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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM163_chr2_134450759_134724000 | 134688541 | A | AAG | intron_variant | MODIFIER | HG03041.hp2 HG03453.hp1 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0170a0001c0001t0001g0178a0001c0001t0002g0179 | 3 | 222 | 0.0135 | 2 | c.322 others(21): Show |
TMEM163 | ENSG00000152128.13 | transcript | ENST00000281924.6 | protein_coding | 2/7 | chr2 | TogoVar | ||||||
TMEM163_chr2_134450759_134724000 | 134701916 | C | CAA | intron_variant | MODIFIER | HG01175.hp1 HG01928.hp1 HG02055.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(1): Show | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0171others(7): Show | 10 | 222 | 0.0451 | 2 | c.322 others(21): Show |
TMEM163 | ENSG00000152128.13 | transcript | ENST00000281924.6 | protein_coding | 2/7 | chr2 | TogoVar | ||||||
TMEM163_chr2_134450759_134724000 | 134710640 | T | TAA | intron_variant | MODIFIER | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0176others(13): Show | 16 | 222 | 0.0721 | 2 | c.322 others(19): Show |
TMEM163 | ENSG00000152128.13 | transcript | ENST00000281924.6 | protein_coding | 2/7 | chr2 | TogoVar | ||||||
TMEM164_chrX_109998114_110182788 | 110015550 | A | AGT | intron_variant | MODIFIER | HG02132.hp1 HG03130.hp1 NA19005.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(1): Show | a0001c0001t0001g0029a0001c0001t0003g0055a0001c0001t0005g0092others(1): Show | 4 | 198 | 0.0202 | 2 | c.390 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110015580 | T | TGC | intron_variant | MODIFIER | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(1): Show | a0001c0001t0003g0036a0001c0001t0004g0008a0001c0001t0004g0034others(5): Show | 8 | 198 | 0.0404 | 2 | c.390 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110017446 | C | CTT | intron_variant | MODIFIER | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0002g0015a0001c0001t0003g0028a0001c0001t0004g0016others(3): Show | 6 | 198 | 0.0303 | 2 | c.390 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110017488 | C | CTT | intron_variant | MODIFIER | HG02630.hp1 HG03195.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0022a0001c0001t0003g0046 | 2 | 198 | 0.0101 | 2 | c.390 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110017492 | C | CTT | intron_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0173 | 1 | 198 | 0.0051 | 2 | c.390 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110021523 | A | ATG | intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0044 | 1 | 198 | 0.0051 | 2 | c.390 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110022199 | A | ATG | intron_variant | MODIFIER | HG02056.hp1 NA19068.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0145a0001c0001t0005g0100 | 2 | 198 | 0.0101 | 2 | c.390 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110024991 | G | GGT | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(87): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0059others(87): Show | 90 | 198 | 0.4546 | 2 | c.390 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110030108 | G | GTT | intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0052 | 1 | 198 | 0.0051 | 2 | c.390 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110035504 | C | CTT | intron_variant | MODIFIER | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0010 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | 198 | 0.0253 | 2 | c.390 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110037984 | A | ATT | intron_variant | MODIFIER | HG02055.hp1 HG02486.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0023 | a0001c0001t0004g0095a0001c0001t0023g0096 | 2 | 198 | 0.0101 | 2 | c.391 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110052745 | G | GTT | intron_variant | MODIFIER | HG01978.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(1): Show | a0001c0001t0002g0136a0001c0001t0008g0077a0001c0001t0011g0026others(1): Show | 4 | 198 | 0.0202 | 2 | c.391 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110056941 | T | TTA | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(40): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(40): Show | 43 | 198 | 0.2172 | 2 | c.391 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110057548 | C | CTT | intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0007 | 1 | 198 | 0.0051 | 2 | c.391 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110058609 | C | CTT | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(31): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(4): Show | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(31): Show | 34 | 198 | 0.1717 | 2 | c.391 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110060266 | G | GAA | intron_variant | MODIFIER | HG02451.hp2 HG03098.hp1 NA19074.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0008 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0008g0078 | 3 | 198 | 0.0152 | 2 | c.391 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110062356 | T | TTG | intron_variant | MODIFIER | HG04199.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0190 | 1 | 198 | 0.0051 | 2 | c.391 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110067151 | T | TGC | intron_variant | MODIFIER | HG02109.hp2 HG03486.hp2 |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0011 | a0001c0001t0010g0010a0001c0001t0011g0009 | 2 | 198 | 0.0101 | 2 | c.391 others(17): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110067154 | G | GCA | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp1 HG01167.hp1 others(39): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0103others(39): Show | 42 | 198 | 0.2121 | 2 | c.391 others(17): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110071716 | C | CAA | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(30): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(30): Show | 33 | 198 | 0.1667 | 2 | c.440 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110072296 | C | CAA | intron_variant | MODIFIER | HG02145.hp1 HG02630.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0028 | a0001c0001t0003g0046a0001c0001t0028g0042 | 2 | 198 | 0.0101 | 2 | c.440 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110084367 | G | GTA | intron_variant | MODIFIER | HG00621.hp1 HG01891.hp1 HG02129.hp1 others(14): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(1): Show | a0001c0001t0001g0040a0001c0001t0001g0099a0001c0001t0001g0128others(14): Show | 17 | 198 | 0.0859 | 2 | c.440 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110084464 | G | GTA | intron_variant | MODIFIER | HG02723.hp1 NA18989.hp1 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0017 | a0001c0001t0003g0027a0001c0001t0007g0019a0001c0001t0017g0179 | 3 | 198 | 0.0152 | 2 | c.440 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110084477 | T | TAG | intron_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0022 | 1 | 198 | 0.0051 | 2 | c.440 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110085336 | A | AAT | intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0188 | 1 | 198 | 0.0051 | 2 | c.440 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110086674 | A | ATG | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(42): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(42): Show | 45 | 198 | 0.2273 | 2 | c.440 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110086688 | G | GTA | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp1 HG01167.hp1 others(46): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(9): Show | a0001c0001t0002g0015a0001c0001t0002g0085a0001c0001t0002g0086others(46): Show | 49 | 198 | 0.2475 | 2 | c.440 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110090311 | A | ATT | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0091 | 1 | 198 | 0.0051 | 2 | c.441 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110098950 | A | ATT | intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0034 | 1 | 198 | 0.0051 | 2 | c.441 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110101580 | A | ATT | intron_variant | MODIFIER | HG02559.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(1): Show | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0037others(2): Show | 5 | 198 | 0.0253 | 2 | c.441 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110105679 | G | GAC | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp1 HG01243.hp1 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0088others(21): Show | 24 | 198 | 0.1212 | 2 | c.441 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110105685 | C | CAG | intron_variant | MODIFIER | HG02258.hp1 HG03486.hp2 |
a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0009a0001c0001t0011g0026 | 2 | 198 | 0.0101 | 2 | c.441 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110105750 | T | TGA | intron_variant | MODIFIER | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(48): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0060others(48): Show | 51 | 198 | 0.2576 | 2 | c.441 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110105792 | A | AGG | intron_variant | MODIFIER | NA19058.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0119 | 1 | 198 | 0.0051 | 2 | c.441 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110106373 | C | CTT | intron_variant | MODIFIER | HG02145.hp1 HG02559.hp2 HG02717.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0027a0001c0001t0028 | a0001c0001t0003g0038a0001c0001t0027g0084a0001c0001t0028g0042 | 3 | 198 | 0.0152 | 2 | c.441 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110108068 | C | CTG | intron_variant | MODIFIER | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0058a0001c0001t0001g0079a0001c0001t0001g0105others(24): Show | 27 | 198 | 0.1364 | 2 | c.441 others(17): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110116822 | T | TTG | intron_variant | MODIFIER | HG01496.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0028others(1): Show | a0001c0001t0001g0122a0001c0001t0001g0156a0001c0001t0004g0045others(2): Show | 5 | 198 | 0.0253 | 2 | c.507 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110116876 | G | GGT | intron_variant | MODIFIER | HG01515.hp1 HG02109.hp2 HG02647.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0002g0098a0001c0001t0003g0012a0001c0001t0004g0007others(2): Show | 5 | 198 | 0.0253 | 2 | c.507 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110126810 | C | CTG | intron_variant | MODIFIER | HG00408.hp2 HG00642.hp1 HG01106.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0002g0015a0001c0001t0002g0083a0001c0001t0002g0103others(15): Show | 18 | 198 | 0.0909 | 2 | c.507 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110134393 | T | TAC | intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0014 | 1 | 198 | 0.0051 | 2 | c.508 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110143804 | G | GGT | intron_variant | MODIFIER | HG02027.hp1 NA19004.hp1 NA19074.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(1): Show | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0197others(3): Show | 6 | 198 | 0.0303 | 2 | c.508 others(17): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
TMEM164_chrX_109998114_110182788 | 110152070 | T | TTG | intron_variant | MODIFIER | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0009a0001c0001t0021others(1): Show | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | 198 | 0.0455 | 2 | c.586 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | TogoVar | ||||||
TMEM164_chrX_109998114_110182788 | 110174375 | C | CCT | 3_prime_UTR_variant | MODIFIER | NA19072.hp1 | a0003 | a0003c0003 | a0003c0003t0016 | a0003c0003t0016g0142 | 1 | 198 | 0.0051 | 2 | c.*92 others(11): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 925 | chrX | TogoVar | |||||
TMEM165_chr4_55390957_55431175 | 55400246 | T | TTA | intron_variant | MODIFIER | HG02145.hp2 HG02976.hp1 HG03540.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | 382 | 0.0079 | 2 | c.207 others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
TMEM165_chr4_55390957_55431175 | 55403492 | C | CTT | intron_variant | MODIFIER | HG00280.hp2 HG00558.hp1 HG00735.hp1 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0265a0001c0001t0002g0135a0001c0001t0002g0136others(12): Show | 15 | 382 | 0.0393 | 2 | c.207 others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
TMEM165_chr4_55390957_55431175 | 55421166 | C | CAA | intron_variant | MODIFIER | HG00673.hp2 HG01099.hp2 HG02818.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0002t0001 | a0001c0001t0001g0001a0001c0001t0001g0265a0001c0001t0003g0314others(2): Show | 6 | 382 | 0.0157 | 2 | c.792 others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
TMEM165_chr4_55390957_55431175 | 55421297 | C | CTT | intron_variant | MODIFIER | NA18612.hp1 NA18939.hp1 NA18959.hp2 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0011 | a0001c0001t0003g0017a0001c0001t0003g0286a0001c0001t0003g0299others(12): Show | 16 | 382 | 0.0419 | 2 | c.793 others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |