Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 441027 |
| ensemblid | ENSG00000249242.8 |
| hgncid | 37263 |
| symbol | TMEM150C |
| name | transmembrane protein 150C |
| refseq_nuc | NM_001080506.3 |
| refseq_prot | NP_001073975.1 |
| ensembl_nuc | ENST00000449862.7 |
| ensembl_prot | ENSP00000403438.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 82483176 |
| end | 82561988 |
| strand | - |
| ver | v1.2 |
| region | chr4:82483176-82561988 |
| region5000 | chr4:82478176-82566988 |
| regionname0 | TMEM150C_chr4_82483176_82561988 |
| regionname5000 | TMEM150C_chr4_82478176_82566988 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 249 | 254 | 87 | 43 | 76 | 14 | 32 | 52 | TMEM150C_chr4_82478176_82566988 | TMEM150C | MDGKK others(244): Show |
chr4 | 82478176 | 82566988 |
| a0002 | 0/0 | 249 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | MDGKK others(244): Show |
chr4 | 82478176 | 82566988 |
| a0003 | 0/0 | 249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | MDGKK others(244): Show |
chr4 | 82478176 | 82566988 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 747 | 253 | 87 | 43 | 76 | 14 | 31 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ATGGA others(742): Show |
chr4 | 82478176 | 82566988 | ||
| a0001c0004 | 0/0 | 747 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ATGGA others(742): Show |
chr4 | 82478176 | 82566988 | ||
| a0002c0003 | 0/0 | 747 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ATGGA others(742): Show |
chr4 | 82478176 | 82566988 | ||
| a0003c0002 | 0/0 | 747 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ATGGA others(742): Show |
chr4 | 82478176 | 82566988 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3178 | 68 | 7 | 14 | 33 | 2 | 11 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3173): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0002 | 0/0 | 3184 | 38 | 1 | 5 | 17 | 4 | 11 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3179): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0003 | 0/0 | 3179 | 31 | 12 | 5 | 11 | 0 | 3 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3174): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0004 | 0/0 | 3179 | 18 | 5 | 7 | 3 | 0 | 3 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3174): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0005 | 0/0 | 3182 | 13 | 13 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3177): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0006 | 0/0 | 3174 | 10 | 10 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3169): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0007 | 0/0 | 3181 | 9 | 7 | 0 | 0 | 2 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3176): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0008 | 0/0 | 3184 | 8 | 0 | 5 | 0 | 3 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3179): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0009 | 0/0 | 3179 | 8 | 8 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3174): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0010 | 0/0 | 3184 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3179): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0011 | 0/0 | 3178 | 5 | 0 | 0 | 4 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3173): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0012 | 0/0 | 3180 | 5 | 1 | 2 | 0 | 2 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3175): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0013 | 0/0 | 3179 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3174): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0014 | 0/0 | 3177 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3172): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0015 | 0/0 | 3178 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3173): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0016 | 0/0 | 3185 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3180): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0017 | 0/0 | 3174 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3169): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0018 | 0/0 | 3180 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3175): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0019 | 0/0 | 3178 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3173): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0020 | 0/0 | 3178 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3173): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0021 | 0/1 | 3184 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3179): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0022 | 0/0 | 3184 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3179): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0023 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3180): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0024 | 0/0 | 3184 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3179): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0025 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3180): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0026 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3180): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0027 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3180): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0028 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3180): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0029 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3178): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0030 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3176): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0031 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3175): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0033 | 0/0 | 3178 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3173): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0034 | 0/0 | 3179 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3174): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0035 | 0/0 | 3178 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3173): Show |
chr4 | 82478176 | 82566988 |
| a0001c0001t0036 | 0/0 | 3178 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3173): Show |
chr4 | 82478176 | 82566988 |
| a0001c0004t0001 | 0/0 | 3178 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3173): Show |
chr4 | 82478176 | 82566988 |
| a0002c0003t0003 | 0/0 | 3179 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3174): Show |
chr4 | 82478176 | 82566988 |
| a0003c0002t0032 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | ACCCG others(3176): Show |
