Item | Value |
---|---|
geneid | 55362 |
ensemblid | ENSG00000137216.19 |
hgncid | 17735 |
symbol | TMEM63B |
name | transmembrane protein 63B |
refseq_nuc | NM_018426.3 |
refseq_prot | NP_060896.1 |
ensembl_nuc | ENST00000323267.11 |
ensembl_prot | ENSP00000327154.6 |
mane_status | MANE Select |
chr | chr6 |
start | 44127554 |
end | 44155519 |
strand | + |
ver | v1.2 |
region | chr6:44127554-44155519 |
region5000 | chr6:44122554-44160519 |
regionname0 | TMEM63B_chr6_44127554_44155519 |
regionname5000 | TMEM63B_chr6_44122554_44160519 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 832 | 333 | 89 | 64 | 127 | 14 | 37 | 97 | TMEM63B_chr6_44122554_44160519 | TMEM63B | MLPFL others(827): Show |
chr6 | 44122554 | 44160519 |
a0002 | 0/0 | 832 | 61 | 1 | 10 | 41 | 1 | 8 | 33 | TMEM63B_chr6_44122554_44160519 | TMEM63B | MLPFL others(827): Show |
chr6 | 44122554 | 44160519 |
a0003 | 0/0 | 832 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | MLPFL others(827): Show |
chr6 | 44122554 | 44160519 |
a0004 | 0/0 | 832 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | MLPFL others(827): Show |
chr6 | 44122554 | 44160519 |
a0005 | 0/0 | 832 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | MLPFL others(827): Show |
chr6 | 44122554 | 44160519 |
a0006 | 0/0 | 827 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | MLPFL others(822): Show |
chr6 | 44122554 | 44160519 |
a0007 | 0/0 | 832 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | MLPFL others(827): Show |
chr6 | 44122554 | 44160519 |
a0008 | 0/0 | 832 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | MLPFL others(827): Show |
chr6 | 44122554 | 44160519 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2496 | 328 | 89 | 63 | 124 | 14 | 36 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0001c0004 | 0/0 | 2496 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0001c0010 | 0/0 | 2496 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0001c0012 | 0/0 | 2496 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0001c0013 | 0/0 | 2496 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0002c0002 | 0/0 | 2496 | 58 | 1 | 9 | 39 | 1 | 8 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0002c0005 | 0/0 | 2496 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0002c0009 | 0/0 | 2496 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0003c0003 | 0/0 | 2496 | 3 | 0 | 0 | 0 | 0 | 3 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0004c0006 | 0/0 | 2496 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0005c0008 | 0/0 | 2496 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0006c0011 | 0/0 | 2483 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2478): Show |
chr6 | 44122554 | 44160519 | ||
a0007c0007 | 0/0 | 2496 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 | ||
a0008c0014 | 0/0 | 2496 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATGCT others(2491): Show |
chr6 | 44122554 | 44160519 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3284 | 176 | 37 | 34 | 74 | 9 | 20 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3279): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0002 | 0/0 | 3288 | 43 | 12 | 7 | 19 | 1 | 4 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0003 | 0/0 | 3288 | 59 | 9 | 12 | 26 | 3 | 9 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0005 | 0/0 | 3285 | 26 | 13 | 9 | 0 | 1 | 3 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3280): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0006 | 0/0 | 3288 | 7 | 7 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0007 | 0/0 | 3287 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3282): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0008 | 0/0 | 3287 | 3 | 2 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3282): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0009 | 0/0 | 3284 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3279): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0010 | 0/0 | 3285 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3280): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0012 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0013 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0016 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0017 | 0/0 | 3285 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3280): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0018 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0001c0001t0019 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0001c0004t0001 | 0/0 | 3284 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3279): Show |
chr6 | 44122554 | 44160519 |
a0001c0004t0002 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0001c0010t0003 | 0/0 | 3288 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0001c0012t0001 | 0/0 | 3284 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3279): Show |
chr6 | 44122554 | 44160519 |
a0001c0013t0003 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0002c0002t0001 | 0/0 | 3284 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3279): Show |
chr6 | 44122554 | 44160519 |
a0002c0002t0002 | 0/0 | 3288 | 22 | 1 | 5 | 15 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0002c0002t0004 | 0/0 | 3288 | 32 | 0 | 4 | 22 | 0 | 6 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0002c0002t0011 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ACACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0002c0002t0014 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0002c0005t0004 | 0/0 | 3288 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0002c0009t0002 | 0/0 | 3288 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0003c0003t0002 | 0/0 | 3288 | 3 | 0 | 0 | 0 | 0 | 3 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0004c0006t0001 | 0/0 | 3284 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3279): Show |
chr6 | 44122554 | 44160519 |
a0005c0008t0002 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
a0006c0011t0015 | 0/0 | 3275 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3270): Show |
chr6 | 44122554 | 44160519 |
a0007c0007t0001 | 0/0 | 3284 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3279): Show |
chr6 | 44122554 | 44160519 |
a0008c0014t0002 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | ATACA others(3283): Show |
chr6 | 44122554 | 44160519 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 37 | 1 | 5 | 26 | 0 | 4 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0002 | 0/0 | 31 | 5 | 14 | 7 | 2 | 3 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0013 | 0/0 | 5 | 3 | 1 | 0 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0007 | 0/0 | 6 | 1 | 0 | 3 | 0 | 2 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0008 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0003 | 0/0 | 14 | 0 | 0 | 12 | 1 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0006 | 0/0 | 7 | 0 | 3 | 1 | 0 | 3 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0009 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0006g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0006g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0007g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0008g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0010g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0012g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0013g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0016g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0017g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0018g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0001t0019g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0010t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0012t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0001c0013t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0010 | 0/0 | 6 | 0 | 2 | 3 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0018 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0004 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0024 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0002t0014g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0005t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0002c0009t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0003c0003t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0003c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0004c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0005c0008t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0006c0011t0015g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0007c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
a0008c0014t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0095 | EUR | GBR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0147 | EUR | GBR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00323 | hp1 | a0004 | c0006 | t0001 | g0001 | EUR | FIN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | FIN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00438 | hp2 | a0002 | c0002 | t0004 | g0188 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00544 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00597 | hp2 | a0001 | c0013 | t0003 | g0154 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00738 | hp1 | a0002 | c0009 | t0002 | g0192 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0139 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01070 | hp2 | a0001 | c0001 | t0017 | g0196 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0114 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01175 | hp1 | a0002 | c0002 | t0004 | g0004 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0106 | AMR | PUR | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0111 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0129 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0162 | EUR | IBS | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01884 | hp2 | a0001 | c0001 | t0016 | g0167 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01943 | hp1 | a0001 | c0010 | t0003 | g0006 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01952 | hp2 | a0002 | c0002 | t0004 | g0004 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02056 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02074 | hp2 | a0002 | c0002 | t0004 | g0180 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02080 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02129 | hp1 | a0001 | c0004 | t0002 | g0181 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02148 | hp1 | a0002 | c0002 | t0004 | g0024 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02155 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | CDX | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02257 | hp1 | a0001 | c0001 | t0019 | g0161 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02293 | hp2 | a0002 | c0002 | t0004 | g0025 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02523 | hp1 | a0002 | c0002 | t0004 | g0194 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0138 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02735 | hp2 | a0002 | c0002 | t0004 | g0177 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02922 | hp2 | a0001 | c0001 | t0018 | g0166 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02976 | hp1 | a0001 | c0001 | t0010 | g0082 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0040 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0037 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0110 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0084 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0195 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03239 | hp2 | a0003 | c0003 | t0002 | g0093 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0041 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ESN | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03540 | hp2 | a0001 | c0001 | t0013 | g0040 | AFR | GWD | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03654 | hp1 | a0002 | c0002 | t0004 | g0173 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | STU | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0149 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0112 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | BEB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03831 | hp2 | a0002 | c0002 | t0004 | g0170 | SAS | BEB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03927 | hp1 | a0001 | c0012 | t0001 | g0121 | SAS | BEB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | BEB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG04115 | hp1 | a0002 | c0002 | t0004 | g0004 | SAS | STU | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0148 | SAS | STU | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | BEB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG04184 | hp2 | a0002 | c0002 | t0004 | g0004 | SAS | BEB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG04199 | hp2 | a0003 | c0003 | t0002 | g0007 | SAS | STU | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG04228 | hp2 | a0003 | c0003 | t0002 | g0096 | SAS | STU | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18939 | hp2 | a0002 | c0002 | t0014 | g0202 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18941 | hp1 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18942 | hp1 | a0002 | c0002 | t0004 | g0197 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18944 | hp2 | a0002 | c0005 | t0004 | g0004 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18946 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18960 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18963 | hp1 | a0005 | c0008 | t0002 | g0094 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18963 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18965 | hp2 | a0006 | c0011 | t0015 | g0100 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18969 | hp1 | a0001 | c0001 | t0007 | g0053 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18970 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18975 | hp1 | a0002 | c0002 | t0011 | g0187 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18993 | hp1 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18994 | hp2 | a0002 | c0002 | t0004 | g0174 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18997 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18999 | hp1 | a0002 | c0002 | t0004 | g0191 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19003 | hp2 | a0002 | c0002 | t0004 | g0176 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19005 | hp2 | a0001 | c0004 | t0001 | g0057 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19009 | hp2 | a0002 | c0002 | t0004 | g0189 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19010 | hp1 | a0007 | c0007 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19011 | hp2 | a0002 | c0002 | t0004 | g0175 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | LWK | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | LWK | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19055 | hp1 | a0002 | c0002 | t0004 | g0171 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19056 | hp2 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19060 | hp2 | a0002 | c0002 | t0004 | g0198 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19067 | hp1 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19074 | hp2 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19081 | hp1 | a0008 | c0014 | t0002 | g0099 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19084 | hp2 | a0002 | c0005 | t0004 | g0004 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19088 | hp1 | a0002 | c0002 | t0004 | g0168 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ASW | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0142 | EUR | TSI | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0010 | EUR | TSI | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA20905 | hp1 | a0002 | c0002 | t0004 | g0172 | SAS | GIH | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0109 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | ACB | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0083 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0037 | AFR | MSL | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | USA | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18955 | hp1 | a0002 | c0002 | t0004 | g0186 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | USA | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | USA | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0071 | REF | REF | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TMEM63B_chr6_44122554_44160519 | TMEM63B | chr6 | 44122554 | 44160519 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:44134726 | G | A | 1 | a0004 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.142G>A | p.Asp48Asn | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 2/24 | 291/3284 | 142/2499 | 48/832 | chr6 | 44134726 | |||
chr6:44135333 | G | C | 1 | a0003 | 3 | HG03239.hp2 HG04199.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.245G>C | p.Arg82Pro | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/24 | 394/3284 | 245/2499 | 82/832 | chr6 | 44135333 | |||
chr6:44135336 | G | A | 1 | a0007 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.248G>A | p.Arg83Gln | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/24 | 397/3284 | 248/2499 | 83/832 | chr6 | 44135336 | |||
chr6:44139483 | G | T | 1 | a0008 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.424G>T | p.Asp142Tyr | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 7/24 | 573/3284 | 424/2499 | 142/832 | chr6 | 44139483 | |||
chr6:44139577 | T | G | 1 | a0005 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.518T>G | p.Val173Gly | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 7/24 | 667/3284 | 518/2499 | 173/832 | chr6 | 44139577 | |||
chr6:44147432 | G | A | 1 | a0002 | 61 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(58): Show |
missense_variant | MODERATE | c.919G>A | p.Val307Met | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 12/24 | 1068/3284 | 919/2499 | 307/832 | chr6 | 44147432 | |||
chr6:44154856 | CCTCATAG others(6): Show |
C | 1 | a0006 | 1 | NA18965.hp2 | frameshift_variant | HIGH | c.2473_2485delCTCATA others(7): Show |
p.Leu825fs | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 2622/3284 | 2473/2499 | 825/832 | chr6 | 44154856 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:44139557 | C | T | 1 | a0002c0005 | 2 | NA18944.hp2 NA19084.hp2 |
synonymous_variant | LOW | c.498C>T | p.Gly166Gly | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 7/24 | 647/3284 | 498/2499 | 166/832 | chr6 | 44139557 | |||
chr6:44140291 | G | T | 1 | a0001c0013 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.642G>T | p.Leu214Leu | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 9/24 | 791/3284 | 642/2499 | 214/832 | chr6 | 44140291 | |||
chr6:44149870 | C | T | 3 | a0001c0012 a0002c0002 a0002c0005 |
61 | HG00423.hp2 HG00438.hp2 HG01167.hp2 others(58): Show |
synonymous_variant | LOW | c.1425C>T | p.Ile475Ile | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 16/24 | 1574/3284 | 1425/2499 | 475/832 | chr6 | 44149870 | |||
chr6:44149927 | C | T | 4 | a0001c0013 a0002c0002 a0002c0005 others(1): Show |
62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
synonymous_variant | LOW | c.1482C>T | p.Ile494Ile | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 16/24 | 1631/3284 | 1482/2499 | 494/832 | chr6 | 44149927 | |||
chr6:44151939 | A | G | 4 | a0001c0004 a0002c0002 a0002c0005 others(1): Show |
63 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(60): Show |
synonymous_variant | LOW | c.1767A>G | p.Pro589Pro | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/24 | 1916/3284 | 1767/2499 | 589/832 | chr6 | 44151939 | |||
chr6:44153767 | G | A | 1 | a0001c0010 | 1 | HG01943.hp1 | synonymous_variant | LOW | c.2034G>A | p.Ser678Ser | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 21/24 | 2183/3284 | 2034/2499 | 678/832 | chr6 | 44153767 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:44127555 | T | C | 1 | a0002c0002t0011 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/24 | 7030 | chr6 | 44127555 | ||||||
chr6:44127590 | G | C | 4 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0012 others(1): Show |
6 | HG02615.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-113G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/24 | 6995 | chr6 | 44127590 | ||||||
chr6:44127606 | C | G | 1 | a0001c0001t0019 | 1 | HG02257.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-97C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/24 | chr6 | 44127606 | |||||||
chr6:44127617 | T | C | 1 | a0002c0002t0014 | 1 | NA18939.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/24 | 6968 | chr6 | 44127617 | ||||||
chr6:44154936 | C | A | 1 | a0006c0011t0015 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 53 | chr6 | 44154936 | ||||||
chr6:44154937 | A | C | 1 | a0006c0011t0015 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*54A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 54 | chr6 | 44154937 | ||||||
chr6:44155035 | T | TC | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(19): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*157dupC | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 158 | INFO_REALIGN_3_PRIME | chr6 | 44155035 | |||||
chr6:44155142 | C | A | 9 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0012 others(6): Show |
68 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*259C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 259 | chr6 | 44155142 | ||||||
chr6:44155265 | C | A | 1 | a0001c0001t0018 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*382C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 382 | chr6 | 44155265 | ||||||
chr6:44155404 | G | A | 2 | a0001c0001t0012 a0001c0001t0016 |
2 | HG01884.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*521G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 521 | chr6 | 44155404 | ||||||
chr6:44155451 | G | GT | 1 | a0001c0001t0005 | 26 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*578dupT | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 579 | INFO_REALIGN_3_PRIME | chr6 | 44155451 | |||||
chr6:44155459 | T | TTGG | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(20): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*577_*578insGGT | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 578 | INFO_REALIGN_3_PRIME | chr6 | 44155459 | |||||
chr6:44155461 | T | G | 1 | a0001c0001t0010 | 2 | HG02976.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*578T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 578 | chr6 | 44155461 | ||||||
chr6:44155462 | G | T | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(20): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*579G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 579 | chr6 | 44155462 | ||||||
chr6:44155463 | G | T | 1 | a0001c0001t0010 | 2 | HG02976.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*580G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 580 | chr6 | 44155463 | ||||||
chr6:44155479 | T | C | 5 | a0001c0001t0007 a0002c0002t0004 a0002c0002t0011 others(2): Show |
40 | HG00438.hp2 HG00544.hp1 HG01175.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*596T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 596 | chr6 | 44155479 | ||||||
chr6:44155481 | G | GT | 1 | a0001c0001t0006 | 7 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*605dupT | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 24/24 | 606 | INFO_REALIGN_3_PRIME | chr6 | 44155481 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:44127953 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-25+275G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44127953 | |||||||
chr6:44128194 | C | T | 2 | a0001c0001t0003g0048 a0001c0001t0003g0205 |
3 | NA18955.hp2 NA19012.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-25+516C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44128194 | |||||||
chr6:44128277 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(37): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-25+599G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44128277 | |||||||
chr6:44128404 | G | A | 3 | a0001c0001t0009g0084 a0001c0001t0010g0082 a0001c0001t0010g0083 |
3 | HG02976.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-25+726G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44128404 | |||||||
chr6:44128544 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-25+866A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44128544 | |||||||
chr6:44129106 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0006g0015 |
5 | HG01255.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+1428G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44129106 | |||||||
chr6:44129139 | G | A | 32 | a0001c0001t0001g0098 a0001c0001t0002g0003 a0001c0001t0002g0007 others(29): Show |
67 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.-25+1461G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44129139 | |||||||
chr6:44129184 | A | G | 5 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0102 others(2): Show |
7 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25+1506A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44129184 | |||||||
chr6:44129199 | C | T | 1 | a0001c0001t0002g0047 | 2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-25+1521C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44129199 | |||||||
chr6:44129206 | A | T | 1 | a0002c0002t0014g0202 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-25+1528A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44129206 | |||||||
chr6:44129365 | CA | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(151): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-25+1704delA | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 44129365 | ||||||
chr6:44129365 | CAA | C | 9 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0201 others(6): Show |
9 | HG01070.hp2 HG02735.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1703_-25+1704d others(4): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 44129365 | ||||||
chr6:44129377 | A | AAAAAGAA others(7): Show |
1 | a0001c0001t0005g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-25+1703_-25+1704i others(16): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 44129377 | ||||||
chr6:44129384 | A | G | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-25+1706A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44129384 | |||||||
chr6:44129711 | G | A | 1 | a0001c0001t0003g0087 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-25+2033G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44129711 | |||||||
chr6:44129735 | T | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(42): Show |
99 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-25+2057T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44129735 | |||||||
chr6:44129745 | C | G | 1 | a0002c0002t0004g0194 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-25+2067C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44129745 | |||||||
chr6:44129995 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-25+2317A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44129995 | |||||||
chr6:44130009 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-25+2331G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130009 | |||||||
chr6:44130409 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0052 |
6 | HG02109.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+2731T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130409 | |||||||
chr6:44130411 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0052 |
6 | HG02109.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+2733C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130411 | |||||||
chr6:44130529 | C | T | 2 | a0002c0002t0002g0193 a0002c0009t0002g0192 |
2 | HG00738.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-25+2851C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130529 | |||||||
chr6:44130538 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0052 |
6 | HG02109.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+2860C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130538 | |||||||
chr6:44130550 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(78): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-25+2872G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130550 | |||||||
chr6:44130617 | T | G | 1 | a0002c0002t0001g0041 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-25+2939T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130617 | |||||||
chr6:44130749 | C | CT | 148 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(145): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-25+3085dupT | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 44130749 | ||||||
chr6:44130749 | C | CTT | 24 | a0001c0001t0001g0030 a0001c0001t0001g0074 a0001c0001t0001g0075 others(21): Show |
26 | HG00438.hp1 HG00438.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-25+3084_-25+3085d others(4): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 44130749 | ||||||
chr6:44130811 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-25+3133G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130811 | |||||||
chr6:44130812 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-25+3134C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130812 | |||||||
chr6:44130825 | G | A | 14 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0182 others(11): Show |
21 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-25+3147G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130825 | |||||||
chr6:44130935 | T | G | 35 | a0001c0001t0001g0042 a0001c0001t0001g0145 a0001c0001t0001g0146 others(32): Show |
45 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.-25+3257T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44130935 | |||||||
chr6:44131062 | C | T | 33 | a0001c0001t0001g0098 a0001c0001t0002g0003 a0001c0001t0002g0007 others(30): Show |
70 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.-25+3384C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131062 | |||||||
chr6:44131207 | C | T | 1 | a0006c0011t0015g0100 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-24-3354C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131207 | |||||||
chr6:44131303 | C | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | NA19007.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-24-3258C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131303 | |||||||
chr6:44131314 | A | T | 1 | a0001c0001t0009g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-24-3247A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131314 | |||||||
chr6:44131547 | T | C | 1 | a0001c0001t0008g0037 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-24-3014T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131547 | |||||||
chr6:44131578 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-24-2983G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131578 | |||||||
chr6:44131675 | C | T | 1 | a0001c0004t0002g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-24-2886C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131675 | |||||||
chr6:44131712 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-24-2849C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131712 | |||||||
chr6:44131734 | A | AC | 168 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(165): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-24-2820dupC | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 44131734 | ||||||
chr6:44131742 | A | C | 22 | a0001c0001t0001g0098 a0001c0001t0001g0128 a0001c0001t0002g0007 others(19): Show |
38 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.-24-2819A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131742 | |||||||
chr6:44131762 | T | C | 1 | a0003c0003t0002g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-24-2799T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131762 | |||||||
chr6:44131824 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(166): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-24-2737G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131824 | |||||||
chr6:44131894 | A | G | 3 | a0001c0001t0003g0147 a0001c0001t0003g0148 a0001c0001t0003g0149 |
3 | HG00140.hp2 HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-24-2667A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44131894 | |||||||
chr6:44132120 | C | G | 1 | a0001c0001t0003g0092 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-24-2441C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44132120 | |||||||
chr6:44132127 | T | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24-2434T>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44132127 | |||||||
chr6:44132310 | T | C | 32 | a0001c0001t0001g0098 a0001c0001t0002g0003 a0001c0001t0002g0007 others(29): Show |
67 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.-24-2251T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44132310 | |||||||
chr6:44132403 | ATAGGAAT others(11): Show |
A | 1 | a0002c0002t0002g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-24-2157_-24-2140d others(20): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44132403 | |||||||
chr6:44132637 | C | T | 1 | a0001c0001t0006g0022 | 3 | HG01891.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-24-1924C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44132637 | |||||||
chr6:44132719 | C | A | 2 | a0001c0001t0010g0082 a0001c0001t0010g0083 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-24-1842C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44132719 | |||||||
chr6:44132723 | GCTC | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(78): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-24-1832_-24-1830d others(5): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 44132723 | ||||||
chr6:44132799 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0152 a0001c0001t0003g0150 others(2): Show |
6 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24-1762G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44132799 | |||||||
chr6:44132937 | G | T | 1 | a0001c0001t0003g0092 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-24-1624G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44132937 | |||||||
chr6:44133028 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-24-1533A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133028 | |||||||
chr6:44133315 | G | A | 3 | a0001c0001t0009g0138 a0001c0001t0012g0040 a0001c0001t0013g0040 |
3 | HG02615.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-24-1246G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133315 | |||||||
chr6:44133539 | T | C | 168 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(165): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-24-1022T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133539 | |||||||
chr6:44133638 | C | T | 38 | a0002c0002t0001g0041 a0002c0002t0002g0010 a0002c0002t0002g0018 others(35): Show |
61 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.-24-923C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133638 | |||||||
chr6:44133685 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(42): Show |
99 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-876C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133685 | |||||||
chr6:44133731 | C | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(42): Show |
99 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-830C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133731 | |||||||
chr6:44133781 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-24-780C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133781 | |||||||
chr6:44133782 | G | A | 1 | a0002c0002t0004g0168 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-24-779G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133782 | |||||||
chr6:44133807 | C | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(163): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-24-754C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133807 | |||||||
chr6:44133818 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-24-743G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133818 | |||||||
chr6:44133867 | A | C | 1 | a0002c0002t0002g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-24-694A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133867 | |||||||
chr6:44133971 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0006g0015 |
5 | HG01255.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-590A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44133971 | |||||||
chr6:44134201 | G | A | 3 | a0001c0001t0002g0049 a0001c0001t0002g0184 a0001c0001t0018g0166 |
3 | HG02615.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-24-360G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44134201 | |||||||
chr6:44134234 | T | G | 2 | a0002c0002t0002g0169 a0002c0002t0002g0185 |
2 | HG02071.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-24-327T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44134234 | |||||||
chr6:44134338 | T | A | 2 | a0001c0001t0001g0085 a0001c0001t0006g0015 |
5 | HG01255.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-223T>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44134338 | |||||||
chr6:44134395 | T | C | 1 | a0001c0001t0005g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-24-166T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 1/23 | chr6 | 44134395 | |||||||
chr6:44134835 | C | CT | 171 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(168): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.159+92_159+93insT | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 2/23 | chr6 | 44134835 | |||||||
chr6:44135107 | G | C | 1 | a0001c0004t0002g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.239+11G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 3/23 | chr6 | 44135107 | |||||||
chr6:44135142 | G | A | 1 | a0001c0001t0007g0053 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.239+46G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 3/23 | chr6 | 44135142 | |||||||
chr6:44135282 | G | C | 32 | a0001c0001t0001g0042 a0001c0001t0001g0152 a0001c0001t0001g0182 others(29): Show |
42 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.240-46G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 3/23 | chr6 | 44135282 | |||||||
chr6:44135293 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.240-35C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 3/23 | chr6 | 44135293 | |||||||
chr6:44135432 | T | G | 1 | a0001c0001t0002g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.278+66T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44135432 | |||||||
chr6:44135456 | G | A | 1 | a0001c0001t0003g0153 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.278+90G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44135456 | |||||||
chr6:44135551 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.278+185C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44135551 | |||||||
chr6:44135576 | C | T | 5 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0184 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.278+210C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44135576 | |||||||
chr6:44135601 | C | T | 1 | a0001c0001t0005g0124 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.278+235C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44135601 | |||||||
chr6:44135685 | G | A | 1 | a0001c0001t0005g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.278+319G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44135685 | |||||||
chr6:44135689 | C | T | 1 | a0008c0014t0002g0099 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.278+323C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44135689 | |||||||
chr6:44135728 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.278+362G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44135728 | |||||||
chr6:44135812 | G | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0152 |
3 | HG00099.hp2 HG00280.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.278+446G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44135812 | |||||||
chr6:44135819 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.278+453T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44135819 | |||||||
chr6:44136008 | G | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0152 a0001c0001t0003g0150 others(2): Show |
6 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.279-341G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44136008 | |||||||
chr6:44136144 | C | G | 1 | a0001c0001t0008g0037 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.279-205C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44136144 | |||||||
chr6:44136145 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(2): Show |
7 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.279-204C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44136145 | |||||||
chr6:44136314 | C | G | 5 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0184 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.279-35C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 4/23 | chr6 | 44136314 | |||||||
chr6:44136549 | T | G | 22 | a0002c0002t0004g0004 a0002c0002t0004g0024 a0002c0002t0004g0025 others(19): Show |
35 | HG00438.hp2 HG01175.hp1 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.369+110T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136549 | |||||||
chr6:44136556 | C | T | 1 | a0001c0001t0001g0036 | 2 | NA18997.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.369+117C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136556 | |||||||
chr6:44136569 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(42): Show |
99 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.369+130G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136569 | |||||||
chr6:44136658 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(128): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.369+219T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136658 | |||||||
chr6:44136712 | C | T | 4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0203 others(1): Show |
6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+273C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136712 | |||||||
chr6:44136744 | G | A | 1 | a0001c0013t0003g0154 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.369+305G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136744 | |||||||
chr6:44136785 | G | A | 1 | a0001c0001t0016g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.369+346G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136785 | |||||||
chr6:44136821 | AGGATCAC others(11): Show |
A | 1 | a0005c0008t0002g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.369+383_369+400del others(18): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136821 | |||||||
chr6:44136836 | C | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(127): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.369+397C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136836 | |||||||
chr6:44136873 | G | A | 1 | a0001c0001t0003g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.369+434G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136873 | |||||||
chr6:44136880 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(128): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.369+441C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136880 | |||||||
chr6:44136991 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(2): Show |
7 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.369+552G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44136991 | |||||||
chr6:44137031 | C | T | 6 | a0001c0001t0001g0132 a0001c0001t0002g0049 a0001c0001t0002g0050 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+592C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137031 | |||||||
chr6:44137053 | CA | C | 3 | a0001c0001t0002g0008 a0001c0001t0002g0072 a0001c0001t0002g0102 |
8 | HG00733.hp1 HG01496.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+622delA | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 44137053 | ||||||
chr6:44137081 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(79): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.369+642C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137081 | |||||||
chr6:44137144 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(128): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.369+705A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137144 | |||||||
chr6:44137151 | G | A | 2 | a0002c0002t0002g0044 a0002c0002t0002g0190 |
3 | HG00423.hp2 NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.369+712G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137151 | |||||||
chr6:44137190 | G | A | 1 | a0001c0004t0002g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.369+751G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137190 | |||||||
chr6:44137376 | G | A | 1 | a0001c0001t0003g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.369+937G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137376 | |||||||
chr6:44137394 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.369+955C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137394 | |||||||
chr6:44137568 | C | G | 39 | a0001c0004t0002g0181 a0002c0002t0001g0041 a0002c0002t0002g0010 others(36): Show |
62 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.370-912C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137568 | |||||||
chr6:44137690 | A | ATT | 30 | a0001c0001t0001g0042 a0001c0001t0001g0152 a0001c0001t0001g0182 others(27): Show |
39 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.370-776_370-775dup others(2): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 44137690 | ||||||
chr6:44137704 | T | A | 1 | a0001c0001t0002g0016 | 4 | HG00408.hp1 HG00609.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-776T>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137704 | |||||||
chr6:44137705 | T | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(122): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.370-775T>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137705 | |||||||
chr6:44137721 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0006g0015 |
5 | HG01255.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-759C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137721 | |||||||
chr6:44137738 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG03017.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.370-742G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137738 | |||||||
chr6:44137765 | C | T | 1 | a0001c0001t0017g0196 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.370-715C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137765 | |||||||
chr6:44137816 | A | G | 22 | a0002c0002t0004g0004 a0002c0002t0004g0024 a0002c0002t0004g0025 others(19): Show |
35 | HG00438.hp2 HG01175.hp1 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.370-664A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137816 | |||||||
chr6:44137833 | G | A | 1 | a0001c0001t0003g0205 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.370-647G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137833 | |||||||
chr6:44137946 | C | T | 32 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(29): Show |
67 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.370-534C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137946 | |||||||
chr6:44137947 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.370-533G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137947 | |||||||
chr6:44137978 | G | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
241 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.370-502G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137978 | |||||||
chr6:44137986 | C | T | 1 | a0001c0001t0016g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.370-494C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44137986 | |||||||
chr6:44138091 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.370-389C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44138091 | |||||||
chr6:44138192 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(42): Show |
99 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.370-288C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44138192 | |||||||
chr6:44138241 | A | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(167): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.370-239A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44138241 | |||||||
chr6:44138244 | G | A | 170 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(167): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.370-236G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44138244 | |||||||
chr6:44138303 | C | T | 4 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0184 others(1): Show |
4 | HG01884.hp1 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-177C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44138303 | |||||||
chr6:44138361 | A | G | 1 | a0001c0001t0009g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.370-119A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44138361 | |||||||
chr6:44138432 | C | T | 1 | a0002c0002t0004g0177 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.370-48C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 5/23 | chr6 | 44138432 | |||||||
chr6:44138630 | C | T | 1 | a0001c0004t0002g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.407+113C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138630 | |||||||
chr6:44138644 | C | T | 1 | a0001c0004t0002g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.407+127C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138644 | |||||||
chr6:44138727 | CCCCTGCC others(17): Show |
C | 1 | a0001c0001t0005g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.407+218_407+241del others(24): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138727 | ||||||
chr6:44138736 | G | GCCC | 20 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0034 others(17): Show |
32 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.407+224_407+226dup others(3): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCC | 26 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0016 others(23): Show |
38 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.407+223_407+226dup others(4): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCC | 21 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0016 others(18): Show |
26 | HG00639.hp2 HG01081.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.407+222_407+226dup others(5): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(9): Show |
2 | a0001c0001t0005g0020 a0001c0001t0005g0110 |
3 | HG02145.hp1 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.407+226_407+227ins others(16): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(11): Show |
1 | a0001c0001t0005g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.407+226_407+227ins others(18): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(3): Show |
1 | a0001c0001t0001g0201 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.407+226_407+227ins others(10): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(4): Show |
2 | a0001c0001t0001g0145 a0001c0001t0005g0017 |
2 | HG02809.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.407+226_407+227ins others(11): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(5): Show |
3 | a0001c0001t0001g0021 a0001c0001t0005g0009 a0001c0001t0005g0112 |
6 | HG00733.hp2 HG01074.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.407+226_407+227ins others(12): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(6): Show |
2 | a0001c0001t0001g0133 a0001c0001t0005g0111 |
2 | HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.407+226_407+227ins others(13): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(7): Show |
4 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0005g0009 others(1): Show |
5 | HG01071.hp1 HG01074.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.407+226_407+227ins others(14): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(8): Show |
3 | a0001c0001t0005g0106 a0001c0001t0005g0124 a0001c0001t0005g0139 |
3 | HG01070.hp1 HG01243.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.407+226_407+227ins others(15): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(9): Show |
2 | a0001c0001t0005g0017 a0001c0001t0005g0105 |
3 | HG02559.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.407+226_407+227ins others(16): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(10): Show |
4 | a0001c0001t0005g0009 a0001c0001t0005g0017 a0001c0001t0005g0113 others(1): Show |
4 | HG02280.hp2 HG02300.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.407+226_407+227ins others(17): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GCCCCCCC others(11): Show |
1 | a0001c0001t0005g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.407+226_407+227ins others(18): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 44138736 | ||||||
chr6:44138736 | G | GTCCCCCC others(3): Show |
3 | a0002c0002t0002g0018 a0002c0002t0002g0169 a0002c0002t0004g0170 |
3 | HG01257.hp2 HG02071.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.407+219_407+220ins others(10): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138736 | G | GTCCCCCC others(4): Show |
3 | a0002c0002t0002g0010 a0002c0002t0002g0179 a0002c0009t0002g0192 |
3 | HG00738.hp1 NA18959.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.407+219_407+220ins others(11): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138736 | G | GTCCCCCC others(5): Show |
6 | a0002c0002t0002g0010 a0002c0002t0002g0165 a0002c0002t0002g0185 others(3): Show |
7 | HG01167.hp2 HG02735.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+219_407+220ins others(12): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138736 | G | GTCCCCCC others(6): Show |
9 | a0002c0002t0002g0010 a0002c0002t0002g0018 a0002c0002t0002g0044 others(6): Show |
10 | HG01168.hp1 HG02055.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.407+219_407+220ins others(13): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138736 | G | GTCCCCCC others(7): Show |
8 | a0002c0002t0002g0018 a0002c0002t0002g0044 a0002c0002t0002g0178 others(5): Show |
10 | HG00423.hp2 HG02148.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.407+219_407+220ins others(14): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138736 | G | GTCCCCCC others(8): Show |
6 | a0002c0002t0002g0018 a0002c0002t0004g0004 a0002c0002t0004g0168 others(3): Show |
8 | HG01175.hp1 HG01192.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.407+219_407+220ins others(15): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138736 | G | GTCCCCCC others(9): Show |
5 | a0002c0002t0002g0010 a0002c0002t0002g0134 a0002c0002t0004g0004 others(2): Show |
5 | HG01175.hp2 HG01952.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.407+219_407+220ins others(16): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138736 | G | GTCCCCCC others(10): Show |
6 | a0002c0002t0002g0200 a0002c0002t0004g0004 a0002c0002t0004g0172 others(3): Show |
6 | HG04184.hp2 NA18942.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.407+219_407+220ins others(17): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138736 | G | GTCCCCCC others(11): Show |
3 | a0002c0002t0004g0024 a0002c0002t0004g0025 a0002c0002t0014g0202 |
3 | NA18939.hp2 NA18941.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.407+219_407+220ins others(18): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138736 | G | GTCCCCCC others(12): Show |
3 | a0002c0002t0004g0171 a0002c0002t0004g0174 a0002c0002t0004g0189 |
3 | NA18994.hp2 NA19009.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.407+219_407+220ins others(19): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138736 | G | GTTCCCCC others(6): Show |
1 | a0002c0002t0004g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.407+219_407+220ins others(13): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138736 | |||||||
chr6:44138740 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.407+223C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138740 | |||||||
chr6:44138744 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0006g0015 |
5 | HG01255.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.407+227G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138744 | |||||||
chr6:44138760 | T | C | 130 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0085 others(127): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.407+243T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138760 | |||||||
chr6:44138811 | C | T | 71 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0085 others(68): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.407+294C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138811 | |||||||
chr6:44138919 | G | A | 1 | a0001c0001t0005g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.407+402G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138919 | |||||||
chr6:44138943 | C | T | 9 | a0002c0002t0004g0025 a0002c0002t0004g0175 a0002c0002t0004g0176 others(6): Show |
11 | HG00438.hp2 HG02074.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.407+426C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138943 | |||||||
chr6:44138978 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0097 |
3 | NA18612.hp2 NA19004.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.407+461C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44138978 | |||||||
chr6:44139011 | T | A | 1 | a0001c0001t0001g0055 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.408-456T>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139011 | |||||||
chr6:44139029 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01081.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.408-438C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139029 | |||||||
chr6:44139045 | C | G | 1 | a0001c0004t0002g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.408-422C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139045 | |||||||
chr6:44139077 | C | G | 4 | a0001c0001t0001g0085 a0001c0001t0006g0015 a0001c0001t0006g0022 others(1): Show |
9 | HG01255.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.408-390C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139077 | |||||||
chr6:44139117 | T | G | 37 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(34): Show |
73 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.408-350T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139117 | |||||||
chr6:44139200 | C | G | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.408-267C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139200 | |||||||
chr6:44139202 | A | G | 28 | a0001c0001t0001g0042 a0001c0001t0001g0152 a0001c0001t0003g0006 others(25): Show |
37 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.408-265A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139202 | |||||||
chr6:44139204 | C | T | 88 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(85): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.408-263C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139204 | |||||||
chr6:44139308 | A | T | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.408-159A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139308 | |||||||
chr6:44139374 | T | G | 1 | a0005c0008t0002g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.408-93T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139374 | |||||||
chr6:44139452 | C | T | 40 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.408-15C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139452 | |||||||
chr6:44139454 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG00408.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.408-13C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139454 | |||||||
chr6:44139455 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.408-12G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139455 | |||||||
chr6:44139455 | G | T | 1 | a0001c0001t0008g0037 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.408-12G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139455 | |||||||
chr6:44139463 | G | A | 45 | a0001c0001t0001g0042 a0001c0001t0001g0152 a0001c0001t0003g0006 others(42): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
splice_region_variant&intron_variant | LOW | c.408-4G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 6/23 | chr6 | 44139463 | |||||||
chr6:44139628 | G | A | 53 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(50): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.550+19G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 7/23 | chr6 | 44139628 | |||||||
chr6:44139768 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.602+9C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 8/23 | chr6 | 44139768 | |||||||
chr6:44139822 | G | A | 40 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.602+63G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 8/23 | chr6 | 44139822 | |||||||
chr6:44139868 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.602+109G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 8/23 | chr6 | 44139868 | |||||||
chr6:44139875 | A | G | 94 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(91): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.602+116A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 8/23 | chr6 | 44139875 | |||||||
chr6:44139903 | C | T | 53 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(50): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.602+144C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 8/23 | chr6 | 44139903 | |||||||
chr6:44140061 | T | C | 53 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(50): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.603-191T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 8/23 | chr6 | 44140061 | |||||||
chr6:44140166 | A | G | 2 | a0001c0001t0005g0114 a0001c0001t0005g0139 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.603-86A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 8/23 | chr6 | 44140166 | |||||||
chr6:44140169 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.603-83G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 8/23 | chr6 | 44140169 | |||||||
chr6:44140413 | T | C | 53 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(50): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.711+53T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 9/23 | chr6 | 44140413 | |||||||
chr6:44140447 | G | T | 1 | a0005c0008t0002g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.711+87G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 9/23 | chr6 | 44140447 | |||||||
chr6:44140478 | A | G | 1 | a0001c0012t0001g0121 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.711+118A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 9/23 | chr6 | 44140478 | |||||||
chr6:44140493 | A | G | 1 | a0001c0001t0005g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.711+133A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 9/23 | chr6 | 44140493 | |||||||
chr6:44140631 | T | A | 1 | a0005c0008t0002g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.711+271T>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 9/23 | chr6 | 44140631 | |||||||
chr6:44140688 | G | A | 1 | a0001c0001t0003g0019 | 3 | NA18970.hp2 NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.711+328G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 9/23 | chr6 | 44140688 | |||||||
chr6:44140757 | T | C | 1 | a0005c0008t0002g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.712-271T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 9/23 | chr6 | 44140757 | |||||||
chr6:44140778 | G | C | 40 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.712-250G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 9/23 | chr6 | 44140778 | |||||||
chr6:44140829 | G | A | 133 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(130): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.712-199G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 9/23 | chr6 | 44140829 | |||||||
chr6:44141111 | C | T | 40 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.782+13C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44141111 | |||||||
chr6:44141200 | G | A | 45 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(42): Show |
70 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.782+102G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44141200 | |||||||
chr6:44141237 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.782+139C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44141237 | |||||||
chr6:44141275 | G | T | 40 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.782+177G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44141275 | |||||||
chr6:44141392 | T | C | 1 | a0001c0004t0001g0057 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.782+294T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44141392 | |||||||
chr6:44141619 | G | T | 53 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(50): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.782+521G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44141619 | |||||||
chr6:44141653 | C | T | 2 | a0001c0001t0003g0038 a0001c0001t0003g0135 |
3 | HG02280.hp1 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.782+555C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44141653 | |||||||
chr6:44141662 | G | A | 1 | a0001c0001t0008g0037 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.782+564G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44141662 | |||||||
chr6:44141991 | G | T | 1 | a0001c0004t0002g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.782+893G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44141991 | |||||||
chr6:44142050 | A | T | 1 | a0001c0001t0008g0037 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.782+952A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142050 | |||||||
chr6:44142109 | G | A | 11 | a0001c0001t0003g0006 a0001c0001t0003g0043 a0001c0001t0003g0143 others(8): Show |
18 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.782+1011G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142109 | |||||||
chr6:44142144 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | NA18953.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.782+1046G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142144 | |||||||
chr6:44142267 | TA | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(73): Show |
145 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.782+1189delA | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44142267 | ||||||
chr6:44142267 | TAA | T | 83 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0145 others(80): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.782+1188_782+1189d others(4): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44142267 | ||||||
chr6:44142267 | TAAA | T | 6 | a0001c0001t0003g0144 a0001c0001t0003g0158 a0001c0001t0003g0162 others(3): Show |
6 | HG01070.hp2 HG01516.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.782+1187_782+1189d others(5): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44142267 | ||||||
chr6:44142277 | A | G | 1 | a0001c0001t0003g0149 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.782+1179A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142277 | |||||||
chr6:44142358 | T | C | 55 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(52): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.782+1260T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142358 | |||||||
chr6:44142415 | A | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(3): Show |
8 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+1317A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142415 | |||||||
chr6:44142444 | C | T | 16 | a0001c0001t0005g0009 a0001c0001t0005g0017 a0001c0001t0005g0020 others(13): Show |
26 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.782+1346C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142444 | |||||||
chr6:44142487 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.782+1389G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142487 | |||||||
chr6:44142494 | C | T | 1 | a0002c0002t0004g0177 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.782+1396C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142494 | |||||||
chr6:44142533 | A | T | 1 | a0001c0001t0008g0037 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.782+1435A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142533 | |||||||
chr6:44142551 | A | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0075 others(1): Show |
8 | HG02257.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.782+1453A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142551 | |||||||
chr6:44142959 | T | C | 1 | a0002c0002t0004g0177 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.782+1861T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142959 | |||||||
chr6:44142965 | C | T | 39 | a0001c0004t0002g0181 a0002c0002t0001g0041 a0002c0002t0002g0010 others(36): Show |
62 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.782+1867C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142965 | |||||||
chr6:44142992 | G | A | 4 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0184 others(1): Show |
4 | HG01884.hp1 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+1894G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44142992 | |||||||
chr6:44143017 | A | G | 4 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0184 others(1): Show |
4 | HG01884.hp1 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+1919A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143017 | |||||||
chr6:44143107 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.782+2009G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143107 | |||||||
chr6:44143212 | G | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(3): Show |
8 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+2114G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143212 | |||||||
chr6:44143326 | C | T | 2 | a0001c0001t0010g0082 a0001c0001t0010g0083 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.782+2228C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143326 | |||||||
chr6:44143563 | GTTTGTTG others(2): Show |
G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(3): Show |
8 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+2472_782+2480d others(11): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44143563 | ||||||
chr6:44143564 | TTTG | T | 41 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(38): Show |
79 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.782+2472_782+2474d others(5): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44143564 | ||||||
chr6:44143567 | G | GTTT | 44 | a0001c0001t0001g0042 a0001c0001t0001g0152 a0001c0001t0003g0006 others(41): Show |
63 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.782+2471_782+2472i others(5): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44143567 | ||||||
chr6:44143567 | GTTGTTTT others(5): Show |
G | 4 | a0001c0001t0003g0136 a0001c0001t0012g0040 a0001c0001t0013g0040 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+2484_782+2495d others(14): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44143567 | ||||||
chr6:44143570 | G | T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.782+2472G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143570 | |||||||
chr6:44143736 | G | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0085 a0001c0001t0009g0138 |
10 | HG01255.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.782+2638G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143736 | |||||||
chr6:44143754 | G | A | 5 | a0001c0001t0005g0017 a0001c0001t0005g0105 a0001c0001t0005g0109 others(2): Show |
8 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+2656G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143754 | |||||||
chr6:44143787 | G | A | 1 | a0002c0002t0002g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.782+2689G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143787 | |||||||
chr6:44143854 | C | T | 4 | a0001c0001t0003g0136 a0001c0001t0012g0040 a0001c0001t0013g0040 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+2756C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143854 | |||||||
chr6:44143855 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.782+2757G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143855 | |||||||
chr6:44143867 | C | T | 1 | a0001c0004t0002g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.782+2769C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44143867 | |||||||
chr6:44144064 | G | A | 32 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(29): Show |
67 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.783-2783G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144064 | |||||||
chr6:44144181 | A | C | 38 | a0002c0002t0001g0041 a0002c0002t0002g0010 a0002c0002t0002g0018 others(35): Show |
61 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.783-2666A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144181 | |||||||
chr6:44144337 | C | T | 4 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0184 others(1): Show |
4 | HG01884.hp1 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.783-2510C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144337 | |||||||
chr6:44144390 | A | G | 1 | a0001c0001t0019g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.783-2457A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144390 | |||||||
chr6:44144657 | C | T | 133 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(130): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.783-2190C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144657 | |||||||
chr6:44144667 | G | A | 51 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0133 others(48): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.783-2180G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144667 | |||||||
chr6:44144672 | C | T | 16 | a0001c0001t0005g0009 a0001c0001t0005g0017 a0001c0001t0005g0020 others(13): Show |
26 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.783-2175C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144672 | |||||||
chr6:44144722 | G | A | 40 | a0001c0001t0001g0116 a0001c0004t0002g0181 a0002c0002t0001g0041 others(37): Show |
63 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.783-2125G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144722 | |||||||
chr6:44144820 | A | C | 1 | a0002c0002t0004g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.783-2027A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144820 | |||||||
chr6:44144821 | C | T | 1 | a0002c0002t0004g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.783-2026C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144821 | |||||||
chr6:44144822 | T | C | 1 | a0002c0002t0004g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.783-2025T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144822 | |||||||
chr6:44144986 | C | T | 32 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(29): Show |
67 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.783-1861C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44144986 | |||||||
chr6:44145204 | G | C | 1 | a0001c0001t0005g0111 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.783-1643G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44145204 | |||||||
chr6:44145274 | C | CA | 51 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0027 others(48): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.783-1556dupA | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44145274 | ||||||
chr6:44145274 | C | CAA | 8 | a0001c0001t0001g0145 a0001c0001t0003g0147 a0001c0001t0003g0148 others(5): Show |
8 | HG00140.hp2 HG01928.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.783-1557_783-1556d others(4): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44145274 | ||||||
chr6:44145274 | CA | C | 43 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0062 others(40): Show |
74 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.783-1556delA | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44145274 | ||||||
chr6:44145301 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | NA19007.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.783-1546C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44145301 | |||||||
chr6:44145343 | A | G | 141 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0062 others(138): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.783-1504A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44145343 | |||||||
chr6:44145379 | G | A | 1 | a0003c0003t0002g0096 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.783-1468G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44145379 | |||||||
chr6:44145500 | G | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0022 |
7 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.783-1347G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44145500 | |||||||
chr6:44145587 | G | A | 1 | a0001c0013t0003g0154 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.783-1260G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44145587 | |||||||
chr6:44145615 | AAAAC | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(5): Show |
15 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.783-1228_783-1225d others(6): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44145615 | ||||||
chr6:44145630 | C | CA | 27 | a0001c0001t0003g0006 a0001c0001t0003g0043 a0001c0001t0003g0045 others(24): Show |
35 | HG00140.hp2 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.783-1211dupA | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44145630 | ||||||
chr6:44145762 | C | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(3): Show |
8 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.783-1085C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44145762 | |||||||
chr6:44145779 | GAAAC | G | 17 | a0001c0001t0005g0009 a0001c0001t0005g0017 a0001c0001t0005g0020 others(14): Show |
27 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.783-1052_783-1049d others(6): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44145779 | ||||||
chr6:44146152 | A | ACAGACAA others(18): Show |
1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-695_783-694ins others(25): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146152 | |||||||
chr6:44146153 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-694G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146153 | |||||||
chr6:44146165 | A | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-682A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146165 | |||||||
chr6:44146178 | A | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-669A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146178 | |||||||
chr6:44146179 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-668T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146179 | |||||||
chr6:44146179 | T | G | 130 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(127): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.783-668T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146179 | |||||||
chr6:44146181 | A | G | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-666A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146181 | |||||||
chr6:44146189 | T | A | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-658T>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146189 | |||||||
chr6:44146191 | T | A | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-656T>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146191 | |||||||
chr6:44146199 | TGCAATTT others(5): Show |
T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-647_783-636del others(12): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146199 | |||||||
chr6:44146212 | A | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-635A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146212 | |||||||
chr6:44146215 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.783-632C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146215 | |||||||
chr6:44146224 | A | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-623A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146224 | |||||||
chr6:44146234 | A | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-613A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146234 | |||||||
chr6:44146249 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0075 others(1): Show |
8 | HG02257.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.783-598T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146249 | |||||||
chr6:44146255 | T | A | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-592T>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146255 | |||||||
chr6:44146278 | A | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-569A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146278 | |||||||
chr6:44146286 | A | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-561A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146286 | |||||||
chr6:44146356 | C | A | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-491C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146356 | |||||||
chr6:44146360 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-487T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146360 | |||||||
chr6:44146361 | A | T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-486A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146361 | |||||||
chr6:44146365 | A | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-482A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146365 | |||||||
chr6:44146378 | C | G | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-469C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146378 | |||||||
chr6:44146382 | A | T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-465A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146382 | |||||||
chr6:44146392 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-455T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146392 | |||||||
chr6:44146394 | G | T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-453G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146394 | |||||||
chr6:44146398 | A | G | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-449A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146398 | |||||||
chr6:44146410 | T | G | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-437T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146410 | |||||||
chr6:44146411 | G | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-436G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146411 | |||||||
chr6:44146415 | A | G | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-432A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146415 | |||||||
chr6:44146419 | A | T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-428A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146419 | |||||||
chr6:44146423 | A | G | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-424A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146423 | |||||||
chr6:44146426 | G | T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-421G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146426 | |||||||
chr6:44146429 | A | T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-418A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146429 | |||||||
chr6:44146439 | G | GGAGATGT others(979): Show |
1 | a0002c0002t0004g0172 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.783-391_783-390ins others(986): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146439 | ||||||
chr6:44146439 | G | GGAGATGT others(979): Show |
4 | a0002c0002t0002g0018 a0002c0002t0002g0179 a0002c0002t0004g0186 others(1): Show |
7 | HG01168.hp1 HG01192.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.783-391_783-390ins others(986): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146439 | ||||||
chr6:44146439 | G | GGAGATGT others(978): Show |
1 | a0002c0002t0004g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.783-391_783-390ins others(985): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146439 | ||||||
chr6:44146439 | G | GGAGATGT others(980): Show |
19 | a0002c0002t0001g0041 a0002c0002t0002g0010 a0002c0002t0002g0044 others(16): Show |
37 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.783-391_783-390ins others(987): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146439 | ||||||
chr6:44146439 | G | GGAGATGT others(980): Show |
1 | a0002c0002t0002g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.783-391_783-390ins others(987): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146439 | ||||||
chr6:44146439 | G | GGAGATGT others(980): Show |
1 | a0002c0002t0004g0173 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.783-391_783-390ins others(987): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146439 | ||||||
chr6:44146439 | G | GGAGATGT others(980): Show |
1 | a0002c0002t0004g0175 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.783-391_783-390ins others(987): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146439 | ||||||
chr6:44146439 | G | GGAGATGT others(980): Show |
1 | a0002c0002t0004g0189 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.783-391_783-390ins others(987): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146439 | ||||||
chr6:44146439 | G | GGAGATGT others(967): Show |
1 | a0001c0004t0002g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.783-391_783-390ins others(974): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146439 | ||||||
chr6:44146439 | G | GGAGATGT others(981): Show |
9 | a0002c0002t0002g0165 a0002c0002t0002g0178 a0002c0002t0002g0190 others(6): Show |
11 | HG02148.hp1 NA18941.hp1 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.783-391_783-390ins others(988): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146439 | ||||||
chr6:44146447 | G | T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-400G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146447 | |||||||
chr6:44146448 | G | C | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-399G>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146448 | |||||||
chr6:44146449 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-398G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146449 | |||||||
chr6:44146459 | C | CT | 17 | a0001c0001t0002g0003 a0001c0001t0002g0090 a0001c0001t0003g0003 others(14): Show |
41 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.783-379dupT | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146459 | ||||||
chr6:44146459 | C | T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-388C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146459 | |||||||
chr6:44146461 | T | G | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-386T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146461 | |||||||
chr6:44146467 | T | TTTCTATA others(3): Show |
1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-379_783-378ins others(10): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 44146467 | ||||||
chr6:44146481 | C | T | 1 | a0001c0001t0003g0150 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.783-366C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146481 | |||||||
chr6:44146512 | G | A | 27 | a0001c0001t0003g0006 a0001c0001t0003g0043 a0001c0001t0003g0045 others(24): Show |
35 | HG00140.hp2 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.783-335G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146512 | |||||||
chr6:44146597 | C | T | 93 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(90): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.783-250C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146597 | |||||||
chr6:44146697 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.783-150C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 10/23 | chr6 | 44146697 | |||||||
chr6:44146976 | T | G | 1 | a0001c0001t0005g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.863+49T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 11/23 | chr6 | 44146976 | |||||||
chr6:44147238 | T | C | 1 | a0001c0001t0002g0072 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.864-139T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 11/23 | chr6 | 44147238 | |||||||
chr6:44147342 | C | T | 23 | a0002c0002t0004g0004 a0002c0002t0004g0024 a0002c0002t0004g0025 others(20): Show |
36 | HG00438.hp2 HG01175.hp1 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.864-35C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 11/23 | chr6 | 44147342 | |||||||
chr6:44147507 | C | T | 1 | a0001c0001t0008g0037 | 2 | HG03195.hp1 HG03471.hp2 |
splice_region_variant&intron_variant | LOW | c.987+7C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 12/23 | chr6 | 44147507 | |||||||
chr6:44147768 | A | C | 40 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.987+268A>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 12/23 | chr6 | 44147768 | |||||||
chr6:44147830 | G | A | 105 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(102): Show |
177 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.987+330G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 12/23 | chr6 | 44147830 | |||||||
chr6:44148005 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.988-247C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 12/23 | chr6 | 44148005 | |||||||
chr6:44148006 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.988-246C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 12/23 | chr6 | 44148006 | |||||||
chr6:44148123 | C | CA | 10 | a0001c0001t0001g0021 a0001c0001t0001g0058 a0001c0001t0001g0060 others(7): Show |
12 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.988-116dupA | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr6 | 44148123 | ||||||
chr6:44148127 | A | G | 40 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.988-125A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 12/23 | chr6 | 44148127 | |||||||
chr6:44148408 | G | A | 2 | a0001c0001t0010g0082 a0001c0001t0010g0083 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1121+23G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 13/23 | chr6 | 44148408 | |||||||
chr6:44149048 | T | TC | 16 | a0001c0001t0005g0009 a0001c0001t0005g0017 a0001c0001t0005g0020 others(13): Show |
26 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1413+105dupC | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr6 | 44149048 | ||||||
chr6:44149057 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1413+112G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149057 | |||||||
chr6:44149137 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1413+192C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149137 | |||||||
chr6:44149213 | C | T | 4 | a0001c0001t0003g0136 a0001c0001t0012g0040 a0001c0001t0013g0040 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413+268C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149213 | |||||||
chr6:44149255 | C | T | 39 | a0001c0004t0002g0181 a0002c0002t0001g0041 a0002c0002t0002g0010 others(36): Show |
62 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1413+310C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149255 | |||||||
chr6:44149256 | A | G | 74 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(71): Show |
107 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1413+311A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149256 | |||||||
chr6:44149298 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1413+353C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149298 | |||||||
chr6:44149335 | G | A | 5 | a0001c0001t0001g0103 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
7 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1413+390G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149335 | |||||||
chr6:44149390 | C | T | 1 | a0002c0002t0004g0174 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1413+445C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149390 | |||||||
chr6:44149409 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(3): Show |
8 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1414-450T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149409 | |||||||
chr6:44149501 | C | T | 4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0203 others(1): Show |
6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414-358C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149501 | |||||||
chr6:44149640 | A | T | 38 | a0002c0002t0001g0041 a0002c0002t0002g0010 a0002c0002t0002g0018 others(35): Show |
61 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.1414-219A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149640 | |||||||
chr6:44149842 | C | T | 4 | a0001c0001t0003g0136 a0001c0001t0012g0040 a0001c0001t0013g0040 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-17C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 15/23 | chr6 | 44149842 | |||||||
chr6:44149990 | A | G | 77 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(74): Show |
110 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1520+25A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 16/23 | chr6 | 44149990 | |||||||
chr6:44150106 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1521-118C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 16/23 | chr6 | 44150106 | |||||||
chr6:44150160 | G | T | 2 | a0001c0001t0002g0184 a0001c0001t0018g0166 |
2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1521-64G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 16/23 | chr6 | 44150160 | |||||||
chr6:44150167 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1521-57C>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 16/23 | chr6 | 44150167 | |||||||
chr6:44150180 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1521-44T>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 16/23 | chr6 | 44150180 | |||||||
chr6:44150334 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1607+24G>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 17/23 | chr6 | 44150334 | |||||||
chr6:44150511 | G | A | 1 | a0001c0001t0003g0092 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1608-53G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 17/23 | chr6 | 44150511 | |||||||
chr6:44150518 | T | G | 1 | a0001c0001t0019g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1608-46T>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 17/23 | chr6 | 44150518 | |||||||
chr6:44150802 | G | A | 2 | a0001c0001t0010g0082 a0001c0001t0010g0083 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1673+173G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 18/23 | chr6 | 44150802 | |||||||
chr6:44150875 | T | C | 116 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(113): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1673+246T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 18/23 | chr6 | 44150875 | |||||||
chr6:44151136 | C | T | 2 | a0001c0001t0010g0082 a0001c0001t0010g0083 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1673+507C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 18/23 | chr6 | 44151136 | |||||||
chr6:44151174 | A | G | 114 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(111): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1673+545A>G | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 18/23 | chr6 | 44151174 | |||||||
chr6:44151388 | C | T | 25 | a0001c0001t0003g0006 a0001c0001t0003g0043 a0001c0001t0003g0045 others(22): Show |
33 | HG00140.hp2 HG00597.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1674-458C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 18/23 | chr6 | 44151388 | |||||||
chr6:44151408 | T | C | 116 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(113): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1674-438T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 18/23 | chr6 | 44151408 | |||||||
chr6:44151601 | C | T | 74 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(71): Show |
107 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1674-245C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 18/23 | chr6 | 44151601 | |||||||
chr6:44151776 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1674-70G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 18/23 | chr6 | 44151776 | |||||||
chr6:44151795 | G | A | 15 | a0002c0002t0001g0041 a0002c0002t0002g0010 a0002c0002t0002g0018 others(12): Show |
25 | HG00423.hp2 HG00738.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1674-51G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 18/23 | chr6 | 44151795 | |||||||
chr6:44152012 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02738.hp1 | splice_region_variant&intron_variant | LOW | c.1836+4C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/23 | chr6 | 44152012 | |||||||
chr6:44152058 | C | A | 1 | a0001c0001t0003g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1836+50C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/23 | chr6 | 44152058 | |||||||
chr6:44152142 | C | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(3): Show |
8 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1836+134C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/23 | chr6 | 44152142 | |||||||
chr6:44152180 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1836+172C>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/23 | chr6 | 44152180 | |||||||
chr6:44152285 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1836+277C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/23 | chr6 | 44152285 | |||||||
chr6:44152406 | C | T | 1 | a0002c0002t0004g0177 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1837-187C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/23 | chr6 | 44152406 | |||||||
chr6:44152415 | C | T | 1 | a0001c0001t0002g0033 | 2 | NA18956.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1837-178C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/23 | chr6 | 44152415 | |||||||
chr6:44152440 | C | T | 2 | a0001c0001t0010g0082 a0001c0001t0010g0083 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1837-153C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/23 | chr6 | 44152440 | |||||||
chr6:44152556 | C | T | 39 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(36): Show |
80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1837-37C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/23 | chr6 | 44152556 | |||||||
chr6:44152557 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1837-36C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 19/23 | chr6 | 44152557 | |||||||
chr6:44152929 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0060 a0001c0001t0001g0065 others(1): Show |
5 | HG02056.hp2 HG02129.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1942+231C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 20/23 | chr6 | 44152929 | |||||||
chr6:44152975 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(3): Show |
8 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1942+277G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 20/23 | chr6 | 44152975 | |||||||
chr6:44153003 | G | A | 2 | a0002c0002t0002g0044 a0002c0002t0002g0190 |
3 | HG00423.hp2 NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1942+305G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 20/23 | chr6 | 44153003 | |||||||
chr6:44153024 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0133 a0001c0001t0001g0145 others(3): Show |
8 | HG01074.hp1 HG01346.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1942+326C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 20/23 | chr6 | 44153024 | |||||||
chr6:44153292 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1943-384C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 20/23 | chr6 | 44153292 | |||||||
chr6:44153477 | A | T | 80 | a0001c0001t0001g0021 a0001c0001t0001g0125 a0001c0001t0001g0133 others(77): Show |
115 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1943-199A>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 20/23 | chr6 | 44153477 | |||||||
chr6:44153479 | T | C | 122 | a0001c0001t0001g0021 a0001c0001t0001g0125 a0001c0001t0001g0133 others(119): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1943-197T>C | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 20/23 | chr6 | 44153479 | |||||||
chr6:44153533 | C | T | 121 | a0001c0001t0001g0021 a0001c0001t0001g0125 a0001c0001t0001g0133 others(118): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1943-143C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 20/23 | chr6 | 44153533 | |||||||
chr6:44153631 | C | T | 1 | a0001c0004t0002g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1943-45C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 20/23 | chr6 | 44153631 | |||||||
chr6:44153920 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2110+77G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 21/23 | chr6 | 44153920 | |||||||
chr6:44154210 | C | T | 42 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
84 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.2226+22C>T | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 22/23 | chr6 | 44154210 | |||||||
chr6:44154302 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0137 |
3 | NA18906.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2227-63G>A | TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 22/23 | chr6 | 44154302 | |||||||
chr6:44154679 | TCTC | T | 127 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(124): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
splice_region_variant&intron_variant | LOW | c.2308-7_2308-5delCC others(1): Show |
TMEM63B | ENSG00000137216.19 | transcript | ENST00000323267.11 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr6 | 44154679 |