Item | Value |
---|---|
geneid | 55151 |
ensemblid | ENSG00000095209.12 |
hgncid | 25535 |
symbol | TMEM38B |
name | transmembrane protein 38B |
refseq_nuc | NM_018112.3 |
refseq_prot | NP_060582.1 |
ensembl_nuc | ENST00000374692.8 |
ensembl_prot | ENSP00000363824.3 |
mane_status | MANE Select |
chr | chr9 |
start | 105694541 |
end | 105776629 |
strand | + |
ver | v1.2 |
region | chr9:105694541-105776629 |
region5000 | chr9:105689541-105781629 |
regionname0 | TMEM38B_chr9_105694541_105776629 |
regionname5000 | TMEM38B_chr9_105689541_105781629 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 291 | 346 | 83 | 66 | 164 | 6 | 25 | 130 | TMEM38B_chr9_105689541_105781629 | TMEM38B | MDSPW others(286): Show |
chr9 | 105689541 | 105781629 |
a0002 | 0/0 | 291 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | MDSPW others(286): Show |
chr9 | 105689541 | 105781629 |
a0003 | 0/0 | 291 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | MDSPW others(286): Show |
chr9 | 105689541 | 105781629 |
a0004 | 0/0 | 291 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | MDSPW others(286): Show |
chr9 | 105689541 | 105781629 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 873 | 339 | 80 | 63 | 163 | 6 | 25 | TMEM38B_chr9_105689541_105781629 | TMEM38B | ATGGA others(868): Show |
chr9 | 105689541 | 105781629 | ||
a0001c0003 | 0/0 | 873 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | ATGGA others(868): Show |
chr9 | 105689541 | 105781629 | ||
a0001c0004 | 0/0 | 873 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | ATGGA others(868): Show |
chr9 | 105689541 | 105781629 | ||
a0001c0006 | 0/0 | 873 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | ATGGA others(868): Show |
chr9 | 105689541 | 105781629 | ||
a0002c0002 | 0/0 | 873 | 8 | 8 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | ATGGA others(868): Show |
chr9 | 105689541 | 105781629 | ||
a0003c0007 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | ATGGA others(868): Show |
chr9 | 105689541 | 105781629 | ||
a0004c0005 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | ATGGA others(868): Show |
chr9 | 105689541 | 105781629 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3545 | 110 | 15 | 23 | 55 | 4 | 11 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0002 | 0/0 | 3544 | 85 | 12 | 10 | 57 | 0 | 6 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0003 | 0/0 | 3545 | 64 | 21 | 18 | 21 | 2 | 2 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0004 | 0/0 | 3544 | 16 | 13 | 1 | 0 | 0 | 2 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0005 | 0/0 | 3544 | 12 | 0 | 4 | 8 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | AGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0006 | 0/0 | 3545 | 11 | 0 | 2 | 9 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0008 | 0/0 | 3545 | 6 | 0 | 3 | 3 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0009 | 0/0 | 3544 | 6 | 5 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0010 | 0/0 | 3544 | 5 | 3 | 1 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0011 | 0/0 | 3546 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3541): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0013 | 0/0 | 3545 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0014 | 0/0 | 3543 | 3 | 0 | 0 | 0 | 0 | 3 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3538): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0015 | 0/0 | 3545 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0016 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0017 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0018 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0019 | 0/0 | 3544 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0020 | 0/0 | 3544 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0021 | 0/0 | 3544 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0022 | 0/0 | 3544 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0023 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0024 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3541): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0026 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0001t0027 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
a0001c0003t0012 | 0/0 | 3544 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0004t0004 | 0/0 | 3544 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0001c0006t0002 | 0/0 | 3544 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0002c0002t0007 | 0/0 | 3544 | 8 | 8 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0003c0007t0025 | 0/0 | 3544 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3539): Show |
chr9 | 105689541 | 105781629 |
a0004c0005t0001 | 0/0 | 3545 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | GGAGC others(3540): Show |
chr9 | 105689541 | 105781629 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0001 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0005g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0005g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0005g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0006g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0008g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0008g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0009g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0009g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0010g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0010g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0010g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0013g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0014g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0014g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0015g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0015g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0016g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0017g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0018g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0019g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0020g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0021g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0022g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0023g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0024g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0026g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0001t0027g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0003t0012g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0003t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0003t0012g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0003t0012g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0004t0004g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0001c0006t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0002c0002t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0002c0002t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0002c0002t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0002c0002t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0002c0002t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0002c0002t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0002c0002t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0002c0002t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0003c0007t0025g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
a0004c0005t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00438 | hp2 | a0001 | c0001 | t0006 | g0086 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00597 | hp1 | a0001 | c0001 | t0008 | g0262 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01099 | hp2 | a0001 | c0004 | t0004 | g0017 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01192 | hp2 | a0001 | c0004 | t0004 | g0017 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01243 | hp2 | a0001 | c0003 | t0012 | g0268 | AMR | PUR | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01255 | hp2 | a0001 | c0001 | t0010 | g0027 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01261 | hp2 | a0001 | c0001 | t0008 | g0259 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0205 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0012 | EUR | IBS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01952 | hp2 | a0001 | c0001 | t0009 | g0217 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01993 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02056 | hp1 | a0001 | c0001 | t0026 | g0263 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02074 | hp2 | a0001 | c0001 | t0008 | g0261 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0220 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02145 | hp2 | a0001 | c0003 | t0012 | g0271 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02148 | hp2 | a0001 | c0001 | t0008 | g0014 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CDX | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02258 | hp2 | a0001 | c0001 | t0013 | g0018 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02280 | hp1 | a0002 | c0002 | t0007 | g0054 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02293 | hp1 | a0001 | c0001 | t0008 | g0014 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0219 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0052 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02622 | hp1 | a0002 | c0002 | t0007 | g0060 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02630 | hp2 | a0003 | c0007 | t0025 | g0223 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02735 | hp1 | a0001 | c0001 | t0014 | g0247 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0253 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02886 | hp2 | a0002 | c0002 | t0007 | g0061 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02895 | hp2 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02965 | hp1 | a0001 | c0001 | t0020 | g0053 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02976 | hp1 | a0001 | c0001 | t0011 | g0273 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0051 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0035 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03098 | hp1 | a0001 | c0001 | t0013 | g0070 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03098 | hp2 | a0002 | c0002 | t0007 | g0062 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03130 | hp1 | a0001 | c0001 | t0024 | g0274 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0148 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03139 | hp2 | a0001 | c0001 | t0019 | g0049 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03195 | hp2 | a0002 | c0002 | t0007 | g0056 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0035 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0149 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03490 | hp1 | a0001 | c0001 | t0014 | g0040 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03490 | hp2 | a0004 | c0005 | t0001 | g0023 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03492 | hp1 | a0001 | c0001 | t0014 | g0040 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0150 | AFR | ESN | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | BEB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG04204 | hp2 | a0001 | c0001 | t0010 | g0065 | SAS | STU | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | YRI | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | YRI | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18612 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | CHB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18747 | hp1 | a0001 | c0001 | t0015 | g0068 | EAS | CHB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18944 | hp1 | a0001 | c0001 | t0016 | g0090 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18946 | hp1 | a0001 | c0006 | t0002 | g0001 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18951 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18966 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18970 | hp1 | a0001 | c0001 | t0021 | g0221 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18971 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0207 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18981 | hp1 | a0001 | c0001 | t0017 | g0104 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18988 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19006 | hp1 | a0001 | c0001 | t0006 | g0083 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0218 | AFR | LWK | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | LWK | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | LWK | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19043 | hp2 | a0002 | c0002 | t0007 | g0058 | AFR | LWK | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19056 | hp1 | a0001 | c0001 | t0018 | g0002 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19063 | hp2 | a0001 | c0001 | t0006 | g0107 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19067 | hp2 | a0001 | c0001 | t0022 | g0209 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19070 | hp1 | a0001 | c0001 | t0015 | g0067 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19082 | hp2 | a0001 | c0001 | t0027 | g0002 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19085 | hp1 | a0001 | c0001 | t0023 | g0227 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19240 | hp1 | a0002 | c0002 | t0007 | g0057 | AFR | YRI | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0264 | AFR | ASW | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA20129 | hp2 | a0002 | c0002 | t0007 | g0055 | AFR | ASW | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0012 | EUR | TSI | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0018 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02486 | hp1 | a0001 | c0003 | t0012 | g0270 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03471 | hp1 | a0001 | c0003 | t0012 | g0269 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
HG03471 | hp2 | a0001 | c0001 | t0010 | g0027 | AFR | MSL | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | USA | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA20300 | hp2 | a0001 | c0001 | t0011 | g0147 | AFR | USA | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | LWK | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0126 | REF | REF | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0111 | REF | REF | TMEM38B_chr9_105689541_105781629 | TMEM38B | chr9 | 105689541 | 105781629 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:105694772 | G | A | 1 | a0004 | 1 | HG03490.hp2 | missense_variant&splice_region_variant | MODERATE | c.112G>A | p.Gly38Arg | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/6 | 232/3545 | 112/876 | 38/291 | chr9 | 105694772 | |||
chr9:105773965 | G | C | 1 | a0002 | 8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
missense_variant | MODERATE | c.761G>C | p.Cys254Ser | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 881/3545 | 761/876 | 254/291 | chr9 | 105773965 | |||
chr9:105774007 | G | A | 1 | a0003 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.803G>A | p.Gly268Glu | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 923/3545 | 803/876 | 268/291 | chr9 | 105774007 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:105705704 | T | C | 1 | a0001c0004 | 2 | HG01099.hp2 HG01192.hp2 |
synonymous_variant | LOW | c.220T>C | p.Leu74Leu | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/6 | 340/3545 | 220/876 | 74/291 | chr9 | 105705704 | |||
chr9:105721684 | T | C | 1 | a0001c0003 | 4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
synonymous_variant | LOW | c.417T>C | p.Asn139Asn | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 3/6 | 537/3545 | 417/876 | 139/291 | chr9 | 105721684 | |||
chr9:105773954 | G | A | 1 | a0001c0006 | 1 | NA18946.hp1 | synonymous_variant | LOW | c.750G>A | p.Pro250Pro | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 870/3545 | 750/876 | 250/291 | chr9 | 105773954 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:105694541 | G | A | 1 | a0001c0001t0005 | 12 | HG01167.hp2 HG01358.hp1 HG01433.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-120G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/6 | 120 | chr9 | 105694541 | ||||||
chr9:105694548 | G | T | 1 | a0001c0001t0027 | 1 | NA19082.hp2 | 5_prime_UTR_variant | MODIFIER | c.-113G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/6 | 113 | chr9 | 105694548 | ||||||
chr9:105694599 | A | C | 1 | a0001c0001t0026 | 1 | HG02056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-62A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/6 | 62 | chr9 | 105694599 | ||||||
chr9:105694607 | A | C | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(16): Show |
212 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(209): Show |
5_prime_UTR_variant | MODIFIER | c.-54A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/6 | 54 | chr9 | 105694607 | ||||||
chr9:105774107 | A | C | 1 | a0002c0002t0007 | 8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*27A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 27 | chr9 | 105774107 | ||||||
chr9:105774115 | T | A | 1 | a0001c0001t0008 | 6 | HG00597.hp1 HG01261.hp2 HG02074.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*35T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 35 | chr9 | 105774115 | ||||||
chr9:105774139 | G | T | 1 | a0003c0007t0025 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*59G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 59 | chr9 | 105774139 | ||||||
chr9:105774145 | AT | A | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(11): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*70delT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 70 | INFO_REALIGN_3_PRIME | chr9 | 105774145 | |||||
chr9:105774164 | G | A | 1 | a0001c0001t0023 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*84G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 84 | chr9 | 105774164 | ||||||
chr9:105774283 | A | T | 2 | a0001c0001t0006 a0001c0001t0018 |
12 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*203A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 203 | chr9 | 105774283 | ||||||
chr9:105774431 | A | G | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(4): Show |
109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*351A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 351 | chr9 | 105774431 | ||||||
chr9:105774439 | A | T | 1 | a0001c0001t0022 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*359A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 359 | chr9 | 105774439 | ||||||
chr9:105774523 | A | C | 1 | a0001c0001t0015 | 2 | NA18747.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*443A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 443 | chr9 | 105774523 | ||||||
chr9:105774530 | A | G | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(11): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*450A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 450 | chr9 | 105774530 | ||||||
chr9:105774581 | T | G | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02965.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*501T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 501 | chr9 | 105774581 | ||||||
chr9:105774587 | T | C | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(4): Show |
109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*507T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 507 | chr9 | 105774587 | ||||||
chr9:105774592 | A | T | 1 | a0001c0001t0022 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 512 | chr9 | 105774592 | ||||||
chr9:105774593 | T | A | 1 | a0001c0001t0022 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*513T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 513 | chr9 | 105774593 | ||||||
chr9:105774596 | A | T | 1 | a0001c0001t0022 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*516A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 516 | chr9 | 105774596 | ||||||
chr9:105774623 | C | T | 6 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0020 others(3): Show |
29 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*543C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 543 | chr9 | 105774623 | ||||||
chr9:105774774 | A | T | 1 | a0001c0001t0018 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*694A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 694 | chr9 | 105774774 | ||||||
chr9:105774791 | T | C | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(11): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*711T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 711 | chr9 | 105774791 | ||||||
chr9:105775011 | C | T | 1 | a0003c0007t0025 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*931C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 931 | chr9 | 105775011 | ||||||
chr9:105775038 | T | C | 1 | a0001c0003t0012 | 4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*958T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 958 | chr9 | 105775038 | ||||||
chr9:105775227 | CAG | C | 1 | a0001c0001t0014 | 3 | HG02735.hp1 HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1151_*1152delGA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1151 | INFO_REALIGN_3_PRIME | chr9 | 105775227 | |||||
chr9:105775235 | C | T | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1155C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1155 | chr9 | 105775235 | ||||||
chr9:105775272 | G | T | 2 | a0001c0001t0011 a0001c0001t0024 |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1192G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1192 | chr9 | 105775272 | ||||||
chr9:105775432 | A | G | 1 | a0001c0001t0013 | 3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1352A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1352 | chr9 | 105775432 | ||||||
chr9:105775488 | G | GT | 2 | a0001c0001t0011 a0001c0001t0024 |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1418dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1419 | INFO_REALIGN_3_PRIME | chr9 | 105775488 | |||||
chr9:105775496 | T | G | 1 | a0001c0001t0009 | 6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1416T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1416 | chr9 | 105775496 | ||||||
chr9:105775521 | A | T | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1441A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1441 | chr9 | 105775521 | ||||||
chr9:105775522 | A | T | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1442A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1442 | chr9 | 105775522 | ||||||
chr9:105775526 | A | T | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1446A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1446 | chr9 | 105775526 | ||||||
chr9:105775528 | A | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1448A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1448 | chr9 | 105775528 | ||||||
chr9:105775529 | T | G | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1449T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1449 | chr9 | 105775529 | ||||||
chr9:105775530 | A | T | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1450A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1450 | chr9 | 105775530 | ||||||
chr9:105775531 | A | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1451A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1451 | chr9 | 105775531 | ||||||
chr9:105775532 | A | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1452A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1452 | chr9 | 105775532 | ||||||
chr9:105775534 | A | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1454 | chr9 | 105775534 | ||||||
chr9:105775537 | A | T | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1457A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1457 | chr9 | 105775537 | ||||||
chr9:105775538 | G | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1458G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1458 | chr9 | 105775538 | ||||||
chr9:105775540 | A | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1460A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1460 | chr9 | 105775540 | ||||||
chr9:105775541 | G | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1461G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1461 | chr9 | 105775541 | ||||||
chr9:105775542 | A | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1462A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1462 | chr9 | 105775542 | ||||||
chr9:105775543 | T | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1463T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1463 | chr9 | 105775543 | ||||||
chr9:105775544 | A | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1464A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1464 | chr9 | 105775544 | ||||||
chr9:105775546 | T | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1466T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1466 | chr9 | 105775546 | ||||||
chr9:105775547 | A | G | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1467A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1467 | chr9 | 105775547 | ||||||
chr9:105775550 | A | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1470A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1470 | chr9 | 105775550 | ||||||
chr9:105775552 | T | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1472T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1472 | chr9 | 105775552 | ||||||
chr9:105775553 | T | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1473T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1473 | chr9 | 105775553 | ||||||
chr9:105775563 | A | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1483A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1483 | chr9 | 105775563 | ||||||
chr9:105775564 | T | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1484T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1484 | chr9 | 105775564 | ||||||
chr9:105775565 | T | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1485T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1485 | chr9 | 105775565 | ||||||
chr9:105775567 | G | T | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1487G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1487 | chr9 | 105775567 | ||||||
chr9:105775569 | A | G | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1489A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1489 | chr9 | 105775569 | ||||||
chr9:105775571 | G | T | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1491G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1491 | chr9 | 105775571 | ||||||
chr9:105775580 | T | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1500T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1500 | chr9 | 105775580 | ||||||
chr9:105775601 | G | C | 1 | a0001c0001t0021 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1521G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1521 | chr9 | 105775601 | ||||||
chr9:105775779 | T | G | 1 | a0001c0001t0016 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1699T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1699 | chr9 | 105775779 | ||||||
chr9:105775851 | T | C | 1 | a0001c0001t0019 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1771T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1771 | chr9 | 105775851 | ||||||
chr9:105775876 | T | C | 1 | a0003c0007t0025 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1796T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1796 | chr9 | 105775876 | ||||||
chr9:105776062 | T | A | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(11): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1982T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 1982 | chr9 | 105776062 | ||||||
chr9:105776095 | C | T | 1 | a0001c0001t0017 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2015C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 2015 | chr9 | 105776095 | ||||||
chr9:105776592 | A | G | 1 | a0001c0003t0012 | 4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2512A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 6/6 | 2512 | chr9 | 105776592 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:105694855 | C | T | 1 | a0001c0001t0004g0281 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.112+83C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105694855 | |||||||
chr9:105694894 | A | T | 6 | a0001c0001t0001g0044 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
7 | HG00673.hp1 HG01891.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+122A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105694894 | |||||||
chr9:105694969 | G | C | 2 | a0001c0001t0002g0015 a0001c0001t0002g0045 |
3 | HG00558.hp2 NA18612.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.112+197G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105694969 | |||||||
chr9:105695074 | G | A | 11 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(8): Show |
13 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.112+302G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105695074 | |||||||
chr9:105695153 | C | CCGCCACT others(12): Show |
4 | a0001c0001t0001g0059 a0002c0002t0007g0060 a0002c0002t0007g0061 others(1): Show |
4 | HG02071.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+420_112+438dup others(19): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105695153 | ||||||
chr9:105695153 | C | CCGCCACT others(31): Show |
5 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(2): Show |
5 | HG02280.hp1 HG03195.hp2 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+401_112+438dup others(38): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105695153 | ||||||
chr9:105695153 | CCGCCACT others(12): Show |
C | 2 | a0001c0001t0011g0273 a0001c0001t0024g0274 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.112+420_112+438del others(19): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105695153 | ||||||
chr9:105695154 | C | G | 12 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(9): Show |
14 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.112+382C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105695154 | |||||||
chr9:105695414 | C | G | 1 | a0001c0001t0003g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112+642C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105695414 | |||||||
chr9:105695525 | A | G | 169 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(166): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.112+753A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105695525 | |||||||
chr9:105695568 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.112+796C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105695568 | |||||||
chr9:105695633 | T | C | 4 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+861T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105695633 | |||||||
chr9:105695736 | A | G | 169 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(166): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.112+964A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105695736 | |||||||
chr9:105695784 | GA | G | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+1015delA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105695784 | ||||||
chr9:105695857 | A | G | 4 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+1085A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105695857 | |||||||
chr9:105695961 | A | T | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+1189A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105695961 | |||||||
chr9:105696476 | G | T | 1 | a0001c0001t0026g0263 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.112+1704G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105696476 | |||||||
chr9:105696595 | C | G | 1 | a0001c0001t0020g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.112+1823C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105696595 | |||||||
chr9:105696687 | A | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0028 others(4): Show |
13 | HG02155.hp1 NA18943.hp1 NA18950.hp1 others(10): Show |
intron_variant | MODIFIER | c.112+1915A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105696687 | |||||||
chr9:105696755 | T | A | 1 | a0001c0003t0012g0268 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.112+1983T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105696755 | |||||||
chr9:105696802 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.112+2030C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105696802 | |||||||
chr9:105697030 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.112+2258T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105697030 | |||||||
chr9:105697137 | G | A | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+2365G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105697137 | |||||||
chr9:105697145 | A | G | 1 | a0001c0001t0020g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.112+2373A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105697145 | |||||||
chr9:105697216 | G | A | 113 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(110): Show |
141 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.112+2444G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105697216 | |||||||
chr9:105697636 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.112+2864G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105697636 | |||||||
chr9:105697679 | C | A | 12 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(9): Show |
14 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.112+2907C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105697679 | |||||||
chr9:105697875 | T | A | 19 | a0001c0001t0003g0153 a0001c0001t0004g0016 a0001c0001t0004g0046 others(16): Show |
21 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.112+3103T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105697875 | |||||||
chr9:105697875 | T | TAAAAAAT others(323): Show |
1 | a0001c0001t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.112+3114_112+3115i others(332): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105697875 | ||||||
chr9:105697989 | CAAT | C | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+3218_112+3220d others(5): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105697989 | |||||||
chr9:105698066 | C | CAT | 56 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(53): Show |
73 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.112+3296_112+3297d others(4): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105698066 | ||||||
chr9:105698116 | A | AT | 159 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(156): Show |
200 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.112+3356dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105698116 | ||||||
chr9:105698116 | A | ATT | 10 | a0001c0001t0002g0222 a0001c0001t0003g0042 a0001c0001t0003g0043 others(7): Show |
14 | HG00597.hp1 HG01261.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+3355_112+3356d others(4): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105698116 | ||||||
chr9:105698168 | C | G | 5 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(2): Show |
5 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+3396C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105698168 | |||||||
chr9:105698508 | T | A | 1 | a0001c0001t0003g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112+3736T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105698508 | |||||||
chr9:105698538 | T | G | 2 | a0001c0001t0015g0067 a0001c0001t0015g0068 |
2 | NA18747.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.112+3766T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105698538 | |||||||
chr9:105698581 | C | G | 169 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(166): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.112+3809C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105698581 | |||||||
chr9:105698693 | A | G | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(175): Show |
225 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.112+3921A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105698693 | |||||||
chr9:105698732 | T | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG02723.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.112+3960T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105698732 | |||||||
chr9:105698854 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.112+4082T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105698854 | |||||||
chr9:105698881 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(7): Show |
13 | HG02027.hp1 HG02071.hp2 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.112+4109C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105698881 | |||||||
chr9:105699057 | A | G | 23 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0066 others(20): Show |
24 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.112+4285A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105699057 | |||||||
chr9:105699311 | T | C | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.112+4539T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105699311 | |||||||
chr9:105699389 | G | A | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG01243.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.112+4617G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105699389 | |||||||
chr9:105699470 | A | T | 1 | a0001c0001t0021g0221 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.112+4698A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105699470 | |||||||
chr9:105699563 | A | T | 171 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(168): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.112+4791A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105699563 | |||||||
chr9:105699728 | A | AT | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(174): Show |
224 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.112+4962dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105699728 | ||||||
chr9:105699771 | T | C | 1 | a0001c0003t0012g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.112+4999T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105699771 | |||||||
chr9:105699867 | C | G | 2 | a0001c0001t0011g0149 a0001c0001t0011g0150 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.112+5095C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105699867 | |||||||
chr9:105699966 | C | T | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+5194C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105699966 | |||||||
chr9:105700011 | CA | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0116 a0001c0001t0003g0224 |
4 | NA18964.hp2 NA18969.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+5240delA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105700011 | |||||||
chr9:105700054 | G | A | 171 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(168): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.112+5282G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105700054 | |||||||
chr9:105700454 | C | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.113-5143C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105700454 | |||||||
chr9:105700643 | G | T | 7 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(4): Show |
7 | HG02717.hp1 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-4954G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105700643 | |||||||
chr9:105700766 | G | A | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-4831G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105700766 | |||||||
chr9:105700827 | A | G | 171 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(168): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.113-4770A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105700827 | |||||||
chr9:105701241 | C | A | 1 | a0001c0001t0004g0152 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.113-4356C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701241 | |||||||
chr9:105701252 | G | A | 27 | a0001c0001t0003g0153 a0001c0001t0004g0016 a0001c0001t0004g0046 others(24): Show |
29 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.113-4345G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701252 | |||||||
chr9:105701299 | G | C | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.113-4298G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701299 | |||||||
chr9:105701332 | G | A | 4 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-4265G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701332 | |||||||
chr9:105701383 | C | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-4214C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701383 | |||||||
chr9:105701421 | C | T | 1 | a0001c0001t0003g0258 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.113-4176C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701421 | |||||||
chr9:105701476 | A | C | 11 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(8): Show |
13 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.113-4121A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701476 | |||||||
chr9:105701530 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.113-4067C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701530 | |||||||
chr9:105701622 | G | A | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.113-3975G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701622 | |||||||
chr9:105701762 | A | T | 4 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-3835A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701762 | |||||||
chr9:105701848 | C | G | 1 | a0001c0001t0002g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.113-3749C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701848 | |||||||
chr9:105701952 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.113-3645C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105701952 | |||||||
chr9:105702147 | T | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.113-3450T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702147 | |||||||
chr9:105702151 | G | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-3446G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702151 | |||||||
chr9:105702221 | C | T | 1 | a0003c0007t0025g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.113-3376C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702221 | |||||||
chr9:105702303 | A | G | 18 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(15): Show |
20 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.113-3294A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702303 | |||||||
chr9:105702461 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.113-3136G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702461 | |||||||
chr9:105702553 | G | A | 55 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(52): Show |
72 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.113-3044G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702553 | |||||||
chr9:105702657 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.113-2940C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702657 | |||||||
chr9:105702671 | GTTAT | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.113-2903_113-2900d others(6): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105702671 | ||||||
chr9:105702823 | G | C | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.113-2774G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702823 | |||||||
chr9:105702830 | C | T | 4 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2767C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702830 | |||||||
chr9:105702871 | A | T | 1 | a0001c0001t0021g0221 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.113-2726A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702871 | |||||||
chr9:105702900 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.113-2697G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702900 | |||||||
chr9:105702960 | C | T | 7 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(4): Show |
7 | HG02717.hp1 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-2637C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105702960 | |||||||
chr9:105703114 | C | A | 1 | a0001c0001t0011g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.113-2483C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703114 | |||||||
chr9:105703305 | T | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.113-2292T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703305 | |||||||
chr9:105703354 | A | G | 1 | a0001c0001t0003g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113-2243A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703354 | |||||||
chr9:105703359 | T | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.113-2238T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703359 | |||||||
chr9:105703574 | G | C | 1 | a0001c0001t0013g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.113-2023G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703574 | |||||||
chr9:105703612 | G | A | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.113-1985G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703612 | |||||||
chr9:105703654 | A | C | 5 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(2): Show |
5 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-1943A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703654 | |||||||
chr9:105703666 | A | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-1931A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703666 | |||||||
chr9:105703744 | G | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.113-1853G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703744 | |||||||
chr9:105703874 | C | T | 3 | a0001c0001t0002g0213 a0001c0001t0003g0254 a0001c0001t0003g0255 |
3 | NA18971.hp2 NA18972.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.113-1723C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703874 | |||||||
chr9:105703892 | GTTGT | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-1698_113-1695d others(6): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105703892 | ||||||
chr9:105703999 | G | A | 3 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
3 | HG02280.hp2 HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.113-1598G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105703999 | |||||||
chr9:105704051 | A | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.113-1546A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704051 | |||||||
chr9:105704064 | A | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.113-1533A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704064 | |||||||
chr9:105704093 | GA | G | 4 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1503delA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704093 | |||||||
chr9:105704158 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.113-1439G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704158 | |||||||
chr9:105704169 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1428A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704169 | |||||||
chr9:105704204 | C | T | 3 | a0001c0001t0009g0035 a0001c0001t0009g0219 a0001c0001t0009g0220 |
4 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-1393C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704204 | |||||||
chr9:105704229 | TA | T | 87 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(84): Show |
115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.113-1358delA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105704229 | ||||||
chr9:105704301 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.113-1296G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704301 | |||||||
chr9:105704338 | T | A | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.113-1259T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704338 | |||||||
chr9:105704383 | C | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.113-1214C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704383 | |||||||
chr9:105704435 | T | C | 6 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 others(3): Show |
6 | NA18959.hp1 NA18966.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-1162T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704435 | |||||||
chr9:105704451 | C | T | 1 | a0001c0001t0004g0159 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.113-1146C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704451 | |||||||
chr9:105704465 | A | G | 23 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0066 others(20): Show |
24 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.113-1132A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704465 | |||||||
chr9:105704481 | CT | C | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-1108delT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105704481 | ||||||
chr9:105704598 | C | T | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.113-999C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704598 | |||||||
chr9:105704705 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.113-892C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704705 | |||||||
chr9:105704734 | G | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG02723.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.113-863G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704734 | |||||||
chr9:105704928 | T | TA | 15 | a0001c0001t0001g0072 a0001c0001t0003g0153 a0001c0001t0004g0152 others(12): Show |
15 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.113-657dupA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 105704928 | ||||||
chr9:105704961 | A | G | 26 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(23): Show |
37 | HG00609.hp2 HG00639.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.113-636A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704961 | |||||||
chr9:105704963 | G | A | 1 | a0003c0007t0025g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.113-634G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105704963 | |||||||
chr9:105705022 | G | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.113-575G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105705022 | |||||||
chr9:105705106 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-491A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105705106 | |||||||
chr9:105705265 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.113-332G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105705265 | |||||||
chr9:105705276 | G | A | 7 | a0001c0001t0002g0003 a0001c0001t0002g0160 a0001c0001t0002g0161 others(4): Show |
11 | HG01081.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.113-321G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105705276 | |||||||
chr9:105705326 | A | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.113-271A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105705326 | |||||||
chr9:105705409 | A | T | 1 | a0001c0001t0003g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.113-188A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105705409 | |||||||
chr9:105705421 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.113-176C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105705421 | |||||||
chr9:105705569 | C | G | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.113-28C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 1/5 | chr9 | 105705569 | |||||||
chr9:105705848 | C | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.269+95C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105705848 | |||||||
chr9:105705902 | G | GT | 22 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0001c0001t0001g0071 others(19): Show |
24 | HG00408.hp1 HG00597.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.269+165dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105705902 | ||||||
chr9:105705902 | G | T | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0003t0012g0268 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+149G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105705902 | |||||||
chr9:105705988 | C | T | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.269+235C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105705988 | |||||||
chr9:105706015 | C | T | 3 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0004t0004g0017 |
4 | HG01099.hp2 HG01192.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+262C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706015 | |||||||
chr9:105706019 | A | C | 1 | a0001c0001t0011g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.269+266A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706019 | |||||||
chr9:105706047 | C | T | 1 | a0001c0001t0002g0210 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.269+294C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706047 | |||||||
chr9:105706252 | T | C | 1 | a0001c0001t0023g0227 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.269+499T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706252 | |||||||
chr9:105706464 | G | A | 9 | a0001c0001t0003g0007 a0001c0001t0003g0038 a0001c0001t0003g0239 others(6): Show |
13 | HG00609.hp2 NA18941.hp1 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.269+711G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706464 | |||||||
chr9:105706503 | T | C | 215 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0044 others(212): Show |
265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.269+750T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706503 | |||||||
chr9:105706504 | G | A | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.269+751G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706504 | |||||||
chr9:105706563 | A | G | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+810A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706563 | |||||||
chr9:105706605 | T | C | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(174): Show |
224 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.269+852T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706605 | |||||||
chr9:105706621 | A | T | 3 | a0001c0001t0009g0035 a0001c0001t0009g0219 a0001c0001t0009g0220 |
4 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.269+868A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706621 | |||||||
chr9:105706664 | A | G | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.269+911A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706664 | |||||||
chr9:105706713 | G | T | 1 | a0001c0001t0009g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.269+960G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706713 | |||||||
chr9:105706727 | G | A | 4 | a0001c0001t0009g0035 a0001c0001t0009g0218 a0001c0001t0009g0219 others(1): Show |
5 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.269+974G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706727 | |||||||
chr9:105706841 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0013g0018 |
3 | HG02109.hp1 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.269+1088T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706841 | |||||||
chr9:105706852 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.269+1099C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706852 | |||||||
chr9:105706966 | C | T | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.269+1213C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706966 | |||||||
chr9:105706978 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.269+1225A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105706978 | |||||||
chr9:105707025 | G | A | 171 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(168): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.269+1272G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707025 | |||||||
chr9:105707041 | G | T | 3 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 |
4 | HG00733.hp2 HG01884.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.269+1288G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707041 | |||||||
chr9:105707069 | T | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.269+1316T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707069 | |||||||
chr9:105707097 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.269+1344A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707097 | |||||||
chr9:105707185 | G | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+1432G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707185 | |||||||
chr9:105707235 | T | G | 1 | a0001c0001t0006g0077 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.269+1482T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707235 | |||||||
chr9:105707243 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.269+1490C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707243 | |||||||
chr9:105707250 | A | C | 7 | a0001c0001t0002g0003 a0001c0001t0002g0160 a0001c0001t0002g0161 others(4): Show |
11 | HG01081.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.269+1497A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707250 | |||||||
chr9:105707324 | T | A | 1 | a0001c0001t0006g0077 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.269+1571T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707324 | |||||||
chr9:105707325 | A | C | 1 | a0001c0001t0006g0077 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.269+1572A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707325 | |||||||
chr9:105707390 | G | T | 55 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(52): Show |
72 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.269+1637G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707390 | |||||||
chr9:105707590 | G | A | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.269+1837G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707590 | |||||||
chr9:105707616 | C | G | 1 | a0001c0001t0001g0020 | 2 | NA19058.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.269+1863C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707616 | |||||||
chr9:105707871 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+2118A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707871 | |||||||
chr9:105707892 | C | T | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.269+2139C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707892 | |||||||
chr9:105707994 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.269+2241C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105707994 | |||||||
chr9:105708030 | TC | T | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.269+2279delC | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105708030 | ||||||
chr9:105708294 | A | G | 2 | a0001c0001t0005g0011 a0001c0001t0005g0207 |
4 | NA18961.hp2 NA18972.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.269+2541A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105708294 | |||||||
chr9:105708488 | G | T | 1 | a0003c0007t0025g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.269+2735G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105708488 | |||||||
chr9:105708587 | G | A | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.269+2834G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105708587 | |||||||
chr9:105708649 | G | A | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.269+2896G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105708649 | |||||||
chr9:105708676 | C | T | 19 | a0001c0001t0003g0153 a0001c0001t0004g0016 a0001c0001t0004g0046 others(16): Show |
21 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.269+2923C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105708676 | |||||||
chr9:105708697 | C | G | 14 | a0001c0001t0002g0004 a0001c0001t0002g0033 a0001c0001t0002g0034 others(11): Show |
22 | HG01167.hp2 HG01358.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.269+2944C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105708697 | |||||||
chr9:105708854 | A | AT | 164 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(161): Show |
211 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.269+3112dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105708854 | ||||||
chr9:105708992 | A | AT | 28 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0003g0153 others(25): Show |
30 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.269+3253dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105708992 | ||||||
chr9:105708992 | AT | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0143 a0001c0001t0001g0276 others(5): Show |
9 | HG01891.hp1 HG02165.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.269+3253delT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105708992 | ||||||
chr9:105709014 | A | C | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+3261A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709014 | |||||||
chr9:105709137 | C | T | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.269+3384C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709137 | |||||||
chr9:105709177 | G | A | 56 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(53): Show |
73 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.269+3424G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709177 | |||||||
chr9:105709282 | C | T | 171 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(168): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.269+3529C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709282 | |||||||
chr9:105709308 | A | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.269+3555A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709308 | |||||||
chr9:105709321 | T | C | 1 | a0001c0001t0009g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.269+3568T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709321 | |||||||
chr9:105709380 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.269+3627A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709380 | |||||||
chr9:105709492 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.269+3739G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709492 | |||||||
chr9:105709604 | A | G | 171 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(168): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.269+3851A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709604 | |||||||
chr9:105709639 | T | C | 1 | a0002c0002t0007g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.269+3886T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709639 | |||||||
chr9:105709671 | G | C | 56 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(53): Show |
73 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.269+3918G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709671 | |||||||
chr9:105709754 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0013g0018 |
3 | HG02109.hp1 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.269+4001C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709754 | |||||||
chr9:105709755 | G | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
7 | HG00673.hp1 HG01891.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.269+4002G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709755 | |||||||
chr9:105709829 | A | G | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.269+4076A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709829 | |||||||
chr9:105709976 | T | A | 1 | a0001c0001t0005g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.269+4223T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709976 | |||||||
chr9:105709981 | A | G | 1 | a0001c0001t0002g0199 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.269+4228A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709981 | |||||||
chr9:105709983 | GA | G | 3 | a0001c0001t0003g0013 a0001c0001t0003g0250 a0001c0001t0003g0251 |
5 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.269+4232delA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105709983 | ||||||
chr9:105709994 | C | T | 3 | a0001c0001t0003g0237 a0001c0001t0003g0238 a0001c0001t0003g0258 |
3 | HG02922.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.269+4241C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105709994 | |||||||
chr9:105710577 | A | T | 56 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(53): Show |
73 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.269+4824A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105710577 | |||||||
chr9:105710862 | A | G | 4 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+5109A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105710862 | |||||||
chr9:105710877 | C | T | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.269+5124C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105710877 | |||||||
chr9:105710954 | G | C | 1 | a0001c0001t0002g0214 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.269+5201G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105710954 | |||||||
chr9:105711122 | G | A | 1 | a0001c0001t0002g0003 | 5 | HG01081.hp1 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.269+5369G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711122 | |||||||
chr9:105711293 | T | C | 1 | a0002c0002t0007g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.269+5540T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711293 | |||||||
chr9:105711302 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
89 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.269+5549G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711302 | |||||||
chr9:105711314 | G | A | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.269+5561G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711314 | |||||||
chr9:105711341 | T | C | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.269+5588T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711341 | |||||||
chr9:105711371 | G | A | 4 | a0001c0001t0002g0174 a0001c0001t0002g0208 a0001c0001t0002g0211 others(1): Show |
4 | NA18949.hp1 NA19003.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+5618G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711371 | |||||||
chr9:105711440 | CA | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.269+5696delA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105711440 | ||||||
chr9:105711473 | A | G | 2 | a0001c0001t0003g0266 a0001c0001t0003g0267 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.269+5720A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711473 | |||||||
chr9:105711573 | C | T | 1 | a0001c0001t0004g0016 | 2 | HG00733.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.269+5820C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711573 | |||||||
chr9:105711663 | A | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.269+5910A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711663 | |||||||
chr9:105711684 | G | C | 80 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.269+5931G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711684 | |||||||
chr9:105711687 | A | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0069 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.269+5934A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711687 | |||||||
chr9:105711820 | C | CA | 13 | a0001c0001t0001g0276 a0001c0001t0002g0174 a0001c0001t0002g0208 others(10): Show |
16 | HG01255.hp2 HG01952.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.269+6083dupA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105711820 | ||||||
chr9:105711838 | A | T | 1 | a0001c0001t0005g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.269+6085A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711838 | |||||||
chr9:105711911 | C | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.269+6158C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105711911 | |||||||
chr9:105712011 | A | G | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.269+6258A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712011 | |||||||
chr9:105712054 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.269+6301A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712054 | |||||||
chr9:105712066 | A | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.269+6313A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712066 | |||||||
chr9:105712116 | C | T | 2 | a0001c0001t0003g0235 a0001c0001t0003g0236 |
2 | HG01123.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.269+6363C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712116 | |||||||
chr9:105712121 | G | T | 1 | a0001c0001t0005g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.269+6368G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712121 | |||||||
chr9:105712257 | C | T | 27 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(24): Show |
30 | HG01243.hp2 HG01255.hp2 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.269+6504C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712257 | |||||||
chr9:105712313 | C | G | 2 | a0001c0003t0012g0269 a0001c0003t0012g0270 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.269+6560C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712313 | |||||||
chr9:105712395 | C | T | 1 | a0001c0001t0005g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.269+6642C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712395 | |||||||
chr9:105712397 | T | C | 1 | a0001c0001t0005g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.269+6644T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712397 | |||||||
chr9:105712398 | A | C | 176 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(173): Show |
223 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.269+6645A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712398 | |||||||
chr9:105712543 | A | C | 1 | a0001c0001t0005g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.269+6790A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712543 | |||||||
chr9:105712834 | C | G | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.269+7081C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712834 | |||||||
chr9:105712879 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.269+7126C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712879 | |||||||
chr9:105712914 | T | G | 1 | a0001c0001t0005g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.269+7161T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105712914 | |||||||
chr9:105713036 | A | G | 6 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0003t0012g0268 others(3): Show |
8 | HG01243.hp2 HG01255.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.269+7283A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105713036 | |||||||
chr9:105713187 | C | T | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.269+7434C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105713187 | |||||||
chr9:105713188 | A | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.269+7435A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105713188 | |||||||
chr9:105713191 | G | A | 1 | a0001c0001t0009g0219 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.269+7438G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105713191 | |||||||
chr9:105713315 | A | T | 4 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+7562A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105713315 | |||||||
chr9:105713432 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.269+7679T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105713432 | |||||||
chr9:105713667 | C | T | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.270-7870C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105713667 | |||||||
chr9:105713670 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.270-7867G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105713670 | |||||||
chr9:105714128 | C | T | 1 | a0001c0001t0004g0281 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.270-7409C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105714128 | |||||||
chr9:105714667 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.270-6870T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105714667 | |||||||
chr9:105714957 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.270-6580A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105714957 | |||||||
chr9:105715006 | C | T | 1 | a0002c0002t0007g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.270-6531C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105715006 | |||||||
chr9:105715367 | C | G | 1 | a0001c0001t0003g0267 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.270-6170C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105715367 | |||||||
chr9:105715522 | T | C | 1 | a0001c0003t0012g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.270-6015T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105715522 | |||||||
chr9:105715525 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.270-6012T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105715525 | |||||||
chr9:105715700 | G | T | 1 | a0001c0001t0002g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.270-5837G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105715700 | |||||||
chr9:105715772 | G | A | 33 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(30): Show |
36 | HG01243.hp2 HG01255.hp2 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.270-5765G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105715772 | |||||||
chr9:105715829 | A | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.270-5708A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105715829 | |||||||
chr9:105715921 | A | G | 1 | a0001c0001t0003g0265 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.270-5616A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105715921 | |||||||
chr9:105715979 | T | C | 1 | a0001c0001t0002g0029 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.270-5558T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105715979 | |||||||
chr9:105715991 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.270-5546C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105715991 | |||||||
chr9:105716030 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.270-5507C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716030 | |||||||
chr9:105716157 | T | A | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.270-5380T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716157 | |||||||
chr9:105716333 | T | C | 5 | a0001c0001t0003g0036 a0001c0001t0003g0228 a0001c0001t0003g0229 others(2): Show |
6 | HG02622.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.270-5204T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716333 | |||||||
chr9:105716374 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0003g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.270-5163_270-5162i others(17): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716374 | |||||||
chr9:105716374 | T | TTGTGTGT others(1): Show |
17 | a0001c0001t0002g0163 a0001c0001t0004g0016 a0001c0001t0004g0046 others(14): Show |
20 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.270-5153_270-5146d others(10): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105716374 | ||||||
chr9:105716374 | T | TTGTGTGT others(3): Show |
85 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(82): Show |
110 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.270-5155_270-5146d others(12): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105716374 | ||||||
chr9:105716374 | T | TTGTGTGT others(5): Show |
15 | a0001c0001t0003g0007 a0001c0001t0003g0038 a0001c0001t0003g0153 others(12): Show |
19 | HG00609.hp2 HG02559.hp2 HG02717.hp1 others(16): Show |
intron_variant | MODIFIER | c.270-5157_270-5146d others(14): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105716374 | ||||||
chr9:105716374 | T | TTGTGTGT others(7): Show |
46 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0036 others(43): Show |
59 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.270-5159_270-5146d others(16): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105716374 | ||||||
chr9:105716374 | T | TTGTGTGT others(9): Show |
3 | a0001c0001t0003g0272 a0001c0003t0012g0269 a0001c0003t0012g0270 |
3 | HG02486.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.270-5161_270-5146d others(18): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105716374 | ||||||
chr9:105716374 | T | TTGTGTGT others(11): Show |
5 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0011g0147 others(2): Show |
7 | HG01255.hp2 HG02145.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.270-5146_270-5145i others(20): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105716374 | ||||||
chr9:105716374 | T | TTGTGTGT others(13): Show |
1 | a0001c0003t0012g0268 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.270-5146_270-5145i others(22): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105716374 | ||||||
chr9:105716374 | T | TTGTGTGT others(17): Show |
3 | a0001c0001t0011g0149 a0001c0001t0011g0150 a0001c0001t0011g0273 |
3 | HG02976.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.270-5146_270-5145i others(26): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105716374 | ||||||
chr9:105716374 | T | TTGTGTGT others(19): Show |
1 | a0001c0001t0024g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.270-5146_270-5145i others(28): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105716374 | ||||||
chr9:105716392 | A | G | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(174): Show |
224 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.270-5145A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716392 | |||||||
chr9:105716621 | A | ACAG | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4916_270-4915i others(5): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716621 | |||||||
chr9:105716623 | T | G | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4914T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716623 | |||||||
chr9:105716624 | T | C | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4913T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716624 | |||||||
chr9:105716626 | G | A | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4911G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716626 | |||||||
chr9:105716627 | A | C | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4910A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716627 | |||||||
chr9:105716628 | A | C | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4909A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716628 | |||||||
chr9:105716633 | G | C | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4904G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716633 | |||||||
chr9:105716635 | GAATCCA | G | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4901_270-4896d others(8): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716635 | |||||||
chr9:105716644 | T | G | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4893T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716644 | |||||||
chr9:105716645 | A | AGAGC | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4892_270-4891i others(6): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716645 | |||||||
chr9:105716648 | T | A | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4889T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716648 | |||||||
chr9:105716651 | A | ACAGAG | 5 | a0001c0001t0005g0011 a0001c0001t0005g0032 a0001c0001t0005g0201 others(2): Show |
8 | NA18952.hp1 NA18954.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.270-4886_270-4885i others(7): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716651 | |||||||
chr9:105716651 | A | ACGGAG | 99 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(96): Show |
123 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.270-4886_270-4885i others(7): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716651 | |||||||
chr9:105716654 | T | G | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4883T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716654 | |||||||
chr9:105716656 | T | TACCCTC | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4881_270-4880i others(8): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716656 | |||||||
chr9:105716660 | T | G | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4877T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716660 | |||||||
chr9:105716661 | C | CAGG | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.270-4876_270-4875i others(5): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716661 | |||||||