chr4 | 82478176 | 82566988 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0008g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0008g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0008g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0008g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0010g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0010g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0011g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0011g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0011g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0011g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0011g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0012g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0012g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0012g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0012g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0013g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0014g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0014g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0014g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0015g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0015g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0016g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0016g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0017g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0017g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0018g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0018g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0019g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0019g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0020g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0020g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0021g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0022g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0023g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0024g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0025g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0026g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0027g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0028g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0029g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0030g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0031g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0033g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0034g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0035g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0001t0036g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0002c0003t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| a0003c0002t0032g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0073 | EUR | GBR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00099 | hp2 | a0001 | c0001 | t0008 | g0161 | EUR | GBR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0140 | EUR | GBR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | FIN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00280 | hp2 | a0001 | c0001 | t0022 | g0050 | EUR | FIN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | FIN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0141 | EUR | FIN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00642 | hp2 | a0001 | c0001 | t0035 | g0016 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00673 | hp2 | a0001 | c0001 | t0011 | g0010 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00735 | hp2 | a0001 | c0001 | t0019 | g0196 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01071 | hp1 | a0002 | c0003 | t0003 | g0190 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0216 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01167 | hp1 | a0001 | c0001 | t0012 | g0070 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01167 | hp2 | a0001 | c0001 | t0014 | g0109 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0192 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0249 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0106 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01243 | hp2 | a0001 | c0001 | t0029 | g0170 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0217 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01257 | hp1 | a0001 | c0001 | t0008 | g0214 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0221 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0230 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01515 | hp1 | a0001 | c0001 | t0008 | g0220 | EUR | IBS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01515 | hp2 | a0001 | c0001 | t0012 | g0069 | EUR | IBS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0219 | EUR | IBS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01516 | hp2 | a0001 | c0001 | t0012 | g0058 | EUR | IBS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0033 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0105 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0125 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0231 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02056 | hp1 | a0001 | c0001 | t0011 | g0011 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02074 | hp1 | a0001 | c0001 | t0011 | g0200 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0211 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | CDX | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0032 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0098 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0099 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0169 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0091 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0030 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0094 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0189 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02818 | hp1 | a0001 | c0001 | t0030 | g0166 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02886 | hp1 | a0001 | c0001 | t0016 | g0146 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02886 | hp2 | a0001 | c0001 | t0024 | g0008 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0027 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02895 | hp2 | a0001 | c0001 | t0028 | g0029 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0087 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0086 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02922 | hp1 | a0001 | c0001 | t0020 | g0088 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0093 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0081 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02970 | hp2 | a0001 | c0001 | t0027 | g0096 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03041 | hp1 | a0001 | c0001 | t0017 | g0246 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0171 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0145 