Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91147 |
| ensemblid | ENSG00000164953.17 |
| hgncid | 28396 |
| symbol | TMEM67 |
| name | transmembrane protein 67 |
| refseq_nuc | NM_153704.6 |
| refseq_prot | NP_714915.3 |
| ensembl_nuc | ENST00000453321.8 |
| ensembl_prot | ENSP00000389998.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 93754894 |
| end | 93818121 |
| strand | + |
| ver | v1.2 |
| region | chr8:93754894-93818121 |
| region5000 | chr8:93749894-93823121 |
| regionname0 | TMEM67_chr8_93754894_93818121 |
| regionname5000 | TMEM67_chr8_93749894_93823121 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 995 | 202 | 70 | 40 | 66 | 4 | 21 | 57 | TMEM67_chr8_93749894_93823121 | TMEM67 | MATRG others(990): Show |
chr8 | 93749894 | 93823121 |
| a0002 | 1/0 | 995 | 110 | 20 | 23 | 45 | 8 | 13 | 40 | TMEM67_chr8_93749894_93823121 | TMEM67 | MATRG others(990): Show |
chr8 | 93749894 | 93823121 |
| a0003 | 0/0 | 995 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | MATRG others(990): Show |
chr8 | 93749894 | 93823121 |
| a0004 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | MATRG others(990): Show |
chr8 | 93749894 | 93823121 |
| a0005 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | MATRG others(990): Show |
chr8 | 93749894 | 93823121 |
| a0006 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | MATRG others(990): Show |
chr8 | 93749894 | 93823121 |
| a0007 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | MATRG others(990): Show |
chr8 | 93749894 | 93823121 |
| a0008 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | MATRG others(990): Show |
chr8 | 93749894 | 93823121 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2985 | 176 | 67 | 35 | 51 | 4 | 18 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0001c0003 | 0/0 | 2985 | 22 | 0 | 4 | 15 | 0 | 3 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0001c0004 | 0/0 | 2985 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0002c0002 | 1/0 | 2985 | 108 | 20 | 23 | 44 | 8 | 12 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0002c0008 | 0/0 | 2985 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0002c0009 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0003c0006 | 0/0 | 2985 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0004c0005 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0005c0010 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0006c0011 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0007c0012 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 | ||
| a0008c0007 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | ATGGC others(2980): Show |
chr8 | 93749894 | 93823121 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4678 | 164 | 56 | 34 | 51 | 4 | 18 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0001c0001t0002 | 0/0 | 4678 | 7 | 6 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0001c0001t0003 | 0/0 | 4678 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0001c0001t0006 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0001c0001t0007 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0001c0003t0001 | 0/0 | 4678 | 22 | 0 | 4 | 15 | 0 | 3 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0001c0004t0001 | 0/0 | 4678 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0002c0002t0001 | 1/0 | 4678 | 103 | 19 | 21 | 44 | 7 | 11 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0002c0002t0004 | 0/0 | 4678 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0002c0002t0005 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0002c0002t0008 | 0/0 | 4678 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0002c0002t0009 | 0/0 | 4678 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0002c0008t0001 | 0/0 | 4678 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0002c0009t0001 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0003c0006t0001 | 0/0 | 4678 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0004c0005t0010 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0005c0010t0002 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0006c0011t0001 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0007c0012t0001 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| a0008c0007t0001 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | GAGGC others(4673): Show |
chr8 | 93749894 | 93823121 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0002g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0004t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0004t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0001c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0008g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0002t0009g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0008t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0002c0009t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0003c0006t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0004c0005t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0005c0010t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0006c0011t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0007c0012t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| a0008c0007t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0280 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00741 | hp1 | a0002 | c0002 | t0004 | g0094 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01109 | hp2 | a0002 | c0002 | t0009 | g0126 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0097 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0247 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01243 | hp2 | a0003 | c0006 | t0001 | g0223 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0187 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0143 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0236 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0234 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0087 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0219 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0055 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0182 | EAS | KHV | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | KHV | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | KHV | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0203 | EAS | KHV | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0221 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02451 | hp2 | a0004 | c0005 | t0010 | g0066 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0227 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02647 | hp2 | a0002 | c0002 | t0005 | g0082 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0218 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02723 | hp2 | a0005 | c0010 | t0002 | g0067 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02738 | hp2 | a0002 | c0002 | t0008 | g0122 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0281 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0054 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0106 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0051 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0133 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0117 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0073 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0164 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0186 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0181 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0243 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0120 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0287 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0279 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0226 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18978 | hp1 | a0006 | c0011 | t0001 | g0270 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18981 | hp1 | a0007 | c0012 | t0001 | g0108 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19056 | hp2 | a0002 | c0009 | t0001 | g0024 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19068 | hp1 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19076 | hp2 | a0008 | c0007 | t0001 | g0214 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19078 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0190 | EUR | TSI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA20752 | hp2 | a0002 | c0002 | t0004 | g0121 | EUR | TSI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0273 | EUR | TSI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | GIH | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA20905 | hp2 | a0002 | c0008 | t0001 | g0083 | SAS | GIH | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0286 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | USA | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | USA | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | USA | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0197 | REF | REF | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0105 | REF | REF | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:93754939 | G | A | 1 | a0004 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.25G>A | p.Val9Met | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/28 | 46/4678 | 25/2988 | 9/995 | chr8 | 93754939 | |||
| chr8:93780659 | G | A | 1 | a0003 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.781G>A | p.Asp261Asn | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 8/28 | 802/4678 | 781/2988 | 261/995 | chr8 | 93780659 | |||
| chr8:93780684 | G | T | 1 | a0007 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.806G>T | p.Gly269Val | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 8/28 | 827/4678 | 806/2988 | 269/995 | chr8 | 93780684 | |||
| chr8:93780885 | T | A | 1 | a0008 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.881T>A | p.Leu294His | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/28 | 902/4678 | 881/2988 | 294/995 | chr8 | 93780885 | |||
| chr8:93795937 | A | G | 6 | a0001 a0003 a0004 others(3): Show |
206 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(203): Show |
missense_variant | MODERATE | c.1810A>G | p.Ile604Val | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/28 | 1831/4678 | 1810/2988 | 604/995 | chr8 | 93795937 | |||
| chr8:93799684 | T | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.2167T>C | p.Tyr723His | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/28 | 2188/4678 | 2167/2988 | 723/995 | chr8 | 93799684 | |||
| chr8:93816388 | G | A | 1 | a0006 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.2924G>A | p.Arg975His | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 2945/4678 | 2924/2988 | 975/995 | chr8 | 93816388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:93804836 | T | C | 1 | a0002c0008 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.2397T>C | p.Asp799Asp | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/28 | 2418/4678 | 2397/2988 | 799/995 | chr8 | 93804836 | |||
| chr8:93809793 | G | A | 1 | a0002c0009 | 1 | NA19056.hp2 | synonymous_variant | LOW | c.2670G>A | p.Lys890Lys | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/28 | 2691/4678 | 2670/2988 | 890/995 | chr8 | 93809793 | |||
| chr8:93815432 | A | C | 1 | a0001c0003 | 22 | HG00673.hp1 HG01192.hp2 HG01928.hp2 others(19): Show |
synonymous_variant | LOW | c.2892A>C | p.Thr964Thr | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/28 | 2913/4678 | 2892/2988 | 964/995 | chr8 | 93815432 | |||
| chr8:93816416 | A | G | 1 | a0001c0004 | 4 | HG01167.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.2952A>G | p.Ala984Ala | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 2973/4678 | 2952/2988 | 984/995 | chr8 | 93816416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:93816471 | T | C | 2 | a0001c0001t0002 a0005c0010t0002 |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*19T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 19 | chr8 | 93816471 | ||||||
| chr8:93816511 | A | T | 1 | a0004c0005t0010 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*59A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 59 | chr8 | 93816511 | ||||||
| chr8:93816993 | A | C | 1 | a0002c0002t0009 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 541 | chr8 | 93816993 | ||||||
| chr8:93817059 | T | C | 1 | a0002c0002t0005 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*607T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 607 | chr8 | 93817059 | ||||||
| chr8:93817132 | G | A | 1 | a0001c0001t0006 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 680 | chr8 | 93817132 | ||||||
| chr8:93817190 | G | T | 1 | a0002c0002t0008 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*738G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 738 | chr8 | 93817190 | ||||||
| chr8:93817304 | C | T | 1 | a0001c0001t0003 | 3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*852C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 852 | chr8 | 93817304 | ||||||
| chr8:93817986 | G | A | 1 | a0001c0001t0007 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1534G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 1534 | chr8 | 93817986 | ||||||
| chr8:93818105 | G | A | 1 | a0002c0002t0004 | 2 | HG00741.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1653G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 1653 | chr8 | 93818105 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:93755202 | C | G | 2 | a0002c0002t0001g0286 a0002c0002t0001g0287 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.223+65C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | chr8 | 93755202 | |||||||
| chr8:93755210 | G | A | 1 | a0002c0002t0001g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.223+73G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | chr8 | 93755210 | |||||||
| chr8:93755696 | A | T | 1 | a0002c0002t0001g0285 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.224-82A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | chr8 | 93755696 | |||||||
| chr8:93755751 | C | CT | 19 | a0001c0001t0001g0267 a0001c0001t0001g0271 a0001c0001t0001g0274 others(16): Show |
19 | HG00408.hp2 HG00673.hp1 HG00741.hp2 others(16): Show |
splice_acceptor_variant&intron_variant | HIGH | c.224-3dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 93755751 | ||||||
| chr8:93755751 | CT | C | 40 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(37): Show |
43 | HG01070.hp1 HG01070.hp2 HG01261.hp2 others(40): Show |
splice_region_variant&intron_variant | LOW | c.224-3delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 93755751 | ||||||
| chr8:93755751 | CTTT | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(1): Show |
7 | HG01255.hp1 HG01358.hp1 HG01993.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.224-5_224-3delTTT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 93755751 | ||||||
| chr8:93755896 | C | G | 3 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0284 |
3 | HG00597.hp2 NA18949.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.312+30C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93755896 | |||||||
| chr8:93756060 | T | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+194T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756060 | |||||||
| chr8:93756125 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG01070.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+259G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756125 | |||||||
| chr8:93756238 | C | T | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.312+372C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756238 | |||||||
| chr8:93756278 | T | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+412T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756278 | |||||||
| chr8:93756385 | A | T | 11 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.312+519A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756385 | |||||||
| chr8:93756461 | GTC | G | 6 | a0002c0002t0001g0024 a0002c0002t0001g0058 a0002c0002t0001g0256 others(3): Show |
6 | NA18977.hp2 NA18984.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+597_312+598del others(2): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93756461 | ||||||
| chr8:93756565 | A | G | 4 | a0002c0002t0001g0023 a0002c0002t0001g0253 a0002c0002t0001g0254 others(1): Show |
5 | NA18961.hp1 NA18977.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.312+699A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756565 | |||||||
| chr8:93756612 | C | G | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.312+746C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756612 | |||||||
| chr8:93756697 | C | A | 1 | a0002c0002t0001g0264 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.312+831C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756697 | |||||||
| chr8:93756699 | A | G | 1 | a0002c0002t0001g0252 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.312+833A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756699 | |||||||
| chr8:93756708 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.312+842A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756708 | |||||||
| chr8:93756926 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.312+1060G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756926 | |||||||
| chr8:93757004 | G | A | 4 | a0002c0002t0001g0072 a0002c0002t0001g0073 a0002c0002t0001g0074 others(1): Show |
4 | HG00733.hp1 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+1138G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757004 | |||||||
| chr8:93757018 | A | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+1152A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757018 | |||||||
| chr8:93757090 | T | TATAA | 26 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(23): Show |
29 | HG00673.hp2 HG01070.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.312+1263_312+1266d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757090 | ||||||
| chr8:93757090 | TATAA | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
104 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.312+1263_312+1266d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757090 | ||||||
| chr8:93757090 | TATAAATA others(1): Show |
T | 86 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0056 others(83): Show |
92 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.312+1259_312+1266d others(10): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757090 | ||||||
| chr8:93757090 | TATAAATA others(5): Show |
T | 1 | a0001c0001t0001g0251 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.312+1255_312+1266d others(14): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757090 | ||||||
| chr8:93757239 | C | G | 17 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.313-1244C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757239 | |||||||
| chr8:93757251 | C | T | 1 | a0001c0003t0001g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.313-1232C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757251 | |||||||
| chr8:93757320 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.313-1163T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757320 | |||||||
| chr8:93757478 | A | G | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-1005A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757478 | |||||||
| chr8:93757635 | C | CA | 15 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0044 others(12): Show |
15 | HG00597.hp2 HG00741.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.313-835dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757635 | ||||||
| chr8:93757647 | A | G | 1 | a0002c0002t0001g0009 | 2 | HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.313-836A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757647 | |||||||
| chr8:93757766 | AT | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.313-703delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757766 | ||||||
| chr8:93758021 | G | T | 2 | a0001c0001t0002g0007 a0001c0001t0002g0029 |
3 | HG01261.hp2 HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.313-462G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93758021 | |||||||
| chr8:93758067 | G | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.313-416G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93758067 | |||||||
| chr8:93758147 | TTTGTG | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
5 | HG00140.hp1 HG01192.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-323_313-319del others(5): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93758147 | ||||||
| chr8:93758387 | C | G | 14 | a0002c0002t0001g0017 a0002c0002t0001g0021 a0002c0002t0001g0054 others(11): Show |
16 | HG01081.hp1 HG01106.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.313-96C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93758387 | |||||||
| chr8:93758933 | A | AT | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+359dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93758933 | ||||||
| chr8:93758937 | A | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+361A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93758937 | |||||||
| chr8:93758964 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+388G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93758964 | |||||||
| chr8:93759091 | G | C | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.406+515G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759091 | |||||||
| chr8:93759152 | T | G | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.406+576T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759152 | |||||||
| chr8:93759302 | T | TA | 67 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
77 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.406+737dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759302 | ||||||
| chr8:93759465 | G | GA | 31 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(28): Show |
34 | HG00597.hp1 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.406+908dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759465 | ||||||
| chr8:93759619 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.406+1043C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759619 | |||||||
| chr8:93759646 | T | A | 1 | a0001c0001t0001g0026 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.406+1070T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759646 | |||||||
| chr8:93759653 | G | GT | 12 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(9): Show |
13 | HG02145.hp2 HG02922.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.406+1090dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759653 | ||||||
| chr8:93759653 | GT | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0144 a0001c0001t0001g0146 others(4): Show |
8 | HG01981.hp1 HG02148.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.406+1090delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759653 | ||||||
| chr8:93759710 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.406+1134G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759710 | |||||||
| chr8:93759920 | A | AT | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1345dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759920 | ||||||
| chr8:93759937 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(12): Show |
19 | HG00140.hp2 HG01081.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.406+1361C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759937 | |||||||
| chr8:93759955 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1379G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759955 | |||||||
| chr8:93759978 | A | ATAAT | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1404_406+1407d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759978 | ||||||
| chr8:93760039 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.406+1463G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760039 | |||||||
| chr8:93760049 | T | G | 4 | a0001c0001t0001g0199 a0001c0001t0001g0205 a0001c0003t0001g0204 others(1): Show |
4 | HG04184.hp1 NA18974.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+1473T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760049 | |||||||
| chr8:93760149 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
99 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.406+1573G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760149 | |||||||
| chr8:93760281 | C | T | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.406+1705C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760281 | |||||||
| chr8:93760359 | A | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1783A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760359 | |||||||
| chr8:93760677 | C | CA | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
120 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.406+2111dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93760677 | ||||||
| chr8:93760810 | G | A | 1 | a0002c0002t0001g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.406+2234G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760810 | |||||||
| chr8:93761046 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
99 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.406+2470C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761046 | |||||||
| chr8:93761107 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.406+2531C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761107 | |||||||
| chr8:93761121 | C | A | 1 | a0001c0001t0001g0151 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.406+2545C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761121 | |||||||
| chr8:93761156 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
126 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.406+2580T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761156 | |||||||
| chr8:93761235 | G | A | 1 | a0002c0002t0001g0103 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.407-2607G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761235 | |||||||
| chr8:93761359 | G | A | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.407-2483G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761359 | |||||||
| chr8:93761562 | G | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0040 |
2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.407-2280G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761562 | |||||||
| chr8:93761723 | T | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-2119T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761723 | |||||||
| chr8:93761750 | A | G | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.407-2092A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761750 | |||||||
| chr8:93761974 | G | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0248 others(3): Show |
7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.407-1868G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761974 | |||||||
| chr8:93761993 | G | A | 6 | a0001c0001t0001g0077 a0002c0002t0001g0078 a0002c0002t0001g0079 others(3): Show |
6 | NA18967.hp2 NA18982.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-1849G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761993 | |||||||
| chr8:93762021 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.407-1821G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762021 | |||||||
| chr8:93762041 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.407-1801G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762041 | |||||||
| chr8:93762052 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.407-1790C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762052 | |||||||
| chr8:93762184 | A | G | 24 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(21): Show |
27 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.407-1658A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762184 | |||||||
| chr8:93762210 | C | T | 75 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0042 others(72): Show |
78 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.407-1632C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762210 | |||||||
| chr8:93762218 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
208 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.407-1624T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762218 | |||||||
| chr8:93762268 | A | G | 1 | a0002c0002t0001g0273 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.407-1574A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762268 | |||||||
| chr8:93762340 | CT | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-1489delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93762340 | ||||||
| chr8:93762365 | AT | A | 26 | a0001c0001t0001g0095 a0001c0001t0002g0006 a0001c0001t0002g0007 others(23): Show |
30 | HG01081.hp1 HG01106.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.407-1466delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93762365 | ||||||
| chr8:93762386 | G | T | 1 | a0002c0002t0001g0087 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.407-1456G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762386 | |||||||
| chr8:93762388 | G | T | 1 | a0002c0002t0001g0087 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.407-1454G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762388 | |||||||
| chr8:93762827 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.407-1015G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762827 | |||||||
| chr8:93762829 | A | G | 1 | a0002c0002t0001g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.407-1013A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762829 | |||||||
| chr8:93762947 | CAG | C | 18 | a0001c0001t0001g0077 a0001c0001t0001g0128 a0002c0002t0001g0009 others(15): Show |
19 | HG00673.hp2 HG01099.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.407-894_407-893del others(2): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762947 | |||||||
| chr8:93763096 | AT | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.407-733delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93763096 | ||||||
| chr8:93763109 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.407-733T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93763109 | |||||||
| chr8:93763570 | C | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-272C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93763570 | |||||||
| chr8:93763636 | T | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(3): Show |
6 | HG02970.hp2 HG03453.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.407-206T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93763636 | |||||||
| chr8:93763959 | G | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0071 |
2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.506+18G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | chr8 | 93763959 | |||||||
| chr8:93763989 | G | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.506+48G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | chr8 | 93763989 | |||||||
| chr8:93764497 | G | T | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.506+556G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | chr8 | 93764497 | |||||||
| chr8:93764501 | A | AACAC | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(5): Show |