chr9:105716702 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.270-4835C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716702 | |||||||
chr9:105716789 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.270-4748T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716789 | |||||||
chr9:105716845 | A | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
330 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(327): Show |
intron_variant | MODIFIER | c.270-4692A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716845 | |||||||
chr9:105716853 | G | A | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(174): Show |
224 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.270-4684G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105716853 | |||||||
chr9:105717009 | G | T | 1 | a0001c0001t0002g0197 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.270-4528G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717009 | |||||||
chr9:105717044 | C | A | 11 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(8): Show |
13 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.270-4493C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717044 | |||||||
chr9:105717149 | A | T | 1 | a0001c0001t0015g0068 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.270-4388A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717149 | |||||||
chr9:105717211 | C | T | 6 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(3): Show |
7 | HG01952.hp2 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.270-4326C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717211 | |||||||
chr9:105717212 | G | A | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.270-4325G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717212 | |||||||
chr9:105717422 | A | AG | 171 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(168): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.270-4115_270-4114i others(3): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717422 | |||||||
chr9:105717504 | T | G | 2 | a0001c0001t0002g0177 a0001c0001t0002g0200 |
2 | HG00408.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.270-4033T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717504 | |||||||
chr9:105717505 | G | T | 3 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0004t0004g0017 |
4 | HG01099.hp2 HG01192.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.270-4032G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717505 | |||||||
chr9:105717660 | A | AT | 171 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(168): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.270-3876dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105717660 | ||||||
chr9:105717876 | A | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.270-3661A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717876 | |||||||
chr9:105717930 | A | C | 176 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(173): Show |
223 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.270-3607A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717930 | |||||||
chr9:105717984 | T | G | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.270-3553T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105717984 | |||||||
chr9:105718052 | C | T | 112 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(109): Show |
142 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.270-3485C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105718052 | |||||||
chr9:105718206 | T | C | 1 | a0001c0001t0003g0042 | 2 | NA18999.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.270-3331T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105718206 | |||||||
chr9:105718241 | G | GT | 9 | a0001c0001t0001g0072 a0001c0001t0001g0106 a0001c0001t0001g0130 others(6): Show |
9 | HG02083.hp1 HG02559.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.270-3281dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105718241 | ||||||
chr9:105718346 | C | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.270-3191C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105718346 | |||||||
chr9:105718391 | A | G | 170 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(167): Show |
217 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.270-3146A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105718391 | |||||||
chr9:105718477 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
130 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.270-3060A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105718477 | |||||||
chr9:105718640 | A | G | 3 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 |
3 | NA18959.hp1 NA18993.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.270-2897A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105718640 | |||||||
chr9:105718670 | A | G | 1 | a0003c0007t0025g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.270-2867A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105718670 | |||||||
chr9:105718846 | G | A | 3 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0004t0004g0017 |
4 | HG01099.hp2 HG01192.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.270-2691G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105718846 | |||||||
chr9:105718882 | G | T | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.270-2655G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105718882 | |||||||
chr9:105718946 | G | T | 1 | a0001c0001t0002g0165 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.270-2591G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105718946 | |||||||
chr9:105719034 | T | C | 1 | a0001c0001t0004g0152 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.270-2503T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105719034 | |||||||
chr9:105719045 | T | C | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.270-2492T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105719045 | |||||||
chr9:105719147 | A | G | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG00140.hp2 HG01070.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.270-2390A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105719147 | |||||||
chr9:105719214 | G | A | 136 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(133): Show |
178 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.270-2323G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105719214 | |||||||
chr9:105719280 | G | T | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.270-2257G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105719280 | |||||||
chr9:105719490 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.270-2047T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105719490 | |||||||
chr9:105719689 | T | A | 1 | a0001c0001t0008g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.270-1848T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105719689 | |||||||
chr9:105719698 | A | G | 1 | a0001c0001t0008g0261 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.270-1839A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105719698 | |||||||
chr9:105719720 | C | T | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.270-1817C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105719720 | |||||||
chr9:105719940 | A | G | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.270-1597A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105719940 | |||||||
chr9:105720084 | A | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.270-1453A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105720084 | |||||||
chr9:105720140 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.270-1397A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105720140 | |||||||
chr9:105720314 | G | A | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(174): Show |
224 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.270-1223G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105720314 | |||||||
chr9:105720338 | CTTTAT | C | 110 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(107): Show |
137 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.270-1193_270-1189d others(7): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 105720338 | ||||||
chr9:105720419 | T | C | 1 | a0001c0003t0012g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.270-1118T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105720419 | |||||||
chr9:105720470 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.270-1067C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105720470 | |||||||
chr9:105720615 | A | G | 110 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(107): Show |
137 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.270-922A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105720615 | |||||||
chr9:105720695 | T | C | 1 | a0001c0001t0004g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.270-842T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105720695 | |||||||
chr9:105720734 | G | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
5 | HG01496.hp2 HG01952.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.270-803G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105720734 | |||||||
chr9:105721129 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.270-408C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105721129 | |||||||
chr9:105721179 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.270-358C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105721179 | |||||||
chr9:105721308 | G | A | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(174): Show |
224 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.270-229G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105721308 | |||||||
chr9:105721434 | C | A | 1 | a0001c0001t0011g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.270-103C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105721434 | |||||||
chr9:105721460 | G | A | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(174): Show |
224 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.270-77G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 2/5 | chr9 | 105721460 | |||||||
chr9:105721989 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.454+268T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 3/5 | chr9 | 105721989 | |||||||
chr9:105722111 | A | G | 183 | a0001c0001t0001g0044 a0001c0001t0001g0276 a0001c0001t0001g0277 others(180): Show |
231 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.454+390A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 3/5 | chr9 | 105722111 | |||||||
chr9:105722445 | A | G | 2 | a0001c0001t0011g0149 a0001c0001t0011g0150 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.455-89A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 3/5 | chr9 | 105722445 | |||||||
chr9:105722449 | T | A | 4 | a0001c0001t0008g0014 a0001c0001t0008g0259 a0001c0001t0008g0261 others(1): Show |
6 | HG00597.hp1 HG01261.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-85T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 3/5 | chr9 | 105722449 | |||||||
chr9:105722741 | G | A | 1 | a0002c0002t0007g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.542+120G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105722741 | |||||||
chr9:105722990 | CTA | C | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+371_542+372del others(2): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105722990 | ||||||
chr9:105723205 | TC | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+585delC | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105723205 | |||||||
chr9:105723277 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0079 a0001c0001t0001g0116 others(1): Show |
5 | HG00609.hp1 NA18964.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.542+656G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105723277 | |||||||
chr9:105723407 | T | A | 11 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(8): Show |
14 | HG01243.hp2 HG01255.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.542+786T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105723407 | |||||||
chr9:105723408 | ATT | A | 107 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(104): Show |
136 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.542+802_542+803del others(2): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105723408 | ||||||
chr9:105723408 | ATTT | A | 8 | a0001c0001t0004g0154 a0001c0001t0009g0035 a0001c0001t0009g0217 others(5): Show |
9 | HG01952.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.542+801_542+803del others(3): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105723408 | ||||||
chr9:105723414 | T | G | 88 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(85): Show |
115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.542+793T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105723414 | |||||||
chr9:105723880 | A | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.542+1259A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105723880 | |||||||
chr9:105723891 | A | G | 2 | a0001c0001t0004g0051 a0001c0001t0004g0052 |
2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.542+1270A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105723891 | |||||||
chr9:105723991 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.542+1370A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105723991 | |||||||
chr9:105724252 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.542+1631G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724252 | |||||||
chr9:105724368 | C | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.542+1747C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724368 | |||||||
chr9:105724420 | C | T | 3 | a0001c0001t0006g0099 a0001c0001t0006g0100 a0001c0001t0006g0107 |
3 | NA18971.hp1 NA19063.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.542+1799C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724420 | |||||||
chr9:105724455 | T | C | 11 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(8): Show |
13 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.542+1834T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724455 | |||||||
chr9:105724469 | A | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+1848A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724469 | |||||||
chr9:105724535 | A | G | 39 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(36): Show |
54 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.542+1914A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724535 | |||||||
chr9:105724577 | C | T | 1 | a0002c0002t0007g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.542+1956C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724577 | |||||||
chr9:105724578 | G | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01433.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.542+1957G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724578 | |||||||
chr9:105724634 | AAAAG | A | 11 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(8): Show |
13 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.542+2016_542+2019d others(6): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105724634 | ||||||
chr9:105724635 | AAAG | A | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
132 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.542+2021_542+2023d others(5): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105724635 | ||||||
chr9:105724775 | C | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.542+2154C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724775 | |||||||
chr9:105724841 | T | G | 1 | a0001c0001t0003g0239 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.542+2220T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724841 | |||||||
chr9:105724849 | C | A | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.542+2228C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105724849 | |||||||
chr9:105725086 | A | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+2465A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105725086 | |||||||
chr9:105725190 | G | A | 1 | a0003c0007t0025g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.542+2569G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105725190 | |||||||
chr9:105725322 | GAT | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+2704_542+2705d others(4): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105725322 | ||||||
chr9:105725324 | T | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.542+2703T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105725324 | |||||||
chr9:105725361 | A | G | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.542+2740A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105725361 | |||||||
chr9:105725399 | A | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.542+2778A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105725399 | |||||||
chr9:105725513 | G | T | 1 | a0001c0001t0003g0248 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.542+2892G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105725513 | |||||||
chr9:105725706 | G | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.542+3085G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105725706 | |||||||
chr9:105725839 | C | T | 1 | a0001c0001t0003g0245 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.542+3218C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105725839 | |||||||
chr9:105725850 | G | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.542+3229G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105725850 | |||||||
chr9:105725861 | T | C | 1 | a0001c0001t0002g0222 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.542+3240T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105725861 | |||||||
chr9:105726075 | C | T | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.542+3454C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105726075 | |||||||
chr9:105726294 | G | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0197 |
2 | NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.542+3673G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105726294 | |||||||
chr9:105726325 | T | C | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+3704T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105726325 | |||||||
chr9:105726518 | G | A | 11 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(8): Show |
14 | HG01243.hp2 HG01255.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.542+3897G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105726518 | |||||||
chr9:105726660 | C | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+4039C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105726660 | |||||||
chr9:105726672 | A | T | 1 | a0001c0001t0011g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.542+4051A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105726672 | |||||||
chr9:105726784 | A | G | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.542+4163A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105726784 | |||||||
chr9:105726892 | G | C | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+4271G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105726892 | |||||||
chr9:105726961 | T | C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+4340T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105726961 | |||||||
chr9:105726990 | A | G | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+4369A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105726990 | |||||||
chr9:105727019 | C | A | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+4398C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105727019 | |||||||
chr9:105727267 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
130 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.542+4646G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105727267 | |||||||
chr9:105727433 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.542+4812A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105727433 | |||||||
chr9:105727542 | A | G | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.542+4921A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105727542 | |||||||
chr9:105727573 | A | G | 7 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+4952A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105727573 | |||||||
chr9:105727579 | C | T | 7 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+4958C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105727579 | |||||||
chr9:105727701 | G | T | 7 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+5080G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105727701 | |||||||
chr9:105727704 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG00140.hp1 HG00639.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.542+5083A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105727704 | |||||||
chr9:105727976 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.542+5355G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105727976 | |||||||
chr9:105728043 | A | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+5422A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728043 | |||||||
chr9:105728087 | T | C | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+5466T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728087 | |||||||
chr9:105728120 | T | C | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+5499T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728120 | |||||||
chr9:105728152 | T | C | 1 | a0001c0001t0010g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.542+5531T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728152 | |||||||
chr9:105728166 | A | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+5545A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728166 | |||||||
chr9:105728264 | C | T | 5 | a0001c0001t0003g0036 a0001c0001t0003g0228 a0001c0001t0003g0229 others(2): Show |
6 | HG02622.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+5643C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728264 | |||||||
chr9:105728339 | G | A | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+5718G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728339 | |||||||
chr9:105728399 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0045 |
3 | HG00558.hp2 NA18612.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.542+5778G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728399 | |||||||
chr9:105728441 | C | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+5820C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728441 | |||||||
chr9:105728491 | A | G | 3 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0004t0004g0017 |
4 | HG01099.hp2 HG01192.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+5870A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728491 | |||||||
chr9:105728594 | G | T | 1 | a0001c0001t0002g0194 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.542+5973G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728594 | |||||||
chr9:105728811 | G | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+6190G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728811 | |||||||
chr9:105728869 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0206 |
3 | HG02523.hp1 NA19064.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.542+6248A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728869 | |||||||
chr9:105728894 | T | C | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+6273T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728894 | |||||||
chr9:105728931 | AT | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.542+6317delT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105728931 | ||||||
chr9:105728996 | G | T | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+6375G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105728996 | |||||||
chr9:105729018 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.542+6397C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729018 | |||||||
chr9:105729077 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.542+6456T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729077 | |||||||
chr9:105729091 | C | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+6470C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729091 | |||||||
chr9:105729108 | G | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+6487G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729108 | |||||||
chr9:105729295 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.542+6674A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729295 | |||||||
chr9:105729297 | A | G | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.542+6676A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729297 | |||||||
chr9:105729346 | T | C | 3 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.542+6725T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729346 | |||||||
chr9:105729414 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.542+6793G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729414 | |||||||
chr9:105729439 | CATCTCTG others(3221): Show |
C | 2 | a0001c0001t0015g0067 a0001c0001t0015g0068 |
2 | NA18747.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.542+6925_542+10152 others(3): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105729439 | ||||||
chr9:105729478 | C | A | 1 | a0001c0001t0003g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.542+6857C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729478 | |||||||
chr9:105729525 | G | A | 1 | a0001c0003t0012g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.542+6904G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729525 | |||||||
chr9:105729624 | A | G | 1 | a0001c0001t0002g0213 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.542+7003A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729624 | |||||||
chr9:105729706 | C | T | 2 | a0001c0001t0003g0039 a0001c0001t0003g0246 |
2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.542+7085C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729706 | |||||||
chr9:105729883 | G | T | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.542+7262G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729883 | |||||||
chr9:105729886 | C | A | 5 | a0001c0001t0003g0036 a0001c0001t0003g0228 a0001c0001t0003g0229 others(2): Show |
6 | HG02622.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+7265C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105729886 | |||||||
chr9:105730046 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+7425C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730046 | |||||||
chr9:105730249 | T | C | 3 | a0001c0001t0009g0035 a0001c0001t0009g0219 a0001c0001t0009g0220 |
4 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.542+7628T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730249 | |||||||