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0103 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03139 | hp2 | a0001 | c0001 | t0020 | g0090 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03195 | hp2 | a0001 | c0001 | t0016 | g0144 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03453 | hp2 | a0003 | c0002 | t0032 | g0024 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0102 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0097 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0092 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03688 | hp2 | a0001 | c0001 | t0018 | g0121 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0195 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03710 | hp2 | a0001 | c0001 | t0025 | g0150 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0057 | SAS | BEB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | BEB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0149 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0238 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG04228 | hp2 | a0001 | c0004 | t0001 | g0055 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0095 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18612 | hp2 | a0001 | c0001 | t0034 | g0241 | EAS | CHB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0001 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0025 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18944 | hp1 | a0001 | c0001 | t0018 | g0245 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18956 | hp1 | a0001 | c0001 | t0011 | g0252 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18967 | hp2 | a0001 | c0001 | t0015 | g0157 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19000 | hp1 | a0001 | c0001 | t0015 | g0167 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19003 | hp1 | a0001 | c0001 | t0026 | g0051 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19011 | hp1 | a0001 | c0001 | t0023 | g0237 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19043 | hp1 | a0001 | c0001 | t0031 | g0153 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19066 | hp1 | a0001 | c0001 | t0036 | g0124 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19068 | hp1 | a0001 | c0001 | t0015 | g0225 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | TSI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | GIH | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | GIH | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01123 | hp1 | a0001 | c0001 | t0019 | g0182 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0218 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02486 | hp1 | a0001 | c0001 | t0033 | g0080 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0085 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | USA | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | USA | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA20300 | hp1 | a0001 | c0001 | t0010 | g0001 | AFR | USA | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0201 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0021 | g0049 | REF | REF | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0163 | REF | REF | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82485587 | G | A | 1 | a0002 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.674C>T | p.Ser225Phe | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 767/3178 | 674/750 | 225/249 | chr4 | 82485587 | |||
| chr4:82485624 | C | T | 1 | a0003 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.637G>A | p.Val213Met | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 730/3178 | 637/750 | 213/249 | chr4 | 82485624 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82490173 | G | A | 1 | a0001c0004 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.429C>T | p.Thr143Thr | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/8 | 522/3178 | 429/750 | 143/249 | chr4 | 82490173 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82483214 | A | G | 1 | a0001c0001t0011 | 5 | HG00673.hp2 HG02056.hp1 HG02074.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2297T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 2297 | chr4 | 82483214 | ||||||
| chr4:82483233 | G | C | 2 | a0001c0001t0004 a0001c0001t0033 |
19 | HG00544.hp2 HG01106.hp1 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2278C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 2278 | chr4 | 82483233 | ||||||
| chr4:82483237 | G | C | 1 | a0001c0001t0019 | 2 | HG00735.hp2 HG01123.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2274C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 2274 | chr4 | 82483237 | ||||||
| chr4:82483388 | G | T | 1 | a0001c0001t0024 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2123C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 2123 | chr4 | 82483388 | ||||||
| chr4:82483613 | T | C | 4 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0017 others(1): Show |
22 | HG00140.hp2 HG00323.hp2 HG01884.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1898A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1898 | chr4 | 82483613 | ||||||
| chr4:82483788 | C | CT | 6 | a0001c0001t0009 a0001c0001t0020 a0001c0001t0023 others(3): Show |
14 | HG02145.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1722dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1722 | chr4 | 82483788 | ||||||
| chr4:82483789 | TTTTTTTC | T | 2 | a0001c0001t0006 a0001c0001t0017 |
12 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1715_*1721delGAAA others(3): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1715 | chr4 | 82483789 | ||||||
| chr4:82483795 | TC | T | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(3): Show |
26 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1715delG | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1715 | chr4 | 82483795 | ||||||
| chr4:82483796 | C | T | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(24): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1715G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1715 | chr4 | 82483796 | ||||||
| chr4:82483798 | T | TTC | 1 | a0001c0001t0012 | 5 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1712_*1713insGA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1712 | chr4 | 82483798 | ||||||
| chr4:82483972 | A | G | 5 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(2): Show |
40 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1539T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1539 | chr4 | 82483972 | ||||||
| chr4:82484079 | C | T | 2 | a0001c0001t0013 a0001c0001t0035 |
5 | HG00642.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1432G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1432 | chr4 | 82484079 | ||||||
| chr4:82484084 | C | T | 2 | a0001c0001t0010 a0001c0001t0024 |