9 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.506+581_506+584dup others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 93764501 | ||||||
| chr8:93764501 | AAC | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
269 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.506+583_506+584del others(2): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 93764501 | ||||||
| chr8:93764754 | T | G | 1 | a0002c0002t0009g0126 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.507-652T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | chr8 | 93764754 | |||||||
| chr8:93765387 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.507-19T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | chr8 | 93765387 | |||||||
| chr8:93765774 | A | G | 3 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0284 |
3 | HG00597.hp2 NA18949.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.651+128A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93765774 | |||||||
| chr8:93765779 | CATT | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0109 others(3): Show |
6 | NA18948.hp1 NA18961.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+135_651+137del others(3): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93765779 | ||||||
| chr8:93765827 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.651+181C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93765827 | |||||||
| chr8:93765955 | G | A | 10 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(7): Show |
10 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.651+309G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93765955 | |||||||
| chr8:93765963 | A | G | 1 | a0002c0002t0001g0125 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.651+317A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93765963 | |||||||
| chr8:93766016 | T | C | 1 | a0001c0001t0006g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.651+370T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766016 | |||||||
| chr8:93766021 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.651+375T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766021 | |||||||
| chr8:93766126 | T | A | 3 | a0001c0001t0001g0134 a0001c0004t0001g0010 a0001c0004t0001g0133 |
4 | HG01167.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+480T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766126 | |||||||
| chr8:93766149 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.651+503A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766149 | |||||||
| chr8:93766204 | A | G | 1 | a0002c0002t0005g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.651+558A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766204 | |||||||
| chr8:93766226 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.651+580C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766226 | |||||||
| chr8:93766265 | C | T | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.651+619C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766265 | |||||||
| chr8:93766343 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.651+697C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766343 | |||||||
| chr8:93766367 | G | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.651+721G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766367 | |||||||
| chr8:93766385 | T | G | 12 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(9): Show |
12 | HG01070.hp2 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.651+739T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766385 | |||||||
| chr8:93767087 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.651+1441C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767087 | |||||||
| chr8:93767547 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.651+1901G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767547 | |||||||
| chr8:93767722 | G | A | 67 | a0001c0001t0001g0020 a0001c0001t0001g0056 a0001c0001t0001g0088 others(64): Show |
69 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.651+2076G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767722 | |||||||
| chr8:93767724 | GA | G | 11 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.651+2079delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767724 | |||||||
| chr8:93767725 | A | AT | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
171 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.651+2095dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93767725 | ||||||
| chr8:93767725 | A | ATT | 7 | a0001c0001t0001g0018 a0001c0001t0001g0068 a0001c0001t0001g0070 others(4): Show |
8 | HG00597.hp1 HG01192.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.651+2094_651+2095d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93767725 | ||||||
| chr8:93767725 | A | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0248 others(3): Show |
7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.651+2079A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767725 | |||||||
| chr8:93767725 | AT | A | 12 | a0001c0001t0001g0077 a0002c0002t0001g0009 a0002c0002t0001g0078 others(9): Show |
13 | HG00673.hp2 HG01952.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.651+2095delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93767725 | ||||||
| chr8:93767777 | T | C | 1 | a0002c0002t0001g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.651+2131T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767777 | |||||||
| chr8:93767863 | CT | C | 9 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+2236delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93767863 | ||||||
| chr8:93767863 | CTT | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
207 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.651+2235_651+2236d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93767863 | ||||||
| chr8:93767870 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.651+2224T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767870 | |||||||
| chr8:93767882 | T | G | 1 | a0001c0001t0001g0142 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.651+2236T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767882 | |||||||
| chr8:93767983 | C | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+2337C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767983 | |||||||
| chr8:93768238 | C | T | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(6): Show |
10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.651+2592C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768238 | |||||||
| chr8:93768279 | TACAC | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
147 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.651+2641_651+2644d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93768279 | ||||||
| chr8:93768315 | T | C | 1 | a0005c0010t0002g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.651+2669T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768315 | |||||||
| chr8:93768491 | A | AT | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+2845_651+2846i others(3): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768491 | |||||||
| chr8:93768612 | A | AAAAATAA others(3): Show |
1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.651+2978_651+2987d others(12): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93768612 | ||||||
| chr8:93768798 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.651+3152C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768798 | |||||||
| chr8:93768947 | A | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG01070.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+3301A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768947 | |||||||
| chr8:93768994 | C | T | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(6): Show |
10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.651+3348C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768994 | |||||||
| chr8:93768995 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.651+3349G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768995 | |||||||
| chr8:93769160 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.652-3429G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769160 | |||||||
| chr8:93769186 | G | T | 1 | a0002c0002t0001g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.652-3403G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769186 | |||||||
| chr8:93769214 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0071 |
2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.652-3375A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769214 | |||||||
| chr8:93769249 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0175 a0001c0001t0001g0178 |
3 | NA18950.hp1 NA18955.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.652-3340C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769249 | |||||||
| chr8:93769334 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.652-3255G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769334 | |||||||
| chr8:93769439 | T | C | 1 | a0002c0002t0001g0187 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.652-3150T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769439 | |||||||
| chr8:93769459 | C | T | 13 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(10): Show |
14 | HG01884.hp2 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.652-3130C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769459 | |||||||
| chr8:93769519 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.652-3070C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769519 | |||||||
| chr8:93769752 | G | A | 19 | a0002c0002t0001g0017 a0002c0002t0001g0021 a0002c0002t0001g0037 others(16): Show |
21 | HG01081.hp1 HG01106.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.652-2837G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769752 | |||||||
| chr8:93769812 | T | G | 1 | a0002c0002t0001g0113 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.652-2777T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769812 | |||||||
| chr8:93769949 | A | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0248 others(3): Show |
7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-2640A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769949 | |||||||
| chr8:93770051 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.652-2538C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770051 | |||||||
| chr8:93770222 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.652-2367A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770222 | |||||||
| chr8:93770239 | C | T | 2 | a0002c0002t0001g0139 a0002c0002t0001g0194 |
2 | HG02451.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.652-2350C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770239 | |||||||
| chr8:93770423 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.652-2166A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770423 | |||||||
| chr8:93770503 | G | A | 67 | a0001c0001t0001g0020 a0001c0001t0001g0056 a0001c0001t0001g0088 others(64): Show |
69 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.652-2086G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770503 | |||||||
| chr8:93770740 | C | T | 1 | a0001c0003t0001g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.652-1849C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770740 | |||||||
| chr8:93771013 | C | CA | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-1561dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93771013 | ||||||
| chr8:93771013 | CA | C | 19 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(16): Show |
20 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.652-1561delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93771013 | ||||||
| chr8:93771118 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.652-1471T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771118 | |||||||
| chr8:93771249 | C | CT | 7 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0002g0006 others(4): Show |
9 | HG01074.hp1 HG01106.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.652-1328dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93771249 | ||||||
| chr8:93771261 | T | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0057 a0001c0001t0001g0107 others(2): Show |
5 | HG02630.hp1 HG02976.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-1328T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771261 | |||||||
| chr8:93771262 | A | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.652-1327A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771262 | |||||||
| chr8:93771293 | T | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.652-1296T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771293 | |||||||
| chr8:93771773 | AG | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0239 a0001c0001t0001g0240 others(3): Show |
7 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-815delG | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771773 | |||||||
| chr8:93771902 | G | A | 2 | a0001c0001t0003g0008 a0001c0001t0003g0185 |
3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.652-687G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771902 | |||||||
| chr8:93771944 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.652-645G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771944 | |||||||
| chr8:93772038 | C | CTG | 3 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0284 |
3 | HG00597.hp2 NA18949.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.652-549_652-548dup others(2): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93772038 | ||||||
| chr8:93772401 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.652-188A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93772401 | |||||||
| chr8:93772669 | A | T | 1 | a0001c0001t0006g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.714+18A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93772669 | |||||||
| chr8:93773066 | G | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+415G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93773066 | |||||||
| chr8:93773324 | G | A | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG00140.hp2 HG02258.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+673G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93773324 | |||||||
| chr8:93773341 | C | T | 24 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(21): Show |
27 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.714+690C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93773341 | |||||||
| chr8:93773744 | T | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+1093T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93773744 | |||||||
| chr8:93773991 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.714+1340T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93773991 | |||||||
| chr8:93774025 | AT | A | 7 | a0001c0001t0001g0248 a0001c0001t0002g0006 a0001c0001t0002g0007 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+1387delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr8 | 93774025 | ||||||
| chr8:93774100 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.714+1449C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774100 | |||||||
| chr8:93774281 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0248 others(3): Show |
7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+1630C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774281 | |||||||
| chr8:93774293 | G | T | 1 | a0001c0003t0001g0206 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.714+1642G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774293 | |||||||
| chr8:93774500 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.714+1849A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774500 | |||||||
| chr8:93774551 | C | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG01884.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.714+1900C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774551 | |||||||
| chr8:93774573 | C | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+1922C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774573 | |||||||
| chr8:93774661 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.714+2010A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774661 | |||||||
| chr8:93774773 | G | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG01884.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+2122G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774773 | |||||||
| chr8:93774810 | C | T | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.714+2159C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774810 | |||||||
| chr8:93775056 | G | C | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.714+2405G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775056 | |||||||
| chr8:93775111 | T | C | 1 | a0002c0002t0001g0085 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.714+2460T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775111 | |||||||
| chr8:93775120 | T | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0092 |
4 | HG01884.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+2469T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775120 | |||||||
| chr8:93775445 | G | A | 3 | a0001c0001t0001g0128 a0002c0002t0001g0098 a0002c0002t0001g0127 |
3 | HG01981.hp2 NA18969.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.714+2794G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775445 | |||||||
| chr8:93775612 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.714+2961C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775612 | |||||||
| chr8:93775785 | A | T | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.714+3134A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775785 | |||||||
| chr8:93775834 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.714+3183A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775834 | |||||||
| chr8:93775840 | T | G | 1 | a0001c0003t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.714+3189T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775840 | |||||||
| chr8:93776238 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
167 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.714+3587A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776238 | |||||||
| chr8:93776265 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.714+3614G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776265 | |||||||
| chr8:93776537 | G | A | 1 | a0002c0002t0001g0268 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.714+3886G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776537 | |||||||
| chr8:93776610 | T | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+3959T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776610 | |||||||
| chr8:93776716 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0092 |
4 | HG01884.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-3877T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776716 | |||||||
| chr8:93776726 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.715-3867T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776726 | |||||||
| chr8:93776727 | T | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.715-3866T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776727 | |||||||
| chr8:93776824 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.715-3769G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776824 | |||||||
| chr8:93776960 | G | A | 2 | a0002c0002t0001g0286 a0002c0002t0001g0287 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.715-3633G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776960 | |||||||
| chr8:93777003 | C | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-3590C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777003 | |||||||
| chr8:93777233 | C | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
167 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.715-3360C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777233 | |||||||
| chr8:93777453 | G | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
167 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.715-3140G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777453 | |||||||
| chr8:93777481 | T | C | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-3112T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777481 | |||||||
| chr8:93777486 | A | C | 1 | a0002c0002t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.715-3107A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777486 | |||||||
| chr8:93777687 | T | A | 17 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.715-2906T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777687 | |||||||
| chr8:93777729 | C | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-2864C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777729 | |||||||
| chr8:93777799 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.715-2794C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777799 | |||||||
| chr8:93777847 | G | A | 3 | a0001c0001t0001g0128 a0002c0002t0001g0098 a0002c0002t0001g0127 |
3 | HG01981.hp2 NA18969.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.715-2746G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777847 | |||||||
| chr8:93777872 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.715-2721T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777872 | |||||||
| chr8:93777972 | T | A | 3 | a0002c0002t0001g0072 a0002c0002t0001g0114 a0002c0002t0001g0129 |
3 | HG00733.hp1 HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.715-2621T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777972 | |||||||
| chr8:93777995 | T | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | NA18972.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.715-2598T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777995 | |||||||
| chr8:93778039 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.715-2554G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778039 | |||||||
| chr8:93778182 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(1): Show |
7 | HG01255.hp1 HG01358.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-2411T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778182 | |||||||
| chr8:93778236 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0036 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.715-2357C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778236 | |||||||
| chr8:93778241 | G | A | 1 | a0001c0003t0001g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.715-2352G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778241 | |||||||
| chr8:93778309 | T | G | 2 | a0002c0002t0001g0037 a0002c0002t0001g0049 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.715-2284T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778309 | |||||||
| chr8:93778450 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.715-2143T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778450 | |||||||
| chr8:93778522 | C | G | 3 | a0002c0002t0001g0072 a0002c0002t0001g0114 a0002c0002t0001g0129 |
3 | HG00733.hp1 HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.715-2071C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778522 | |||||||
| chr8:93778556 | T | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-2037T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778556 | |||||||
| chr8:93778644 | C | G | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1949C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778644 | |||||||
| chr8:93778644 | C | T | 2 | a0002c0002t0001g0112 a0002c0002t0001g0124 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.715-1949C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778644 | |||||||
| chr8:93778945 | G | T | 1 | a0001c0001t0002g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.715-1648G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778945 | |||||||
| chr8:93779038 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0070 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.715-1555A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779038 | |||||||
| chr8:93779168 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-1425C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779168 | |||||||
| chr8:93779191 | T | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.715-1402T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779191 | |||||||
| chr8:93779192 | C | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.715-1401C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779192 | |||||||
| chr8:93779287 | C | T | 2 | a0002c0002t0001g0110 a0007c0012t0001g0108 |
2 | NA18948.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.715-1306C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779287 | |||||||
| chr8:93779403 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.715-1190T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779403 | |||||||
| chr8:93779426 | G | A | 6 | a0002c0002t0001g0024 a0002c0002t0001g0058 a0002c0002t0001g0256 others(3): Show |
6 | NA18977.hp2 NA18984.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-1167G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779426 | |||||||
| chr8:93779544 | G | A | 1 | a0002c0002t0001g0115 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.715-1049G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779544 | |||||||
| chr8:93780046 | C | G | 27 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0101 others(24): Show |
27 | HG00408.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.715-547C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780046 | |||||||
| chr8:93780046 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.715-547C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780046 | |||||||
| chr8:93780162 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0040 |
2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.715-431G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780162 | |||||||
| chr8:93780173 | C | T | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-420C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780173 | |||||||
| chr8:93780475 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.715-118G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780475 | |||||||
| chr8:93780535 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.715-58A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780535 | |||||||
| chr8:93780548 | CTGTTCAG others(5): Show |
C | 1 | a0001c0001t0001g0153 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.715-40_715-29delCA others(10): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr8 | 93780548 | ||||||
| chr8:93780844 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0002g0065 |
3 | HG03195.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.870-30C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 8/27 | chr8 | 93780844 | |||||||
| chr8:93780845 | A | G | 7 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0057 others(4): Show |
7 | HG01070.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-29A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 8/27 | chr8 | 93780845 | |||||||
| chr8:93781193 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.978+211A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781193 | |||||||
| chr8:93781378 | T | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(6): Show |
10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.979-280T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781378 | |||||||
| chr8:93781426 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.979-232A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781426 | |||||||
| chr8:93781494 | T | C | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.979-164T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781494 | |||||||
| chr8:93781498 | GT | G | 17 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.979-159delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781498 | |||||||
| chr8:93781551 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG01070.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.979-107A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781551 | |||||||
| chr8:93781826 | G | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0027 |
6 | HG01255.hp1 HG01358.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065+82G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93781826 | |||||||
| chr8:93781895 | TTTTG | T | 2 | a0001c0001t0003g0008 a0001c0001t0003g0185 |
3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1065+175_1065+178d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr8 | 93781895 | ||||||
| chr8:93781926 | C | CT | 15 | a0002c0002t0001g0017 a0002c0002t0001g0021 a0002c0002t0001g0054 others(12): Show |
17 | HG01081.hp1 HG01106.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1065+192dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr8 | 93781926 | ||||||
| chr8:93781926 | C | T | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1065+182C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93781926 | |||||||
| chr8:93781926 | CT | C | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065+192delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr8 | 93781926 | ||||||
| chr8:93781927 | T | C | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1065+183T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93781927 | |||||||
| chr8:93782005 | G | A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01070.hp2 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1065+261G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782005 | |||||||
| chr8:93782047 | G | T | 1 | a0007c0012t0001g0108 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1065+303G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782047 | |||||||
| chr8:93782070 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1066-325C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782070 | |||||||
| chr8:93782221 | A | T | 1 | a0008c0007t0001g0214 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1066-174A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782221 | |||||||
| chr8:93782368 | T | A | 1 | a0007c0012t0001g0108 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1066-27T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782368 | |||||||
| chr8:93782392 | C | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
splice_region_variant&intron_variant | LOW | c.1066-3C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782392 | |||||||
| chr8:93782561 | T | G | 1 | a0007c0012t0001g0108 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1131+101T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782561 | |||||||
| chr8:93782571 | G | GT | 11 | a0001c0001t0001g0031 a0001c0001t0001g0154 a0001c0003t0001g0182 others(8): Show |
12 | HG01081.hp1 HG01109.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131+130dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr8 | 93782571 | ||||||
| chr8:93782571 | GT | G | 12 | a0001c0001t0001g0027 a0001c0001t0001g0147 a0001c0001t0001g0230 others(9): Show |
14 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1131+130delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr8 | 93782571 | ||||||
| chr8:93782577 | T | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1131+117T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782577 | |||||||
| chr8:93782730 | C | G | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1131+270C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782730 | |||||||
| chr8:93782834 | C | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1131+374C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782834 | |||||||
| chr8:93782835 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0004c0005t0010g0066 |
3 | HG00738.hp1 HG01099.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1131+375G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782835 | |||||||
| chr8:93782864 | C | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1131+404C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782864 | |||||||
| chr8:93782875 | G | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131+415G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782875 | |||||||
| chr8:93782908 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1131+448T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782908 | |||||||
| chr8:93783196 | C | T | 4 | a0001c0001t0001g0128 a0002c0002t0001g0098 a0002c0002t0001g0127 others(1): Show |
4 | HG01981.hp2 HG04115.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1131+736C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783196 | |||||||
| chr8:93783282 | G | A | 1 | a0002c0002t0001g0252 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1131+822G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783282 | |||||||
| chr8:93783288 | G | A | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1131+828G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783288 | |||||||
| chr8:93783451 | C | T | 1 | a0001c0001t0006g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1131+991C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783451 | |||||||
| chr8:93783496 | T | G | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | NA18968.hp2 NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1131+1036T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783496 | |||||||
| chr8:93783817 | A | AG | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1131+1357_1131+135 others(5): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783817 | |||||||
| chr8:93783831 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1131+1371T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783831 | |||||||
| chr8:93783893 | G | T | 1 | a0001c0001t0001g0278 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1132-1329G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783893 | |||||||
| chr8:93784029 | C | A | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1132-1193C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784029 | |||||||
| chr8:93784376 | G | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1132-846G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784376 | |||||||
| chr8:93784421 | G | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG01884.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132-801G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784421 | |||||||
| chr8:93784498 | A | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1132-724A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784498 | |||||||
| chr8:93784584 | C | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0277 |
2 | HG00408.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1132-638C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784584 | |||||||
| chr8:93784745 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1132-477A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784745 | |||||||
| chr8:93784860 | G | T | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1132-362G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784860 | |||||||
| chr8:93785424 | C | T | 24 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(21): Show |
27 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1288+46C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 12/27 | chr8 | 93785424 | |||||||
| chr8:93785660 | G | A | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1288+282G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 12/27 | chr8 | 93785660 | |||||||
| chr8:93785744 | G | A | 2 | a0002c0002t0001g0078 a0002c0002t0001g0266 |
2 | NA18967.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1288+366G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 12/27 | chr8 | 93785744 | |||||||
| chr8:93785801 | C | T | 17 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1289-422C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 12/27 | chr8 | 93785801 | |||||||
| chr8:93785811 | C | T | 1 | a0002c0002t0001g0170 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1289-412C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 12/27 | chr8 | 93785811 | |||||||
| chr8:93786456 | G | A | 1 | a0005c0010t0002g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1412+110G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93786456 | |||||||
| chr8:93786547 | G | A | 12 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(9): Show |
12 | HG01070.hp2 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1412+201G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93786547 | |||||||
| chr8:93786637 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1412+291G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93786637 | |||||||
| chr8:93787197 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG01070.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1413-647G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93787197 | |||||||
| chr8:93787301 | T | A | 1 | a0001c0003t0001g0219 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1413-543T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93787301 | |||||||
| chr8:93787409 | G | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0092 |
4 | HG01884.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413-435G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93787409 | |||||||
| chr8:93787625 | A | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0229 |
2 | NA18954.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1413-219A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93787625 | |||||||
| chr8:93787967 | T | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1518+18T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93787967 | |||||||
| chr8:93788031 | G | A | 2 | a0002c0002t0001g0112 a0002c0002t0001g0124 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1518+82G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788031 | |||||||
| chr8:93788033 | CT | C | 8 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(5): Show |
10 | HG01261.hp2 HG01515.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1518+98delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr8 | 93788033 | ||||||
| chr8:93788219 | T | C | 1 | a0001c0001t0006g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1518+270T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788219 | |||||||
| chr8:93788423 | C | T | 1 | a0002c0002t0001g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1518+474C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788423 | |||||||
| chr8:93788495 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0040 |
2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1518+546G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788495 | |||||||
| chr8:93788649 | A | C | 2 | a0002c0002t0001g0192 a0002c0002t0001g0193 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1518+700A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788649 | |||||||
| chr8:93788890 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1518+941A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788890 | |||||||
| chr8:93788941 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1518+992G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788941 | |||||||
| chr8:93788984 | T | C | 14 | a0002c0002t0001g0017 a0002c0002t0001g0021 a0002c0002t0001g0054 others(11): Show |
16 | HG01081.hp1 HG01106.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1518+1035T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788984 | |||||||
| chr8:93789094 | T | C | 1 | a0002c0002t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1518+1145T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789094 | |||||||
| chr8:93789098 | T | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0248 others(3): Show |
7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1518+1149T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789098 | |||||||
| chr8:93789130 | A | G | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01934.hp2 HG01952.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1518+1181A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789130 | |||||||
| chr8:93789281 | C | T | 1 | a0002c0002t0001g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1518+1332C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789281 | |||||||
| chr8:93789497 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1518+1548C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789497 | |||||||
| chr8:93789523 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1518+1574T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789523 | |||||||
| chr8:93789651 | AAT | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0035 others(17): Show |
21 | HG00738.hp2 HG01070.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1519-1593_1519-159 others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr8 | 93789651 | ||||||
| chr8:93789653 | T | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
191 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1519-1610T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789653 | |||||||
| chr8:93789655 | T | A | 28 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0030 others(25): Show |
32 | HG01070.hp2 HG01261.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.1519-1608T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789655 | |||||||
| chr8:93789667 | TA | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
200 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1519-1595delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789667 | |||||||
| chr8:93789668 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1519-1595A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789668 | |||||||
| chr8:93789669 | TA | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(41): Show |
49 | HG00140.hp1 HG01192.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.1519-1593delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789669 | |||||||
| chr8:93789670 | A | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(205): Show |
228 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1519-1593A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789670 | |||||||
| chr8:93789670 | AT | A | 10 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0076 others(7): Show |
13 | HG01261.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1519-1583delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr8 | 93789670 | ||||||
| chr8:93789672 | T | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0249 |
3 | HG02717.hp1 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1519-1591T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789672 | |||||||
| chr8:93789691 | A | C | 1 | a0001c0001t0001g0018 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1519-1572A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789691 | |||||||
| chr8:93789790 | G | T | 1 | a0002c0002t0008g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1519-1473G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789790 | |||||||
| chr8:93789797 | G | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519-1466G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789797 | |||||||
| chr8:93789804 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1519-1459C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789804 | |||||||
| chr8:93789947 | A | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1519-1316A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789947 | |||||||
| chr8:93790070 | GA | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1519-1182delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr8 | 93790070 | ||||||
| chr8:93790076 | A | G | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1519-1187A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790076 | |||||||
| chr8:93790084 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1519-1179C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790084 | |||||||
| chr8:93790140 | T | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0036 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1519-1123T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790140 | |||||||
| chr8:93790318 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1519-945C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790318 | |||||||
| chr8:93790572 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1519-691A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790572 | |||||||
| chr8:93790575 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1519-688A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790575 | |||||||
| chr8:93790645 | T | C | 1 | a0002c0002t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1519-618T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790645 | |||||||
| chr8:93790697 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1519-566C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790697 | |||||||
| chr8:93790801 | C | T | 4 | a0001c0001t0001g0202 a0001c0001t0001g0213 a0001c0001t0001g0278 others(1): Show |
4 | HG00597.hp1 NA18946.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519-462C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790801 | |||||||
| chr8:93791372 | G | A | 24 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(21): Show |
27 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1575+53G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93791372 | |||||||
| chr8:93791387 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1575+68A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93791387 | |||||||
| chr8:93791669 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1575+350G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93791669 | |||||||
| chr8:93791829 | C | T | 1 | a0002c0002t0001g0021 | 2 | HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1575+510C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93791829 | |||||||
| chr8:93791939 | G | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1575+620G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93791939 | |||||||
| chr8:93792050 | T | G | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1575+731T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792050 | |||||||
| chr8:93792101 | A | T | 17 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1575+782A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792101 | |||||||
| chr8:93792120 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG01070.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+801C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792120 | |||||||
| chr8:93792313 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1576-885G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792313 | |||||||