chr9:105730404 | A | T | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.542+7783A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730404 | |||||||
chr9:105730430 | G | A | 92 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(89): Show |
119 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.542+7809G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730430 | |||||||
chr9:105730454 | C | T | 87 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(84): Show |
115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.542+7833C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730454 | |||||||
chr9:105730505 | C | T | 7 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+7884C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730505 | |||||||
chr9:105730529 | C | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+7908C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730529 | |||||||
chr9:105730538 | C | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+7917C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730538 | |||||||
chr9:105730592 | G | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+7971G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730592 | |||||||
chr9:105730646 | G | T | 7 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+8025G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730646 | |||||||
chr9:105730771 | A | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+8150A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730771 | |||||||
chr9:105730779 | C | T | 4 | a0001c0001t0011g0149 a0001c0001t0011g0150 a0001c0001t0011g0273 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+8158C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730779 | |||||||
chr9:105730792 | G | A | 11 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(8): Show |
13 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.542+8171G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730792 | |||||||
chr9:105730949 | T | C | 1 | a0001c0001t0001g0020 | 2 | NA19058.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.542+8328T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105730949 | |||||||
chr9:105731052 | G | T | 1 | a0001c0001t0009g0217 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.542+8431G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731052 | |||||||
chr9:105731102 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.542+8481G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731102 | |||||||
chr9:105731103 | C | G | 1 | a0001c0001t0003g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.542+8482C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731103 | |||||||
chr9:105731158 | G | C | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.542+8537G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731158 | |||||||
chr9:105731227 | C | A | 1 | a0001c0001t0002g0004 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.542+8606C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731227 | |||||||
chr9:105731295 | TTTA | T | 25 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(22): Show |
27 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.542+8700_542+8702d others(5): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105731295 | ||||||
chr9:105731295 | TTTATTA | T | 87 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(84): Show |
115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.542+8697_542+8702d others(8): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105731295 | ||||||
chr9:105731347 | G | A | 1 | a0001c0003t0012g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.542+8726G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731347 | |||||||
chr9:105731421 | T | C | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+8800T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731421 | |||||||
chr9:105731470 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.542+8849C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731470 | |||||||
chr9:105731552 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.542+8931T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731552 | |||||||
chr9:105731709 | T | C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+9088T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731709 | |||||||
chr9:105731755 | A | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.542+9134A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731755 | |||||||
chr9:105731819 | C | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+9198C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105731819 | |||||||
chr9:105732060 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.542+9439G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732060 | |||||||
chr9:105732065 | G | A | 1 | a0001c0001t0002g0001 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.542+9444G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732065 | |||||||
chr9:105732116 | T | C | 1 | a0001c0001t0004g0159 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.542+9495T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732116 | |||||||
chr9:105732247 | A | C | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+9626A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732247 | |||||||
chr9:105732260 | C | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+9639C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732260 | |||||||
chr9:105732282 | T | G | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.542+9661T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732282 | |||||||
chr9:105732336 | G | T | 3 | a0001c0001t0001g0023 a0001c0001t0004g0046 a0001c0001t0004g0047 |
3 | HG01884.hp2 HG02922.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.542+9715G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732336 | |||||||
chr9:105732460 | T | A | 1 | a0003c0007t0025g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.542+9839T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732460 | |||||||
chr9:105732487 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.542+9866A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732487 | |||||||
chr9:105732601 | C | T | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.542+9980C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732601 | |||||||
chr9:105732660 | TG | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.542+10041delG | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105732660 | ||||||
chr9:105732741 | G | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG02723.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.542+10120G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732741 | |||||||
chr9:105732870 | A | T | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.542+10249A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732870 | |||||||
chr9:105732884 | A | G | 10 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 others(7): Show |
10 | HG00438.hp1 NA18747.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.542+10263A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105732884 | |||||||
chr9:105733059 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.542+10438A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733059 | |||||||
chr9:105733163 | C | T | 1 | a0001c0001t0017g0104 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.542+10542C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733163 | |||||||
chr9:105733165 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.542+10544A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733165 | |||||||
chr9:105733180 | C | T | 1 | a0001c0001t0010g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.542+10559C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733180 | |||||||
chr9:105733225 | A | G | 33 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(30): Show |
35 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.542+10604A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733225 | |||||||
chr9:105733239 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.542+10618A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733239 | |||||||
chr9:105733421 | C | CT | 6 | a0001c0001t0001g0071 a0001c0001t0003g0013 a0001c0001t0003g0243 others(3): Show |
8 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.542+10815dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105733421 | ||||||
chr9:105733421 | C | CTT | 14 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0219 others(11): Show |
15 | HG01952.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.542+10814_542+1081 others(6): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105733421 | ||||||
chr9:105733421 | C | CTTT | 84 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(81): Show |
111 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.542+10813_542+1081 others(7): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105733421 | ||||||
chr9:105733421 | C | CTTTT | 10 | a0001c0001t0002g0031 a0001c0001t0002g0176 a0001c0001t0002g0189 others(7): Show |
11 | HG00673.hp2 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.542+10812_542+1081 others(8): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105733421 | ||||||
chr9:105733421 | C | T | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.542+10800C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733421 | |||||||
chr9:105733423 | T | TTTC | 8 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(5): Show |
9 | HG00733.hp2 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.542+10804_542+1080 others(7): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105733423 | ||||||
chr9:105733439 | G | A | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+10818G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733439 | |||||||
chr9:105733459 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.542+10838G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733459 | |||||||
chr9:105733576 | G | A | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.542+10955G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733576 | |||||||
chr9:105733630 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+11009A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733630 | |||||||
chr9:105733642 | CTTTG | C | 7 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+11028_542+1103 others(8): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105733642 | ||||||
chr9:105733713 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.542+11092G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733713 | |||||||
chr9:105733825 | G | A | 283 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(280): Show |
352 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.542+11204G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733825 | |||||||
chr9:105733882 | C | G | 5 | a0001c0001t0004g0048 a0001c0001t0004g0050 a0001c0001t0004g0281 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.542+11261C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733882 | |||||||
chr9:105733895 | A | T | 18 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(15): Show |
20 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.542+11274A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105733895 | |||||||
chr9:105734000 | T | G | 1 | a0001c0001t0009g0217 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.542+11379T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105734000 | |||||||
chr9:105734107 | T | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+11486T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105734107 | |||||||
chr9:105734199 | C | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+11578C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105734199 | |||||||
chr9:105734221 | T | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.542+11600T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105734221 | |||||||
chr9:105734359 | CAT | C | 5 | a0001c0001t0004g0048 a0001c0001t0004g0050 a0001c0001t0004g0281 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.542+11739_542+1174 others(6): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105734359 | |||||||
chr9:105734540 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.542+11919G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105734540 | |||||||
chr9:105734651 | T | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.542+12030T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105734651 | |||||||
chr9:105734865 | CT | C | 122 | a0001c0001t0001g0119 a0001c0001t0001g0133 a0001c0001t0002g0001 others(119): Show |
152 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.542+12259delT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105734865 | ||||||
chr9:105734883 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+12262C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105734883 | |||||||
chr9:105734889 | A | T | 1 | a0001c0001t0003g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.542+12268A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105734889 | |||||||
chr9:105735179 | A | G | 1 | a0001c0001t0003g0036 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.542+12558A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735179 | |||||||
chr9:105735238 | T | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.542+12617T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735238 | |||||||
chr9:105735294 | T | C | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.542+12673T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735294 | |||||||
chr9:105735373 | T | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.543-12700T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735373 | |||||||
chr9:105735471 | G | T | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.543-12602G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735471 | |||||||
chr9:105735508 | TG | T | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-12562delG | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105735508 | ||||||
chr9:105735658 | A | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.543-12415A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735658 | |||||||
chr9:105735827 | C | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0143 |
4 | NA19003.hp1 NA19065.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.543-12246C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735827 | |||||||
chr9:105735846 | A | G | 2 | a0001c0001t0002g0180 a0001c0001t0002g0197 |
2 | NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.543-12227A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735846 | |||||||
chr9:105735867 | T | A | 28 | a0001c0001t0003g0153 a0001c0001t0004g0016 a0001c0001t0004g0046 others(25): Show |
30 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.543-12206T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735867 | |||||||
chr9:105735876 | A | T | 80 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.543-12197A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735876 | |||||||
chr9:105735906 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.543-12167G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735906 | |||||||
chr9:105735971 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.543-12102A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105735971 | |||||||
chr9:105736014 | A | T | 1 | a0001c0003t0012g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.543-12059A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105736014 | |||||||
chr9:105736046 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0023g0227 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.543-12018_543-1200 others(18): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105736046 | ||||||
chr9:105736055 | G | T | 4 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-12018G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105736055 | |||||||
chr9:105736055 | GT | G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(105): Show |
137 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.543-12004delT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105736055 | ||||||
chr9:105736056 | T | G | 1 | a0001c0001t0004g0159 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.543-12017T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105736056 | |||||||
chr9:105736077 | A | G | 1 | a0002c0002t0007g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.543-11996A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105736077 | |||||||
chr9:105736090 | A | G | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.543-11983A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105736090 | |||||||
chr9:105736142 | G | C | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.543-11931G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105736142 | |||||||
chr9:105736461 | G | A | 1 | a0001c0001t0003g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.543-11612G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105736461 | |||||||
chr9:105736539 | C | T | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.543-11534C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105736539 | |||||||
chr9:105736922 | G | A | 80 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.543-11151G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105736922 | |||||||
chr9:105736932 | C | G | 5 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(2): Show |
5 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.543-11141C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105736932 | |||||||
chr9:105737090 | G | A | 1 | a0001c0001t0004g0159 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.543-10983G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105737090 | |||||||
chr9:105737104 | C | T | 1 | a0001c0001t0003g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.543-10969C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105737104 | |||||||
chr9:105737341 | G | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-10732G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105737341 | |||||||
chr9:105737345 | AAG | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.543-10725_543-1072 others(6): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105737345 | ||||||
chr9:105737380 | C | T | 1 | a0001c0001t0003g0234 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.543-10693C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105737380 | |||||||
chr9:105737414 | C | T | 7 | a0001c0001t0002g0003 a0001c0001t0002g0160 a0001c0001t0002g0161 others(4): Show |
11 | HG01081.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.543-10659C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105737414 | |||||||
chr9:105737570 | G | A | 18 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(15): Show |
20 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.543-10503G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105737570 | |||||||
chr9:105737578 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.543-10495C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105737578 | |||||||
chr9:105737768 | A | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.543-10305A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105737768 | |||||||
chr9:105738039 | C | T | 28 | a0001c0001t0003g0153 a0001c0001t0004g0016 a0001c0001t0004g0046 others(25): Show |
30 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.543-10034C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738039 | |||||||
chr9:105738040 | A | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.543-10033A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738040 | |||||||
chr9:105738070 | C | T | 1 | a0001c0001t0015g0067 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.543-10003C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738070 | |||||||
chr9:105738085 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.543-9988T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738085 | |||||||
chr9:105738185 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0029 a0001c0001t0002g0156 others(3): Show |
9 | HG01257.hp2 HG01258.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.543-9888C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738185 | |||||||
chr9:105738319 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0132 |
2 | HG01358.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.543-9754C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738319 | |||||||
chr9:105738387 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.543-9686A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738387 | |||||||
chr9:105738398 | C | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.543-9675C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738398 | |||||||
chr9:105738472 | A | C | 1 | a0001c0001t0014g0247 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.543-9601A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738472 | |||||||
chr9:105738516 | T | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.543-9557T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738516 | |||||||
chr9:105738653 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.543-9420C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738653 | |||||||
chr9:105738715 | C | CT | 7 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0142 others(4): Show |
7 | HG00597.hp2 HG00642.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.543-9337dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105738715 | ||||||
chr9:105738715 | C | CTTTTT | 88 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(85): Show |
115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.543-9341_543-9337d others(7): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105738715 | ||||||
chr9:105738715 | C | CTTTTTT | 26 | a0001c0001t0002g0030 a0001c0001t0002g0166 a0001c0001t0002g0168 others(23): Show |
28 | HG00741.hp1 HG01261.hp1 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.543-9342_543-9337d others(8): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105738715 | ||||||
chr9:105738755 | G | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-9318G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738755 | |||||||
chr9:105738819 | G | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-9254G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738819 | |||||||
chr9:105738857 | A | G | 4 | a0001c0001t0011g0149 a0001c0001t0011g0150 a0001c0001t0011g0273 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-9216A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105738857 | |||||||
chr9:105739035 | A | G | 55 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(52): Show |
72 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.543-9038A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739035 | |||||||
chr9:105739154 | A | G | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-8919A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739154 | |||||||
chr9:105739305 | CT | C | 17 | a0001c0001t0003g0153 a0001c0001t0004g0152 a0001c0001t0004g0154 others(14): Show |
17 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.543-8754delT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105739305 | ||||||
chr9:105739376 | C | G | 1 | a0001c0001t0011g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.543-8697C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739376 | |||||||
chr9:105739415 | C | CA | 5 | a0001c0001t0004g0048 a0001c0001t0004g0050 a0001c0001t0004g0281 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.543-8650dupA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105739415 | ||||||
chr9:105739503 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.543-8570T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739503 | |||||||
chr9:105739527 | G | C | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.543-8546G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739527 | |||||||
chr9:105739554 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.543-8519G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739554 | |||||||
chr9:105739558 | C | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.543-8515C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739558 | |||||||
chr9:105739620 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.543-8453G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739620 | |||||||
chr9:105739780 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.543-8293C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739780 | |||||||
chr9:105739797 | T | A | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.543-8276T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739797 | |||||||
chr9:105739807 | G | A | 80 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.543-8266G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739807 | |||||||
chr9:105739824 | C | T | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.543-8249C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739824 | |||||||
chr9:105739888 | T | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(7): Show |
13 | HG02027.hp1 HG02071.hp2 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.543-8185T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105739888 | |||||||
chr9:105740008 | G | A | 3 | a0001c0001t0009g0035 a0001c0001t0009g0219 a0001c0001t0009g0220 |
4 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.543-8065G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105740008 | |||||||
chr9:105740142 | G | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.543-7931G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105740142 | |||||||
chr9:105740181 | C | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.543-7892C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105740181 | |||||||
chr9:105740254 | C | T | 2 | a0001c0003t0012g0269 a0001c0003t0012g0270 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.543-7819C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105740254 | |||||||
chr9:105740260 | G | GT | 95 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(92): Show |
124 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.543-7795dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105740260 | ||||||
chr9:105740260 | G | GTT | 11 | a0001c0001t0002g0166 a0001c0001t0002g0173 a0001c0001t0002g0186 others(8): Show |
12 | HG02145.hp1 HG02145.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.543-7796_543-7795d others(4): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105740260 | ||||||
chr9:105740260 | GT | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
198 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.543-7795delT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105740260 | ||||||
chr9:105740269 | T | G | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.543-7804T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105740269 | |||||||
chr9:105740492 | C | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.543-7581C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105740492 | |||||||
chr9:105740504 | C | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.543-7569C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105740504 | |||||||
chr9:105740546 | G | A | 182 | a0001c0001t0001g0044 a0001c0001t0001g0276 a0001c0001t0001g0277 others(179): Show |
230 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.543-7527G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105740546 | |||||||
chr9:105740974 | G | GTA | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.543-7099_543-7098i others(4): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105740974 | |||||||
chr9:105740975 | A | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.543-7098A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105740975 | |||||||
chr9:105741049 | A | G | 1 | a0001c0001t0004g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543-7024A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105741049 | |||||||
chr9:105741138 | T | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.543-6935T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105741138 | |||||||
chr9:105741239 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.543-6834G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105741239 | |||||||
chr9:105741297 | A | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.543-6776A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105741297 | |||||||
chr9:105741335 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.543-6738T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105741335 | |||||||
chr9:105741610 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.543-6463C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105741610 | |||||||
chr9:105741612 | A | G | 1 | a0001c0001t0008g0261 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.543-6461A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105741612 | |||||||
chr9:105741901 | A | G | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-6172A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105741901 | |||||||
chr9:105742014 | G | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA18965.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.543-6059G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742014 | |||||||
chr9:105742119 | AATGAAAG | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.543-5952_543-5946d others(9): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105742119 | ||||||
chr9:105742196 | T | C | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.543-5877T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742196 | |||||||
chr9:105742255 | G | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.543-5818G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742255 | |||||||
chr9:105742284 | A | G | 1 | a0001c0001t0002g0188 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.543-5789A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742284 | |||||||
chr9:105742309 | G | A | 15 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(12): Show |
15 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.543-5764G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742309 | |||||||
chr9:105742340 | C | T | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.543-5733C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742340 | |||||||
chr9:105742512 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.543-5561T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742512 | |||||||
chr9:105742636 | C | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-5437C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742636 | |||||||
chr9:105742656 | A | T | 1 | a0001c0003t0012g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.543-5417A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742656 | |||||||
chr9:105742694 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.543-5379A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742694 | |||||||
chr9:105742832 | T | A | 1 | a0001c0001t0001g0019 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.543-5241T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742832 | |||||||
chr9:105742835 | T | A | 1 | a0001c0001t0001g0019 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.543-5238T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742835 | |||||||
chr9:105742947 | T | C | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.543-5126T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742947 | |||||||
chr9:105742963 | A | G | 1 | a0001c0001t0003g0260 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.543-5110A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105742963 | |||||||
chr9:105743003 | C | T | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.543-5070C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105743003 | |||||||
chr9:105743043 | A | G | 2 | a0001c0001t0004g0154 a0001c0001t0004g0155 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.543-5030A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105743043 | |||||||
chr9:105743078 | A | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0260 |
3 | NA18978.hp2 NA18989.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.543-4995A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105743078 | |||||||
chr9:105743334 | A | C | 1 | a0001c0001t0003g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.543-4739A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105743334 | |||||||
chr9:105743345 | C | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.543-4728C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105743345 | |||||||
chr9:105743612 | G | A | 1 | a0001c0001t0006g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.543-4461G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105743612 | |||||||
chr9:105743615 | A | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.543-4458A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105743615 | |||||||
chr9:105743739 | G | A | 1 | a0001c0001t0003g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.543-4334G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105743739 | |||||||
chr9:105743779 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.543-4294G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105743779 | |||||||
chr9:105743998 | T | C | 2 | a0001c0003t0012g0268 a0001c0003t0012g0271 |
2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.543-4075T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105743998 | |||||||
chr9:105744008 | G | T | 105 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(102): Show |
135 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.543-4065G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744008 | |||||||
chr9:105744162 | A | G | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.543-3911A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744162 | |||||||
chr9:105744177 | T | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-3896T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744177 | |||||||
chr9:105744195 | CAAGAAAA others(13): Show |
C | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.543-3872_543-3853d others(22): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105744195 | ||||||
chr9:105744355 | A | G | 1 | a0001c0001t0003g0236 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.543-3718A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744355 | |||||||
chr9:105744435 | G | C | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3638G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744435 | |||||||
chr9:105744436 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3637G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744436 | |||||||
chr9:105744437 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3636A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744437 | |||||||
chr9:105744438 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3635T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744438 | |||||||
chr9:105744439 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-3634C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744439 | |||||||
chr9:105744440 | G | A | 1 | a0001c0003t0012g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.543-3633G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744440 | |||||||
chr9:105744447 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3626T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744447 | |||||||
chr9:105744453 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3620C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744453 | |||||||
chr9:105744454 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3619G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744454 | |||||||
chr9:105744456 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3617A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744456 | |||||||
chr9:105744458 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3615C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744458 | |||||||
chr9:105744459 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3614C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744459 | |||||||
chr9:105744462 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3611G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744462 | |||||||
chr9:105744464 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3609A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744464 | |||||||
chr9:105744466 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3607G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744466 | |||||||
chr9:105744467 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3606A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744467 | |||||||
chr9:105744469 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3604G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744469 | |||||||
chr9:105744470 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3603G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744470 | |||||||
chr9:105744474 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3599A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744474 | |||||||
chr9:105744477 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3596T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744477 | |||||||
chr9:105744478 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3595G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744478 | |||||||
chr9:105744480 | G | C | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3593G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744480 | |||||||
chr9:105744483 | GAATATAT others(6): Show |
G | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3589_543-3577d others(15): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744483 | |||||||
chr9:105744499 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3574T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744499 | |||||||
chr9:105744505 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3568T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744505 | |||||||
chr9:105744507 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3566C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744507 | |||||||
chr9:105744511 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3562C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744511 | |||||||
chr9:105744512 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3561C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744512 | |||||||
chr9:105744514 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3559T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744514 | |||||||
chr9:105744515 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3558C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744515 | |||||||
chr9:105744516 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3557T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744516 | |||||||
chr9:105744522 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3551T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744522 | |||||||
chr9:105744526 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3547A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744526 | |||||||
chr9:105744538 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3535T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744538 | |||||||
chr9:105744541 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3532A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744541 | |||||||
chr9:105744545 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3528T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744545 | |||||||
chr9:105744550 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3523G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744550 | |||||||
chr9:105744553 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3520A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744553 | |||||||
chr9:105744555 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3518G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744555 | |||||||
chr9:105744557 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3516A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744557 | |||||||
chr9:105744558 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3515A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744558 | |||||||
chr9:105744560 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.543-3513T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744560 | |||||||
chr9:105744633 | C | T | 15 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(12): Show |
15 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.543-3440C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744633 | |||||||
chr9:105744692 | C | T | 15 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(12): Show |
15 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.543-3381C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744692 | |||||||
chr9:105744812 | C | A | 1 | a0001c0001t0003g0038 | 2 | NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.543-3261C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105744812 | |||||||
chr9:105745037 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0097 |
2 | HG01515.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.543-3036G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745037 | |||||||
chr9:105745092 | A | G | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.543-2981A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745092 | |||||||
chr9:105745101 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.543-2972C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745101 | |||||||
chr9:105745190 | T | G | 7 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-2883T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745190 | |||||||
chr9:105745335 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.543-2738C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745335 | |||||||
chr9:105745354 | T | C | 1 | a0001c0001t0010g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.543-2719T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745354 | |||||||
chr9:105745359 | C | G | 7 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(4): Show |
7 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-2714C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745359 | |||||||
chr9:105745365 | G | T | 1 | a0001c0003t0012g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.543-2708G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745365 | |||||||
chr9:105745384 | T | A | 1 | a0001c0001t0003g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.543-2689T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745384 | |||||||
chr9:105745413 | C | T | 3 | a0002c0002t0007g0056 a0002c0002t0007g0057 a0002c0002t0007g0061 |
3 | HG02886.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.543-2660C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745413 | |||||||
chr9:105745416 | T | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.543-2657T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745416 | |||||||
chr9:105745473 | G | C | 1 | a0001c0001t0003g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.543-2600G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745473 | |||||||
chr9:105745521 | C | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.543-2552C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745521 | |||||||
chr9:105745578 | G | A | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(112): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.543-2495G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745578 | |||||||
chr9:105745615 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.543-2458A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745615 | |||||||
chr9:105745620 | T | G | 1 | a0001c0001t0002g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.543-2453T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745620 | |||||||
chr9:105745644 | A | G | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.543-2429A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745644 | |||||||
chr9:105745686 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.543-2387G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745686 | |||||||
chr9:105745856 | G | T | 3 | a0001c0001t0003g0233 a0001c0001t0003g0235 a0001c0001t0003g0236 |
3 | HG00642.hp1 HG01123.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.543-2217G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745856 | |||||||
chr9:105745876 | A | T | 3 | a0001c0001t0003g0233 a0001c0001t0003g0235 a0001c0001t0003g0236 |
3 | HG00642.hp1 HG01123.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.543-2197A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745876 | |||||||
chr9:105745880 | G | C | 3 | a0001c0001t0003g0233 a0001c0001t0003g0235 a0001c0001t0003g0236 |
3 | HG00642.hp1 HG01123.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.543-2193G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745880 | |||||||
chr9:105745882 | A | G | 3 | a0001c0001t0003g0233 a0001c0001t0003g0235 a0001c0001t0003g0236 |
3 | HG00642.hp1 HG01123.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.543-2191A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105745882 | |||||||
chr9:105746061 | C | G | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.543-2012C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746061 | |||||||
chr9:105746078 | A | C | 1 | a0001c0001t0004g0158 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.543-1995A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746078 | |||||||
chr9:105746172 | A | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.543-1901A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746172 | |||||||
chr9:105746230 | A | ATTTG | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.543-1841_543-1838d others(6): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 105746230 | ||||||
chr9:105746664 | C | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.543-1409C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746664 | |||||||
chr9:105746676 | C | T | 1 | a0001c0001t0009g0217 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.543-1397C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746676 | |||||||
chr9:105746702 | T | C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.543-1371T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746702 | |||||||
chr9:105746759 | C | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.543-1314C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746759 | |||||||
chr9:105746877 | C | T | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.543-1196C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746877 | |||||||
chr9:105746889 | C | T | 1 | a0003c0007t0025g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.543-1184C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746889 | |||||||
chr9:105746909 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.543-1164C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746909 | |||||||
chr9:105746920 | C | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.543-1153C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746920 | |||||||
chr9:105746936 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.543-1137A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746936 | |||||||
chr9:105746939 | G | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.543-1134G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105746939 | |||||||
chr9:105747019 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.543-1054G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747019 | |||||||
chr9:105747019 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.543-1054G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747019 | |||||||
chr9:105747099 | T | G | 1 | a0003c0007t0025g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.543-974T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747099 | |||||||
chr9:105747123 | A | G | 1 | a0002c0002t0007g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.543-950A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747123 | |||||||
chr9:105747204 | C | T | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.543-869C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747204 | |||||||
chr9:105747323 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.543-750G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747323 | |||||||
chr9:105747361 | T | C | 182 | a0001c0001t0001g0044 a0001c0001t0001g0276 a0001c0001t0001g0277 others(179): Show |
230 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.543-712T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747361 | |||||||
chr9:105747374 | A | G | 3 | a0001c0001t0003g0233 a0001c0001t0003g0235 a0001c0001t0003g0236 |
3 | HG00642.hp1 HG01123.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.543-699A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747374 | |||||||
chr9:105747402 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.543-671T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747402 | |||||||
chr9:105747404 | T | A | 1 | a0001c0001t0001g0079 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.543-669T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747404 | |||||||
chr9:105747426 | C | T | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.543-647C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747426 | |||||||
chr9:105747446 | G | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-627G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747446 | |||||||
chr9:105747456 | G | T | 1 | a0001c0001t0009g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.543-617G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747456 | |||||||
chr9:105747482 | T | G | 1 | a0001c0001t0003g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.543-591T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747482 | |||||||
chr9:105747615 | C | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.543-458C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747615 | |||||||
chr9:105747713 | T | C | 4 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-360T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747713 | |||||||
chr9:105747908 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.543-165G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 4/5 | chr9 | 105747908 | |||||||
chr9:105748228 | G | A | 1 | a0001c0001t0010g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.660+38G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105748228 | |||||||
chr9:105748397 | CAGG | C | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+209_660+211del others(3): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105748397 | ||||||
chr9:105748485 | T | TA | 107 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(104): Show |
137 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.660+296dupA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105748485 | ||||||
chr9:105748679 | G | T | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.660+489G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105748679 | |||||||
chr9:105748806 | T | G | 15 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(12): Show |
15 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.660+616T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105748806 | |||||||
chr9:105748845 | G | A | 1 | a0001c0001t0004g0159 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.660+655G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105748845 | |||||||
chr9:105748858 | A | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0120 a0001c0001t0001g0131 others(2): Show |
6 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+668A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105748858 | |||||||
chr9:105748882 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+692G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105748882 | |||||||
chr9:105749348 | T | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+1158T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105749348 | |||||||
chr9:105749349 | G | A | 4 | a0001c0001t0011g0149 a0001c0001t0011g0150 a0001c0001t0011g0273 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+1159G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105749349 | |||||||
chr9:105749367 | C | T | 1 | a0001c0001t0004g0159 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.660+1177C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105749367 | |||||||
chr9:105749375 | A | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+1185A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105749375 | |||||||
chr9:105749483 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.660+1293A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105749483 | |||||||
chr9:105749519 | A | C | 1 | a0001c0001t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.660+1329A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105749519 | |||||||
chr9:105749543 | T | C | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+1353T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105749543 | |||||||
chr9:105749625 | A | AT | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.660+1437dupT | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105749625 | ||||||
chr9:105749833 | G | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+1643G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105749833 | |||||||
chr9:105749871 | G | C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.660+1681G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105749871 | |||||||
chr9:105749989 | T | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+1799T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105749989 | |||||||
chr9:105750018 | A | C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.660+1828A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750018 | |||||||
chr9:105750221 | A | C | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+2031A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750221 | |||||||
chr9:105750345 | C | T | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+2155C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750345 | |||||||
chr9:105750484 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0145 |
3 | NA18964.hp1 NA18989.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.660+2294C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750484 | |||||||
chr9:105750539 | G | A | 1 | a0001c0001t0003g0224 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.660+2349G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750539 | |||||||
chr9:105750631 | A | AAACAAAT | 111 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(108): Show |
141 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.660+2445_660+2446i others(9): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105750631 | ||||||
chr9:105750631 | A | T | 3 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0152 |
3 | HG01884.hp2 HG02895.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.660+2441A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750631 | |||||||
chr9:105750633 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA18965.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.660+2443A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750633 | |||||||
chr9:105750647 | T | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+2457T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750647 | |||||||
chr9:105750844 | T | G | 1 | a0001c0001t0003g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.660+2654T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750844 | |||||||
chr9:105750859 | A | C | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+2669A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750859 | |||||||
chr9:105750915 | C | T | 7 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.660+2725C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750915 | |||||||
chr9:105750999 | G | T | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+2809G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105750999 | |||||||
chr9:105751025 | G | A | 86 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(83): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.660+2835G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751025 | |||||||
chr9:105751114 | G | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.660+2924G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751114 | |||||||
chr9:105751224 | G | A | 3 | a0001c0001t0003g0037 a0001c0001t0003g0232 a0001c0001t0003g0257 |
4 | HG01884.hp1 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.660+3034G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751224 | |||||||
chr9:105751264 | A | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0276 a0001c0001t0001g0277 others(2): Show |
6 | HG01891.hp1 HG02630.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+3074A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751264 | |||||||
chr9:105751272 | G | A | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.660+3082G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751272 | |||||||
chr9:105751274 | A | C | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+3084A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751274 | |||||||
chr9:105751372 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+3182G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751372 | |||||||
chr9:105751584 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.660+3394A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751584 | |||||||
chr9:105751673 | A | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+3483A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751673 | |||||||
chr9:105751743 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0142 |
2 | HG01106.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.660+3553C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751743 | |||||||
chr9:105751854 | G | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.660+3664G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751854 | |||||||
chr9:105751957 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG00140.hp1 HG00639.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.660+3767G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105751957 | |||||||
chr9:105752001 | C | T | 1 | a0001c0003t0012g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.660+3811C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752001 | |||||||
chr9:105752236 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.660+4046T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752236 | |||||||
chr9:105752252 | G | T | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+4062G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752252 | |||||||
chr9:105752283 | G | A | 27 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(24): Show |
29 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.660+4093G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752283 | |||||||
chr9:105752379 | C | T | 3 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.660+4189C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752379 | |||||||
chr9:105752384 | A | C | 8 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(5): Show |
9 | HG00733.hp2 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+4194A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752384 | |||||||
chr9:105752396 | T | A | 1 | a0001c0003t0012g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.660+4206T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752396 | |||||||
chr9:105752419 | C | T | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+4229C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752419 | |||||||
chr9:105752583 | G | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.660+4393G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752583 | |||||||
chr9:105752602 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG00140.hp1 HG00639.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.660+4412G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752602 | |||||||
chr9:105752797 | A | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
7 | HG00673.hp1 HG01891.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.660+4607A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752797 | |||||||
chr9:105752861 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+4671A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105752861 | |||||||
chr9:105753002 | A | G | 12 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(9): Show |
14 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.660+4812A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105753002 | |||||||
chr9:105753028 | G | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.660+4838G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105753028 | |||||||
chr9:105753037 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.660+4847C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105753037 | |||||||
chr9:105753181 | G | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+4991G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105753181 | |||||||
chr9:105753219 | T | C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.660+5029T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105753219 | |||||||
chr9:105753476 | A | T | 1 | a0001c0001t0016g0090 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.660+5286A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105753476 | |||||||
chr9:105753846 | C | T | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.660+5656C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105753846 | |||||||
chr9:105754016 | T | C | 27 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(24): Show |
29 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.660+5826T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754016 | |||||||
chr9:105754020 | T | G | 2 | a0001c0003t0012g0268 a0001c0003t0012g0271 |
2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.660+5830T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754020 | |||||||
chr9:105754052 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+5862G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754052 | |||||||
chr9:105754145 | C | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+5955C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754145 | |||||||
chr9:105754195 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.660+6005A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754195 | |||||||
chr9:105754251 | T | C | 2 | a0001c0001t0004g0048 a0001c0001t0004g0050 |
2 | HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.660+6061T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754251 | |||||||
chr9:105754281 | C | G | 1 | a0001c0003t0012g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.660+6091C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754281 | |||||||
chr9:105754300 | C | T | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+6110C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754300 | |||||||
chr9:105754380 | T | C | 4 | a0001c0001t0004g0048 a0001c0001t0004g0050 a0001c0001t0019g0049 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+6190T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754380 | |||||||
chr9:105754417 | T | G | 1 | a0001c0001t0002g0203 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.660+6227T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754417 | |||||||
chr9:105754491 | A | G | 1 | a0001c0001t0002g0187 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.660+6301A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754491 | |||||||
chr9:105754498 | G | C | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.660+6308G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754498 | |||||||
chr9:105754499 | G | T | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.660+6309G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754499 | |||||||
chr9:105754511 | C | T | 3 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.660+6321C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754511 | |||||||
chr9:105754607 | A | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+6417A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754607 | |||||||
chr9:105754699 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.660+6509A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754699 | |||||||
chr9:105754783 | C | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.660+6593C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754783 | |||||||
chr9:105754885 | A | G | 87 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(84): Show |
115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.660+6695A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754885 | |||||||
chr9:105754913 | C | G | 1 | a0001c0001t0003g0267 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.660+6723C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754913 | |||||||
chr9:105754980 | A | G | 27 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(24): Show |
29 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.660+6790A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105754980 | |||||||
chr9:105755068 | A | G | 2 | a0001c0003t0012g0269 a0001c0003t0012g0270 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.660+6878A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755068 | |||||||
chr9:105755085 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.660+6895C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755085 | |||||||
chr9:105755107 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+6917G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755107 | |||||||
chr9:105755181 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.660+6991T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755181 | |||||||
chr9:105755252 | T | C | 1 | a0001c0001t0003g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.660+7062T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755252 | |||||||
chr9:105755391 | T | C | 1 | a0001c0003t0012g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.660+7201T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755391 | |||||||
chr9:105755441 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.660+7251C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755441 | |||||||
chr9:105755482 | TAAA | T | 80 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.660+7296_660+7298d others(5): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105755482 | ||||||
chr9:105755488 | A | G | 1 | a0001c0001t0015g0067 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.660+7298A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755488 | |||||||
chr9:105755545 | A | G | 1 | a0001c0001t0008g0261 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.660+7355A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755545 | |||||||
chr9:105755581 | T | G | 3 | a0001c0001t0003g0037 a0001c0001t0003g0232 a0001c0001t0003g0257 |
4 | HG01884.hp1 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.660+7391T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755581 | |||||||
chr9:105755585 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.660+7395A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755585 | |||||||
chr9:105755682 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.660+7492A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755682 | |||||||
chr9:105755747 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0115 |
2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.660+7557C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755747 | |||||||
chr9:105755903 | G | C | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+7713G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105755903 | |||||||
chr9:105756159 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.660+7969T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105756159 | |||||||
chr9:105756393 | T | TATA | 2 | a0001c0001t0001g0073 a0001c0001t0013g0018 |
3 | HG02109.hp1 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.660+8206_660+8208d others(5): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105756393 | ||||||
chr9:105756394 | A | G | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG02723.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.660+8204A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105756394 | |||||||
chr9:105756424 | A | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+8234A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105756424 | |||||||
chr9:105756634 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.660+8444T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105756634 | |||||||
chr9:105756739 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+8549G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105756739 | |||||||
chr9:105756785 | T | C | 1 | a0001c0001t0002g0029 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.660+8595T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105756785 | |||||||
chr9:105757321 | A | G | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+9131A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105757321 | |||||||
chr9:105757608 | C | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+9418C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105757608 | |||||||
chr9:105757747 | C | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+9557C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105757747 | |||||||
chr9:105757869 | G | A | 3 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.660+9679G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105757869 | |||||||
chr9:105757987 | T | C | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.660+9797T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105757987 | |||||||
chr9:105758019 | A | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+9829A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105758019 | |||||||
chr9:105758062 | G | A | 27 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(24): Show |
29 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.660+9872G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105758062 | |||||||
chr9:105758093 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.660+9903G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105758093 | |||||||
chr9:105758107 | C | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(66): Show |
88 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.660+9917C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105758107 | |||||||
chr9:105758663 | A | C | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.660+10473A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105758663 | |||||||
chr9:105758791 | C | A | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+10601C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105758791 | |||||||
chr9:105759040 | A | C | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+10850A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105759040 | |||||||
chr9:105759087 | G | A | 3 | a0001c0001t0003g0038 a0001c0001t0003g0239 a0001c0001t0003g0242 |
4 | NA18945.hp2 NA18950.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+10897G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105759087 | |||||||
chr9:105759121 | C | T | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.660+10931C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105759121 | |||||||
chr9:105759219 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG00140.hp1 HG00639.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.660+11029T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105759219 | |||||||
chr9:105759409 | C | T | 7 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.660+11219C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105759409 | |||||||
chr9:105759412 | A | G | 82 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.660+11222A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105759412 | |||||||
chr9:105759643 | C | T | 3 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.660+11453C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105759643 | |||||||
chr9:105759894 | C | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.660+11704C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105759894 | |||||||
chr9:105759966 | A | G | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+11776A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105759966 | |||||||
chr9:105760052 | C | A | 113 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(110): Show |
143 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.660+11862C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105760052 | |||||||
chr9:105760075 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.660+11885C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105760075 | |||||||
chr9:105760091 | C | G | 5 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(2): Show |
5 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.660+11901C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105760091 | |||||||
chr9:105760119 | G | A | 1 | a0001c0001t0006g0083 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.660+11929G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105760119 | |||||||
chr9:105760183 | A | G | 1 | a0001c0001t0003g0245 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.660+11993A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105760183 | |||||||
chr9:105760259 | A | G | 6 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(3): Show |
7 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+12069A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105760259 | |||||||
chr9:105760460 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+12270C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105760460 | |||||||
chr9:105760635 | G | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0072 others(4): Show |
11 | HG02165.hp1 NA18945.hp1 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.660+12445G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105760635 | |||||||
chr9:105760701 | C | CAAGCAAC others(5): Show |
1 | a0001c0001t0022g0209 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.660+12512_660+1252 others(16): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105760701 | ||||||
chr9:105760748 | G | A | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+12558G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105760748 | |||||||
chr9:105760986 | C | T | 3 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.660+12796C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105760986 | |||||||
chr9:105761015 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.660+12825T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105761015 | |||||||
chr9:105761429 | G | T | 57 | a0001c0001t0001g0071 a0001c0001t0003g0007 a0001c0001t0003g0012 others(54): Show |
74 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.661-12436G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105761429 | |||||||
chr9:105761540 | T | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-12325T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105761540 | |||||||
chr9:105761712 | C | T | 12 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(9): Show |
14 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.661-12153C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105761712 | |||||||
chr9:105761795 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.661-12070A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105761795 | |||||||
chr9:105761982 | C | T | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-11883C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105761982 | |||||||
chr9:105762015 | G | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0197 |
2 | NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.661-11850G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762015 | |||||||
chr9:105762202 | G | T | 1 | a0001c0001t0021g0221 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.661-11663G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762202 | |||||||
chr9:105762247 | A | T | 113 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(110): Show |
143 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.661-11618A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762247 | |||||||
chr9:105762257 | T | A | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG02723.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.661-11608T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762257 | |||||||
chr9:105762258 | A | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(74): Show |
102 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.661-11607A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762258 | |||||||
chr9:105762408 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.661-11457T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762408 | |||||||
chr9:105762451 | C | T | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-11414C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762451 | |||||||
chr9:105762481 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.661-11384C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762481 | |||||||
chr9:105762484 | A | G | 3 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0022g0209 |
3 | NA18994.hp2 NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.661-11381A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762484 | |||||||
chr9:105762522 | C | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG01243.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.661-11343C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762522 | |||||||
chr9:105762525 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.661-11340G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762525 | |||||||
chr9:105762552 | C | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.661-11313C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762552 | |||||||
chr9:105762572 | A | AT | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.661-11293_661-1129 others(5): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762572 | |||||||
chr9:105762573 | C | A | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.661-11292C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762573 | |||||||
chr9:105762591 | C | A | 113 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(110): Show |
143 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.661-11274C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762591 | |||||||
chr9:105762617 | A | C | 1 | a0001c0001t0004g0275 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.661-11248A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762617 | |||||||
chr9:105762643 | A | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-11222A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762643 | |||||||
chr9:105762663 | G | C | 1 | a0001c0001t0003g0042 | 2 | NA18999.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.661-11202G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762663 | |||||||
chr9:105762677 | T | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-11188T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762677 | |||||||
chr9:105762692 | A | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0125 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.661-11173A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762692 | |||||||
chr9:105762706 | C | T | 3 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0058 |
3 | HG02280.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.661-11159C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762706 | |||||||
chr9:105762720 | A | G | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.661-11145A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762720 | |||||||
chr9:105762721 | T | G | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.661-11144T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762721 | |||||||
chr9:105762881 | A | G | 1 | a0001c0001t0002g0199 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.661-10984A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762881 | |||||||
chr9:105762893 | A | G | 1 | a0001c0001t0003g0244 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.661-10972A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762893 | |||||||
chr9:105762914 | C | A | 1 | a0003c0007t0025g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661-10951C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762914 | |||||||
chr9:105762930 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661-10935A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762930 | |||||||
chr9:105762954 | G | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.661-10911G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105762954 | |||||||
chr9:105763148 | C | G | 6 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0003t0012g0268 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-10717C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763148 | |||||||
chr9:105763182 | T | C | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG02723.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.661-10683T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763182 | |||||||
chr9:105763220 | G | C | 3 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.661-10645G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763220 | |||||||
chr9:105763223 | A | G | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.661-10642A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763223 | |||||||
chr9:105763291 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.661-10574G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763291 | |||||||
chr9:105763396 | A | G | 1 | a0001c0001t0003g0234 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.661-10469A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763396 | |||||||
chr9:105763416 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-10449C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763416 | |||||||
chr9:105763417 | A | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-10448A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763417 | |||||||
chr9:105763623 | C | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0116 a0001c0001t0003g0224 |
4 | NA18964.hp2 NA18969.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-10242C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763623 | |||||||
chr9:105763636 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.661-10229G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763636 | |||||||
chr9:105763701 | A | G | 2 | a0001c0001t0003g0041 a0001c0001t0003g0252 |
3 | HG01070.hp1 HG01071.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.661-10164A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763701 | |||||||
chr9:105763717 | C | T | 3 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0185 |
3 | HG00741.hp1 HG01261.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.661-10148C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763717 | |||||||
chr9:105763720 | T | A | 3 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0185 |
3 | HG00741.hp1 HG01261.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.661-10145T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763720 | |||||||
chr9:105763760 | T | C | 182 | a0001c0001t0001g0044 a0001c0001t0001g0071 a0001c0001t0001g0276 others(179): Show |
230 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.661-10105T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763760 | |||||||
chr9:105763832 | G | A | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-10033G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763832 | |||||||
chr9:105763930 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.661-9935C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763930 | |||||||
chr9:105763931 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA18965.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.661-9934G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105763931 | |||||||
chr9:105764075 | C | T | 1 | a0001c0001t0011g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.661-9790C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764075 | |||||||
chr9:105764131 | AAT | A | 111 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(108): Show |
141 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.661-9733_661-9732d others(4): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764131 | |||||||
chr9:105764229 | T | C | 3 | a0001c0001t0003g0237 a0001c0001t0003g0238 a0001c0001t0003g0258 |
3 | HG02922.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.661-9636T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764229 | |||||||
chr9:105764337 | T | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01070.hp2 HG01346.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-9528T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764337 | |||||||
chr9:105764412 | A | G | 11 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(8): Show |
13 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.661-9453A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764412 | |||||||
chr9:105764482 | A | G | 2 | a0001c0001t0003g0041 a0001c0001t0003g0252 |
3 | HG01070.hp1 HG01071.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.661-9383A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764482 | |||||||
chr9:105764516 | A | C | 3 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 |
4 | HG00733.hp2 HG01884.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-9349A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764516 | |||||||
chr9:105764522 | C | T | 3 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 |
4 | HG00733.hp2 HG01884.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-9343C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764522 | |||||||
chr9:105764555 | G | A | 10 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0003g0039 others(7): Show |
12 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.661-9310G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764555 | |||||||
chr9:105764571 | G | T | 2 | a0001c0001t0014g0040 a0001c0001t0014g0247 |
3 | HG02735.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.661-9294G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764571 | |||||||
chr9:105764650 | A | G | 3 | a0001c0001t0009g0035 a0001c0001t0009g0219 a0001c0001t0009g0220 |
4 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-9215A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764650 | |||||||
chr9:105764721 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.661-9144C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764721 | |||||||
chr9:105764746 | T | C | 82 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.661-9119T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764746 | |||||||
chr9:105764764 | C | G | 2 | a0001c0003t0012g0268 a0001c0003t0012g0271 |
2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.661-9101C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764764 | |||||||
chr9:105764813 | A | G | 1 | a0001c0001t0003g0240 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.661-9052A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764813 | |||||||
chr9:105764870 | T | G | 1 | a0001c0001t0003g0250 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.661-8995T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764870 | |||||||
chr9:105764885 | T | G | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-8980T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764885 | |||||||
chr9:105764923 | C | T | 8 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(5): Show |
9 | HG00733.hp2 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.661-8942C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764923 | |||||||
chr9:105764981 | G | A | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
353 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.661-8884G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105764981 | |||||||
chr9:105765007 | T | G | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.661-8858T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765007 | |||||||
chr9:105765104 | C | T | 2 | a0001c0001t0004g0051 a0001c0001t0004g0052 |
2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.661-8761C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765104 | |||||||
chr9:105765174 | A | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-8691A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765174 | |||||||
chr9:105765176 | T | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.661-8689T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765176 | |||||||
chr9:105765230 | T | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-8635T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765230 | |||||||
chr9:105765277 | C | T | 60 | a0001c0001t0001g0071 a0001c0001t0003g0007 a0001c0001t0003g0012 others(57): Show |
77 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.661-8588C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765277 | |||||||
chr9:105765384 | C | G | 9 | a0001c0001t0002g0010 a0001c0001t0002g0015 a0001c0001t0002g0029 others(6): Show |
13 | HG00558.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.661-8481C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765384 | |||||||
chr9:105765391 | T | G | 1 | a0001c0001t0002g0200 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.661-8474T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765391 | |||||||
chr9:105765628 | T | C | 11 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(8): Show |
13 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.661-8237T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765628 | |||||||
chr9:105765693 | G | A | 1 | a0001c0001t0017g0104 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.661-8172G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765693 | |||||||
chr9:105765775 | T | C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-8090T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765775 | |||||||
chr9:105765781 | C | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.661-8084C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765781 | |||||||
chr9:105765890 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.661-7975C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765890 | |||||||
chr9:105765958 | C | T | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-7907C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765958 | |||||||
chr9:105765975 | A | G | 1 | a0001c0001t0006g0141 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.661-7890A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105765975 | |||||||
chr9:105766006 | T | A | 1 | a0001c0001t0004g0158 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.661-7859T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766006 | |||||||
chr9:105766044 | G | A | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-7821G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766044 | |||||||
chr9:105766083 | G | T | 1 | a0001c0001t0002g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.661-7782G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766083 | |||||||
chr9:105766107 | A | C | 1 | a0001c0001t0002g0197 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.661-7758A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766107 | |||||||
chr9:105766160 | A | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-7705A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766160 | |||||||
chr9:105766162 | A | G | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-7703A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766162 | |||||||
chr9:105766209 | T | C | 1 | a0001c0001t0002g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.661-7656T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766209 | |||||||
chr9:105766237 | A | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-7628A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766237 | |||||||
chr9:105766314 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.661-7551A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766314 | |||||||
chr9:105766353 | G | C | 3 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
3 | HG02280.hp2 HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.661-7512G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766353 | |||||||
chr9:105766552 | C | T | 11 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(8): Show |
13 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.661-7313C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766552 | |||||||
chr9:105766571 | T | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-7294T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766571 | |||||||
chr9:105766662 | A | G | 1 | a0001c0003t0012g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.661-7203A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766662 | |||||||
chr9:105766662 | A | T | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661-7203A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766662 | |||||||
chr9:105766750 | T | A | 1 | a0001c0001t0002g0191 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.661-7115T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766750 | |||||||
chr9:105766754 | A | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-7111A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766754 | |||||||
chr9:105766847 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0144 |
5 | NA18943.hp1 NA19003.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-7018A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766847 | |||||||
chr9:105766877 | C | G | 4 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-6988C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105766877 | |||||||
chr9:105767082 | C | G | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.661-6783C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767082 | |||||||
chr9:105767163 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.661-6702A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767163 | |||||||
chr9:105767211 | C | A | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-6654C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767211 | |||||||
chr9:105767295 | A | G | 2 | a0002c0002t0007g0054 a0002c0002t0007g0055 |
2 | HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.661-6570A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767295 | |||||||
chr9:105767321 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.661-6544A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767321 | |||||||
chr9:105767481 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-6384C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767481 | |||||||
chr9:105767530 | G | T | 8 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(5): Show |
9 | HG00733.hp2 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.661-6335G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767530 | |||||||
chr9:105767584 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.661-6281T>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767584 | |||||||
chr9:105767619 | A | G | 80 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.661-6246A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767619 | |||||||
chr9:105767629 | C | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-6236C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767629 | |||||||
chr9:105767748 | A | G | 1 | a0001c0001t0021g0221 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.661-6117A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767748 | |||||||
chr9:105767834 | G | A | 1 | a0001c0001t0010g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.661-6031G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767834 | |||||||
chr9:105767928 | T | C | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG01243.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.661-5937T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767928 | |||||||
chr9:105767963 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0102 a0001c0001t0001g0124 others(1): Show |
5 | HG01496.hp1 HG01952.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-5902T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105767963 | |||||||
chr9:105768076 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.661-5789T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105768076 | |||||||
chr9:105768294 | T | C | 1 | a0001c0001t0004g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.661-5571T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105768294 | |||||||
chr9:105768357 | A | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-5508A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105768357 | |||||||
chr9:105768462 | A | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-5403A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105768462 | |||||||
chr9:105768567 | TAAC | T | 5 | a0001c0001t0009g0035 a0001c0001t0009g0217 a0001c0001t0009g0218 others(2): Show |
6 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-5295_661-5293d others(5): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105768567 | ||||||
chr9:105768614 | C | G | 3 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.661-5251C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105768614 | |||||||
chr9:105768687 | A | C | 1 | a0001c0001t0003g0250 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.661-5178A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105768687 | |||||||
chr9:105768740 | TAATGTCT others(2): Show |
T | 1 | a0001c0001t0003g0013 | 3 | HG00741.hp2 HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.661-5123_661-5115d others(11): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105768740 | ||||||
chr9:105768849 | C | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-5016C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105768849 | |||||||
chr9:105768883 | A | G | 2 | a0001c0001t0003g0235 a0001c0001t0003g0236 |
2 | HG01123.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.661-4982A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105768883 | |||||||
chr9:105769008 | A | G | 8 | a0002c0002t0007g0054 a0002c0002t0007g0055 a0002c0002t0007g0056 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.661-4857A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105769008 | |||||||
chr9:105769046 | A | T | 1 | a0001c0003t0012g0268 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.661-4819A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105769046 | |||||||
chr9:105769073 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.661-4792A>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105769073 | |||||||
chr9:105769216 | CAT | C | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.661-4646_661-4645d others(4): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105769216 | ||||||
chr9:105769418 | T | A | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-4447T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105769418 | |||||||
chr9:105769434 | G | A | 1 | a0002c0002t0007g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.661-4431G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105769434 | |||||||
chr9:105769509 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.661-4356T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105769509 | |||||||
chr9:105769577 | C | A | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
353 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.661-4288C>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105769577 | |||||||
chr9:105769724 | T | TAGC | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.661-4139_661-4138i others(5): Show |
TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105769724 | ||||||
chr9:105769749 | C | T | 1 | a0001c0001t0003g0224 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.661-4116C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105769749 | |||||||
chr9:105769964 | G | A | 4 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0260 others(1): Show |
6 | HG02056.hp1 NA18978.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-3901G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105769964 | |||||||
chr9:105770110 | G | A | 87 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(84): Show |
115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.661-3755G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105770110 | |||||||
chr9:105770129 | A | G | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-3736A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105770129 | |||||||
chr9:105770131 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.661-3734T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105770131 | |||||||
chr9:105770248 | C | G | 1 | a0001c0001t0003g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.661-3617C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105770248 | |||||||
chr9:105770298 | T | C | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-3567T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105770298 | |||||||
chr9:105770357 | A | G | 1 | a0001c0001t0004g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.661-3508A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105770357 | |||||||
chr9:105770433 | A | G | 1 | a0001c0001t0003g0228 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.661-3432A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105770433 | |||||||
chr9:105770688 | G | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-3177G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105770688 | |||||||
chr9:105770822 | A | C | 27 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(24): Show |
29 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.661-3043A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105770822 | |||||||
chr9:105770856 | T | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.661-3009T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105770856 | |||||||
chr9:105771533 | C | G | 1 | a0001c0001t0006g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.661-2332C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105771533 | |||||||
chr9:105771673 | T | TA | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-2186dupA | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 105771673 | ||||||
chr9:105771825 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.661-2040A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105771825 | |||||||
chr9:105771945 | C | T | 1 | a0002c0002t0007g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.661-1920C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105771945 | |||||||
chr9:105772188 | T | A | 1 | a0001c0001t0002g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.661-1677T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772188 | |||||||
chr9:105772224 | T | C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(111): Show |
144 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.661-1641T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772224 | |||||||
chr9:105772298 | C | G | 1 | a0001c0001t0002g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.661-1567C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772298 | |||||||
chr9:105772409 | A | G | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-1456A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772409 | |||||||
chr9:105772593 | G | A | 7 | a0001c0001t0004g0152 a0001c0001t0004g0154 a0001c0001t0004g0155 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.661-1272G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772593 | |||||||
chr9:105772665 | T | A | 119 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(116): Show |
149 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.661-1200T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772665 | |||||||
chr9:105772666 | T | A | 1 | a0001c0001t0002g0045 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.661-1199T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772666 | |||||||
chr9:105772686 | T | C | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
4 | HG01255.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-1179T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772686 | |||||||
chr9:105772703 | T | A | 1 | a0001c0001t0022g0209 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.661-1162T>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772703 | |||||||
chr9:105772756 | G | C | 6 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(3): Show |
6 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-1109G>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772756 | |||||||
chr9:105772934 | A | C | 1 | a0001c0001t0002g0031 | 2 | NA18960.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.661-931A>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772934 | |||||||
chr9:105772977 | T | C | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.661-888T>C | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772977 | |||||||
chr9:105772979 | C | T | 5 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(2): Show |
5 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-886C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772979 | |||||||
chr9:105772991 | A | G | 80 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.661-874A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105772991 | |||||||
chr9:105773049 | A | G | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.661-816A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105773049 | |||||||
chr9:105773278 | A | G | 4 | a0001c0003t0012g0268 a0001c0003t0012g0269 a0001c0003t0012g0270 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-587A>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105773278 | |||||||
chr9:105773481 | G | T | 27 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0047 others(24): Show |
29 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.661-384G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105773481 | |||||||
chr9:105773503 | G | A | 1 | a0001c0001t0020g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.661-362G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105773503 | |||||||
chr9:105773551 | C | T | 4 | a0001c0001t0011g0149 a0001c0001t0011g0150 a0001c0001t0011g0273 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-314C>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105773551 | |||||||
chr9:105773740 | G | A | 4 | a0001c0001t0004g0048 a0001c0001t0004g0050 a0001c0001t0019g0049 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-125G>A | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105773740 | |||||||
chr9:105773740 | G | T | 1 | a0001c0001t0011g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.661-125G>T | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105773740 | |||||||
chr9:105773818 | C | G | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.661-47C>G | TMEM38B | ENSG00000095209.12 | transcript | ENST00000374692.8 | protein_coding | 5/5 | chr9 | 105773818 |