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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
HTR6_chr1_19659875_19685966 | 19671809 | T | TGGAAATG others(6086): Show |
intron_variant | MODIFIER | NA19070.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 | 1 | 400 | 0.0025 | 6093 | c.714 others(6110): Show |
HTR6 | ENSG00000158748.4 | transcript | ENST00000289753.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6086): Show |
intron_variant | MODIFIER | HG01074.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0131 | 1 | 344 | 0.0029 | 6093 | c.120 others(6110): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NRXN3_chr14_78165373_79873291 | 79626233 | T | TTAGGGGG others(6086): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0004 | 1 | 24 | 0.0417 | 6093 | c.344 others(6114): Show |
NRXN3 | ENSG00000021645.20 | transcript | ENST00000335750.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
SHC3_chr9_89000771_89183818 | 89159080 | T | TGAAAACC others(6086): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0171 | 1 | 188 | 0.0053 | 6093 | c.474 others(6112): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | TogoVar | |||||||
SIK3_chr11_116838402_117103428 | 116994892 | G | GCAGCAAG others(6086): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0206 | 1 | 366 | 0.0027 | 6093 | c.274 others(6112): Show |
SIK3 | ENSG00000160584.17 | transcript | ENST00000445177.6 | protein_coding | 1/24 | chr11 | TogoVar | |||||||
SLC9A9_chr3_143260222_143853468 | 143402916 | T | TTTTTGTT others(6086): Show |
intron_variant | MODIFIER | HG01934.hp2 NA18950.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0003 | a0001c0001t0002g0017 a0001c0002t0003g0023 |
2 | 108 | 0.0185 | 6093 | c.147 others(6114): Show |
SLC9A9 | ENSG00000181804.15 | transcript | ENST00000316549.11 | protein_coding | 12/15 | chr3 | TogoVar | |||||||
SLC9A9_chr3_143260222_143853468 | 143402916 | T | TTTTTGTT others(6086): Show |
intron_variant | MODIFIER | HG00408.hp1 NA18966.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0003 | a0001c0001t0002g0049 a0001c0002t0003g0046 |
2 | 108 | 0.0185 | 6093 | c.147 others(6114): Show |
SLC9A9 | ENSG00000181804.15 | transcript | ENST00000316549.11 | protein_coding | 12/15 | chr3 | TogoVar | |||||||
SLC9A9_chr3_143260222_143853468 | 143402916 | T | TTTTTGTT others(6086): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0021 | 1 | 108 | 0.0093 | 6093 | c.147 others(6114): Show |
SLC9A9 | ENSG00000181804.15 | transcript | ENST00000316549.11 | protein_coding | 12/15 | chr3 | TogoVar | |||||||
SLC9A9_chr3_143260222_143853468 | 143402916 | T | TTTTTGTT others(6086): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0043 | 1 | 108 | 0.0093 | 6093 | c.147 others(6114): Show |
SLC9A9 | ENSG00000181804.15 | transcript | ENST00000316549.11 | protein_coding | 12/15 | chr3 | TogoVar | |||||||
SYK_chr9_90796819_90903549 | 90868723 | A | AGATAAGC others(6086): Show |
intron_variant | MODIFIER | NA18993.hp2 | a0001 | a0001c0003 | a0001c0003t0008 | a0001c0003t0008g0302 | 1 | 376 | 0.0027 | 6093 | c.915 others(6110): Show |
SYK | ENSG00000165025.15 | transcript | ENST00000375754.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
TENM1_chrX_124370903_125209312 | 124787395 | G | GCTATACA others(6086): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0025 | a0001c0025t0028 | a0001c0025t0028g0137 | 1 | 140 | 0.0071 | 6093 | c.536 others(6112): Show |
TENM1 | ENSG00000009694.14 | transcript | ENST00000422452.4 | protein_coding | 6/34 | chrX | TogoVar | |||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6087): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 | 1 | 234 | 0.0043 | 6094 | c.829 others(6113): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6087): Show |
intron_variant | MODIFIER | HG02273.hp1 NA18956.hp1 NA19030.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0147 a0001c0001t0001g0171 a0001c0001t0001g0188 others(2): Show |
5 | 234 | 0.0214 | 6094 | c.829 others(6113): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6087): Show |
intron_variant | MODIFIER | HG03491.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0108 | 1 | 234 | 0.0043 | 6094 | c.829 others(6113): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6087): Show |
intron_variant | MODIFIER | NA18955.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 234 | 0.0043 | 6094 | c.829 others(6113): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6087): Show |
intron_variant | MODIFIER | NA18990.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0218 | 1 | 234 | 0.0043 | 6094 | c.829 others(6113): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
IPCEF1_chr6_154149496_154361803 | 154263429 | T | TAGGGAGT others(6087): Show |
intron_variant | MODIFIER | HG00099.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0188 | 1 | 264 | 0.0038 | 6094 | c.36+ others(6109): Show |
IPCEF1 | ENSG00000074706.14 | transcript | ENST00000367220.9 | protein_coding | 3/11 | chr6 | TogoVar | |||||||
MAP3K9_chr14_70717526_70814513 | 70731059 | T | TAAGAATA others(6087): Show |
intron_variant | MODIFIER | HG01993.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0072 | 1 | 374 | 0.0027 | 6094 | c.283 others(6111): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6087): Show |
intron_variant | MODIFIER | HG02109.hp2 HG02622.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0127 a0001c0001t0001g0270 |
2 | 344 | 0.0058 | 6094 | c.120 others(6111): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6087): Show |
intron_variant | MODIFIER | HG01975.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0265 | 1 | 344 | 0.0029 | 6094 | c.120 others(6111): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6087): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100 | 1 | 344 | 0.0029 | 6094 | c.120 others(6111): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
RERG_chr12_15102783_15226417 | 15116527 | A | ATGCAGGA others(6087): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0113 | 1 | 300 | 0.0033 | 6094 | c.118 others(6111): Show |
RERG | ENSG00000134533.6 | transcript | ENST00000256953.6 | protein_coding | 3/4 | chr12 | TogoVar | |||||||
SLC22A15_chr1_115971513_116075054 | 116005396 | T | TCTCCATA others(6087): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0244 | 1 | 308 | 0.0033 | 6094 | c.300 others(6113): Show |
SLC22A15 | ENSG00000163393.13 | transcript | ENST00000369503.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TLL1_chr4_165868237_166109457 | 166072333 | A | ATAATAAT others(6087): Show |
intron_variant | MODIFIER | NA19000.hp2 | a0002 | a0002c0002 | a0002c0002t0062 | a0002c0002t0062g0091 | 1 | 250 | 0.0040 | 6094 | c.218 others(6113): Show |
TLL1 | ENSG00000038295.8 | transcript | ENST00000061240.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCDC178_chr18_32932406_33445721 | 33247304 | T | TTAAAATG others(6088): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0012 | a0012c0004 | a0012c0004t0001 | a0012c0004t0001g0005 | 1 | 58 | 0.0172 | 6095 | c.141 others(6114): Show |
CCDC178 | ENSG00000166960.17 | transcript | ENST00000383096.8 | protein_coding | 14/22 | chr18 | TogoVar | |||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG00673.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0167 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0168 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG02132.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0177 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | NA18983.hp1 NA19080.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0197 a0001c0001t0001g0199 |
2 | 234 | 0.0086 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG00735.hp1 HG01928.hp1 HG02080.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0104 a0001c0001t0001g0176 a0001c0001t0001g0185 others(9): Show |
12 | 234 | 0.0513 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | NA18950.hp1 NA18960.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | 234 | 0.0086 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG02027.hp1 HG02040.hp1 NA18951.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0105 a0001c0001t0001g0203 a0001c0001t0001g0207 others(1): Show |
4 | 234 | 0.0171 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | NA18945.hp1 NA18954.hp2 NA18963.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0001g0201 |
3 | 234 | 0.0128 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG03453.hp1 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0159 a0001c0001t0001g0164 |
2 | 234 | 0.0086 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0165 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0208 a0001c0001t0001g0233 |
2 | 234 | 0.0086 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0158 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00597.hp1 HG01071.hp1 others(28): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0152 a0001c0001t0001g0153 others(28): Show |
31 | 234 | 0.1325 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0169 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0162 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0196 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG02015.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0219 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0228 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0151 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | NA18946.hp1 NA19065.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | 234 | 0.0086 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6088): Show |
intron_variant | MODIFIER | NA19082.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0216 | 1 | 234 | 0.0043 | 6095 | c.829 others(6114): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6088): Show |
intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0097 | 1 | 344 | 0.0029 | 6095 | c.120 others(6112): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6088): Show |
intron_variant | MODIFIER | NA18747.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0245 | 1 | 344 | 0.0029 | 6095 | c.120 others(6112): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6088): Show |
intron_variant | MODIFIER | HG01433.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0197 | 1 | 344 | 0.0029 | 6095 | c.120 others(6112): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6088): Show |
intron_variant | MODIFIER | HG00597.hp1 NA18941.hp1 NA18981.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0090 a0001c0001t0001g0121 a0001c0001t0001g0157 others(7): Show |
10 | 344 | 0.0291 | 6095 | c.120 others(6112): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar |