Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79912 |
| ensemblid | ENSG00000121350.16 |
| hgncid | 26162 |
| symbol | PYROXD1 |
| name | pyridine nucleotide-disulphide oxidoreductase domain 1 |
| refseq_nuc | NM_024854.5 |
| refseq_prot | NP_079130.2 |
| ensembl_nuc | ENST00000240651.14 |
| ensembl_prot | ENSP00000240651.9 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 21437655 |
| end | 21471250 |
| strand | + |
| ver | v1.2 |
| region | chr12:21437655-21471250 |
| region5000 | chr12:21432655-21476250 |
| regionname0 | PYROXD1_chr12_21437655_21471250 |
| regionname5000 | PYROXD1_chr12_21432655_21476250 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 500 | 412 | 91 | 68 | 197 | 16 | 38 | 155 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | MEAAR others(495): Show |
chr12 | 21432655 | 21476250 |
| a0002 | 0/0 | 500 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | MEAAR others(495): Show |
chr12 | 21432655 | 21476250 |
| a0003 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | MEAAR others(495): Show |
chr12 | 21432655 | 21476250 |
| a0004 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | MEAAR others(495): Show |
chr12 | 21432655 | 21476250 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1500 | 407 | 89 | 67 | 195 | 16 | 38 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | ATGGA others(1495): Show |
chr12 | 21432655 | 21476250 | ||
| a0001c0002 | 0/0 | 1500 | 3 | 2 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | ATGGA others(1495): Show |
chr12 | 21432655 | 21476250 | ||
| a0001c0005 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | ATGGA others(1495): Show |
chr12 | 21432655 | 21476250 | ||
| a0001c0006 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | ATGGA others(1495): Show |
chr12 | 21432655 | 21476250 | ||
| a0002c0003 | 0/0 | 1500 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | ATGGA others(1495): Show |
chr12 | 21432655 | 21476250 | ||
| a0003c0007 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | ATGGA others(1495): Show |
chr12 | 21432655 | 21476250 | ||
| a0004c0004 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | ATGGA others(1495): Show |
chr12 | 21432655 | 21476250 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4075 | 128 | 24 | 27 | 58 | 7 | 12 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0002 | 0/0 | 4078 | 97 | 1 | 19 | 59 | 6 | 12 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4073): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0003 | 0/0 | 4074 | 68 | 2 | 5 | 55 | 1 | 5 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4069): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0004 | 0/0 | 4073 | 17 | 11 | 1 | 1 | 0 | 4 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4068): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0005 | 0/0 | 4076 | 13 | 13 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4071): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0006 | 0/0 | 4075 | 11 | 0 | 2 | 9 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0007 | 0/0 | 4070 | 10 | 9 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4065): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0008 | 0/0 | 4078 | 6 | 4 | 1 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4073): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0009 | 0/0 | 4077 | 6 | 1 | 2 | 0 | 1 | 2 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4072): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0010 | 0/0 | 4071 | 5 | 0 | 3 | 0 | 1 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4066): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0012 | 0/0 | 4079 | 5 | 0 | 0 | 5 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4074): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0013 | 0/0 | 4076 | 4 | 1 | 2 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4071): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0014 | 1/0 | 4075 | 4 | 3 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0015 | 0/0 | 4075 | 3 | 3 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0016 | 0/0 | 4075 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0017 | 0/0 | 4075 | 2 | 0 | 1 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0018 | 0/0 | 4075 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0019 | 0/0 | 4075 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0020 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4072): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0021 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0022 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4068): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0023 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4068): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0024 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4069): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0025 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4068): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0026 | 0/0 | 4074 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4069): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0027 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4073): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0028 | 0/0 | 4051 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4046): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0029 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0030 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0031 | 0/0 | 3767 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(3762): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0032 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0033 | 0/1 | 4070 | 1 | 0 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4065): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0034 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0035 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0036 | 0/0 | 4078 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4073): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0037 | 0/0 | 4078 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4073): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0038 | 0/0 | 4076 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4071): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0040 | 0/0 | 4078 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4073): Show |
chr12 | 21432655 | 21476250 |
| a0001c0001t0041 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4073): Show |
chr12 | 21432655 | 21476250 |
| a0001c0002t0011 | 0/0 | 4075 | 3 | 2 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0001c0005t0004 | 0/0 | 4073 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4068): Show |
chr12 | 21432655 | 21476250 |
| a0001c0006t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0002c0003t0011 | 0/0 | 4075 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0003c0007t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4070): Show |
chr12 | 21432655 | 21476250 |
| a0004c0004t0039 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | GGCTG others(4073): Show |
chr12 | 21432655 | 21476250 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 26 | 3 | 5 | 12 | 2 | 4 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0001 | 0/0 | 28 | 0 | 2 | 19 | 3 | 4 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0006 | 0/0 | 8 | 0 | 7 | 0 | 1 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0018 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0049 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0003 | 0/0 | 20 | 0 | 0 | 20 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0004 | 0/0 | 17 | 0 | 0 | 16 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0015 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0004g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0005g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0005g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0006g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0006g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0007g0005 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0008g0001 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0009g0016 | 0/0 | 4 | 1 | 0 | 0 | 1 | 2 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0009g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0010g0027 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0010g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0010g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0012g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0012g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0012g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0012g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0013g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0013g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0014g0026 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0014g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0015g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0015g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0016g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0017g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0017g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0018g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0019g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0019g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0020g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0020g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0021g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0022g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0023g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0024g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0025g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0026g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0027g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0028g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0029g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0030g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0031g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0032g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0033g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0034g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0035g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0036g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0037g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0038g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0040g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0001t0041g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0002t0011g0028 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0005t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0001c0006t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0002c0003t0011g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0003c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| a0004c0004t0039g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0016 | EUR | FIN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | FIN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00597 | hp2 | a0001 | c0001 | t0012 | g0187 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00639 | hp1 | a0001 | c0001 | t0017 | g0004 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00639 | hp2 | a0001 | c0001 | t0040 | g0001 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0146 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01069 | hp1 | a0001 | c0001 | t0036 | g0001 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0047 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01106 | hp2 | a0001 | c0001 | t0009 | g0047 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01175 | hp1 | a0001 | c0001 | t0013 | g0069 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01243 | hp2 | a0001 | c0002 | t0011 | g0028 | AMR | PUR | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01261 | hp1 | a0001 | c0001 | t0013 | g0012 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01346 | hp2 | a0001 | c0001 | t0010 | g0027 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01361 | hp1 | a0001 | c0001 | t0010 | g0027 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01496 | hp2 | a0001 | c0001 | t0037 | g0001 | AMR | CLM | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0027 | EUR | IBS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0049 | EUR | IBS | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01884 | hp1 | a0001 | c0001 | t0020 | g0193 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01891 | hp2 | a0001 | c0001 | t0015 | g0143 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0148 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0185 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | CDX | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | CDX | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0048 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02280 | hp2 | a0001 | c0001 | t0020 | g0154 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02451 | hp1 | a0001 | c0001 | t0030 | g0023 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02451 | hp2 | a0001 | c0001 | t0041 | g0001 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | KHV | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0186 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0181 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02630 | hp1 | a0001 | c0001 | t0022 | g0137 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02647 | hp1 | a0001 | c0001 | t0031 | g0057 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02647 | hp2 | a0002 | c0003 | t0011 | g0050 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02717 | hp1 | a0001 | c0001 | t0035 | g0139 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02723 | hp1 | a0002 | c0003 | t0011 | g0050 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02723 | hp2 | a0001 | c0001 | t0013 | g0058 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02809 | hp1 | a0001 | c0001 | t0021 | g0142 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02886 | hp1 | a0001 | c0001 | t0029 | g0040 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02897 | hp1 | a0001 | c0001 | t0025 | g0009 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0184 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02970 | hp1 | a0001 | c0001 | t0019 | g0156 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0048 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03209 | hp2 | a0001 | c0001 | t0023 | g0043 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03486 | hp1 | a0001 | c0001 | t0016 | g0041 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0134 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0135 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03540 | hp1 | a0001 | c0001 | t0027 | g0159 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0026 | AFR | GWD | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03579 | hp1 | a0001 | c0002 | t0011 | g0028 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0166 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | STU | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03704 | hp2 | a0001 | c0001 | t0009 | g0016 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03710 | hp2 | a0001 | c0001 | t0009 | g0016 | SAS | PJL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03927 | hp2 | a0001 | c0001 | t0010 | g0145 | SAS | BEB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0113 | SAS | STU | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0132 | SAS | BEB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | BEB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | STU | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0149 | AFR | YRI | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18522 | hp2 | a0001 | c0001 | t0016 | g0041 | AFR | YRI | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | CHB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | YRI | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18941 | hp1 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18943 | hp1 | a0001 | c0001 | t0017 | g0024 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18974 | hp1 | a0001 | c0001 | t0038 | g0162 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18977 | hp1 | a0001 | c0001 | t0018 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18978 | hp1 | a0001 | c0001 | t0013 | g0007 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18978 | hp2 | a0001 | c0001 | t0012 | g0167 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18989 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18993 | hp1 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18994 | hp1 | a0001 | c0001 | t0028 | g0060 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18994 | hp2 | a0001 | c0006 | t0001 | g0013 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18997 | hp1 | a0001 | c0001 | t0012 | g0171 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19009 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19030 | hp1 | a0001 | c0002 | t0011 | g0028 | AFR | LWK | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0140 | AFR | LWK | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19055 | hp1 | a0001 | c0001 | t0018 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19059 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19062 | hp1 | a0003 | c0007 | t0001 | g0108 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19067 | hp1 | a0001 | c0005 | t0004 | g0133 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19076 | hp1 | a0001 | c0001 | t0032 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19077 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19082 | hp2 | a0001 | c0001 | t0024 | g0045 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19086 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | YRI | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ASW | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0015 | EUR | TSI | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA20905 | hp2 | a0001 | c0001 | t0026 | g0025 | SAS | GIH | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0026 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | ACB | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | MSL | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | USA | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | USA | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | USA | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA21309 | hp1 | a0001 | c0001 | t0034 | g0155 | AFR | LWK | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| NA21309 | hp2 | a0004 | c0004 | t0039 | g0180 | AFR | LWK | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0033 | g0147 | REF | REF | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0014 | g0026 | REF | REF | PYROXD1_chr12_21432655_21476250 | PYROXD1 | chr12 | 21432655 | 21476250 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21437812 | C | A | 1 | a0004 | 1 | NA21309.hp2 | missense_variant&splice_region_variant | MODERATE | c.82C>A | p.Gln28Lys | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/12 | 158/4075 | 82/1503 | 28/500 | chr12 | 21437812 | |||
| chr12:21455259 | A | G | 1 | a0003 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.616A>G | p.Ile206Val | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/12 | 692/4075 | 616/1503 | 206/500 | chr12 | 21455259 | |||
| chr12:21455266 | A | T | 1 | a0004 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.623A>T | p.His208Leu | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/12 | 699/4075 | 623/1503 | 208/500 | chr12 | 21455266 | |||
| chr12:21461108 | G | C | 1 | a0002 | 2 | HG02647.hp2 HG02723.hp1 |
missense_variant | MODERATE | c.834G>C | p.Lys278Asn | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/12 | 910/4075 | 834/1503 | 278/500 | chr12 | 21461108 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21455198 | C | T | 2 | a0001c0002 a0002c0003 |
5 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
synonymous_variant | LOW | c.555C>T | p.Phe185Phe | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/12 | 631/4075 | 555/1503 | 185/500 | chr12 | 21455198 | |||
| chr12:21461117 | T | C | 1 | a0001c0005 | 1 | NA19067.hp1 | synonymous_variant | LOW | c.843T>C | p.Thr281Thr | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/12 | 919/4075 | 843/1503 | 281/500 | chr12 | 21461117 | |||
| chr12:21462117 | C | T | 1 | a0001c0006 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.990C>T | p.Asn330Asn | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/12 | 1066/4075 | 990/1503 | 330/500 | chr12 | 21462117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21437666 | C | T | 1 | a0001c0001t0009 | 6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-65C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/12 | 65 | chr12 | 21437666 | ||||||
| chr12:21437675 | T | G | 2 | a0001c0001t0007 a0001c0001t0021 |
11 | HG00741.hp1 HG02055.hp1 HG02559.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-56T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/12 | 56 | chr12 | 21437675 | ||||||
| chr12:21437685 | C | A | 1 | a0001c0001t0022 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-46C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/12 | 46 | chr12 | 21437685 | ||||||
| chr12:21437687 | T | C | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(18): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-44T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/12 | chr12 | 21437687 | |||||||
| chr12:21468762 | A | T | 1 | a0001c0001t0032 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 8 | chr12 | 21468762 | ||||||
| chr12:21468803 | A | G | 9 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0018 others(6): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*49A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 49 | chr12 | 21468803 | ||||||
| chr12:21468883 | A | C | 11 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(8): Show |
126 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*129A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 129 | chr12 | 21468883 | ||||||
| chr12:21468902 | A | G | 1 | a0001c0001t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*148A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 148 | chr12 | 21468902 | ||||||
| chr12:21468957 | T | C | 4 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0036 others(1): Show |
104 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*203T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 203 | chr12 | 21468957 | ||||||
| chr12:21469096 | A | C | 1 | a0001c0001t0030 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*342A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 342 | chr12 | 21469096 | ||||||
| chr12:21469117 | A | C | 4 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0026 others(1): Show |
72 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*363A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 363 | chr12 | 21469117 | ||||||
| chr12:21469163 | T | C | 1 | a0001c0001t0036 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*409T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 409 | chr12 | 21469163 | ||||||
| chr12:21469168 | A | G | 1 | a0001c0001t0041 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 414 | chr12 | 21469168 | ||||||
| chr12:21469286 | C | T | 3 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0021 |
14 | HG00741.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*532C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 532 | chr12 | 21469286 | ||||||
| chr12:21469409 | T | C | 1 | a0001c0001t0018 | 2 | NA18977.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*655T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 655 | chr12 | 21469409 | ||||||
| chr12:21469435 | A | C | 1 | a0001c0001t0040 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 681 | chr12 | 21469435 | ||||||
| chr12:21469440 | ATTC | A | 2 | a0001c0001t0006 a0001c0001t0038 |
12 | HG01952.hp1 HG01978.hp1 HG02135.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*693_*695delTTC | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 693 | INFO_REALIGN_3_PRIME | chr12 | 21469440 | |||||
| chr12:21469443 | C | A | 1 | a0001c0001t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*689C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 689 | chr12 | 21469443 | ||||||
| chr12:21469493 | A | G | 1 | a0001c0001t0026 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*739A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 739 | chr12 | 21469493 | ||||||
| chr12:21469514 | AC | A | 6 | a0001c0001t0004 a0001c0001t0022 a0001c0001t0023 others(3): Show |
22 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*761delC | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 761 | chr12 | 21469514 | ||||||
| chr12:21469557 | GGTTATGT others(302): Show |
G | 1 | a0001c0001t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*860_*1168del | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 860 | INFO_REALIGN_3_PRIME | chr12 | 21469557 | |||||
| chr12:21469561 | A | C | 1 | a0002c0003t0011 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*807A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 807 | chr12 | 21469561 | ||||||
| chr12:21469621 | T | A | 1 | a0001c0001t0032 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*867T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 867 | chr12 | 21469621 | ||||||
| chr12:21469651 | T | A | 1 | a0001c0001t0032 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*897T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 897 | chr12 | 21469651 | ||||||
| chr12:21469686 | AT | A | 2 | a0001c0001t0003 a0001c0001t0010 |
7 | HG00408.hp2 HG00735.hp2 HG01346.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*942delT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 942 | INFO_REALIGN_3_PRIME | chr12 | 21469686 | |||||
| chr12:21469761 | A | G | 6 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0016 others(3): Show |
51 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1007A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1007 | chr12 | 21469761 | ||||||
| chr12:21469812 | C | T | 1 | a0001c0001t0019 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1058C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1058 | chr12 | 21469812 | ||||||
| chr12:21469888 | T | C | 1 | a0001c0001t0010 | 5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1134T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1134 | chr12 | 21469888 | ||||||
| chr12:21469917 | T | G | 1 | a0001c0001t0023 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1163T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1163 | chr12 | 21469917 | ||||||
| chr12:21469929 | ATGAACTT others(17): Show |
A | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1176_*1199delTGAA others(20): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1176 | chr12 | 21469929 | ||||||
| chr12:21469987 | G | T | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1233G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1233 | chr12 | 21469987 | ||||||
| chr12:21469990 | T | A | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1236T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1236 | chr12 | 21469990 | ||||||
| chr12:21469993 | T | C | 3 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0021 |
13 | HG00741.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1239T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1239 | chr12 | 21469993 | ||||||
| chr12:21469997 | G | A | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1243G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1243 | chr12 | 21469997 | ||||||
| chr12:21469998 | G | T | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1244G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1244 | chr12 | 21469998 | ||||||
| chr12:21470005 | A | T | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1251A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1251 | chr12 | 21470005 | ||||||
| chr12:21470006 | T | C | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1252T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1252 | chr12 | 21470006 | ||||||
| chr12:21470007 | A | T | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1253A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1253 | chr12 | 21470007 | ||||||
| chr12:21470036 | T | A | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1282T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1282 | chr12 | 21470036 | ||||||
| chr12:21470050 | A | G | 1 | a0001c0001t0037 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1296A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1296 | chr12 | 21470050 | ||||||
| chr12:21470073 | A | C | 1 | a0001c0001t0035 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1319 | chr12 | 21470073 | ||||||
| chr12:21470073 | A | T | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1319 | chr12 | 21470073 | ||||||
| chr12:21470118 | C | A | 1 | a0001c0001t0028 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1364C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1364 | chr12 | 21470118 | ||||||
| chr12:21470175 | A | C | 1 | a0001c0001t0025 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1421 | chr12 | 21470175 | ||||||
| chr12:21470188 | T | G | 10 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(7): Show |
125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1434T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1434 | chr12 | 21470188 | ||||||
| chr12:21470193 | A | C | 1 | a0001c0001t0029 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1439A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1439 | chr12 | 21470193 | ||||||
| chr12:21470245 | T | C | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0017 others(7): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1491T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1491 | chr12 | 21470245 | ||||||
| chr12:21470350 | C | CA | 3 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0031 |
18 | HG01175.hp1 HG01261.hp1 HG02145.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1612dupA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1613 | INFO_REALIGN_3_PRIME | chr12 | 21470350 | |||||
| chr12:21470350 | C | CAA | 2 | a0001c0001t0009 a0001c0001t0020 |
8 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1611_*1612dupAA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1613 | INFO_REALIGN_3_PRIME | chr12 | 21470350 | |||||
| chr12:21470350 | C | CAAA | 9 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(6): Show |
120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1610_*1612dupAAA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1613 | INFO_REALIGN_3_PRIME | chr12 | 21470350 | |||||
| chr12:21470350 | C | CAAAA | 2 | a0001c0001t0012 a0001c0001t0038 |
6 | HG00597.hp2 NA18974.hp1 NA18978.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1609_*1612dupAAAA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1613 | INFO_REALIGN_3_PRIME | chr12 | 21470350 | |||||
| chr12:21470350 | CA | C | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0022 others(4): Show |
90 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1612delA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1612 | INFO_REALIGN_3_PRIME | chr12 | 21470350 | |||||
| chr12:21470577 | A | G | 5 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0015 others(2): Show |
20 | HG00735.hp2 HG00741.hp1 HG01346.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1823A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1823 | chr12 | 21470577 | ||||||
| chr12:21470581 | CACTTG | C | 1 | a0001c0001t0007 | 10 | HG00741.hp1 HG02055.hp1 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1835_*1839delTTGA others(1): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 1835 | INFO_REALIGN_3_PRIME | chr12 | 21470581 | |||||
| chr12:21470951 | AAATT | A | 1 | a0001c0001t0010 | 5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2201_*2204delTAAT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 2201 | INFO_REALIGN_3_PRIME | chr12 | 21470951 | |||||
| chr12:21471035 | A | G | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0017 others(7): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*2281A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 2281 | chr12 | 21471035 | ||||||
| chr12:21471165 | G | T | 1 | a0001c0001t0029 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2411G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 2411 | chr12 | 21471165 | ||||||
| chr12:21471179 | C | T | 4 | a0001c0001t0019 a0001c0001t0034 a0001c0002t0011 others(1): Show |
8 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2425C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 12/12 | 2425 | chr12 | 21471179 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21437854 | C | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.84+40C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21437854 | |||||||
| chr12:21437859 | A | C | 2 | a0001c0001t0004g0138 a0001c0001t0022g0137 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.84+45A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21437859 | |||||||
| chr12:21437945 | T | C | 1 | a0001c0001t0031g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.84+131T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21437945 | |||||||
| chr12:21437950 | C | T | 1 | a0001c0001t0020g0193 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.84+136C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21437950 | |||||||
| chr12:21438095 | G | C | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+281G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438095 | |||||||
| chr12:21438129 | C | T | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+315C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438129 | |||||||
| chr12:21438139 | A | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.84+325A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438139 | |||||||
| chr12:21438287 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.84+473A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438287 | |||||||
| chr12:21438313 | A | G | 46 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(43): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.84+499A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438313 | |||||||
| chr12:21438365 | CT | C | 4 | a0001c0001t0003g0024 a0001c0001t0003g0110 a0001c0001t0003g0111 others(1): Show |
5 | NA18943.hp1 NA18947.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+552delT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438365 | |||||||
| chr12:21438539 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.84+725G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438539 | |||||||
| chr12:21438566 | A | G | 1 | a0001c0001t0003g0046 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.84+752A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438566 | |||||||
| chr12:21438851 | G | A | 4 | a0001c0001t0007g0005 a0001c0001t0015g0048 a0001c0001t0015g0143 others(1): Show |
14 | HG00741.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.84+1037G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438851 | |||||||
| chr12:21438851 | G | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.84+1037G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438851 | |||||||
| chr12:21438860 | G | T | 1 | a0001c0001t0002g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.84+1046G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438860 | |||||||
| chr12:21438880 | GTA | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.84+1071_84+1072del others(2): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 21438880 | ||||||
| chr12:21438894 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.84+1080G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438894 | |||||||
| chr12:21438913 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.84+1099G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438913 | |||||||
| chr12:21438987 | T | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.84+1173T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21438987 | |||||||
| chr12:21439111 | A | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0141 a0001c0001t0002g0188 others(3): Show |
9 | HG00558.hp1 HG02074.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-1257A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439111 | |||||||
| chr12:21439160 | G | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.85-1208G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439160 | |||||||
| chr12:21439266 | A | C | 46 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(43): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.85-1102A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439266 | |||||||
| chr12:21439423 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.85-945G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439423 | |||||||
| chr12:21439472 | A | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.85-896A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439472 | |||||||
| chr12:21439612 | A | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.85-756A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439612 | |||||||
| chr12:21439746 | T | A | 1 | a0001c0001t0002g0049 | 2 | HG01517.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.85-622T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439746 | |||||||
| chr12:21439813 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.85-555T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439813 | |||||||
| chr12:21439844 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.85-524A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439844 | |||||||
| chr12:21439909 | G | C | 1 | a0001c0001t0003g0112 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.85-459G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439909 | |||||||
| chr12:21439959 | A | G | 46 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(43): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.85-409A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21439959 | |||||||
| chr12:21440005 | A | G | 1 | a0001c0001t0012g0187 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.85-363A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21440005 | |||||||
| chr12:21440073 | G | C | 3 | a0001c0001t0010g0027 a0001c0001t0010g0145 a0001c0001t0010g0146 |
5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-295G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21440073 | |||||||
| chr12:21440103 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.85-265T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21440103 | |||||||
| chr12:21440112 | A | G | 1 | a0001c0001t0031g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.85-256A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21440112 | |||||||
| chr12:21440337 | C | G | 2 | a0001c0001t0014g0140 a0001c0001t0035g0139 |
2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.85-31C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 1/11 | chr12 | 21440337 | |||||||
| chr12:21440470 | G | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.165+22G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21440470 | |||||||
| chr12:21440503 | G | T | 1 | a0001c0001t0003g0131 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.165+55G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21440503 | |||||||
| chr12:21440527 | A | AT | 5 | a0001c0001t0005g0030 a0001c0001t0005g0183 a0001c0001t0005g0184 others(2): Show |
7 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+86dupT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 21440527 | ||||||
| chr12:21440591 | A | G | 4 | a0001c0001t0007g0005 a0001c0001t0015g0048 a0001c0001t0015g0143 others(1): Show |
14 | HG00741.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+143A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21440591 | |||||||
| chr12:21440661 | T | A | 1 | a0001c0001t0006g0148 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.165+213T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21440661 | |||||||
| chr12:21440666 | CA | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.165+219delA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21440666 | |||||||
| chr12:21440782 | A | G | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(61): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.165+334A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21440782 | |||||||
| chr12:21440831 | C | T | 1 | a0001c0001t0031g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.165+383C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21440831 | |||||||
| chr12:21440832 | T | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.165+384T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21440832 | |||||||
| chr12:21440875 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.165+427G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21440875 | |||||||
| chr12:21440984 | A | G | 1 | a0001c0001t0019g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.165+536A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21440984 | |||||||
| chr12:21441094 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.165+646C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441094 | |||||||
| chr12:21441171 | C | T | 40 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(37): Show |
88 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.165+723C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441171 | |||||||
| chr12:21441173 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.165+725C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441173 | |||||||
| chr12:21441258 | C | T | 1 | a0001c0001t0034g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.165+810C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441258 | |||||||
| chr12:21441275 | G | A | 1 | a0001c0001t0013g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165+827G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441275 | |||||||
| chr12:21441390 | A | G | 40 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(37): Show |
88 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.165+942A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441390 | |||||||
| chr12:21441393 | A | G | 1 | a0003c0007t0001g0108 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.165+945A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441393 | |||||||
| chr12:21441395 | G | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.165+947G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441395 | |||||||
| chr12:21441402 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.165+954A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441402 | |||||||
| chr12:21441408 | AG | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0059 others(4): Show |
14 | HG00423.hp1 HG02129.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.165+961delG | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441408 | |||||||
| chr12:21441443 | ACTT | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.165+998_165+1000de others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 21441443 | ||||||
| chr12:21441450 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.165+1002T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441450 | |||||||
| chr12:21441554 | T | C | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1106T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441554 | |||||||
| chr12:21441642 | T | A | 2 | a0001c0002t0011g0028 a0002c0003t0011g0050 |
5 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1194T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441642 | |||||||
| chr12:21441658 | G | C | 5 | a0001c0001t0019g0149 a0001c0001t0019g0156 a0001c0001t0034g0155 others(2): Show |
8 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+1210G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441658 | |||||||
| chr12:21441685 | G | C | 1 | a0001c0001t0031g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.165+1237G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441685 | |||||||
| chr12:21441744 | T | TTGTC | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.165+1296_165+1297i others(6): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441744 | |||||||
| chr12:21441782 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.165+1334C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441782 | |||||||
| chr12:21441834 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.165+1386A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441834 | |||||||
| chr12:21441901 | G | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(61): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.165+1453G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441901 | |||||||
| chr12:21441920 | A | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.165+1472A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441920 | |||||||
| chr12:21441998 | A | G | 1 | a0001c0001t0008g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.165+1550A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21441998 | |||||||
| chr12:21442049 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.165+1601G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442049 | |||||||
| chr12:21442124 | G | A | 1 | a0001c0001t0003g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+1676G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442124 | |||||||
| chr12:21442130 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.165+1682G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442130 | |||||||
| chr12:21442133 | A | T | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1685A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442133 | |||||||
| chr12:21442156 | C | T | 1 | a0001c0001t0016g0041 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.165+1708C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442156 | |||||||
| chr12:21442202 | T | A | 12 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0150 others(9): Show |
15 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.165+1754T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442202 | |||||||
| chr12:21442306 | C | T | 1 | a0001c0001t0020g0154 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.165+1858C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442306 | |||||||
| chr12:21442456 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.165+2008A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442456 | |||||||
| chr12:21442480 | A | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.165+2032A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442480 | |||||||
| chr12:21442558 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.165+2110T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442558 | |||||||
| chr12:21442564 | G | A | 2 | a0001c0002t0011g0028 a0002c0003t0011g0050 |
5 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+2116G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442564 | |||||||
| chr12:21442618 | TGGAA | T | 9 | a0001c0001t0007g0005 a0001c0001t0009g0016 a0001c0001t0009g0047 others(6): Show |
25 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.165+2171_165+2174d others(6): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442618 | |||||||
| chr12:21442699 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.165+2251T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442699 | |||||||
| chr12:21442790 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.165+2342G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442790 | |||||||
| chr12:21442823 | T | C | 1 | a0001c0001t0005g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.165+2375T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442823 | |||||||
| chr12:21442924 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0109 a0001c0001t0029g0040 |
3 | HG02109.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.166-2423C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442924 | |||||||
| chr12:21442938 | C | T | 1 | a0001c0001t0020g0193 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.166-2409C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21442938 | |||||||
| chr12:21443036 | A | G | 7 | a0001c0001t0007g0005 a0001c0001t0010g0027 a0001c0001t0010g0145 others(4): Show |
19 | HG00735.hp2 HG00741.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.166-2311A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443036 | |||||||
| chr12:21443084 | T | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.166-2263T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443084 | |||||||
| chr12:21443142 | A | T | 3 | a0001c0001t0010g0027 a0001c0001t0010g0145 a0001c0001t0010g0146 |
5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-2205A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443142 | |||||||
| chr12:21443158 | A | G | 4 | a0001c0001t0004g0043 a0001c0001t0004g0044 a0001c0001t0004g0129 others(1): Show |
5 | HG01255.hp1 HG02055.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-2189A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443158 | |||||||
| chr12:21443170 | A | G | 11 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0043 others(8): Show |
18 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.166-2177A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443170 | |||||||
| chr12:21443181 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.166-2166G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443181 | |||||||
| chr12:21443231 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 |
3 | NA18973.hp1 NA19079.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.166-2116T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443231 | |||||||
| chr12:21443507 | A | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.166-1840A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443507 | |||||||
| chr12:21443509 | C | T | 2 | a0001c0001t0019g0149 a0001c0001t0019g0156 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.166-1838C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443509 | |||||||
| chr12:21443518 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.166-1829T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443518 | |||||||
| chr12:21443539 | T | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG01361.hp2 HG02735.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.166-1808T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443539 | |||||||
| chr12:21443642 | A | C | 1 | a0001c0001t0020g0193 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.166-1705A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443642 | |||||||
| chr12:21443648 | T | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | NA18973.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.166-1699T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443648 | |||||||
| chr12:21443705 | A | G | 1 | a0001c0001t0019g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.166-1642A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443705 | |||||||
| chr12:21443849 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.166-1498A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443849 | |||||||
| chr12:21443857 | G | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.166-1490G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21443857 | |||||||
| chr12:21444010 | A | G | 1 | a0004c0004t0039g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.166-1337A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444010 | |||||||
| chr12:21444013 | T | C | 1 | a0001c0001t0003g0114 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.166-1334T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444013 | |||||||
| chr12:21444141 | G | C | 1 | a0002c0003t0011g0050 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.166-1206G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444141 | |||||||
| chr12:21444312 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.166-1035A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444312 | |||||||
| chr12:21444571 | G | T | 2 | a0001c0002t0011g0028 a0002c0003t0011g0050 |
5 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-776G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444571 | |||||||
| chr12:21444580 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.166-767G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444580 | |||||||
| chr12:21444583 | C | T | 1 | a0001c0001t0002g0020 | 4 | HG00423.hp2 NA18954.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-764C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444583 | |||||||
| chr12:21444608 | A | G | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-739A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444608 | |||||||
| chr12:21444635 | G | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0052 a0001c0001t0002g0158 |
11 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-712G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444635 | |||||||
| chr12:21444670 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.166-677T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444670 | |||||||
| chr12:21444679 | AAGG | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.166-667_166-665del others(3): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444679 | |||||||
| chr12:21444756 | C | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.166-591C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444756 | |||||||
| chr12:21444932 | G | A | 40 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(37): Show |
88 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.166-415G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21444932 | |||||||
| chr12:21445261 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.166-86G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21445261 | |||||||
| chr12:21445330 | C | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(61): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.166-17C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21445330 | |||||||
| chr12:21445337 | A | G | 2 | a0001c0001t0003g0025 a0001c0001t0026g0025 |
3 | HG02602.hp1 HG03491.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.166-10A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 2/11 | chr12 | 21445337 | |||||||
| chr12:21445540 | C | G | 12 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0150 others(9): Show |
15 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.285+74C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21445540 | |||||||
| chr12:21445558 | C | G | 5 | a0001c0001t0019g0149 a0001c0001t0019g0156 a0001c0001t0034g0155 others(2): Show |
8 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+92C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21445558 | |||||||
| chr12:21445592 | A | G | 12 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0150 others(9): Show |
15 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.285+126A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21445592 | |||||||
| chr12:21445767 | T | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(149): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.285+301T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21445767 | |||||||
| chr12:21445857 | A | G | 1 | a0001c0001t0034g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.285+391A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21445857 | |||||||
| chr12:21445948 | C | T | 5 | a0001c0001t0019g0149 a0001c0001t0019g0156 a0001c0001t0034g0155 others(2): Show |
8 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+482C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21445948 | |||||||
| chr12:21445950 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.285+484G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21445950 | |||||||
| chr12:21445952 | T | C | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG01070.hp2 HG01074.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+486T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21445952 | |||||||
| chr12:21446017 | T | G | 5 | a0001c0001t0019g0149 a0001c0001t0019g0156 a0001c0001t0034g0155 others(2): Show |
8 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+551T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446017 | |||||||
| chr12:21446072 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.285+606A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446072 | |||||||
| chr12:21446209 | G | A | 1 | a0001c0001t0027g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+743G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446209 | |||||||
| chr12:21446292 | G | A | 2 | a0001c0001t0005g0151 a0001c0001t0005g0152 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.285+826G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446292 | |||||||
| chr12:21446316 | C | T | 1 | a0001c0002t0011g0028 | 3 | HG01243.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.285+850C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446316 | |||||||
| chr12:21446323 | CT | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.285+859delT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 21446323 | ||||||
| chr12:21446368 | T | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.285+902T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446368 | |||||||
| chr12:21446371 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.285+905G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446371 | |||||||
| chr12:21446410 | G | A | 1 | a0001c0001t0003g0115 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.285+944G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446410 | |||||||
| chr12:21446415 | A | T | 1 | a0004c0004t0039g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.285+949A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446415 | |||||||
| chr12:21446416 | C | T | 1 | a0004c0004t0039g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.285+950C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446416 | |||||||
| chr12:21446439 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.285+973A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446439 | |||||||
| chr12:21446511 | A | AT | 6 | a0001c0001t0002g0178 a0001c0001t0005g0030 a0001c0001t0005g0183 others(3): Show |
8 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.285+1060dupT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 21446511 | ||||||
| chr12:21446511 | AT | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.285+1060delT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 21446511 | ||||||
| chr12:21446686 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.285+1220C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446686 | |||||||
| chr12:21446702 | A | G | 12 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0150 others(9): Show |
15 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.285+1236A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446702 | |||||||
| chr12:21446714 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
11 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.285+1248C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446714 | |||||||
| chr12:21446783 | C | T | 9 | a0001c0001t0007g0005 a0001c0001t0009g0016 a0001c0001t0009g0047 others(6): Show |
25 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.285+1317C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446783 | |||||||
| chr12:21446845 | T | G | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+1379T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446845 | |||||||
| chr12:21446915 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.285+1449A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446915 | |||||||
| chr12:21446932 | T | C | 3 | a0001c0001t0010g0027 a0001c0001t0010g0145 a0001c0001t0010g0146 |
5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+1466T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21446932 | |||||||
| chr12:21447006 | C | A | 9 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0043 others(6): Show |
16 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.285+1540C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447006 | |||||||
| chr12:21447106 | T | C | 1 | a0001c0001t0035g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.285+1640T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447106 | |||||||
| chr12:21447110 | C | T | 7 | a0001c0001t0007g0005 a0001c0001t0010g0027 a0001c0001t0010g0145 others(4): Show |
19 | HG00735.hp2 HG00741.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.285+1644C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447110 | |||||||
| chr12:21447211 | G | T | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+1745G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447211 | |||||||
| chr12:21447241 | T | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.285+1775T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447241 | |||||||
| chr12:21447305 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.285+1839A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447305 | |||||||
| chr12:21447351 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.285+1885G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447351 | |||||||
| chr12:21447472 | G | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.285+2006G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447472 | |||||||
| chr12:21447478 | C | T | 1 | a0001c0001t0019g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.285+2012C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447478 | |||||||
| chr12:21447505 | G | A | 4 | a0001c0001t0007g0005 a0001c0001t0015g0048 a0001c0001t0015g0143 others(1): Show |
14 | HG00741.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.285+2039G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447505 | |||||||
| chr12:21447509 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.285+2043T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447509 | |||||||
| chr12:21447520 | C | A | 1 | a0001c0001t0013g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286-2043C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447520 | |||||||
| chr12:21447586 | A | G | 2 | a0001c0001t0015g0048 a0001c0001t0015g0143 |
3 | HG01891.hp2 HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.286-1977A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447586 | |||||||
| chr12:21447634 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.286-1929T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447634 | |||||||
| chr12:21447676 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.286-1887C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447676 | |||||||
| chr12:21447705 | T | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.286-1858T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447705 | |||||||
| chr12:21447714 | C | T | 1 | a0001c0001t0031g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286-1849C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447714 | |||||||
| chr12:21447768 | C | T | 1 | a0001c0001t0005g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.286-1795C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447768 | |||||||
| chr12:21447769 | G | A | 1 | a0001c0001t0031g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286-1794G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447769 | |||||||
| chr12:21447803 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.286-1760G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447803 | |||||||
| chr12:21447904 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.286-1659A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447904 | |||||||
| chr12:21447906 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.286-1657A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447906 | |||||||
| chr12:21447919 | A | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.286-1644A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447919 | |||||||
| chr12:21447931 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.286-1632T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447931 | |||||||
| chr12:21447940 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.286-1623G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447940 | |||||||
| chr12:21447963 | A | G | 3 | a0001c0001t0010g0027 a0001c0001t0010g0145 a0001c0001t0010g0146 |
5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-1600A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21447963 | |||||||
| chr12:21447981 | T | TA | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.286-1568dupA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 21447981 | ||||||
| chr12:21447981 | T | TAA | 6 | a0001c0001t0001g0066 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG01106.hp1 HG01175.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-1569_286-1568d others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 21447981 | ||||||
| chr12:21448003 | G | A | 2 | a0001c0001t0005g0051 a0001c0001t0005g0153 |
3 | HG02559.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.286-1560G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448003 | |||||||
| chr12:21448018 | C | T | 46 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(43): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.286-1545C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448018 | |||||||
| chr12:21448019 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.286-1544G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448019 | |||||||
| chr12:21448216 | C | T | 1 | a0001c0001t0003g0128 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.286-1347C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448216 | |||||||
| chr12:21448280 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.286-1283G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448280 | |||||||
| chr12:21448282 | C | T | 1 | a0001c0001t0004g0129 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.286-1281C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448282 | |||||||
| chr12:21448557 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.286-1006C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448557 | |||||||
| chr12:21448563 | T | A | 1 | a0001c0001t0019g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.286-1000T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448563 | |||||||
| chr12:21448569 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.286-994T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448569 | |||||||
| chr12:21448697 | A | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(55): Show |
126 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.286-866A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448697 | |||||||
| chr12:21448723 | A | G | 1 | a0001c0001t0031g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286-840A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448723 | |||||||
| chr12:21448756 | A | G | 2 | a0001c0001t0005g0151 a0001c0001t0005g0152 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.286-807A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448756 | |||||||
| chr12:21448828 | T | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.286-735T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448828 | |||||||
| chr12:21448936 | A | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0038 others(4): Show |
12 | HG01074.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.286-627A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448936 | |||||||
| chr12:21448998 | A | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.286-565A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21448998 | |||||||
| chr12:21449070 | T | C | 1 | a0002c0003t0011g0050 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.286-493T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21449070 | |||||||
| chr12:21449086 | G | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0176 |
5 | HG00323.hp2 HG00733.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-477G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21449086 | |||||||
| chr12:21449211 | A | G | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-352A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21449211 | |||||||
| chr12:21449238 | T | A | 2 | a0001c0001t0006g0029 a0001c0001t0006g0163 |
4 | NA18940.hp2 NA18993.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-325T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21449238 | |||||||
| chr12:21449303 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0013g0012 |
4 | HG00733.hp2 HG00735.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-260T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21449303 | |||||||
| chr12:21449364 | AT | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.286-196delT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 21449364 | ||||||
| chr12:21449394 | T | G | 1 | a0001c0002t0011g0028 | 3 | HG01243.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.286-169T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21449394 | |||||||
| chr12:21449496 | TAAAGTGA others(39): Show |
T | 1 | a0001c0005t0004g0133 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.286-65_286-20delAA others(44): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 21449496 | ||||||
| chr12:21449503 | A | G | 1 | a0001c0001t0008g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.286-60A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 3/11 | chr12 | 21449503 | |||||||
| chr12:21449858 | C | CT | 6 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0005g0152 others(3): Show |
10 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.414+184dupT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 21449858 | ||||||
| chr12:21449858 | CTTTTTTT others(5): Show |
C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.414+173_414+184del others(12): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 21449858 | ||||||
| chr12:21449862 | T | C | 5 | a0001c0001t0019g0149 a0001c0001t0019g0156 a0001c0001t0034g0155 others(2): Show |
8 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+171T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21449862 | |||||||
| chr12:21449880 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.414+189C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21449880 | |||||||
| chr12:21449881 | G | A | 17 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0043 others(14): Show |
25 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.414+190G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21449881 | |||||||
| chr12:21449926 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.414+235C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21449926 | |||||||
| chr12:21449927 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0080 |
3 | HG00642.hp1 HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.414+236G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21449927 | |||||||
| chr12:21450009 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.414+318C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450009 | |||||||
| chr12:21450021 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.414+330C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450021 | |||||||
| chr12:21450024 | ATT | A | 79 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(76): Show |
169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.414+350_414+351del others(2): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 21450024 | ||||||
| chr12:21450024 | ATTTT | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.414+348_414+351del others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 21450024 | ||||||
| chr12:21450104 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.414+413C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450104 | |||||||
| chr12:21450105 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.414+414G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450105 | |||||||
| chr12:21450120 | G | GGCC | 15 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0043 others(12): Show |
22 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.414+430_414+432dup others(3): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 21450120 | ||||||
| chr12:21450212 | G | C | 4 | a0001c0001t0007g0005 a0001c0001t0015g0048 a0001c0001t0015g0143 others(1): Show |
14 | HG00741.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.414+521G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450212 | |||||||
| chr12:21450369 | A | G | 1 | a0001c0001t0002g0056 | 2 | NA18956.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.414+678A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450369 | |||||||
| chr12:21450410 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.414+719A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450410 | |||||||
| chr12:21450495 | C | A | 46 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(43): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.414+804C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450495 | |||||||
| chr12:21450555 | T | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.414+864T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450555 | |||||||
| chr12:21450631 | G | A | 1 | a0001c0001t0003g0110 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.414+940G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450631 | |||||||
| chr12:21450763 | C | T | 6 | a0001c0001t0004g0045 a0001c0001t0004g0132 a0001c0001t0004g0134 others(3): Show |
6 | HG03491.hp2 HG03492.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+1072C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450763 | |||||||
| chr12:21450814 | T | C | 5 | a0001c0001t0019g0149 a0001c0001t0019g0156 a0001c0001t0034g0155 others(2): Show |
8 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+1123T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450814 | |||||||
| chr12:21450839 | C | G | 3 | a0001c0001t0005g0051 a0001c0001t0005g0150 a0001c0001t0005g0153 |
4 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+1148C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450839 | |||||||
| chr12:21450867 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.414+1176T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450867 | |||||||
| chr12:21450885 | A | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.414+1194A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450885 | |||||||
| chr12:21450901 | C | T | 7 | a0001c0001t0005g0030 a0001c0001t0005g0151 a0001c0001t0005g0152 others(4): Show |
9 | HG02145.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-1180C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450901 | |||||||
| chr12:21450939 | A | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0062 a0001c0001t0001g0079 |
4 | NA18612.hp2 NA18951.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1142A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450939 | |||||||
| chr12:21450943 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(42): Show |
89 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.415-1138G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21450943 | |||||||
| chr12:21451034 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.415-1047A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451034 | |||||||
| chr12:21451075 | G | C | 2 | a0001c0001t0003g0025 a0001c0001t0026g0025 |
3 | HG02602.hp1 HG03491.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.415-1006G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451075 | |||||||
| chr12:21451087 | A | G | 1 | a0001c0001t0008g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.415-994A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451087 | |||||||
| chr12:21451174 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.415-907G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451174 | |||||||
| chr12:21451227 | C | CT | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-853dupT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 21451227 | ||||||
| chr12:21451228 | TC | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.415-852delC | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451228 | |||||||
| chr12:21451229 | C | T | 84 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(81): Show |
174 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.415-852C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451229 | |||||||
| chr12:21451230 | T | C | 1 | a0001c0005t0004g0133 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.415-851T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451230 | |||||||
| chr12:21451247 | C | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.415-834C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451247 | |||||||
| chr12:21451265 | A | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(43): Show |
90 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.415-816A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451265 | |||||||
| chr12:21451443 | A | G | 2 | a0001c0001t0007g0005 a0001c0001t0021g0142 |
11 | HG00741.hp1 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-638A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451443 | |||||||
| chr12:21451445 | A | AT | 4 | a0001c0001t0007g0005 a0001c0001t0015g0048 a0001c0001t0015g0143 others(1): Show |
14 | HG00741.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.415-625dupT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 21451445 | ||||||
| chr12:21451546 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.415-535A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451546 | |||||||
| chr12:21451578 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.415-503C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451578 | |||||||
| chr12:21451584 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.415-497A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451584 | |||||||
| chr12:21451682 | C | CTTCTCA | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.415-395_415-390dup others(6): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 21451682 | ||||||
| chr12:21451701 | T | G | 1 | a0001c0001t0019g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.415-380T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451701 | |||||||
| chr12:21451787 | A | G | 1 | a0001c0001t0004g0042 | 2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.415-294A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451787 | |||||||
| chr12:21451806 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.415-275C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451806 | |||||||
| chr12:21451845 | A | G | 15 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0043 others(12): Show |
22 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.415-236A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451845 | |||||||
| chr12:21451873 | A | T | 4 | a0001c0001t0019g0149 a0001c0001t0019g0156 a0001c0001t0034g0155 others(1): Show |
6 | HG01243.hp2 HG02970.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-208A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451873 | |||||||
| chr12:21451913 | A | G | 1 | a0001c0001t0004g0129 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.415-168A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 4/11 | chr12 | 21451913 | |||||||
| chr12:21452182 | C | CAT | 13 | a0001c0001t0007g0005 a0001c0001t0009g0016 a0001c0001t0009g0047 others(10): Show |
31 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.488+29_488+30dupAT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 21452182 | ||||||
| chr12:21452197 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0090 |
3 | HG02717.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.488+43A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452197 | |||||||
| chr12:21452200 | A | G | 12 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0150 others(9): Show |
15 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.488+46A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452200 | |||||||
| chr12:21452223 | A | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.488+69A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452223 | |||||||
| chr12:21452303 | A | G | 1 | a0001c0001t0001g0033 | 2 | NA18954.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.488+149A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452303 | |||||||
| chr12:21452310 | T | G | 1 | a0001c0001t0013g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.488+156T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452310 | |||||||
| chr12:21452326 | C | T | 2 | a0001c0001t0019g0149 a0001c0001t0019g0156 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.488+172C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452326 | |||||||
| chr12:21452385 | A | G | 5 | a0001c0001t0005g0030 a0001c0001t0005g0183 a0001c0001t0005g0184 others(2): Show |
7 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+231A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452385 | |||||||
| chr12:21452432 | G | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.488+278G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452432 | |||||||
| chr12:21452530 | T | C | 14 | a0001c0001t0007g0005 a0001c0001t0009g0016 a0001c0001t0009g0047 others(11): Show |
33 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.488+376T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452530 | |||||||
| chr12:21452543 | A | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.488+389A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452543 | |||||||
| chr12:21452552 | A | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.488+398A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452552 | |||||||
| chr12:21452573 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.488+419C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452573 | |||||||
| chr12:21452584 | C | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.488+430C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452584 | |||||||
| chr12:21452688 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.488+534C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452688 | |||||||
| chr12:21452821 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.488+667A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452821 | |||||||
| chr12:21452879 | CTT | C | 9 | a0001c0001t0007g0005 a0001c0001t0009g0016 a0001c0001t0009g0047 others(6): Show |
25 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.488+727_488+728del others(2): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 21452879 | ||||||
| chr12:21452898 | A | G | 1 | a0001c0001t0004g0132 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.488+744A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21452898 | |||||||
| chr12:21453129 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.488+975G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453129 | |||||||
| chr12:21453181 | A | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(30): Show |
51 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.488+1027A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453181 | |||||||
| chr12:21453193 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.488+1039G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453193 | |||||||
| chr12:21453197 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.488+1043T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453197 | |||||||
| chr12:21453286 | G | A | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.488+1132G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453286 | |||||||
| chr12:21453325 | C | G | 1 | a0001c0001t0003g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.488+1171C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453325 | |||||||
| chr12:21453474 | A | G | 1 | a0001c0001t0002g0055 | 2 | NA19007.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.488+1320A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453474 | |||||||
| chr12:21453508 | CCTTT | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.488+1357_488+1360d others(6): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 21453508 | ||||||
| chr12:21453576 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.488+1422T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453576 | |||||||
| chr12:21453615 | A | G | 12 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0150 others(9): Show |
15 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.488+1461A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453615 | |||||||
| chr12:21453631 | C | G | 2 | a0001c0001t0007g0005 a0001c0001t0021g0142 |
11 | HG00741.hp1 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.488+1477C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453631 | |||||||
| chr12:21453784 | G | C | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.489-1348G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453784 | |||||||
| chr12:21453835 | A | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.489-1297A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453835 | |||||||
| chr12:21453839 | A | G | 1 | a0001c0005t0004g0133 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.489-1293A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453839 | |||||||
| chr12:21453857 | T | A | 1 | a0001c0001t0003g0118 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.489-1275T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453857 | |||||||
| chr12:21453875 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.489-1257A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453875 | |||||||
| chr12:21453953 | T | G | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.489-1179T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453953 | |||||||
| chr12:21453973 | A | G | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.489-1159A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21453973 | |||||||
| chr12:21454010 | A | G | 1 | a0001c0001t0010g0146 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.489-1122A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454010 | |||||||
| chr12:21454018 | CTA | C | 43 | a0001c0001t0001g0038 a0001c0001t0001g0099 a0001c0001t0003g0003 others(40): Show |
92 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.489-1112_489-1111d others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 21454018 | ||||||
| chr12:21454060 | T | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
5 | NA18939.hp1 NA18940.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-1072T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454060 | |||||||
| chr12:21454064 | G | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.489-1068G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454064 | |||||||
| chr12:21454218 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.489-914A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454218 | |||||||
| chr12:21454312 | T | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0164 a0001c0001t0012g0171 |
8 | HG02080.hp1 HG02129.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.489-820T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454312 | |||||||
| chr12:21454368 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.489-764G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454368 | |||||||
| chr12:21454440 | A | G | 1 | a0001c0001t0016g0041 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.489-692A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454440 | |||||||
| chr12:21454553 | A | C | 3 | a0001c0001t0005g0051 a0001c0001t0005g0150 a0001c0001t0005g0153 |
4 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.489-579A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454553 | |||||||
| chr12:21454578 | T | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.489-554T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454578 | |||||||
| chr12:21454580 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.489-552T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454580 | |||||||
| chr12:21454625 | T | G | 1 | a0001c0001t0022g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.489-507T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454625 | |||||||
| chr12:21454637 | G | A | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.489-495G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454637 | |||||||
| chr12:21454745 | G | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.489-387G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454745 | |||||||
| chr12:21454865 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.489-267C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454865 | |||||||
| chr12:21454908 | C | G | 1 | a0001c0001t0006g0169 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.489-224C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454908 | |||||||
| chr12:21454945 | T | C | 1 | a0001c0001t0003g0046 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.489-187T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454945 | |||||||
| chr12:21454969 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.489-163C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454969 | |||||||
| chr12:21454982 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.489-150C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21454982 | |||||||
| chr12:21455077 | G | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.489-55G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21455077 | |||||||
| chr12:21455109 | A | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.489-23A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 5/11 | chr12 | 21455109 | |||||||
| chr12:21455355 | G | A | 1 | a0001c0001t0003g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.649+63G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455355 | |||||||
| chr12:21455436 | T | TTCTATTT others(12): Show |
1 | a0001c0001t0019g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.649+146_649+164dup others(19): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 21455436 | ||||||
| chr12:21455457 | G | C | 1 | a0001c0001t0019g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.649+165G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455457 | |||||||
| chr12:21455458 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.649+166T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455458 | |||||||
| chr12:21455462 | T | A | 1 | a0001c0001t0002g0188 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.649+170T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455462 | |||||||
| chr12:21455462 | T | TTATATAT others(14): Show |
1 | a0001c0001t0019g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.649+179_649+180ins others(21): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 21455462 | ||||||
| chr12:21455462 | TTA | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.649+185_649+186del others(2): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 21455462 | ||||||
| chr12:21455585 | G | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.649+293G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455585 | |||||||
| chr12:21455614 | AT | A | 5 | a0001c0001t0005g0030 a0001c0001t0005g0183 a0001c0001t0005g0184 others(2): Show |
7 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.649+329delT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 21455614 | ||||||
| chr12:21455619 | T | G | 4 | a0001c0001t0005g0030 a0001c0001t0005g0183 a0001c0001t0005g0185 others(1): Show |
6 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.649+327T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455619 | |||||||
| chr12:21455647 | T | C | 2 | a0001c0002t0011g0028 a0002c0003t0011g0050 |
5 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.650-348T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455647 | |||||||
| chr12:21455651 | T | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.650-344T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455651 | |||||||
| chr12:21455660 | TAAAC | T | 3 | a0001c0001t0010g0027 a0001c0001t0010g0145 a0001c0001t0010g0146 |
5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.650-332_650-329del others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 21455660 | ||||||
| chr12:21455684 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.650-311G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455684 | |||||||
| chr12:21455699 | T | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.650-296T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455699 | |||||||
| chr12:21455750 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.650-245G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455750 | |||||||
| chr12:21455798 | C | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.650-197C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455798 | |||||||
| chr12:21455838 | A | C | 1 | a0001c0001t0012g0171 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.650-157A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455838 | |||||||
| chr12:21455957 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.650-38T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 6/11 | chr12 | 21455957 | |||||||
| chr12:21456193 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.750+98T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456193 | |||||||
| chr12:21456246 | T | G | 47 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(44): Show |
95 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.750+151T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456246 | |||||||
| chr12:21456288 | G | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.750+193G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456288 | |||||||
| chr12:21456346 | C | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(42): Show |
89 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.750+251C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456346 | |||||||
| chr12:21456354 | C | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.750+259C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456354 | |||||||
| chr12:21456369 | G | T | 1 | a0001c0001t0012g0171 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.750+274G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456369 | |||||||
| chr12:21456389 | C | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.750+294C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456389 | |||||||
| chr12:21456427 | T | G | 1 | a0001c0002t0011g0028 | 3 | HG01243.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.750+332T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456427 | |||||||
| chr12:21456438 | C | T | 1 | a0001c0001t0003g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.750+343C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456438 | |||||||
| chr12:21456448 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.750+353G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456448 | |||||||
| chr12:21456451 | A | G | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.750+356A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456451 | |||||||
| chr12:21456459 | G | C | 1 | a0001c0001t0012g0171 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.750+364G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456459 | |||||||
| chr12:21456460 | T | G | 1 | a0001c0001t0012g0171 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.750+365T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456460 | |||||||
| chr12:21456618 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.750+523G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456618 | |||||||
| chr12:21456666 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.750+571G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456666 | |||||||
| chr12:21456673 | G | A | 3 | a0001c0001t0034g0155 a0001c0002t0011g0028 a0002c0003t0011g0050 |
6 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+578G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456673 | |||||||
| chr12:21456750 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0035 others(19): Show |
33 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.750+655A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456750 | |||||||
| chr12:21456799 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.750+704A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456799 | |||||||
| chr12:21456827 | C | CAACT | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.750+734_750+735ins others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21456827 | ||||||
| chr12:21456839 | A | G | 41 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(38): Show |
89 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.750+744A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456839 | |||||||
| chr12:21456880 | C | A | 1 | a0001c0001t0034g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.750+785C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456880 | |||||||
| chr12:21456973 | G | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.750+878G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456973 | |||||||
| chr12:21456988 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.750+893C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21456988 | |||||||
| chr12:21457002 | A | G | 27 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0035 others(24): Show |
39 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.750+907A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457002 | |||||||
| chr12:21457088 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.750+993T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457088 | |||||||
| chr12:21457093 | G | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.750+998G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457093 | |||||||
| chr12:21457109 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.750+1014C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457109 | |||||||
| chr12:21457133 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.750+1038C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457133 | |||||||
| chr12:21457163 | TAAC | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.750+1070_750+1072d others(5): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21457163 | ||||||
| chr12:21457188 | C | G | 4 | a0001c0001t0002g0054 a0001c0001t0002g0161 a0001c0001t0002g0178 others(1): Show |
5 | NA18957.hp1 NA18975.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.750+1093C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457188 | |||||||
| chr12:21457190 | A | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.750+1095A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457190 | |||||||
| chr12:21457310 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.750+1215T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457310 | |||||||
| chr12:21457399 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.750+1304G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457399 | |||||||
| chr12:21457428 | T | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(132): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.750+1333T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457428 | |||||||
| chr12:21457431 | ATCTT | A | 31 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(28): Show |
72 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.750+1338_750+1341d others(6): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21457431 | ||||||
| chr12:21457433 | C | CT | 12 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0150 others(9): Show |
15 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.750+1353dupT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21457433 | ||||||
| chr12:21457433 | CT | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.750+1353delT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21457433 | ||||||
| chr12:21457480 | A | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.750+1385A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457480 | |||||||
| chr12:21457712 | G | C | 3 | a0001c0001t0034g0155 a0001c0002t0011g0028 a0002c0003t0011g0050 |
6 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+1617G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457712 | |||||||
| chr12:21457737 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.750+1642A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457737 | |||||||
| chr12:21457759 | A | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.750+1664A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457759 | |||||||
| chr12:21457811 | A | ATCCAGTC others(20): Show |
119 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.750+1721_750+1747d others(29): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21457811 | ||||||
| chr12:21457825 | C | CACCAGGC others(20): Show |
1 | a0001c0001t0031g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.750+1747_750+1748i others(29): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21457825 | ||||||
| chr12:21457866 | T | G | 3 | a0001c0001t0010g0027 a0001c0001t0010g0145 a0001c0001t0010g0146 |
5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.750+1771T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457866 | |||||||
| chr12:21457906 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.750+1811T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21457906 | |||||||
| chr12:21458061 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.750+1966C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458061 | |||||||
| chr12:21458093 | A | C | 1 | a0001c0001t0002g0176 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.750+1998A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458093 | |||||||
| chr12:21458143 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.750+2048G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458143 | |||||||
| chr12:21458243 | A | G | 2 | a0001c0002t0011g0028 a0002c0003t0011g0050 |
5 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.750+2148A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458243 | |||||||
| chr12:21458249 | A | G | 2 | a0001c0001t0019g0149 a0001c0001t0019g0156 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.750+2154A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458249 | |||||||
| chr12:21458325 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.750+2230C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458325 | |||||||
| chr12:21458454 | C | A | 1 | a0001c0001t0013g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.750+2359C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458454 | |||||||
| chr12:21458538 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.750+2443G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458538 | |||||||
| chr12:21458655 | T | G | 1 | a0002c0003t0011g0050 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.751-2370T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458655 | |||||||
| chr12:21458696 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.751-2329G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458696 | |||||||
| chr12:21458815 | T | A | 1 | a0001c0001t0031g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.751-2210T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458815 | |||||||
| chr12:21458994 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.751-2031C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21458994 | |||||||
| chr12:21459047 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.751-1978T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459047 | |||||||
| chr12:21459110 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0010g0027 a0001c0001t0010g0145 others(2): Show |
8 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.751-1915C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459110 | |||||||
| chr12:21459211 | A | G | 1 | a0001c0001t0003g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.751-1814A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459211 | |||||||
| chr12:21459249 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.751-1776A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459249 | |||||||
| chr12:21459308 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0093 |
2 | HG01255.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.751-1717G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459308 | |||||||
| chr12:21459403 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.751-1622C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459403 | |||||||
| chr12:21459425 | T | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0062 a0001c0001t0001g0079 others(1): Show |
5 | NA18612.hp2 NA18951.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.751-1600T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459425 | |||||||
| chr12:21459429 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.751-1596C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459429 | |||||||
| chr12:21459498 | A | C | 3 | a0001c0001t0003g0015 a0001c0001t0003g0117 a0001c0001t0003g0125 |
6 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.751-1527A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459498 | |||||||
| chr12:21459527 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.751-1498C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459527 | |||||||
| chr12:21459625 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.751-1400T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459625 | |||||||
| chr12:21459667 | A | G | 9 | a0001c0001t0003g0003 a0001c0001t0003g0112 a0001c0001t0003g0119 others(6): Show |
28 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.751-1358A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459667 | |||||||
| chr12:21459772 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.751-1253A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459772 | |||||||
| chr12:21459870 | C | T | 1 | a0001c0001t0005g0051 | 2 | HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.751-1155C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459870 | |||||||
| chr12:21459899 | A | C | 46 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(43): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.751-1126A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459899 | |||||||
| chr12:21459980 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.751-1045C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459980 | |||||||
| chr12:21459996 | A | G | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.751-1029A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21459996 | |||||||
| chr12:21460070 | T | C | 9 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0043 others(6): Show |
16 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.751-955T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460070 | |||||||
| chr12:21460077 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.751-948A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460077 | |||||||
| chr12:21460180 | T | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.751-845T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460180 | |||||||
| chr12:21460188 | A | T | 1 | a0001c0001t0002g0191 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.751-837A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460188 | |||||||
| chr12:21460214 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.751-811C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460214 | |||||||
| chr12:21460234 | T | TATTA | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.751-790_751-787dup others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21460234 | ||||||
| chr12:21460238 | A | G | 2 | a0001c0001t0019g0149 a0001c0001t0019g0156 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.751-787A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460238 | |||||||
| chr12:21460256 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.751-769C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460256 | |||||||
| chr12:21460336 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.751-689G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460336 | |||||||
| chr12:21460373 | A | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(43): Show |
90 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.751-652A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460373 | |||||||
| chr12:21460379 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.751-646G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460379 | |||||||
| chr12:21460420 | A | T | 2 | a0001c0001t0020g0154 a0001c0001t0020g0193 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.751-605A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460420 | |||||||
| chr12:21460421 | T | A | 2 | a0001c0001t0020g0154 a0001c0001t0020g0193 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.751-604T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460421 | |||||||
| chr12:21460427 | TTA | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(71): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.751-596_751-595del others(2): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21460427 | ||||||
| chr12:21460428 | TA | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0084 a0001c0001t0001g0103 others(1): Show |
9 | HG02132.hp2 HG02145.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.751-596delA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460428 | |||||||
| chr12:21460429 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.751-596A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460429 | |||||||
| chr12:21460431 | TTA | T | 41 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(38): Show |
89 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.751-592_751-591del others(2): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21460431 | ||||||
| chr12:21460432 | T | A | 1 | a0001c0001t0001g0013 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.751-593T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460432 | |||||||
| chr12:21460433 | A | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.751-592A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460433 | |||||||
| chr12:21460497 | C | T | 2 | a0001c0002t0011g0028 a0002c0003t0011g0050 |
5 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.751-528C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460497 | |||||||
| chr12:21460516 | C | T | 3 | a0001c0001t0010g0027 a0001c0001t0010g0145 a0001c0001t0010g0146 |
5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.751-509C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460516 | |||||||
| chr12:21460526 | C | T | 1 | a0001c0001t0009g0047 | 2 | HG01081.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.751-499C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460526 | |||||||
| chr12:21460538 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.751-487C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460538 | |||||||
| chr12:21460568 | C | T | 31 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(28): Show |
72 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.751-457C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460568 | |||||||
| chr12:21460691 | C | G | 1 | a0001c0001t0003g0131 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.751-334C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460691 | |||||||
| chr12:21460745 | A | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.751-280A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460745 | |||||||
| chr12:21460824 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.751-201T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460824 | |||||||
| chr12:21460890 | CAATGTGG others(18): Show |
C | 5 | a0001c0001t0019g0149 a0001c0001t0019g0156 a0001c0001t0034g0155 others(2): Show |
8 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.751-131_751-107del others(25): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 21460890 | ||||||
| chr12:21460892 | A | G | 1 | a0001c0001t0002g0001 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.751-133A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460892 | |||||||
| chr12:21460933 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.751-92A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460933 | |||||||
| chr12:21460949 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.751-76G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460949 | |||||||
| chr12:21460989 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.751-36T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 7/11 | chr12 | 21460989 | |||||||
| chr12:21461207 | CAATTT | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.880+57_880+61delTT others(3): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 21461207 | ||||||
| chr12:21461244 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.880+90G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461244 | |||||||
| chr12:21461319 | ACTGT | A | 12 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0150 others(9): Show |
15 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.880+170_880+173del others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 21461319 | ||||||
| chr12:21461322 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.880+168G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461322 | |||||||
| chr12:21461328 | T | G | 1 | a0001c0002t0011g0028 | 3 | HG01243.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.880+174T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461328 | |||||||
| chr12:21461650 | G | A | 5 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0138 others(2): Show |
11 | HG01884.hp2 HG02630.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.881-358G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461650 | |||||||
| chr12:21461667 | A | G | 40 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(37): Show |
88 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.881-341A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461667 | |||||||
| chr12:21461685 | G | C | 3 | a0001c0001t0034g0155 a0001c0002t0011g0028 a0002c0003t0011g0050 |
6 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.881-323G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461685 | |||||||
| chr12:21461836 | A | C | 1 | a0001c0001t0002g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.881-172A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461836 | |||||||
| chr12:21461888 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.881-120A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461888 | |||||||
| chr12:21461903 | T | C | 1 | a0001c0001t0004g0129 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.881-105T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461903 | |||||||
| chr12:21461921 | T | C | 1 | a0001c0001t0002g0053 | 2 | NA18955.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.881-87T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461921 | |||||||
| chr12:21461942 | T | TA | 3 | a0001c0001t0001g0040 a0001c0001t0001g0109 a0001c0001t0029g0040 |
3 | HG02109.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.881-65dupA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 21461942 | ||||||
| chr12:21461969 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.881-39A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461969 | |||||||
| chr12:21461991 | G | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0090 a0001c0001t0021g0142 |
4 | HG02717.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-17G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 8/11 | chr12 | 21461991 | |||||||
| chr12:21462222 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.993+102G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/11 | chr12 | 21462222 | |||||||
| chr12:21462273 | A | G | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(61): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.993+153A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/11 | chr12 | 21462273 | |||||||
| chr12:21462314 | T | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.993+194T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/11 | chr12 | 21462314 | |||||||
| chr12:21462315 | G | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0036 others(8): Show |
16 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.993+195G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/11 | chr12 | 21462315 | |||||||
| chr12:21462323 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.993+203G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/11 | chr12 | 21462323 | |||||||
| chr12:21462334 | T | C | 12 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0150 others(9): Show |
15 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.993+214T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/11 | chr12 | 21462334 | |||||||
| chr12:21462384 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.993+264C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/11 | chr12 | 21462384 | |||||||
| chr12:21462460 | CA | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(203): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.994-267delA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 21462460 | ||||||
| chr12:21462460 | CAA | C | 5 | a0001c0001t0019g0149 a0001c0001t0019g0156 a0001c0001t0034g0155 others(2): Show |
8 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.994-268_994-267del others(2): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 21462460 | ||||||
| chr12:21462730 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.994-10T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 9/11 | chr12 | 21462730 | |||||||
| chr12:21462920 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1116+58G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21462920 | |||||||
| chr12:21462960 | T | G | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116+98T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21462960 | |||||||
| chr12:21462983 | C | CAG | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1116+122_1116+123d others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21462983 | ||||||
| chr12:21463001 | A | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.1116+139A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463001 | |||||||
| chr12:21463002 | A | T | 1 | a0001c0001t0003g0124 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1116+140A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463002 | |||||||
| chr12:21463132 | CAGG | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1116+273_1116+275d others(5): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21463132 | ||||||
| chr12:21463171 | C | T | 30 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(27): Show |
70 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1116+309C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463171 | |||||||
| chr12:21463289 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(43): Show |
90 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1116+427G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463289 | |||||||
| chr12:21463325 | C | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(61): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1116+463C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463325 | |||||||
| chr12:21463371 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1116+509C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463371 | |||||||
| chr12:21463599 | C | T | 1 | a0001c0002t0011g0028 | 3 | HG01243.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1116+737C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463599 | |||||||
| chr12:21463623 | C | T | 2 | a0001c0001t0007g0005 a0001c0001t0021g0142 |
11 | HG00741.hp1 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1116+761C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463623 | |||||||
| chr12:21463624 | G | A | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(61): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1116+762G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463624 | |||||||
| chr12:21463664 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1116+802C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463664 | |||||||
| chr12:21463692 | C | CAA | 37 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(34): Show |
85 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.1116+846_1116+847d others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21463692 | ||||||
| chr12:21463692 | C | CAAAA | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(31): Show |
51 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1116+844_1116+847d others(6): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21463692 | ||||||
| chr12:21463692 | C | CAAAAA | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(40): Show |
87 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1116+843_1116+847d others(7): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21463692 | ||||||
| chr12:21463692 | CA | C | 86 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(83): Show |
173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1116+847delA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21463692 | ||||||
| chr12:21463803 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1116+941G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463803 | |||||||
| chr12:21463816 | T | C | 3 | a0001c0001t0003g0015 a0001c0001t0003g0117 a0001c0001t0003g0125 |
6 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116+954T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463816 | |||||||
| chr12:21463907 | T | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(61): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1116+1045T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21463907 | |||||||
| chr12:21464049 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1116+1187G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464049 | |||||||
| chr12:21464079 | C | G | 1 | a0001c0001t0001g0032 | 2 | NA18945.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1116+1217C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464079 | |||||||
| chr12:21464134 | T | TA | 9 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0043 others(6): Show |
16 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1116+1272_1116+127 others(5): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464134 | |||||||
| chr12:21464137 | G | GT | 47 | a0001c0001t0002g0157 a0001c0001t0002g0190 a0001c0001t0003g0003 others(44): Show |
107 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1116+1288dupT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21464137 | ||||||
| chr12:21464137 | G | T | 9 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0043 others(6): Show |
16 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1116+1275G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464137 | |||||||
| chr12:21464137 | GTT | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1116+1287_1116+128 others(6): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21464137 | ||||||
| chr12:21464209 | G | GA | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116+1353dupA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21464209 | ||||||
| chr12:21464209 | GA | G | 40 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(37): Show |
88 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1116+1353delA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21464209 | ||||||
| chr12:21464210 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1116+1348A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464210 | |||||||
| chr12:21464211 | A | G | 40 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(37): Show |
88 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1116+1349A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464211 | |||||||
| chr12:21464256 | T | TAGGCCCC others(20): Show |
1 | a0001c0001t0028g0060 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1116+1396_1116+142 others(31): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21464256 | ||||||
| chr12:21464425 | G | C | 1 | a0001c0001t0021g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1116+1563G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464425 | |||||||
| chr12:21464441 | G | GA | 14 | a0001c0001t0003g0121 a0001c0001t0003g0127 a0001c0001t0005g0030 others(11): Show |
17 | HG01884.hp1 HG02145.hp1 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.1116+1590dupA | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21464441 | ||||||
| chr12:21464526 | C | T | 5 | a0001c0001t0019g0149 a0001c0001t0019g0156 a0001c0001t0034g0155 others(2): Show |
8 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1116+1664C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464526 | |||||||
| chr12:21464565 | C | T | 1 | a0001c0001t0002g0018 | 4 | HG01358.hp1 HG02683.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116+1703C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464565 | |||||||
| chr12:21464724 | G | GT | 120 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(117): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1116+1874dupT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21464724 | ||||||
| chr12:21464724 | G | GTT | 3 | a0001c0001t0034g0155 a0001c0002t0011g0028 a0002c0003t0011g0050 |
6 | HG01243.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116+1873_1116+187 others(6): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21464724 | ||||||
| chr12:21464734 | T | TA | 7 | a0001c0001t0003g0025 a0001c0001t0005g0051 a0001c0001t0005g0150 others(4): Show |
9 | HG02258.hp2 HG02559.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1116+1872_1116+187 others(5): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464734 | |||||||
| chr12:21464734 | T | TTA | 78 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1116+1873_1116+187 others(6): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21464734 | ||||||
| chr12:21464743 | A | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(29): Show |
50 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1116+1881A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464743 | |||||||
| chr12:21464743 | ATAT | A | 3 | a0001c0001t0010g0027 a0001c0001t0010g0145 a0001c0001t0010g0146 |
5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116+1883_1116+188 others(7): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 21464743 | ||||||
| chr12:21464779 | A | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1116+1917A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464779 | |||||||
| chr12:21464804 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1116+1942C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464804 | |||||||
| chr12:21464807 | T | G | 40 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(37): Show |
88 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1116+1945T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464807 | |||||||
| chr12:21464838 | G | A | 9 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0043 others(6): Show |
16 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1116+1976G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464838 | |||||||
| chr12:21464984 | A | G | 2 | a0001c0001t0007g0005 a0001c0001t0021g0142 |
11 | HG00741.hp1 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1116+2122A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21464984 | |||||||
| chr12:21465004 | A | C | 1 | a0001c0001t0005g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1116+2142A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465004 | |||||||
| chr12:21465132 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG01361.hp2 HG02735.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1116+2270G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465132 | |||||||
| chr12:21465216 | C | G | 1 | a0001c0001t0002g0182 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1117-2265C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465216 | |||||||
| chr12:21465248 | A | G | 1 | a0001c0001t0002g0056 | 2 | NA18956.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1117-2233A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465248 | |||||||
| chr12:21465329 | A | C | 2 | a0001c0001t0019g0149 a0001c0001t0019g0156 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1117-2152A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465329 | |||||||
| chr12:21465442 | T | G | 1 | a0001c0001t0013g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1117-2039T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465442 | |||||||
| chr12:21465473 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1117-2008G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465473 | |||||||
| chr12:21465489 | T | C | 1 | a0001c0001t0019g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1117-1992T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465489 | |||||||
| chr12:21465518 | T | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1117-1963T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465518 | |||||||
| chr12:21465569 | A | C | 1 | a0001c0001t0015g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1117-1912A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465569 | |||||||
| chr12:21465576 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.1117-1905G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465576 | |||||||
| chr12:21465579 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1117-1902C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465579 | |||||||
| chr12:21465608 | C | T | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1117-1873C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465608 | |||||||
| chr12:21465620 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1117-1861T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465620 | |||||||
| chr12:21465636 | G | A | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1117-1845G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465636 | |||||||
| chr12:21465646 | A | G | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1117-1835A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465646 | |||||||
| chr12:21465694 | A | G | 40 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(37): Show |
88 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1117-1787A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465694 | |||||||
| chr12:21465694 | A | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1117-1787A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465694 | |||||||
| chr12:21465780 | T | C | 1 | a0001c0002t0011g0028 | 3 | HG01243.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1117-1701T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465780 | |||||||
| chr12:21465982 | T | C | 1 | a0001c0001t0031g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1117-1499T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21465982 | |||||||
| chr12:21466024 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1117-1457A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466024 | |||||||
| chr12:21466080 | C | T | 1 | a0001c0001t0010g0145 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1117-1401C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466080 | |||||||
| chr12:21466142 | C | T | 2 | a0001c0001t0019g0149 a0001c0001t0019g0156 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1117-1339C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466142 | |||||||
| chr12:21466147 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1117-1334C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466147 | |||||||
| chr12:21466183 | G | T | 1 | a0001c0001t0008g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1117-1298G>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466183 | |||||||
| chr12:21466242 | A | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(55): Show |
126 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1117-1239A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466242 | |||||||
| chr12:21466291 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1117-1190A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466291 | |||||||
| chr12:21466331 | C | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1117-1150C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466331 | |||||||
| chr12:21466356 | G | C | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1117-1125G>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466356 | |||||||
| chr12:21466410 | T | C | 46 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(43): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1117-1071T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466410 | |||||||
| chr12:21466474 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1117-1007G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466474 | |||||||
| chr12:21466518 | A | G | 57 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(54): Show |
125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1117-963A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466518 | |||||||
| chr12:21466572 | T | C | 4 | a0001c0001t0007g0005 a0001c0001t0015g0048 a0001c0001t0015g0143 others(1): Show |
14 | HG00741.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1117-909T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466572 | |||||||
| chr12:21466646 | C | T | 1 | a0001c0001t0034g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1117-835C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466646 | |||||||
| chr12:21466697 | A | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1117-784A>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466697 | |||||||
| chr12:21466737 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1117-744T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466737 | |||||||
| chr12:21466767 | T | C | 1 | a0001c0001t0019g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1117-714T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466767 | |||||||
| chr12:21466828 | G | A | 4 | a0001c0001t0007g0005 a0001c0001t0015g0048 a0001c0001t0015g0143 others(1): Show |
14 | HG00741.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1117-653G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466828 | |||||||
| chr12:21466891 | T | G | 31 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(28): Show |
72 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1117-590T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466891 | |||||||
| chr12:21466955 | T | A | 2 | a0001c0001t0019g0149 a0001c0001t0019g0156 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1117-526T>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21466955 | |||||||
| chr12:21467037 | A | T | 1 | a0001c0001t0004g0044 | 2 | HG01255.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1117-444A>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21467037 | |||||||
| chr12:21467154 | G | A | 2 | a0001c0001t0020g0154 a0001c0001t0020g0193 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1117-327G>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21467154 | |||||||
| chr12:21467187 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1117-294T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 10/11 | chr12 | 21467187 | |||||||
| chr12:21467829 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1254+211T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | chr12 | 21467829 | |||||||
| chr12:21467962 | T | G | 2 | a0001c0001t0009g0016 a0001c0001t0009g0047 |
6 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+344T>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | chr12 | 21467962 | |||||||
| chr12:21467971 | C | G | 2 | a0001c0001t0019g0149 a0001c0001t0019g0156 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1254+353C>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | chr12 | 21467971 | |||||||
| chr12:21467974 | T | TTATCTTA others(13): Show |
2 | a0001c0001t0007g0005 a0001c0001t0021g0142 |
11 | HG00741.hp1 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1254+357_1254+376d others(22): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr12 | 21467974 | ||||||
| chr12:21468017 | G | GT | 122 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(119): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1254+410dupT | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr12 | 21468017 | ||||||
| chr12:21468017 | G | GTT | 4 | a0001c0001t0001g0007 a0001c0001t0001g0084 a0001c0001t0003g0113 others(1): Show |
9 | HG02132.hp2 HG04115.hp1 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1254+409_1254+410d others(4): Show |
PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr12 | 21468017 | ||||||
| chr12:21468431 | C | T | 12 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0150 others(9): Show |
15 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1255-75C>T | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | chr12 | 21468431 | |||||||
| chr12:21468476 | T | C | 1 | a0001c0001t0002g0164 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1255-30T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | chr12 | 21468476 | |||||||
| chr12:21468485 | C | A | 46 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(43): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1255-21C>A | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | chr12 | 21468485 | |||||||
| chr12:21468498 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG02132.hp1 | splice_region_variant&intron_variant | LOW | c.1255-8A>G | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | chr12 | 21468498 | |||||||
| chr12:21468503 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0078 |
7 | NA18965.hp1 NA18988.hp1 NA18992.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1255-3T>C | PYROXD1 | ENSG00000121350.16 | transcript | ENST00000240651.14 | protein_coding | 11/11 | chr12 | 21468503 |