ENSG00000157800.18 | transcript | ENST00000326232.14 | protein_coding | 1/14 | chr7 | TogoVar | |||||||
STK24_chr13_98440185_98582107 | 98473274 | G | GGAGAGGA others(722): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0091 | a0001c0001t0091g0286 | 1 | 3 | 0.3333 | 729 | c.597 others(746): Show |
STK24 | ENSG00000102572.15 | transcript | ENST00000539966.6 | protein_coding | 5/10 | chr13 | TogoVar | |||||||
TMEM120B_chr12_121707752_121787068 | 121747289 | G | GCTGGGGT others(722): Show |
intron_variant | MODIFIER | NA19090.hp2 | a0001 | a0001c0001 | a0001c0001t0069 | a0001c0001t0069g0019 | 1 | 264 | 0.0038 | 729 | c.189 others(746): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
TMEM178B_chr7_141069064_141485380 | 141337038 | C | CCATCACC others(722): Show |
intron_variant | MODIFIER | HG03704.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0005 | 1 | 38 | 0.0263 | 729 | c.497 others(750): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TNS1_chr2_217794791_218007995 | 217805592 | C | CCACCACA others(722): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0034 | a0034c0097 | a0034c0097t0048 | a0034c0097t0048g0150 | 1 | 49 | 0.0204 | 729 | c.537 others(746): Show |
TNS1 | ENSG00000079308.21 | transcript | ENST00000682258.1 | protein_coding | 32/32 | chr2 | TogoVar | |||||||
TWIST2_chr2_238843085_238915534 | 238870987 | A | ACACCCCA others(722): Show |
intron_variant | MODIFIER | NA19063.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037 | 1 | 272 | 0.0037 | 729 | c.*35 others(748): Show |
TWIST2 | ENSG00000233608.5 | transcript | ENST00000612363.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TXNDC16_chr14_52425596_52557505 | 52530465 | T | TAATAATA others(722): Show |
intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 | 1 | 83 | 0.0120 | 729 | c.392 others(746): Show |
TXNDC16 | ENSG00000087301.9 | transcript | ENST00000281741.9 | protein_coding | 6/20 | chr14 | TogoVar | |||||||
UMAD1_chr7_7635752_7884223 | 7679065 | T | TATAAATA others(722): Show |
intron_variant | MODIFIER | NA19001.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0195 | 1 | 141 | 0.0071 | 729 | c.82+ others(744): Show |
UMAD1 | ENSG00000219545.12 | transcript | ENST00000682710.1 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
VCX_chrX_7838171_7849143 | 7844242 | G | GGGGAGGG others(722): Show |
downstream_gene_variant | MODIFIER | NA18959.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010 | 1 | 277 | 0.0036 | 729 | c.*22 others(738): Show |
VCX | ENSG00000182583.13 | transcript | ENST00000688183.1 | protein_coding | 100 | chrX | TogoVar | |||||||
VEGFB_chr11_64229584_64244264 | 64237115 | G | GGGAGAGG others(722): Show |
intron_variant | MODIFIER | NA18984.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0108 | 1 | 318 | 0.0031 | 729 | c.375 others(742): Show |
VEGFB | ENSG00000173511.10 | transcript | ENST00000309422.7 | protein_coding | 4/6 | chr11 | TogoVar | |||||||
ZNF16_chr8_144925358_144955880 | 144946810 | G | GCTGTGTC others(722): Show |
intron_variant | MODIFIER | NA19059.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0093 | 1 | 283 | 0.0035 | 729 | c.-9- others(742): Show |
ZNF16 | ENSG00000170631.15 | transcript | ENST00000394909.7 | protein_coding | 1/2 | chr8 | TogoVar | |||||||
ZNF627_chr19_11592483_11624161 | 11613145 | C | CCCTCCCC others(722): Show |
intron_variant | MODIFIER | HG01517.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0136 | 1 | 9 | 0.1111 | 729 | c.4-1 others(742): Show |
ZNF627 | ENSG00000198551.10 | transcript | ENST00000361113.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |