Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55069 |
| ensemblid | ENSG00000106609.16 |
| hgncid | 25476 |
| symbol | TMEM248 |
| name | transmembrane protein 248 |
| refseq_nuc | NM_017994.5 |
| refseq_prot | NP_060464.1 |
| ensembl_nuc | ENST00000341567.8 |
| ensembl_prot | ENSP00000340668.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 66921225 |
| end | 66958551 |
| strand | + |
| ver | v1.2 |
| region | chr7:66921225-66958551 |
| region5000 | chr7:66916225-66963551 |
| regionname0 | TMEM248_chr7_66921225_66958551 |
| regionname5000 | TMEM248_chr7_66916225_66963551 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 314 | 394 | 73 | 66 | 195 | 16 | 42 | 149 | TMEM248_chr7_66916225_66963551 | TMEM248 | MFSIN others(309): Show |
chr7 | 66916225 | 66963551 |
| a0002 | 0/0 | 314 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TMEM248_chr7_66916225_66963551 | TMEM248 | MFSIN others(309): Show |
chr7 | 66916225 | 66963551 |
| a0003 | 0/0 | 314 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | MFGIN others(309): Show |
chr7 | 66916225 | 66963551 |
| a0004 | 0/0 | 314 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | MFSIN others(309): Show |
chr7 | 66916225 | 66963551 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 942 | 394 | 73 | 66 | 195 | 16 | 42 | TMEM248_chr7_66916225_66963551 | TMEM248 | ATGTT others(937): Show |
chr7 | 66916225 | 66963551 | ||
| a0002c0002 | 0/0 | 942 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ATGTT others(937): Show |
chr7 | 66916225 | 66963551 | ||
| a0003c0004 | 0/0 | 942 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ATGTT others(937): Show |
chr7 | 66916225 | 66963551 | ||
| a0004c0003 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ATGTT others(937): Show |
chr7 | 66916225 | 66963551 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4229 | 106 | 22 | 18 | 39 | 9 | 17 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4224): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0002 | 0/0 | 4231 | 72 | 18 | 14 | 33 | 0 | 7 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0003 | 0/0 | 4231 | 55 | 4 | 7 | 34 | 3 | 7 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0004 | 0/0 | 4231 | 53 | 1 | 10 | 37 | 2 | 3 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0005 | 0/0 | 4231 | 28 | 4 | 4 | 18 | 2 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0006 | 0/0 | 4231 | 26 | 0 | 2 | 24 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0007 | 0/0 | 4227 | 13 | 13 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4222): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0008 | 0/0 | 4230 | 8 | 1 | 4 | 0 | 0 | 3 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4225): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0009 | 0/0 | 4232 | 7 | 0 | 0 | 7 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4227): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0010 | 0/0 | 4231 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0011 | 0/0 | 4231 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0012 | 0/0 | 4231 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0013 | 0/0 | 4229 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4224): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0014 | 0/0 | 4231 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCA others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0015 | 0/0 | 4231 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0016 | 0/0 | 4231 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0017 | 0/0 | 4231 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0018 | 0/0 | 4231 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0019 | 0/0 | 4231 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0020 | 0/1 | 4229 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4224): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0021 | 0/0 | 4231 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0022 | 0/0 | 4229 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4224): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0023 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4224): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0024 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4224): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0025 | 0/0 | 4231 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0026 | 0/0 | 4231 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0027 | 0/0 | 4229 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4224): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0028 | 0/0 | 4231 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0029 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4224): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0030 | 0/0 | 4231 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0001c0001t0031 | 0/0 | 4231 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0002c0002t0002 | 0/0 | 4231 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0003c0004t0002 | 0/0 | 4231 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| a0004c0003t0004 | 0/0 | 4231 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | ACCCG others(4226): Show |
chr7 | 66916225 | 66963551 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0001 | 0/0 | 10 | 0 | 4 | 4 | 0 | 2 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0005g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0008g0007 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0008g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0008g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0009g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0009g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0010g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0011g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0012g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0013g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0014g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0015g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0016g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0017g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0018g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0019g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0020g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0021g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0022g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0023g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0024g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0025g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0026g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0027g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0028g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0029g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0030g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0001c0001t0031g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0003c0004t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| a0004c0003t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0316 | EUR | GBR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0077 | EUR | FIN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00438 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00438 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0337 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00673 | hp1 | a0001 | c0001 | t0009 | g0253 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | CHS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0323 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00738 | hp2 | a0001 | c0001 | t0031 | g0223 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01074 | hp1 | a0001 | c0001 | t0027 | g0148 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0187 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0061 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0062 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0064 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01256 | hp2 | a0001 | c0001 | t0015 | g0046 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0331 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0060 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01358 | hp1 | a0001 | c0001 | t0018 | g0325 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01358 | hp2 | a0001 | c0001 | t0028 | g0298 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0055 | EUR | IBS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0322 | EUR | IBS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0321 | EUR | IBS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0119 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0118 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0014 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01928 | hp2 | a0001 | c0001 | t0026 | g0001 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0014 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01943 | hp1 | a0001 | c0001 | t0014 | g0296 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0178 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0177 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0182 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | CDX | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | CDX | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | CDX | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0121 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0113 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0317 | AMR | PEL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02451 | hp2 | a0001 | c0001 | t0029 | g0208 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0093 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0246 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0001 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02818 | hp2 | a0001 | c0001 | t0011 | g0004 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0018 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0265 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0018 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | ESN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0120 | AFR | MSL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0111 | AFR | MSL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | ESN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ESN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | MSL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | MSL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03239 | hp1 | a0001 | c0001 | t0012 | g0273 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | MSL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03486 | hp2 | a0001 | c0001 | t0030 | g0215 | AFR | MSL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03491 | hp1 | a0001 | c0001 | t0022 | g0168 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | ESN | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03540 | hp1 | a0001 | c0001 | t0023 | g0211 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03654 | hp2 | a0001 | c0001 | t0025 | g0032 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | STU | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0297 | SAS | STU | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0087 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0242 | SAS | BEB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | BEB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | BEB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | BEB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0295 | SAS | BEB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0181 | SAS | STU | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG04184 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | BEB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | BEB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | STU | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | STU | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG04228 | hp1 | a0001 | c0001 | t0017 | g0110 | SAS | STU | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG04228 | hp2 | a0001 | c0001 | t0008 | g0007 | SAS | STU | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0115 | AFR | YRI | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0114 | AFR | YRI | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0336 | EAS | CHB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | CHB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | CHB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18906 | hp1 | a0001 | c0001 | t0024 | g0130 | AFR | YRI | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0116 | AFR | YRI | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0105 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0329 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18954 | hp2 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18963 | hp1 | a0001 | c0001 | t0010 | g0037 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0320 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18975 | hp1 | a0001 | c0001 | t0006 | g0106 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18977 | hp2 | a0001 | c0001 | t0009 | g0238 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18979 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0107 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0319 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18985 | hp2 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18990 | hp1 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0108 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18993 | hp2 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0318 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19002 | hp2 | a0001 | c0001 | t0016 | g0083 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19003 | hp2 | a0001 | c0001 | t0010 | g0037 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0330 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0101 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19043 | hp1 | a0001 | c0001 | t0019 | g0088 | AFR | LWK | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19043 | hp2 | a0003 | c0004 | t0002 | g0122 | AFR | LWK | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19054 | hp1 | a0001 | c0001 | t0006 | g0095 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19055 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19057 | hp1 | a0001 | c0001 | t0006 | g0102 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0334 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0333 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19068 | hp1 | a0004 | c0003 | t0004 | g0067 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19072 | hp2 | a0001 | c0001 | t0006 | g0109 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19077 | hp1 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19081 | hp1 | a0001 | c0001 | t0006 | g0097 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0335 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19085 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | YRI | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ASW | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | TSI | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0029 | EUR | TSI | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | TSI | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0029 | EUR | TSI | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02486 | hp2 | a0001 | c0001 | t0021 | g0195 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | MSL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | USA | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | USA | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | USA | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | USA | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | LWK | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | LWK | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0020 | g0165 | REF | REF | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0142 | REF | REF | TMEM248_chr7_66916225_66963551 | TMEM248 | chr7 | 66916225 | 66963551 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66941872 | A | G | 1 | a0003 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.7A>G | p.Ser3Gly | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/7 | 262/4229 | 7/945 | 3/314 | chr7 | 66941872 | |||
| chr7:66945036 | A | T | 1 | a0004 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.220A>T | p.Thr74Ser | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/7 | 475/4229 | 220/945 | 74/314 | chr7 | 66945036 | |||
| chr7:66945244 | A | G | 1 | a0002 | 2 | NA18973.hp2 NA19056.hp2 |
missense_variant | MODERATE | c.428A>G | p.His143Arg | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/7 | 683/4229 | 428/945 | 143/314 | chr7 | 66945244 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66921229 | G | A | 1 | a0001c0001t0014 | 1 | HG01943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-251G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/7 | 20637 | chr7 | 66921229 | ||||||
| chr7:66921348 | T | G | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
5_prime_UTR_variant | MODIFIER | c.-132T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/7 | 20518 | chr7 | 66921348 | ||||||
| chr7:66955709 | A | G | 1 | a0001c0001t0019 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*187A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 187 | chr7 | 66955709 | ||||||
| chr7:66955833 | C | T | 1 | a0001c0001t0006 | 26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*311C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 311 | chr7 | 66955833 | ||||||
| chr7:66955836 | C | T | 1 | a0001c0001t0018 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*314C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 314 | chr7 | 66955836 | ||||||
| chr7:66955870 | C | G | 1 | a0001c0001t0031 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*348C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 348 | chr7 | 66955870 | ||||||
| chr7:66955952 | C | T | 1 | a0001c0001t0013 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*430C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 430 | chr7 | 66955952 | ||||||
| chr7:66956156 | C | A | 4 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0016 others(1): Show |
56 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*634C>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 634 | chr7 | 66956156 | ||||||
| chr7:66956246 | A | G | 1 | a0001c0001t0030 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*724A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 724 | chr7 | 66956246 | ||||||
| chr7:66956345 | G | A | 1 | a0001c0001t0019 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*823G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 823 | chr7 | 66956345 | ||||||
| chr7:66956456 | TTCTA | T | 1 | a0001c0001t0007 | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*939_*942delTCTA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 939 | INFO_REALIGN_3_PRIME | chr7 | 66956456 | |||||
| chr7:66956459 | T | G | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(21): Show |
263 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*937T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 937 | chr7 | 66956459 | ||||||
| chr7:66956550 | A | G | 1 | a0001c0001t0029 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1028A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1028 | chr7 | 66956550 | ||||||
| chr7:66956570 | A | G | 1 | a0001c0001t0028 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1048 | chr7 | 66956570 | ||||||
| chr7:66956701 | G | C | 4 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(1): Show |
65 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1179G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1179 | chr7 | 66956701 | ||||||
| chr7:66956706 | G | A | 1 | a0001c0001t0015 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1184G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1184 | chr7 | 66956706 | ||||||
| chr7:66956748 | A | C | 1 | a0001c0001t0027 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1226A>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1226 | chr7 | 66956748 | ||||||
| chr7:66956893 | T | C | 1 | a0001c0001t0012 | 2 | HG02735.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1371T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1371 | chr7 | 66956893 | ||||||
| chr7:66956895 | G | GA | 1 | a0001c0001t0008 | 8 | HG01106.hp2 HG01952.hp2 HG01975.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1375dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1376 | INFO_REALIGN_3_PRIME | chr7 | 66956895 | |||||
| chr7:66957141 | G | A | 1 | a0001c0001t0021 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1619G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1619 | chr7 | 66957141 | ||||||
| chr7:66957216 | A | ACT | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(22): Show |
276 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*1697_*1698dupCT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1699 | INFO_REALIGN_3_PRIME | chr7 | 66957216 | |||||
| chr7:66957320 | C | T | 1 | a0001c0001t0006 | 26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1798C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1798 | chr7 | 66957320 | ||||||
| chr7:66957502 | C | T | 1 | a0001c0001t0024 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1980C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 1980 | chr7 | 66957502 | ||||||
| chr7:66957592 | T | A | 1 | a0001c0001t0011 | 2 | HG02818.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2070T>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 2070 | chr7 | 66957592 | ||||||
| chr7:66957867 | T | TA | 1 | a0001c0001t0009 | 7 | HG00438.hp1 HG00673.hp1 NA18954.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2349dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 2350 | INFO_REALIGN_3_PRIME | chr7 | 66957867 | |||||
| chr7:66957979 | C | T | 1 | a0001c0001t0010 | 2 | NA18963.hp1 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2457C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 2457 | chr7 | 66957979 | ||||||
| chr7:66958146 | G | A | 1 | a0001c0001t0022 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2624G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 2624 | chr7 | 66958146 | ||||||
| chr7:66958179 | G | A | 1 | a0001c0001t0025 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2657G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 2657 | chr7 | 66958179 | ||||||
| chr7:66958208 | C | G | 1 | a0001c0001t0026 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2686C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 2686 | chr7 | 66958208 | ||||||
| chr7:66958334 | A | G | 1 | a0001c0001t0016 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2812A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 2812 | chr7 | 66958334 | ||||||
| chr7:66958474 | T | C | 1 | a0001c0001t0023 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2952T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 2952 | chr7 | 66958474 | ||||||
| chr7:66958518 | A | G | 1 | a0001c0001t0017 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2996A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 7/7 | 2996 | chr7 | 66958518 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66921823 | T | C | 4 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0040 others(1): Show |
4 | NA18943.hp2 NA18949.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+362T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66921823 | |||||||
| chr7:66921832 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+371G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66921832 | |||||||
| chr7:66921904 | C | T | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19+443C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66921904 | |||||||
| chr7:66922034 | T | G | 79 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(76): Show |
88 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-19+573T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922034 | |||||||
| chr7:66922087 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-19+626A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922087 | |||||||
| chr7:66922224 | A | G | 1 | a0001c0001t0005g0337 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-19+763A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922224 | |||||||
| chr7:66922270 | G | T | 4 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0002g0314 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+809G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922270 | |||||||
| chr7:66922280 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-19+819C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922280 | |||||||
| chr7:66922498 | C | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(48): Show |
63 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-19+1037C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922498 | |||||||
| chr7:66922530 | T | C | 1 | a0001c0001t0003g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-19+1069T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922530 | |||||||
| chr7:66922703 | T | TCTAAGTG others(2): Show |
103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-19+1242_-19+1243i others(11): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922703 | |||||||
| chr7:66922704 | T | A | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-19+1243T>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922704 | |||||||
| chr7:66922755 | G | A | 57 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(54): Show |
60 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-19+1294G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922755 | |||||||
| chr7:66922854 | C | T | 4 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+1393C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922854 | |||||||
| chr7:66922912 | G | A | 21 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(18): Show |
27 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19+1451G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66922912 | |||||||
| chr7:66923031 | C | T | 1 | a0001c0001t0002g0263 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-19+1570C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66923031 | |||||||
| chr7:66923095 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(48): Show |
63 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-19+1634A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66923095 | |||||||
| chr7:66923148 | CTT | C | 11 | a0001c0001t0001g0117 a0001c0001t0007g0015 a0001c0001t0007g0016 others(8): Show |
13 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+1698_-19+1699d others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66923148 | ||||||
| chr7:66923402 | A | G | 1 | a0001c0001t0017g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-19+1941A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66923402 | |||||||
| chr7:66923711 | T | C | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-19+2250T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66923711 | |||||||
| chr7:66923741 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+2280C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66923741 | |||||||
| chr7:66923892 | T | C | 1 | a0001c0001t0002g0312 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19+2431T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66923892 | |||||||
| chr7:66923897 | G | T | 1 | a0001c0001t0005g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19+2436G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66923897 | |||||||
| chr7:66923927 | A | G | 1 | a0001c0001t0003g0262 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-19+2466A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66923927 | |||||||
| chr7:66924286 | C | G | 1 | a0001c0001t0001g0030 | 2 | HG02083.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-19+2825C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66924286 | |||||||
| chr7:66924342 | C | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-19+2881C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66924342 | |||||||
| chr7:66924443 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+2982C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66924443 | |||||||
| chr7:66924529 | T | G | 1 | a0003c0004t0002g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+3068T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66924529 | |||||||
| chr7:66924647 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-19+3186C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66924647 | |||||||
| chr7:66924779 | C | T | 79 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(76): Show |
88 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-19+3318C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66924779 | |||||||
| chr7:66924832 | C | T | 1 | a0001c0001t0002g0314 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-19+3371C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66924832 | |||||||
| chr7:66924844 | G | A | 1 | a0001c0001t0017g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-19+3383G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66924844 | |||||||
| chr7:66925040 | G | A | 2 | a0001c0001t0001g0264 a0001c0001t0007g0265 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-19+3579G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925040 | |||||||
| chr7:66925249 | G | T | 1 | a0001c0001t0002g0309 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-19+3788G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925249 | |||||||
| chr7:66925267 | C | T | 54 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0009 others(51): Show |
65 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-19+3806C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925267 | |||||||
| chr7:66925268 | A | G | 261 | a0001c0001t0001g0026 a0001c0001t0001g0117 a0001c0001t0001g0196 others(258): Show |
301 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.-19+3807A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925268 | |||||||
| chr7:66925386 | C | G | 1 | a0001c0001t0002g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-19+3925C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925386 | |||||||
| chr7:66925402 | C | G | 1 | a0001c0001t0003g0258 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-19+3941C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925402 | |||||||
| chr7:66925508 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+4047A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925508 | |||||||
| chr7:66925554 | G | A | 1 | a0001c0001t0003g0219 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-19+4093G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925554 | |||||||
| chr7:66925687 | G | GTTTTTTC | 137 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0032 others(134): Show |
160 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-19+4233_-19+4239d others(9): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66925687 | ||||||
| chr7:66925695 | T | TTTTTTC | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19+4239_-19+4240i others(8): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66925695 | ||||||
| chr7:66925700 | T | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG00609.hp2 HG02071.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-19+4239T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925700 | |||||||
| chr7:66925737 | A | G | 156 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(153): Show |
180 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.-19+4276A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925737 | |||||||
| chr7:66925882 | C | G | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG01167.hp2 HG01168.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-19+4421C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925882 | |||||||
| chr7:66925885 | C | T | 1 | a0001c0001t0003g0029 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-19+4424C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66925885 | |||||||
| chr7:66926084 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-19+4623C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66926084 | |||||||
| chr7:66926095 | C | T | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-19+4634C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66926095 | |||||||
| chr7:66926146 | A | G | 1 | a0001c0001t0002g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-19+4685A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66926146 | |||||||
| chr7:66926440 | T | C | 1 | a0001c0001t0002g0268 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-19+4979T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66926440 | |||||||
| chr7:66926639 | C | CA | 22 | a0001c0001t0002g0042 a0001c0001t0006g0003 a0001c0001t0006g0005 others(19): Show |
28 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+5193dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66926639 | ||||||
| chr7:66926639 | C | CAA | 81 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(78): Show |
87 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.-19+5192_-19+5193d others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66926639 | ||||||
| chr7:66926639 | CA | C | 6 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0002g0306 others(3): Show |
6 | HG00609.hp1 HG01934.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+5193delA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66926639 | ||||||
| chr7:66926756 | AT | A | 57 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(54): Show |
60 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-19+5297delT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66926756 | ||||||
| chr7:66926800 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-19+5339C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66926800 | |||||||
| chr7:66927007 | A | G | 1 | a0001c0001t0008g0187 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-19+5546A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927007 | |||||||
| chr7:66927076 | T | G | 2 | a0001c0001t0002g0313 a0001c0001t0002g0315 |
2 | HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-19+5615T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927076 | |||||||
| chr7:66927193 | C | A | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19+5732C>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927193 | |||||||
| chr7:66927245 | G | C | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+5784G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927245 | |||||||
| chr7:66927436 | A | G | 4 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0263 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+5975A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927436 | |||||||
| chr7:66927436 | A | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-19+5975A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927436 | |||||||
| chr7:66927495 | T | C | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-19+6034T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927495 | |||||||
| chr7:66927624 | G | GT | 41 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 others(38): Show |
46 | HG00642.hp1 HG00673.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.-19+6178dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66927624 | ||||||
| chr7:66927624 | G | T | 3 | a0001c0001t0001g0184 a0001c0001t0002g0042 a0001c0001t0007g0121 |
3 | HG02109.hp1 HG02257.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-19+6163G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927624 | |||||||
| chr7:66927639 | T | A | 1 | a0001c0001t0005g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19+6178T>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927639 | |||||||
| chr7:66927639 | T | TA | 54 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(51): Show |
57 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-19+6179dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66927639 | ||||||
| chr7:66927804 | C | T | 54 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(51): Show |
56 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-19+6343C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927804 | |||||||
| chr7:66927805 | A | G | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-19+6344A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927805 | |||||||
| chr7:66927982 | A | G | 2 | a0001c0001t0003g0251 a0001c0001t0003g0252 |
2 | NA18612.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-19+6521A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66927982 | |||||||
| chr7:66928400 | A | G | 55 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0009 others(52): Show |
66 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-19+6939A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66928400 | |||||||
| chr7:66928530 | A | G | 6 | a0001c0001t0004g0085 a0001c0001t0004g0086 a0001c0001t0004g0089 others(3): Show |
6 | NA18945.hp1 NA18960.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+7069A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66928530 | |||||||
| chr7:66928582 | C | G | 2 | a0001c0001t0004g0084 a0001c0001t0016g0083 |
2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-19+7121C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66928582 | |||||||
| chr7:66928775 | AT | A | 51 | a0001c0001t0001g0316 a0001c0001t0002g0001 a0001c0001t0002g0032 others(48): Show |
63 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-19+7324delT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66928775 | ||||||
| chr7:66928806 | G | A | 20 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(17): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+7345G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66928806 | |||||||
| chr7:66929083 | C | T | 4 | a0001c0001t0005g0334 a0001c0001t0005g0335 a0001c0001t0005g0336 others(1): Show |
5 | NA18612.hp1 NA18963.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+7622C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66929083 | |||||||
| chr7:66929217 | A | G | 1 | a0001c0001t0003g0250 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-19+7756A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66929217 | |||||||
| chr7:66929426 | A | AT | 68 | a0001c0001t0001g0025 a0001c0001t0001g0125 a0001c0001t0001g0169 others(65): Show |
82 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-19+7993dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATT | 14 | a0001c0001t0001g0174 a0001c0001t0002g0193 a0001c0001t0002g0194 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+7992_-19+7993d others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTT | 9 | a0001c0001t0004g0049 a0001c0001t0006g0003 a0001c0001t0006g0005 others(6): Show |
14 | HG04228.hp1 NA18939.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19+7988_-19+7993d others(8): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT | 6 | a0001c0001t0006g0014 a0001c0001t0006g0098 a0001c0001t0006g0099 others(3): Show |
7 | HG01928.hp1 HG01934.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+7987_-19+7993d others(9): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(2): Show |
12 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0050 others(9): Show |
13 | HG00558.hp1 HG01515.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+7985_-19+7993d others(11): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(3): Show |
10 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0005g0035 others(7): Show |
12 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19+7984_-19+7993d others(12): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(4): Show |
11 | a0001c0001t0004g0013 a0001c0001t0004g0051 a0001c0001t0004g0052 others(8): Show |
13 | HG02145.hp2 HG02280.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+7983_-19+7993d others(13): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(5): Show |
3 | a0001c0001t0005g0330 a0001c0001t0005g0331 a0001c0001t0005g0332 |
3 | HG01257.hp2 NA18950.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-19+7982_-19+7993d others(14): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0004g0089 a0001c0001t0005g0333 |
2 | NA18980.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-19+7981_-19+7993d others(15): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0004g0053 a0001c0001t0004g0085 a0001c0001t0004g0090 |
3 | NA18945.hp1 NA19005.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-19+7980_-19+7993d others(16): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0005g0335 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-19+7979_-19+7993d others(17): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0004g0092 a0001c0001t0019g0088 |
2 | NA19043.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-19+7978_-19+7993d others(18): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0004g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-19+7977_-19+7993d others(19): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0004g0054 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-19+7976_-19+7993d others(20): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0004g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-19+7975_-19+7993d others(21): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(13): Show |
5 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0058 others(2): Show |
5 | HG00642.hp2 HG01175.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+7974_-19+7993d others(22): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(14): Show |
4 | a0001c0001t0004g0060 a0001c0001t0004g0061 a0001c0001t0004g0062 others(1): Show |
4 | HG01109.hp2 HG01168.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+7973_-19+7993d others(23): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(15): Show |
2 | a0001c0001t0004g0064 a0001c0001t0004g0086 |
2 | HG01169.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-19+7972_-19+7993d others(24): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(18): Show |
4 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0068 others(1): Show |
4 | NA18944.hp1 NA18971.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+7969_-19+7993d others(27): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(19): Show |
7 | a0001c0001t0004g0069 a0001c0001t0004g0070 a0001c0001t0004g0071 others(4): Show |
7 | HG02074.hp1 NA18956.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+7968_-19+7993d others(28): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(21): Show |
1 | a0001c0001t0004g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-19+7966_-19+7993d others(30): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(22): Show |
1 | a0001c0001t0004g0077 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-19+7993_-19+7994i others(31): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(24): Show |
2 | a0001c0001t0004g0078 a0001c0001t0004g0079 |
2 | NA18989.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-19+7993_-19+7994i others(33): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(28): Show |
2 | a0001c0001t0004g0080 a0001c0001t0004g0081 |
2 | NA18975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-19+7993_-19+7994i others(37): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | A | ATTTTTTT others(30): Show |
1 | a0001c0001t0004g0082 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-19+7993_-19+7994i others(39): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | AT | A | 17 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0196 others(14): Show |
19 | HG00738.hp2 HG02109.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-19+7993delT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | ATTTTTT | A | 9 | a0001c0001t0001g0117 a0001c0001t0007g0015 a0001c0001t0007g0016 others(6): Show |
11 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+7988_-19+7993d others(8): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0126 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-19+7982_-19+7993d others(14): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929426 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0004g0044 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-19+7981_-19+7993d others(15): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66929426 | ||||||
| chr7:66929522 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+8061C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66929522 | |||||||
| chr7:66929582 | G | A | 1 | a0003c0004t0002g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+8121G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66929582 | |||||||
| chr7:66929664 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-19+8203C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66929664 | |||||||
| chr7:66929686 | G | T | 1 | a0001c0001t0003g0029 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-19+8225G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66929686 | |||||||
| chr7:66929735 | C | T | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19+8274C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66929735 | |||||||
| chr7:66929899 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-19+8438G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66929899 | |||||||
| chr7:66929995 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-19+8534A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66929995 | |||||||
| chr7:66930064 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0129 |
3 | HG00280.hp1 HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-19+8603G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66930064 | |||||||
| chr7:66930162 | A | G | 7 | a0001c0001t0002g0008 a0001c0001t0002g0191 a0001c0001t0002g0192 others(4): Show |
9 | HG01243.hp1 HG02055.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+8701A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66930162 | |||||||
| chr7:66930376 | C | G | 1 | a0001c0001t0012g0273 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-19+8915C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66930376 | |||||||
| chr7:66930422 | G | A | 1 | a0001c0001t0007g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19+8961G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66930422 | |||||||
| chr7:66930449 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-19+8988C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66930449 | |||||||
| chr7:66930505 | A | G | 3 | a0001c0001t0003g0028 a0001c0001t0003g0241 a0001c0001t0031g0223 |
4 | HG00738.hp2 HG01361.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+9044A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66930505 | |||||||
| chr7:66930536 | C | T | 4 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0003g0251 others(1): Show |
4 | HG02155.hp2 NA18612.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+9075C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66930536 | |||||||
| chr7:66930539 | A | C | 1 | a0001c0001t0006g0103 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-19+9078A>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66930539 | |||||||
| chr7:66930585 | G | C | 4 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0263 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+9124G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66930585 | |||||||
| chr7:66930755 | G | A | 12 | a0001c0001t0001g0026 a0001c0001t0001g0196 a0001c0001t0001g0197 others(9): Show |
13 | HG00544.hp2 HG02015.hp2 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+9294G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66930755 | |||||||
| chr7:66931111 | T | G | 1 | a0001c0001t0017g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-19+9650T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66931111 | |||||||
| chr7:66931132 | A | G | 1 | a0001c0001t0003g0240 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-19+9671A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66931132 | |||||||
| chr7:66931217 | C | T | 1 | a0001c0001t0005g0335 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-19+9756C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66931217 | |||||||
| chr7:66931297 | C | CA | 33 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0129 others(30): Show |
33 | HG00423.hp2 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.-19+9860dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931297 | ||||||
| chr7:66931297 | CA | C | 16 | a0001c0001t0001g0023 a0001c0001t0001g0128 a0001c0001t0001g0163 others(13): Show |
17 | HG00735.hp2 HG01243.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19+9860delA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931297 | ||||||
| chr7:66931297 | CAA | C | 25 | a0001c0001t0001g0024 a0001c0001t0001g0164 a0001c0001t0005g0035 others(22): Show |
29 | HG00642.hp1 HG01256.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-19+9859_-19+9860d others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931297 | ||||||
| chr7:66931297 | CAAAA | C | 23 | a0001c0001t0004g0076 a0001c0001t0005g0011 a0001c0001t0005g0043 others(20): Show |
30 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19+9857_-19+9860d others(6): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931297 | ||||||
| chr7:66931297 | CAAAAA | C | 64 | a0001c0001t0001g0117 a0001c0001t0004g0012 a0001c0001t0004g0013 others(61): Show |
68 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-19+9856_-19+9860d others(7): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931297 | ||||||
| chr7:66931392 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-19+9931T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66931392 | |||||||
| chr7:66931490 | A | AT | 26 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0004g0075 others(23): Show |
32 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.-19+10039dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931490 | ||||||
| chr7:66931792 | C | CT | 102 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(99): Show |
107 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-18-10026dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931792 | ||||||
| chr7:66931792 | C | CTT | 15 | a0001c0001t0001g0123 a0001c0001t0001g0136 a0001c0001t0001g0159 others(12): Show |
15 | HG01261.hp1 HG01358.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-10027_-18-1002 others(6): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931792 | ||||||
| chr7:66931792 | C | CTTT | 6 | a0001c0001t0001g0137 a0001c0001t0001g0161 a0001c0001t0001g0162 others(3): Show |
7 | HG01192.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18-10028_-18-1002 others(7): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931792 | ||||||
| chr7:66931792 | CT | C | 54 | a0001c0001t0001g0188 a0001c0001t0002g0008 a0001c0001t0002g0193 others(51): Show |
69 | HG00438.hp2 HG01167.hp2 HG01257.hp2 others(66): Show |
intron_variant | MODIFIER | c.-18-10026delT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931792 | ||||||
| chr7:66931792 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0310 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18-10038_-18-1002 others(17): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66931792 | ||||||
| chr7:66931821 | T | C | 20 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(17): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-10027T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66931821 | |||||||
| chr7:66931831 | G | A | 4 | a0001c0001t0004g0012 a0001c0001t0004g0047 a0001c0001t0004g0056 others(1): Show |
5 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-10017G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66931831 | |||||||
| chr7:66931923 | G | A | 79 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(76): Show |
88 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-18-9925G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66931923 | |||||||
| chr7:66931953 | C | T | 79 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(76): Show |
88 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-18-9895C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66931953 | |||||||
| chr7:66931970 | A | T | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18-9878A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66931970 | |||||||
| chr7:66931994 | C | T | 1 | a0001c0001t0002g0302 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-18-9854C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66931994 | |||||||
| chr7:66932011 | A | G | 1 | a0001c0001t0003g0236 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-18-9837A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932011 | |||||||
| chr7:66932040 | A | G | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-18-9808A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932040 | |||||||
| chr7:66932104 | G | A | 3 | a0001c0001t0003g0028 a0001c0001t0003g0241 a0001c0001t0031g0223 |
4 | HG00738.hp2 HG01361.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-9744G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932104 | |||||||
| chr7:66932183 | A | G | 1 | a0001c0001t0012g0273 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-18-9665A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932183 | |||||||
| chr7:66932224 | CTG | C | 11 | a0001c0001t0001g0117 a0001c0001t0007g0015 a0001c0001t0007g0016 others(8): Show |
13 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-9620_-18-9619d others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66932224 | ||||||
| chr7:66932337 | C | T | 1 | a0001c0001t0006g0106 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-18-9511C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932337 | |||||||
| chr7:66932344 | G | A | 1 | a0001c0001t0005g0337 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-18-9504G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932344 | |||||||
| chr7:66932427 | T | A | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-18-9421T>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932427 | |||||||
| chr7:66932517 | C | CT | 59 | a0001c0001t0001g0149 a0001c0001t0002g0307 a0001c0001t0002g0310 others(56): Show |
61 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-18-9315dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66932517 | ||||||
| chr7:66932602 | GCCTCCCA others(338): Show |
G | 20 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(17): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-9225_-18-8881d others(2): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66932602 | ||||||
| chr7:66932642 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-18-9206A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932642 | |||||||
| chr7:66932749 | C | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(48): Show |
63 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-18-9099C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932749 | |||||||
| chr7:66932797 | T | C | 1 | a0001c0001t0003g0231 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-18-9051T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932797 | |||||||
| chr7:66932976 | A | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(48): Show |
63 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-18-8872A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66932976 | |||||||
| chr7:66933003 | C | T | 1 | a0001c0001t0003g0249 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18-8845C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933003 | |||||||
| chr7:66933020 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0132 a0001c0001t0001g0139 others(1): Show |
4 | HG00099.hp1 HG03927.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-8828G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933020 | |||||||
| chr7:66933093 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-18-8755C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933093 | |||||||
| chr7:66933193 | A | T | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-18-8655A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933193 | |||||||
| chr7:66933281 | T | C | 105 | a0001c0001t0001g0196 a0001c0001t0001g0201 a0001c0001t0004g0012 others(102): Show |
117 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-18-8567T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933281 | |||||||
| chr7:66933315 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0161 others(1): Show |
4 | HG01261.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-8533G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933315 | |||||||
| chr7:66933326 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18-8522C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933326 | |||||||
| chr7:66933380 | T | G | 3 | a0001c0001t0002g0008 a0001c0001t0002g0191 a0001c0001t0002g0192 |
5 | HG02055.hp2 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-8468T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933380 | |||||||
| chr7:66933407 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(48): Show |
63 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-18-8441A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933407 | |||||||
| chr7:66933477 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-18-8371A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933477 | |||||||
| chr7:66933603 | C | T | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-18-8245C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933603 | |||||||
| chr7:66933713 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0017g0110 |
2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-18-8135C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933713 | |||||||
| chr7:66933724 | A | G | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-18-8124A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933724 | |||||||
| chr7:66933753 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-18-8095C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933753 | |||||||
| chr7:66933878 | T | C | 1 | a0001c0001t0003g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-18-7970T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66933878 | |||||||
| chr7:66933965 | C | CT | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18-7872dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66933965 | ||||||
| chr7:66934030 | C | T | 58 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(55): Show |
61 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-18-7818C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66934030 | |||||||
| chr7:66934031 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0259 |
2 | HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-7817G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66934031 | |||||||
| chr7:66934071 | C | T | 1 | a0001c0001t0007g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-18-7777C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66934071 | |||||||
| chr7:66934264 | A | G | 226 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0032 others(223): Show |
263 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.-18-7584A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66934264 | |||||||
| chr7:66934523 | C | T | 50 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0009 others(47): Show |
61 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-18-7325C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66934523 | |||||||
| chr7:66934662 | G | T | 36 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(33): Show |
47 | HG00408.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.-18-7186G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66934662 | |||||||
| chr7:66934909 | G | A | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0140 others(4): Show |
8 | HG00099.hp2 HG00741.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18-6939G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66934909 | |||||||
| chr7:66935133 | T | C | 105 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0004g0012 others(102): Show |
117 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-18-6715T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66935133 | |||||||
| chr7:66935157 | C | T | 54 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(51): Show |
56 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-18-6691C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66935157 | |||||||
| chr7:66935608 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18-6240C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66935608 | |||||||
| chr7:66935609 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0161 others(1): Show |
4 | HG01261.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-6239G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66935609 | |||||||
| chr7:66935679 | A | G | 1 | a0001c0001t0003g0235 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-18-6169A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66935679 | |||||||
| chr7:66935842 | C | T | 1 | a0001c0001t0003g0245 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-18-6006C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66935842 | |||||||
| chr7:66935981 | C | T | 4 | a0001c0001t0006g0005 a0001c0001t0006g0096 a0001c0001t0006g0099 others(1): Show |
6 | NA18947.hp1 NA18970.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-5867C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66935981 | |||||||
| chr7:66936013 | G | T | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18-5835G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66936013 | |||||||
| chr7:66936221 | G | T | 12 | a0001c0001t0001g0026 a0001c0001t0001g0196 a0001c0001t0001g0197 others(9): Show |
13 | HG00544.hp2 HG02015.hp2 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-5627G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66936221 | |||||||
| chr7:66936267 | G | A | 1 | a0001c0001t0005g0318 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-18-5581G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66936267 | |||||||
| chr7:66936409 | A | T | 5 | a0001c0001t0005g0321 a0001c0001t0005g0322 a0001c0001t0005g0323 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-5439A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66936409 | |||||||
| chr7:66936470 | A | G | 105 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0004g0012 others(102): Show |
117 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-18-5378A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66936470 | |||||||
| chr7:66936516 | C | CT | 7 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0002g0314 others(4): Show |
8 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-5322dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66936516 | ||||||
| chr7:66936552 | G | C | 1 | a0001c0001t0003g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-18-5296G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66936552 | |||||||
| chr7:66936564 | C | T | 57 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(54): Show |
60 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-18-5284C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66936564 | |||||||
| chr7:66936591 | CTCT | C | 6 | a0001c0001t0004g0055 a0001c0001t0004g0057 a0001c0001t0004g0058 others(3): Show |
6 | HG00280.hp2 HG00642.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-5250_-18-5248d others(5): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66936591 | ||||||
| chr7:66937035 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-18-4813T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937035 | |||||||
| chr7:66937230 | T | C | 2 | a0001c0001t0002g0277 a0001c0001t0002g0289 |
2 | NA18962.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-18-4618T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937230 | |||||||
| chr7:66937337 | T | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(48): Show |
63 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-18-4511T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937337 | |||||||
| chr7:66937771 | C | T | 2 | a0001c0001t0005g0011 a0001c0001t0005g0043 |
3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-18-4077C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937771 | |||||||
| chr7:66937774 | G | A | 59 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(56): Show |
62 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.-18-4074G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937774 | |||||||
| chr7:66937831 | C | G | 1 | a0001c0001t0017g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18-4017C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937831 | |||||||
| chr7:66937849 | T | C | 1 | a0001c0001t0003g0227 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-18-3999T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937849 | |||||||
| chr7:66937871 | T | C | 1 | a0001c0001t0002g0283 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-18-3977T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937871 | |||||||
| chr7:66937879 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-18-3969T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937879 | |||||||
| chr7:66937902 | G | C | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(48): Show |
63 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-18-3946G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937902 | |||||||
| chr7:66937994 | G | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0209 a0001c0001t0001g0212 |
3 | HG02109.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-18-3854G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66937994 | |||||||
| chr7:66938022 | G | A | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-3826G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66938022 | |||||||
| chr7:66938170 | A | G | 21 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(18): Show |
27 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18-3678A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66938170 | |||||||
| chr7:66938233 | G | T | 155 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(152): Show |
179 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.-18-3615G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66938233 | |||||||
| chr7:66938327 | G | A | 1 | a0001c0001t0003g0250 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-18-3521G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66938327 | |||||||
| chr7:66938600 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-18-3248C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66938600 | |||||||
| chr7:66938603 | G | GTTCAACT others(11): Show |
1 | a0001c0001t0024g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-18-3240_-18-3223d others(20): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66938603 | ||||||
| chr7:66938696 | C | T | 1 | a0001c0001t0008g0187 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-18-3152C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66938696 | |||||||
| chr7:66938864 | C | G | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18-2984C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66938864 | |||||||
| chr7:66938907 | G | C | 1 | a0001c0001t0021g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-2941G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66938907 | |||||||
| chr7:66938934 | A | C | 3 | a0001c0001t0004g0013 a0001c0001t0004g0051 a0001c0001t0004g0052 |
4 | NA18941.hp1 NA18948.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-2914A>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66938934 | |||||||
| chr7:66939030 | C | T | 1 | a0001c0001t0002g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-18-2818C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939030 | |||||||
| chr7:66939048 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18-2800C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939048 | |||||||
| chr7:66939058 | C | CCATTTAA others(14): Show |
1 | a0001c0001t0001g0127 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-18-2784_-18-2764d others(23): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66939058 | ||||||
| chr7:66939158 | C | G | 54 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(51): Show |
56 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-18-2690C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939158 | |||||||
| chr7:66939222 | T | C | 1 | a0001c0001t0004g0075 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-18-2626T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939222 | |||||||
| chr7:66939255 | G | T | 1 | a0001c0001t0004g0074 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-18-2593G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939255 | |||||||
| chr7:66939281 | G | A | 20 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(17): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-2567G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939281 | |||||||
| chr7:66939290 | C | T | 12 | a0001c0001t0001g0026 a0001c0001t0001g0196 a0001c0001t0001g0197 others(9): Show |
13 | HG00544.hp2 HG02015.hp2 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-2558C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939290 | |||||||
| chr7:66939333 | C | T | 1 | a0001c0001t0005g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-2515C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939333 | |||||||
| chr7:66939350 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(48): Show |
63 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-18-2498A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939350 | |||||||
| chr7:66939390 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18-2458G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939390 | |||||||
| chr7:66939390 | G | C | 1 | a0001c0001t0017g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18-2458G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939390 | |||||||
| chr7:66939556 | T | C | 1 | a0001c0001t0019g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-18-2292T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939556 | |||||||
| chr7:66939570 | C | T | 1 | a0001c0001t0005g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-2278C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939570 | |||||||
| chr7:66939669 | G | A | 1 | a0001c0001t0017g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18-2179G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939669 | |||||||
| chr7:66939721 | T | G | 20 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(17): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-2127T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939721 | |||||||
| chr7:66939783 | T | C | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-18-2065T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66939783 | |||||||
| chr7:66940173 | C | T | 1 | a0001c0001t0003g0227 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-18-1675C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940173 | |||||||
| chr7:66940195 | C | A | 7 | a0001c0001t0001g0175 a0001c0001t0008g0007 a0001c0001t0008g0177 others(4): Show |
9 | HG00741.hp1 HG01106.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-1653C>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940195 | |||||||
| chr7:66940200 | C | T | 1 | a0001c0001t0021g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-1648C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940200 | |||||||
| chr7:66940257 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18-1591G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940257 | |||||||
| chr7:66940268 | T | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-18-1580T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940268 | |||||||
| chr7:66940398 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG01167.hp2 HG01168.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-18-1450C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940398 | |||||||
| chr7:66940517 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18-1331C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940517 | |||||||
| chr7:66940561 | C | T | 1 | a0001c0001t0021g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-1287C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940561 | |||||||
| chr7:66940699 | A | G | 1 | a0001c0001t0021g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-1149A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940699 | |||||||
| chr7:66940915 | T | G | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18-933T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940915 | |||||||
| chr7:66940925 | T | TA | 12 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0113 others(9): Show |
14 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18-922dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66940925 | ||||||
| chr7:66940969 | T | G | 104 | a0001c0001t0002g0042 a0001c0001t0004g0012 a0001c0001t0004g0013 others(101): Show |
116 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-18-879T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66940969 | |||||||
| chr7:66941111 | G | T | 1 | a0001c0001t0005g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-737G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66941111 | |||||||
| chr7:66941167 | G | C | 1 | a0001c0001t0006g0104 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-18-681G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66941167 | |||||||
| chr7:66941374 | G | A | 7 | a0001c0001t0002g0008 a0001c0001t0002g0191 a0001c0001t0002g0192 others(4): Show |
9 | HG01243.hp1 HG02055.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-474G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66941374 | |||||||
| chr7:66941378 | C | CA | 7 | a0001c0001t0001g0164 a0001c0001t0001g0170 a0001c0001t0002g0218 others(4): Show |
7 | HG00735.hp1 HG01256.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18-455dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941378 | ||||||
| chr7:66941378 | CA | C | 5 | a0001c0001t0001g0204 a0001c0001t0003g0004 a0001c0001t0005g0322 others(2): Show |
6 | HG01515.hp2 HG02015.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-455delA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941378 | ||||||
| chr7:66941394 | G | A | 1 | a0001c0001t0005g0043 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18-454G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66941394 | |||||||
| chr7:66941394 | GA | G | 57 | a0001c0001t0001g0150 a0001c0001t0003g0002 a0001c0001t0004g0012 others(54): Show |
61 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-18-443delA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941394 | ||||||
| chr7:66941395 | A | G | 3 | a0001c0001t0004g0070 a0001c0001t0004g0074 a0001c0001t0005g0043 |
3 | HG02145.hp2 NA18956.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-18-453A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66941395 | |||||||
| chr7:66941449 | G | A | 1 | a0001c0001t0004g0087 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-18-399G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66941449 | |||||||
| chr7:66941561 | A | AAC | 25 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0117 others(22): Show |
29 | HG00738.hp2 HG01071.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18-251_-18-250dup others(2): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941561 | ||||||
| chr7:66941561 | A | AACAC | 23 | a0001c0001t0001g0139 a0001c0001t0001g0199 a0001c0001t0001g0209 others(20): Show |
29 | HG00099.hp1 HG00438.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18-253_-18-250dup others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941561 | ||||||
| chr7:66941561 | A | AACACAC | 4 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0006g0093 others(1): Show |
5 | HG02145.hp2 HG02280.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-255_-18-250dup others(6): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941561 | ||||||
| chr7:66941561 | A | AC | 3 | a0001c0001t0001g0164 a0001c0001t0004g0084 a0001c0001t0007g0121 |
3 | HG01256.hp1 HG02257.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.-18-287_-18-286ins others(1): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66941561 | |||||||
| chr7:66941561 | A | C | 1 | a0001c0001t0007g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-18-287A>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66941561 | |||||||
| chr7:66941561 | AAC | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0191 a0001c0001t0002g0192 others(100): Show |
119 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-18-251_-18-250del others(2): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941561 | ||||||
| chr7:66941561 | AACAC | A | 8 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0004g0055 others(5): Show |
8 | HG00280.hp2 HG00642.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-253_-18-250del others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941561 | ||||||
| chr7:66941561 | AACACAC | A | 3 | a0001c0001t0002g0271 a0001c0001t0002g0297 a0001c0001t0002g0301 |
3 | HG03688.hp2 NA19083.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-18-255_-18-250del others(6): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941561 | ||||||
| chr7:66941561 | AACACACA others(1): Show |
A | 33 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(30): Show |
44 | HG00408.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-18-257_-18-250del others(8): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941561 | ||||||
| chr7:66941561 | AACACACA others(3): Show |
A | 1 | a0001c0001t0005g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-259_-18-250del others(10): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 66941561 | ||||||
| chr7:66941836 | C | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0179 a0001c0001t0001g0183 |
3 | HG01175.hp2 HG01361.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-18-12C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 1/6 | chr7 | 66941836 | |||||||
| chr7:66942043 | T | C | 1 | a0001c0001t0019g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.159+19T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66942043 | |||||||
| chr7:66942143 | G | T | 51 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0009 others(48): Show |
62 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.159+119G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66942143 | |||||||
| chr7:66942418 | A | T | 1 | a0001c0001t0021g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.159+394A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66942418 | |||||||
| chr7:66942477 | G | A | 1 | a0001c0001t0004g0085 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.159+453G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66942477 | |||||||
| chr7:66942531 | C | T | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.159+507C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66942531 | |||||||
| chr7:66942548 | T | C | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.159+524T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66942548 | |||||||
| chr7:66942785 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.159+761C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66942785 | |||||||
| chr7:66942955 | T | C | 4 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0303 others(1): Show |
4 | HG00597.hp1 NA19007.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+931T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66942955 | |||||||
| chr7:66943202 | C | G | 6 | a0001c0001t0004g0085 a0001c0001t0004g0086 a0001c0001t0004g0089 others(3): Show |
6 | NA18945.hp1 NA18960.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.159+1178C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66943202 | |||||||
| chr7:66943206 | G | A | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.159+1182G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66943206 | |||||||
| chr7:66943222 | C | G | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+1198C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66943222 | |||||||
| chr7:66943383 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.159+1359C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66943383 | |||||||
| chr7:66943650 | T | A | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.160-1326T>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66943650 | |||||||
| chr7:66943691 | ATG | A | 20 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(17): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.160-1283_160-1282d others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 66943691 | ||||||
| chr7:66943791 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160-1185A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66943791 | |||||||
| chr7:66943795 | C | CT | 30 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0126 others(27): Show |
33 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.160-1167dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 66943795 | ||||||
| chr7:66943795 | CT | C | 30 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(27): Show |
35 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.160-1167delT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 66943795 | ||||||
| chr7:66943888 | C | G | 1 | a0001c0001t0003g0251 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.160-1088C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66943888 | |||||||
| chr7:66943889 | C | G | 1 | a0001c0001t0003g0249 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.160-1087C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66943889 | |||||||
| chr7:66943943 | C | T | 1 | a0001c0001t0029g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.160-1033C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66943943 | |||||||
| chr7:66943993 | C | G | 79 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(76): Show |
88 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.160-983C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66943993 | |||||||
| chr7:66944084 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.160-892C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66944084 | |||||||
| chr7:66944103 | C | CT | 29 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0132 others(26): Show |
29 | HG00099.hp1 HG00621.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.160-854dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 66944103 | ||||||
| chr7:66944103 | CT | C | 95 | a0001c0001t0001g0150 a0001c0001t0002g0001 a0001c0001t0002g0032 others(92): Show |
113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.160-854delT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 66944103 | ||||||
| chr7:66944103 | CTT | C | 28 | a0001c0001t0004g0012 a0001c0001t0004g0045 a0001c0001t0004g0047 others(25): Show |
32 | HG00642.hp1 HG00735.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.160-855_160-854del others(2): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 66944103 | ||||||
| chr7:66944293 | C | T | 6 | a0001c0001t0002g0270 a0001c0001t0002g0276 a0001c0001t0002g0287 others(3): Show |
6 | HG03942.hp1 NA18971.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-683C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66944293 | |||||||
| chr7:66944294 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.160-682G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66944294 | |||||||
| chr7:66944383 | G | A | 1 | a0001c0001t0029g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.160-593G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66944383 | |||||||
| chr7:66944393 | C | T | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.160-583C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66944393 | |||||||
| chr7:66944426 | C | T | 1 | a0001c0001t0021g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160-550C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66944426 | |||||||
| chr7:66944712 | A | T | 1 | a0001c0001t0003g0231 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.160-264A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66944712 | |||||||
| chr7:66944894 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(48): Show |
63 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.160-82A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66944894 | |||||||
| chr7:66944919 | G | A | 2 | a0001c0001t0003g0239 a0001c0001t0003g0248 |
2 | HG01433.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.160-57G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 2/6 | chr7 | 66944919 | |||||||
| chr7:66945650 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0293 |
3 | HG00738.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.445+389A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66945650 | |||||||
| chr7:66946005 | A | G | 1 | a0001c0001t0019g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.445+744A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66946005 | |||||||
| chr7:66946085 | C | CA | 51 | a0001c0001t0001g0146 a0001c0001t0002g0001 a0001c0001t0002g0032 others(48): Show |
63 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.445+839dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr7 | 66946085 | ||||||
| chr7:66946085 | CA | C | 60 | a0001c0001t0003g0230 a0001c0001t0003g0232 a0001c0001t0004g0012 others(57): Show |
63 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.445+839delA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr7 | 66946085 | ||||||
| chr7:66946117 | G | T | 1 | a0001c0001t0021g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.445+856G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66946117 | |||||||
| chr7:66946170 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.445+909G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66946170 | |||||||
| chr7:66946210 | C | T | 79 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(76): Show |
88 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.445+949C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66946210 | |||||||
| chr7:66946249 | G | A | 1 | a0001c0001t0003g0221 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.445+988G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66946249 | |||||||
| chr7:66946265 | AAAAG | A | 20 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(17): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.445+1008_445+1011d others(6): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr7 | 66946265 | ||||||
| chr7:66946530 | A | G | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.445+1269A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66946530 | |||||||
| chr7:66946616 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.445+1355T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66946616 | |||||||
| chr7:66946635 | G | T | 1 | a0001c0001t0005g0318 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.445+1374G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66946635 | |||||||
| chr7:66947059 | A | T | 56 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0022 others(53): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.446-1485A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66947059 | |||||||
| chr7:66947070 | C | T | 1 | a0001c0001t0013g0018 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.446-1474C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66947070 | |||||||
| chr7:66947214 | C | CA | 101 | a0001c0001t0001g0137 a0001c0001t0001g0146 a0001c0001t0001g0154 others(98): Show |
108 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.446-1309dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr7 | 66947214 | ||||||
| chr7:66947214 | C | CAA | 7 | a0001c0001t0004g0045 a0001c0001t0004g0059 a0001c0001t0004g0065 others(4): Show |
7 | HG01175.hp1 HG01978.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.446-1310_446-1309d others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr7 | 66947214 | ||||||
| chr7:66947236 | C | A | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.446-1308C>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66947236 | |||||||
| chr7:66947259 | C | G | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.446-1285C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66947259 | |||||||
| chr7:66947400 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.446-1144G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66947400 | |||||||
| chr7:66947787 | T | A | 260 | a0001c0001t0001g0026 a0001c0001t0001g0117 a0001c0001t0001g0196 others(257): Show |
300 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.446-757T>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66947787 | |||||||
| chr7:66947803 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.446-741G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66947803 | |||||||
| chr7:66948148 | G | C | 20 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(17): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.446-396G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66948148 | |||||||
| chr7:66948347 | C | T | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.446-197C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66948347 | |||||||
| chr7:66948356 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.446-188G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66948356 | |||||||
| chr7:66948389 | G | A | 1 | a0001c0001t0017g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.446-155G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 3/6 | chr7 | 66948389 | |||||||
| chr7:66948707 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.596+13G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66948707 | |||||||
| chr7:66948983 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.596+289G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66948983 | |||||||
| chr7:66949009 | G | C | 1 | a0001c0001t0017g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.596+315G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66949009 | |||||||
| chr7:66949141 | T | A | 1 | a0001c0001t0019g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.596+447T>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66949141 | |||||||
| chr7:66949141 | T | TA | 21 | a0001c0001t0002g0275 a0001c0001t0002g0301 a0001c0001t0002g0305 others(18): Show |
27 | HG01928.hp1 HG01934.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.596+462dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr7 | 66949141 | ||||||
| chr7:66949156 | A | G | 1 | a0001c0001t0017g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.596+462A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66949156 | |||||||
| chr7:66949331 | A | G | 1 | a0001c0001t0009g0253 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.596+637A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66949331 | |||||||
| chr7:66949346 | G | T | 1 | a0001c0001t0004g0039 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.596+652G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66949346 | |||||||
| chr7:66949483 | A | C | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.596+789A>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66949483 | |||||||
| chr7:66949532 | A | G | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0030g0215 |
3 | HG02615.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.596+838A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66949532 | |||||||
| chr7:66949606 | T | TAAAC | 340 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0019 others(337): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.596+914_596+915ins others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr7 | 66949606 | ||||||
| chr7:66949700 | C | A | 9 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0113 others(6): Show |
11 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.596+1006C>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66949700 | |||||||
| chr7:66949803 | G | GT | 57 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(54): Show |
60 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.596+1117dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr7 | 66949803 | ||||||
| chr7:66949892 | T | C | 24 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.597-1060T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66949892 | |||||||
| chr7:66949942 | C | T | 1 | a0001c0001t0007g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.597-1010C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66949942 | |||||||
| chr7:66950082 | T | C | 141 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(138): Show |
164 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.597-870T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66950082 | |||||||
| chr7:66950149 | A | T | 104 | a0001c0001t0002g0042 a0001c0001t0004g0012 a0001c0001t0004g0013 others(101): Show |
116 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.597-803A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66950149 | |||||||
| chr7:66950185 | C | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
17 | HG00099.hp2 HG00741.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.597-767C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66950185 | |||||||
| chr7:66950215 | C | CA | 18 | a0001c0001t0003g0244 a0001c0001t0004g0069 a0001c0001t0005g0036 others(15): Show |
20 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.597-722dupA | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr7 | 66950215 | ||||||
| chr7:66950215 | C | CAA | 9 | a0001c0001t0005g0035 a0001c0001t0005g0318 a0001c0001t0005g0319 others(6): Show |
10 | HG02155.hp1 NA18939.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.597-723_597-722dup others(2): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr7 | 66950215 | ||||||
| chr7:66950378 | T | G | 1 | a0001c0001t0004g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.597-574T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66950378 | |||||||
| chr7:66950463 | T | G | 1 | a0001c0001t0005g0324 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.597-489T>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66950463 | |||||||
| chr7:66950614 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.597-338G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66950614 | |||||||
| chr7:66950622 | C | A | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.597-330C>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66950622 | |||||||
| chr7:66950833 | C | T | 4 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0263 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-119C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 4/6 | chr7 | 66950833 | |||||||
| chr7:66951561 | G | C | 1 | a0001c0001t0001g0202 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.780+426G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66951561 | |||||||
| chr7:66951628 | A | G | 20 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(17): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.780+493A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66951628 | |||||||
| chr7:66951738 | C | T | 1 | a0001c0001t0002g0309 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.780+603C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66951738 | |||||||
| chr7:66951768 | C | T | 23 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(20): Show |
26 | HG00642.hp1 HG01257.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.780+633C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66951768 | |||||||
| chr7:66951780 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.780+645C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66951780 | |||||||
| chr7:66952055 | C | T | 50 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0009 others(47): Show |
61 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.780+920C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66952055 | |||||||
| chr7:66952223 | G | A | 1 | a0001c0001t0030g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.781-1003G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66952223 | |||||||
| chr7:66952539 | G | T | 1 | a0001c0001t0005g0324 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.781-687G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66952539 | |||||||
| chr7:66952561 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.781-665C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66952561 | |||||||
| chr7:66952696 | C | A | 103 | a0001c0001t0002g0042 a0001c0001t0004g0012 a0001c0001t0004g0013 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.781-530C>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66952696 | |||||||
| chr7:66952697 | G | A | 7 | a0001c0001t0002g0008 a0001c0001t0002g0191 a0001c0001t0002g0192 others(4): Show |
9 | HG01243.hp1 HG02055.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.781-529G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66952697 | |||||||
| chr7:66952760 | G | T | 1 | a0001c0001t0021g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-466G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66952760 | |||||||
| chr7:66953019 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.781-207A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953019 | |||||||
| chr7:66953031 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.781-195G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953031 | |||||||
| chr7:66953081 | A | T | 1 | a0001c0001t0004g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-145A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953081 | |||||||
| chr7:66953083 | A | T | 1 | a0001c0001t0004g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-143A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953083 | |||||||
| chr7:66953086 | G | C | 1 | a0001c0001t0004g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-140G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953086 | |||||||
| chr7:66953088 | G | T | 1 | a0001c0001t0004g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-138G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953088 | |||||||
| chr7:66953090 | A | G | 1 | a0001c0001t0004g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-136A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953090 | |||||||
| chr7:66953091 | A | T | 1 | a0001c0001t0004g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-135A>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953091 | |||||||
| chr7:66953092 | C | G | 1 | a0001c0001t0004g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-134C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953092 | |||||||
| chr7:66953093 | C | A | 1 | a0001c0001t0004g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-133C>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953093 | |||||||
| chr7:66953095 | C | G | 1 | a0001c0001t0004g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-131C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953095 | |||||||
| chr7:66953096 | C | T | 1 | a0001c0001t0004g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-130C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | chr7 | 66953096 | |||||||
| chr7:66953146 | CTG | C | 9 | a0001c0001t0004g0013 a0001c0001t0004g0051 a0001c0001t0004g0052 others(6): Show |
10 | HG02074.hp1 NA18941.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.781-78_781-77delGT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr7 | 66953146 | ||||||
| chr7:66953636 | G | A | 23 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0317 others(20): Show |
26 | HG00642.hp1 HG01257.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.924+267G>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66953636 | |||||||
| chr7:66953727 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.924+358C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66953727 | |||||||
| chr7:66953763 | T | C | 337 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0019 others(334): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.924+394T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66953763 | |||||||
| chr7:66953939 | C | CT | 17 | a0001c0001t0001g0117 a0001c0001t0001g0136 a0001c0001t0001g0144 others(14): Show |
17 | HG01071.hp2 HG02615.hp2 HG02738.hp1 others(14): Show |
intron_variant | MODIFIER | c.924+594dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 66953939 | ||||||
| chr7:66953939 | CT | C | 10 | a0001c0001t0001g0155 a0001c0001t0001g0209 a0001c0001t0002g0042 others(7): Show |
10 | HG01975.hp1 HG02109.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.924+594delT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 66953939 | ||||||
| chr7:66953939 | CTT | C | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(48): Show |
65 | HG00408.hp2 HG00642.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.924+593_924+594del others(2): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 66953939 | ||||||
| chr7:66953939 | CTTT | C | 26 | a0001c0001t0002g0284 a0001c0001t0002g0306 a0001c0001t0004g0041 others(23): Show |
32 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.924+592_924+594del others(3): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 66953939 | ||||||
| chr7:66953939 | CTTTT | C | 55 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(52): Show |
58 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.924+591_924+594del others(4): Show |
TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 66953939 | ||||||
| chr7:66953944 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.924+575T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66953944 | |||||||
| chr7:66953963 | T | A | 1 | a0001c0001t0021g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.924+594T>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66953963 | |||||||
| chr7:66954092 | T | C | 104 | a0001c0001t0002g0042 a0001c0001t0004g0012 a0001c0001t0004g0013 others(101): Show |
116 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.924+723T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66954092 | |||||||
| chr7:66954155 | G | T | 21 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(18): Show |
27 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.924+786G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66954155 | |||||||
| chr7:66954158 | A | G | 1 | a0001c0001t0006g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.924+789A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66954158 | |||||||
| chr7:66954247 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0157 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.924+878A>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66954247 | |||||||
| chr7:66954383 | A | AT | 12 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0002g0277 others(9): Show |
13 | HG01978.hp1 HG01978.hp2 NA18940.hp1 others(10): Show |
intron_variant | MODIFIER | c.924+1034dupT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 66954383 | ||||||
| chr7:66954383 | AT | A | 8 | a0001c0001t0001g0169 a0001c0001t0002g0281 a0001c0001t0003g0029 others(5): Show |
9 | HG00558.hp2 HG02486.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.924+1034delT | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 66954383 | ||||||
| chr7:66954396 | T | A | 1 | a0001c0001t0003g0009 | 3 | HG01167.hp1 HG01169.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.924+1027T>A | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66954396 | |||||||
| chr7:66954470 | C | T | 1 | a0001c0001t0017g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.925-1032C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66954470 | |||||||
| chr7:66954709 | G | C | 5 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0202 others(2): Show |
5 | NA18954.hp1 NA18961.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.925-793G>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66954709 | |||||||
| chr7:66954785 | T | C | 20 | a0001c0001t0006g0003 a0001c0001t0006g0005 a0001c0001t0006g0014 others(17): Show |
26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.925-717T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66954785 | |||||||
| chr7:66954801 | C | G | 4 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0002g0314 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.925-701C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66954801 | |||||||
| chr7:66954831 | T | C | 103 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0038 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.925-671T>C | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66954831 | |||||||
| chr7:66955054 | C | G | 104 | a0001c0001t0002g0042 a0001c0001t0004g0012 a0001c0001t0004g0013 others(101): Show |
116 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.925-448C>G | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66955054 | |||||||
| chr7:66955066 | C | T | 1 | a0001c0001t0002g0285 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.925-436C>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66955066 | |||||||
| chr7:66955130 | G | T | 1 | a0001c0001t0005g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925-372G>T | TMEM248 | ENSG00000106609.16 | transcript | ENST00000341567.8 | protein_coding | 6/6 | chr7 | 66955130 |