| chr8:93792388 | G | T | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1576-810G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792388 | |||||||
| chr8:93792478 | A | G | 2 | a0002c0002t0001g0264 a0002c0002t0001g0284 |
2 | NA18949.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1576-720A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792478 | |||||||
| chr8:93792562 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1576-636C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792562 | |||||||
| chr8:93792599 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1576-599A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792599 | |||||||
| chr8:93792691 | A | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-507A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792691 | |||||||
| chr8:93792773 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1576-425C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792773 | |||||||
| chr8:93792773 | CT | C | 14 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0041 others(11): Show |
15 | HG01516.hp1 HG02280.hp1 HG02922.hp2 others(12): Show |
intron_variant | MODIFIER | c.1576-410delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr8 | 93792773 | ||||||
| chr8:93792831 | C | T | 2 | a0002c0002t0001g0037 a0002c0002t0001g0049 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1576-367C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792831 | |||||||
| chr8:93792962 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1576-236C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792962 | |||||||
| chr8:93792973 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1576-225G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792973 | |||||||
| chr8:93792974 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1576-224T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792974 | |||||||
| chr8:93792984 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1576-214G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792984 | |||||||
| chr8:93792985 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1576-213A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792985 | |||||||
| chr8:93793017 | T | C | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
311 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1576-181T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93793017 | |||||||
| chr8:93793023 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1576-175G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93793023 | |||||||
| chr8:93793114 | G | T | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1576-84G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93793114 | |||||||
| chr8:93793326 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1674+30T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93793326 | |||||||
| chr8:93793390 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1674+94G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93793390 | |||||||
| chr8:93793421 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1674+125G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93793421 | |||||||
| chr8:93793886 | T | G | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1674+590T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93793886 | |||||||
| chr8:93794036 | C | T | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+740C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794036 | |||||||
| chr8:93794097 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1674+801G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794097 | |||||||
| chr8:93794166 | A | G | 10 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(7): Show |
10 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1674+870A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794166 | |||||||
| chr8:93794427 | G | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1675-982G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794427 | |||||||
| chr8:93794530 | G | T | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1675-879G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794530 | |||||||
| chr8:93794629 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1675-780G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794629 | |||||||
| chr8:93794667 | G | C | 1 | a0001c0001t0001g0212 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1675-742G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794667 | |||||||
| chr8:93794728 | T | C | 17 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(14): Show |
19 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1675-681T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794728 | |||||||
| chr8:93795021 | C | T | 1 | a0002c0002t0001g0287 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1675-388C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93795021 | |||||||
| chr8:93795023 | A | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1675-386A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93795023 | |||||||
| chr8:93795212 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG01884.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1675-197G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93795212 | |||||||
| chr8:93795517 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1773+10T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | chr8 | 93795517 | |||||||
| chr8:93795583 | T | C | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1773+76T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | chr8 | 93795583 | |||||||
| chr8:93795768 | G | T | 1 | a0001c0001t0001g0262 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1774-133G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | chr8 | 93795768 | |||||||
| chr8:93795811 | C | CA | 12 | a0001c0001t0001g0064 a0001c0001t0001g0134 a0001c0001t0001g0259 others(9): Show |
13 | HG01167.hp1 HG01167.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1774-81dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr8 | 93795811 | ||||||
| chr8:93795828 | G | A | 4 | a0002c0002t0001g0054 a0002c0002t0001g0188 a0002c0002t0001g0189 others(1): Show |
4 | HG02738.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1774-73G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | chr8 | 93795828 | |||||||
| chr8:93795856 | A | C | 2 | a0001c0001t0002g0007 a0004c0005t0010g0066 |
3 | HG01261.hp2 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1774-45A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | chr8 | 93795856 | |||||||
| chr8:93796339 | G | A | 2 | a0001c0001t0002g0065 a0004c0005t0010g0066 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1860+352G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796339 | |||||||
| chr8:93796340 | A | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0248 others(3): Show |
7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1860+353A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796340 | |||||||
| chr8:93796405 | T | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1860+418T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796405 | |||||||
| chr8:93796500 | T | C | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1860+513T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796500 | |||||||
| chr8:93796589 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1861-545G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796589 | |||||||
| chr8:93796627 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1861-507G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796627 | |||||||
| chr8:93796658 | C | T | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1861-476C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796658 | |||||||
| chr8:93796720 | G | A | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1861-414G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796720 | |||||||
| chr8:93796957 | C | T | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(6): Show |
10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1861-177C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796957 | |||||||
| chr8:93797067 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1861-67A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93797067 | |||||||
| chr8:93797652 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2100+182T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93797652 | |||||||
| chr8:93797708 | A | G | 6 | a0001c0001t0001g0099 a0002c0002t0001g0102 a0002c0002t0001g0113 others(3): Show |
6 | HG00738.hp2 HG00741.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2100+238A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93797708 | |||||||
| chr8:93797865 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2100+395C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93797865 | |||||||
| chr8:93798282 | CTA | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0070 |
3 | HG01070.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2100+814_2100+815d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798282 | ||||||
| chr8:93798942 | A | AGT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
98 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.2101-635_2101-634d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | ||||||
| chr8:93798942 | A | AGTGT | 26 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0048 others(23): Show |
27 | HG01070.hp2 HG01243.hp2 HG02293.hp2 others(24): Show |
intron_variant | MODIFIER | c.2101-637_2101-634d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | ||||||
| chr8:93798942 | A | AGTGTGT | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0057 others(9): Show |
12 | HG01243.hp1 HG01261.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2101-639_2101-634d others(8): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | ||||||
| chr8:93798942 | A | AGTGTGTG others(1): Show |
7 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0061 others(4): Show |
7 | HG02717.hp1 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2101-641_2101-634d others(10): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | ||||||
| chr8:93798942 | A | AGTGTGTG others(3): Show |
3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0216 |
3 | HG01884.hp2 HG01978.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2101-643_2101-634d others(12): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | ||||||
| chr8:93798942 | AGT | A | 48 | a0001c0001t0001g0015 a0001c0001t0001g0099 a0001c0001t0001g0104 others(45): Show |
53 | HG00558.hp2 HG00738.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.2101-635_2101-634d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | ||||||
| chr8:93798942 | AGTGT | A | 18 | a0001c0001t0001g0071 a0001c0001t0001g0109 a0001c0001t0002g0007 others(15): Show |
18 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2101-637_2101-634d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | ||||||
| chr8:93798942 | AGTGTGT | A | 28 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(25): Show |
31 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.2101-639_2101-634d others(8): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | ||||||
| chr8:93798942 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0156 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2101-643_2101-634d others(12): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | ||||||
| chr8:93798942 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0001g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2101-645_2101-634d others(14): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | ||||||
| chr8:93798983 | GT | G | 3 | a0001c0001t0001g0077 a0002c0002t0001g0081 a0002c0002t0001g0084 |
3 | HG02004.hp1 NA19001.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2101-632delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798983 | ||||||
| chr8:93798984 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0031 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2101-634_2101-633i others(13): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93798984 | |||||||
| chr8:93799070 | C | A | 1 | a0005c0010t0002g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2101-548C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93799070 | |||||||
| chr8:93799425 | A | C | 12 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(9): Show |
12 | HG01070.hp2 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2101-193A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93799425 | |||||||
| chr8:93799452 | T | C | 43 | a0001c0001t0001g0050 a0001c0001t0001g0099 a0001c0001t0001g0104 others(40): Show |
49 | HG00558.hp2 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2101-166T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93799452 | |||||||
| chr8:93799870 | A | G | 1 | a0002c0002t0001g0103 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2241+112A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93799870 | |||||||
| chr8:93799904 | C | CTT | 8 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0052 others(5): Show |
9 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2241+166_2241+167d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93799904 | ||||||
| chr8:93799904 | CT | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
190 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.2241+167delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93799904 | ||||||
| chr8:93799904 | CTTT | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2241+165_2241+167d others(5): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93799904 | ||||||
| chr8:93800421 | G | A | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2241+663G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800421 | |||||||
| chr8:93800431 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0036 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2241+673G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800431 | |||||||
| chr8:93800508 | A | G | 2 | a0002c0002t0001g0125 a0007c0012t0001g0108 |
2 | HG02622.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2241+750A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800508 | |||||||
| chr8:93800753 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2241+995C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800753 | |||||||
| chr8:93800764 | T | C | 3 | a0002c0002t0001g0143 a0002c0002t0001g0192 a0002c0002t0001g0193 |
3 | HG01257.hp2 HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2241+1006T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800764 | |||||||
| chr8:93800781 | C | G | 1 | a0001c0001t0001g0251 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2241+1023C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800781 | |||||||
| chr8:93800850 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0237 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2241+1092A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800850 | |||||||
| chr8:93800864 | A | T | 17 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2241+1106A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800864 | |||||||
| chr8:93801047 | G | T | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2241+1289G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801047 | |||||||
| chr8:93801071 | A | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2241+1313A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801071 | |||||||
| chr8:93801216 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
311 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.2241+1458A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801216 | |||||||
| chr8:93801218 | T | C | 1 | a0002c0008t0001g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2241+1460T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801218 | |||||||
| chr8:93801306 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2241+1548T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801306 | |||||||
| chr8:93801400 | A | AT | 14 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0076 others(11): Show |
16 | HG01123.hp1 HG01169.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.2241+1660dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93801400 | ||||||
| chr8:93801400 | AT | A | 32 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0088 others(29): Show |
32 | HG00408.hp2 HG00597.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.2241+1660delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93801400 | ||||||
| chr8:93801433 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2241+1675C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801433 | |||||||
| chr8:93801620 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2241+1862A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801620 | |||||||
| chr8:93801828 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0036 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2242-1776A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801828 | |||||||
| chr8:93802193 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2242-1411T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93802193 | |||||||
| chr8:93802196 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2242-1408C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93802196 | |||||||
| chr8:93802222 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2242-1382C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93802222 | |||||||
| chr8:93802232 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2242-1372A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93802232 | |||||||
| chr8:93802324 | ATCT | A | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG00140.hp2 HG02258.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2242-1275_2242-127 others(7): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93802324 | ||||||
| chr8:93803161 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2242-443C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803161 | |||||||
| chr8:93803275 | A | G | 1 | a0002c0002t0001g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2242-329A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803275 | |||||||
| chr8:93803420 | C | T | 6 | a0001c0003t0001g0055 a0001c0003t0001g0182 a0001c0003t0001g0203 others(3): Show |
6 | HG01192.hp2 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2242-184C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803420 | |||||||
| chr8:93803431 | C | T | 1 | a0002c0002t0001g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2242-173C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803431 | |||||||
| chr8:93803526 | T | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2242-78T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803526 | |||||||
| chr8:93803573 | T | C | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2242-31T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803573 | |||||||
| chr8:93803576 | T | C | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2242-28T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803576 | |||||||
| chr8:93803879 | AT | A | 10 | a0001c0001t0001g0136 a0001c0001t0001g0159 a0001c0001t0001g0208 others(7): Show |
10 | HG00733.hp2 HG01099.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2322+210delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93803879 | ||||||
| chr8:93803879 | ATTT | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2322+208_2322+210d others(5): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93803879 | ||||||
| chr8:93803911 | A | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2322+227A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93803911 | |||||||
| chr8:93804148 | A | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2322+464A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804148 | |||||||
| chr8:93804169 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
75 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.2322+485G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804169 | |||||||
| chr8:93804298 | C | CTCTTT | 15 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0088 others(12): Show |
16 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2323-452_2323-448d others(7): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804298 | ||||||
| chr8:93804310 | C | CT | 21 | a0001c0001t0001g0031 a0001c0001t0001g0077 a0001c0001t0001g0128 others(18): Show |
23 | HG00673.hp2 HG01109.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.2323-430dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804310 | ||||||
| chr8:93804310 | C | CTTTT | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2323-433_2323-430d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804310 | ||||||
| chr8:93804310 | CT | C | 25 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0052 others(22): Show |
26 | HG01099.hp1 HG01243.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.2323-430delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804310 | ||||||
| chr8:93804310 | CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0057 others(4): Show |
7 | HG01070.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2323-440_2323-430d others(13): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804310 | ||||||
| chr8:93804311 | T | TTTTC | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
139 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.2323-448_2323-447i others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804311 | ||||||
| chr8:93804312 | T | TTTC | 9 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0160 others(6): Show |
10 | HG01109.hp1 HG01167.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2323-448_2323-447i others(5): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804312 | ||||||
| chr8:93804366 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2323-396C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804366 | |||||||
| chr8:93804381 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.2323-381C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804381 | |||||||
| chr8:93804481 | A | AT | 30 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0027 others(27): Show |
34 | HG00140.hp2 HG01081.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.2323-261dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804481 | ||||||
| chr8:93804518 | C | T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01070.hp2 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2323-244C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804518 | |||||||
| chr8:93804548 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2323-214C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804548 | |||||||
| chr8:93804595 | A | C | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2323-167A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804595 | |||||||
| chr8:93804929 | T | A | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2439+51T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93804929 | |||||||
| chr8:93804949 | T | A | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2439+71T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93804949 | |||||||
| chr8:93805126 | C | T | 11 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2439+248C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805126 | |||||||
| chr8:93805350 | G | A | 1 | a0002c0002t0001g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2439+472G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805350 | |||||||
| chr8:93805446 | T | A | 1 | a0001c0004t0001g0133 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2439+568T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805446 | |||||||
| chr8:93805447 | G | T | 1 | a0001c0004t0001g0133 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2439+569G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805447 | |||||||
| chr8:93805453 | G | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0036 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2439+575G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805453 | |||||||
| chr8:93805580 | C | CA | 9 | a0001c0001t0001g0035 a0001c0001t0001g0057 a0001c0001t0001g0100 others(6): Show |
11 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2439+720dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93805580 | ||||||
| chr8:93805580 | CA | C | 21 | a0001c0001t0001g0022 a0001c0001t0001g0060 a0001c0001t0001g0092 others(18): Show |
22 | HG01167.hp1 HG01167.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.2439+720delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93805580 | ||||||
| chr8:93805630 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2439+752A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805630 | |||||||
| chr8:93805946 | G | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(6): Show |
10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2439+1068G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805946 | |||||||
| chr8:93806113 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2439+1235C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806113 | |||||||
| chr8:93806146 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2439+1268T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806146 | |||||||
| chr8:93806190 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2439+1312G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806190 | |||||||
| chr8:93806356 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2439+1478G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806356 | |||||||
| chr8:93806405 | G | A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01070.hp2 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2439+1527G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806405 | |||||||
| chr8:93806850 | A | C | 2 | a0002c0002t0001g0114 a0002c0002t0001g0129 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.2439+1972A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806850 | |||||||
| chr8:93806857 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2439+1979T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806857 | |||||||
| chr8:93807103 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2440-1737T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807103 | |||||||
| chr8:93807113 | T | G | 11 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2440-1727T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807113 | |||||||
| chr8:93807445 | T | C | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2440-1395T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807445 | |||||||
| chr8:93807618 | A | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2440-1222A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807618 | |||||||
| chr8:93807738 | A | G | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(6): Show |
10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2440-1102A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807738 | |||||||
| chr8:93807874 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2440-966A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807874 | |||||||
| chr8:93807885 | A | G | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(6): Show |
10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2440-955A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807885 | |||||||
| chr8:93807887 | A | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2440-953A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807887 | |||||||
| chr8:93807949 | G | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2440-891G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807949 | |||||||
| chr8:93808130 | A | C | 4 | a0002c0002t0001g0024 a0002c0002t0001g0058 a0002c0002t0001g0258 others(1): Show |
4 | NA18984.hp2 NA19010.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-710A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808130 | |||||||
| chr8:93808257 | T | C | 1 | a0002c0002t0001g0187 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2440-583T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808257 | |||||||
| chr8:93808338 | A | T | 1 | a0001c0001t0002g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2440-502A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808338 | |||||||
| chr8:93808368 | A | ATCTACTA others(33): Show |
1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2440-463_2440-462i others(42): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808368 | ||||||
| chr8:93808374 | T | C | 1 | a0002c0002t0009g0126 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2440-466T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808374 | |||||||
| chr8:93808378 | A | T | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
311 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.2440-462A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808378 | |||||||
| chr8:93808443 | T | C | 4 | a0001c0001t0001g0056 a0001c0001t0001g0233 a0001c0001t0001g0237 others(1): Show |
4 | HG00741.hp2 HG02004.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-397T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808443 | |||||||
| chr8:93808458 | T | C | 3 | a0001c0001t0001g0128 a0002c0002t0001g0098 a0002c0002t0001g0127 |
3 | HG01981.hp2 NA18969.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2440-382T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808458 | |||||||
| chr8:93808464 | T | TATCTATT others(32): Show |
163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
182 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.2440-373_2440-335d others(41): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(49): Show |
1 | a0002c0002t0001g0114 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2440-335_2440-334i others(58): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(60): Show |
1 | a0001c0001t0001g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2440-335_2440-334i others(69): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(127): Show |
6 | a0001c0001t0001g0077 a0002c0002t0001g0078 a0002c0002t0001g0079 others(3): Show |
6 | NA18967.hp2 NA18982.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(136): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(88): Show |
1 | a0002c0002t0001g0115 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2440-335_2440-334i others(97): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(105): Show |
1 | a0002c0002t0001g0190 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2440-335_2440-334i others(114): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(105): Show |
14 | a0002c0002t0001g0017 a0002c0002t0001g0054 a0002c0002t0001g0139 others(11): Show |
15 | HG01106.hp2 HG01255.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(114): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(133): Show |
1 | a0002c0002t0001g0021 | 2 | HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2440-335_2440-334i others(142): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(211): Show |
1 | a0002c0002t0001g0268 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2440-335_2440-334i others(220): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(183): Show |
1 | a0002c0002t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2440-335_2440-334i others(192): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(155): Show |
11 | a0001c0003t0001g0279 a0002c0002t0001g0037 a0002c0002t0001g0038 others(8): Show |
11 | HG00597.hp2 HG01891.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(164): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(127): Show |
47 | a0001c0001t0001g0050 a0001c0001t0001g0099 a0001c0001t0001g0104 others(44): Show |
53 | HG00558.hp2 HG00673.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(136): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(166): Show |
1 | a0002c0002t0001g0039 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2440-335_2440-334i others(175): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(123): Show |
2 | a0002c0002t0001g0112 a0002c0002t0001g0124 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2440-335_2440-334i others(132): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(99): Show |
2 | a0002c0002t0001g0131 a0002c0002t0009g0126 |
2 | HG01109.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.2440-335_2440-334i others(108): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(71): Show |
18 | a0001c0001t0001g0022 a0001c0001t0001g0076 a0001c0001t0001g0091 others(15): Show |
19 | HG00140.hp2 HG01081.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(80): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808464 | T | TATCTATT others(68): Show |
1 | a0001c0001t0001g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2440-366_2440-365i others(77): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | ||||||
| chr8:93808480 | T | TTATCTAT others(17): Show |
1 | a0002c0002t0001g0009 | 2 | HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2440-350_2440-349i others(26): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808480 | ||||||
| chr8:93808484 | C | CTATAATA others(28): Show |
11 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(37): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808484 | ||||||
| chr8:93808505 | T | TATTTATC others(170): Show |
1 | a0002c0002t0001g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2440-335_2440-334i others(179): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808505 | |||||||
| chr8:93808506 | G | T | 1 | a0002c0002t0001g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2440-334G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808506 | |||||||
| chr8:93808518 | T | C | 1 | a0002c0002t0001g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2440-322T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808518 | |||||||
| chr8:93808529 | A | G | 19 | a0001c0001t0001g0077 a0001c0001t0001g0128 a0002c0002t0001g0009 others(16): Show |
20 | HG00673.hp2 HG00733.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2440-311A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808529 | |||||||
| chr8:93808547 | T | C | 1 | a0002c0002t0001g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2440-293T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808547 | |||||||
| chr8:93808594 | G | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0071 |
2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2440-246G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808594 | |||||||
| chr8:93808599 | G | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0240 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2440-241G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808599 | |||||||
| chr8:93808610 | G | T | 1 | a0002c0002t0001g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2440-230G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808610 | |||||||
| chr8:93808834 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp1 | splice_region_variant&intron_variant | LOW | c.2440-6T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808834 | |||||||
| chr8:93809203 | A | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2661+42A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809203 | |||||||
| chr8:93809297 | T | G | 1 | a0001c0001t0001g0278 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2661+136T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809297 | |||||||
| chr8:93809422 | A | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2661+261A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809422 | |||||||
| chr8:93809511 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2662-274T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809511 | |||||||
| chr8:93809517 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2662-268T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809517 | |||||||
| chr8:93809549 | A | G | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2662-236A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809549 | |||||||
| chr8:93809574 | C | A | 1 | a0002c0002t0001g0081 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2662-211C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809574 | |||||||
| chr8:93809643 | G | A | 19 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0046 others(16): Show |
21 | HG00408.hp1 HG00558.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.2662-142G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809643 | |||||||
| chr8:93809685 | A | G | 2 | a0001c0001t0001g0050 a0002c0002t0001g0016 |
3 | HG01928.hp1 HG01943.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2662-100A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809685 | |||||||
| chr8:93809971 | CT | C | 11 | a0001c0001t0001g0208 a0001c0001t0001g0249 a0001c0001t0002g0006 others(8): Show |
13 | HG01167.hp2 HG01261.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.2764+100delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93809971 | ||||||
| chr8:93809987 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2764+100T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93809987 | |||||||
| chr8:93809991 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2764+104C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93809991 | |||||||
| chr8:93810026 | T | C | 1 | a0002c0002t0001g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2764+139T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93810026 | |||||||
| chr8:93810036 | T | C | 1 | a0001c0003t0001g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2764+149T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93810036 | |||||||
| chr8:93810126 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2764+239G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93810126 | |||||||
| chr8:93810181 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2764+294G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93810181 | |||||||
| chr8:93810259 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.2764+372A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93810259 | |||||||
| chr8:93811043 | T | C | 1 | a0004c0005t0010g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2764+1156T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811043 | |||||||
| chr8:93811325 | GCAAAGAC | G | 66 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0040 others(63): Show |
68 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.2764+1439_2764+144 others(11): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811325 | |||||||
| chr8:93811335 | T | C | 66 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0040 others(63): Show |
68 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.2764+1448T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811335 | |||||||
| chr8:93811337 | A | C | 66 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0040 others(63): Show |
68 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.2764+1450A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811337 | |||||||
| chr8:93811344 | C | G | 17 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(14): Show |
18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2764+1457C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811344 | |||||||
| chr8:93811586 | G | A | 3 | a0002c0002t0001g0110 a0002c0002t0001g0252 a0007c0012t0001g0108 |
3 | NA18948.hp1 NA18981.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2764+1699G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811586 | |||||||
| chr8:93811663 | A | G | 1 | a0001c0003t0001g0225 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2764+1776A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811663 | |||||||
| chr8:93811785 | G | T | 2 | a0002c0002t0001g0112 a0002c0002t0001g0124 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2764+1898G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811785 | |||||||
| chr8:93811794 | G | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(2): Show |
7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2764+1907G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811794 | |||||||
| chr8:93811906 | T | G | 1 | a0002c0002t0001g0039 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2764+2019T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811906 | |||||||
| chr8:93812056 | G | A | 3 | a0001c0004t0001g0010 a0001c0004t0001g0097 a0001c0004t0001g0133 |
4 | HG01167.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2764+2169G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812056 | |||||||
| chr8:93812089 | T | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2764+2202T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812089 | |||||||
| chr8:93812108 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2764+2221C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812108 | |||||||
| chr8:93812149 | C | CA | 9 | a0001c0001t0001g0238 a0001c0001t0002g0006 a0001c0001t0002g0007 others(6): Show |
11 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2764+2278dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93812149 | ||||||
| chr8:93812377 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2764+2490G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812377 | |||||||
| chr8:93812704 | G | T | 1 | a0002c0002t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2765-2601G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812704 | |||||||
| chr8:93812991 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2765-2314C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812991 | |||||||
| chr8:93813149 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2765-2156C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93813149 | |||||||
| chr8:93813247 | C | T | 1 | a0002c0002t0001g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2765-2058C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93813247 | |||||||
| chr8:93813596 | A | T | 2 | a0002c0002t0001g0087 a0002c0002t0005g0082 |
2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2765-1709A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93813596 | |||||||
| chr8:93814135 | C | CTTT | 4 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(1): Show |
6 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2765-1150_2765-114 others(7): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814135 | ||||||
| chr8:93814135 | CT | C | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
277 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.2765-1148delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814135 | ||||||
| chr8:93814135 | CTT | C | 10 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0162 others(7): Show |
10 | HG01099.hp2 HG02273.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2765-1149_2765-114 others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814135 | ||||||
| chr8:93814163 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
3 | HG02717.hp2 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2765-1142G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814163 | |||||||
| chr8:93814239 | A | G | 1 | a0001c0003t0001g0222 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2765-1066A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814239 | |||||||
| chr8:93814296 | T | C | 11 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2765-1009T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814296 | |||||||
| chr8:93814299 | G | C | 11 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2765-1006G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814299 | |||||||
| chr8:93814300 | T | C | 11 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2765-1005T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814300 | |||||||
| chr8:93814385 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2765-920C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814385 | |||||||
| chr8:93814438 | A | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2765-867A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814438 | |||||||
| chr8:93814468 | G | GT | 6 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0248 others(3): Show |
7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2765-828dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814468 | ||||||
| chr8:93814469 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2765-836T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814469 | |||||||
| chr8:93814523 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2765-782C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814523 | |||||||
| chr8:93814566 | A | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2765-739A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814566 | |||||||
| chr8:93814568 | G | A | 1 | a0001c0003t0001g0226 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2765-737G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814568 | |||||||
| chr8:93814630 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
167 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.2765-675C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814630 | |||||||
| chr8:93814652 | C | CT | 7 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0068 others(4): Show |
7 | HG00673.hp2 HG01070.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2765-638dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814652 | ||||||
| chr8:93814652 | C | CTT | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(6): Show |
10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2765-639_2765-638d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814652 | ||||||
| chr8:93815246 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2765-59A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93815246 | |||||||
| chr8:93815772 | C | T | 1 | a0003c0006t0001g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2907+325C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | chr8 | 93815772 | |||||||
| chr8:93815829 | A | AAGGGAAG others(8): Show |
175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
194 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.2907+384_2907+385i others(17): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr8 | 93815829 | ||||||
| chr8:93815854 | C | G | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2907+407C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | chr8 | 93815854 | |||||||
| chr8:93816315 | G | A | 1 | a0002c0002t0001g0074 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2908-57G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | chr8 | 93816315 | |||||||
| chr8:93816329 | C | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0028 others(4): Show |
9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2908-43C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | chr8 | 93816329 | |||||||
| chr8:93816337 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2908-35A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | chr8 | 93816337 |