6 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1427G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1427 | chr4 | 82484084 | ||||||
| chr4:82484230 | T | C | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(22): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*1281A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1281 | chr4 | 82484230 | ||||||
| chr4:82484237 | A | G | 1 | a0001c0001t0023 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1274T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1274 | chr4 | 82484237 | ||||||
| chr4:82484411 | C | CA | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(10): Show |
82 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1099dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1099 | chr4 | 82484411 | ||||||
| chr4:82484411 | CA | C | 2 | a0001c0001t0014 a0001c0001t0020 |
5 | HG01167.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1099delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1099 | chr4 | 82484411 | ||||||
| chr4:82484805 | T | A | 2 | a0001c0001t0004 a0001c0001t0034 |
19 | HG00544.hp2 HG01106.hp1 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*706A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 706 | chr4 | 82484805 | ||||||
| chr4:82485011 | G | A | 1 | a0001c0001t0006 | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*500C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 500 | chr4 | 82485011 | ||||||
| chr4:82485041 | G | A | 1 | a0001c0001t0033 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*470C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 470 | chr4 | 82485041 | ||||||
| chr4:82485052 | T | C | 6 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0020 others(3): Show |
18 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*459A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 459 | chr4 | 82485052 | ||||||
| chr4:82485058 | A | G | 1 | a0001c0001t0022 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*453T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 453 | chr4 | 82485058 | ||||||
| chr4:82485064 | A | T | 1 | a0001c0001t0033 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 447 | chr4 | 82485064 | ||||||
| chr4:82485143 | C | T | 1 | a0001c0001t0016 | 2 | HG02886.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*368G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 368 | chr4 | 82485143 | ||||||
| chr4:82485247 | C | T | 6 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0016 others(3): Show |
25 | HG00140.hp2 HG00323.hp2 HG01884.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 264 | chr4 | 82485247 | ||||||
| chr4:82485334 | T | C | 1 | a0001c0001t0008 | 8 | HG00099.hp2 HG01071.hp2 HG01123.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 177 | chr4 | 82485334 | ||||||
| chr4:82485367 | A | G | 3 | a0001c0001t0004 a0001c0001t0033 a0001c0001t0034 |
20 | HG00544.hp2 HG01106.hp1 HG01168.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*144T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 144 | chr4 | 82485367 | ||||||
| chr4:82485396 | A | ATG | 7 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0017 others(4): Show |
26 | HG00140.hp2 HG00323.hp2 HG01884.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*113_*114dupCA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 114 | chr4 | 82485396 | ||||||
| chr4:82485396 | A | ATGTG | 2 | a0001c0001t0005 a0001c0001t0029 |
14 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*111_*114dupCACA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 114 | chr4 | 82485396 | ||||||
| chr4:82485396 | A | ATGTGTG | 11 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(8): Show |
60 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*109_*114dupCACACA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 114 | chr4 | 82485396 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82485944 | T | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0148 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.542-225A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82485944 | |||||||
| chr4:82486002 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.542-283A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486002 | |||||||
| chr4:82486014 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.542-295A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486014 | |||||||
| chr4:82486232 | G | A | 40 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0035 others(37): Show |
40 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.542-513C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486232 | |||||||
| chr4:82486257 | T | A | 2 | a0001c0001t0016g0144 a0001c0001t0016g0146 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.542-538A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486257 | |||||||
| chr4:82486335 | T | TA | 64 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0052 others(61): Show |
64 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.542-617dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486335 | |||||||
| chr4:82486335 | T | TAA | 7 | a0001c0001t0001g0037 a0001c0001t0001g0164 a0001c0001t0003g0005 others(4): Show |
7 | HG00642.hp2 HG02165.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.542-618_542-617dup others(2): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486335 | |||||||
| chr4:82486335 | T | TAAAAA | 8 | a0001c0001t0009g0019 a0001c0001t0009g0030 a0001c0001t0009g0103 others(5): Show |
8 | HG01167.hp1 HG01515.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.542-621_542-617dup others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486335 | |||||||
| chr4:82486335 | TA | T | 15 | a0001c0001t0001g0063 a0001c0001t0001g0110 a0001c0001t0001g0242 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.542-617delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486335 | |||||||
| chr4:82486335 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0002g0022 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.542-631_542-617del others(15): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486335 | |||||||
| chr4:82486403 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.542-684C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486403 | |||||||
| chr4:82486488 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG00738.hp2 HG01192.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-769G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486488 | |||||||
| chr4:82486555 | C | T | 182 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.542-836G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486555 | |||||||
| chr4:82486569 | G | A | 5 | a0001c0001t0009g0019 a0001c0001t0009g0030 a0001c0001t0009g0087 others(2): Show |
5 | HG02622.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-850C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486569 | |||||||
| chr4:82486691 | A | G | 40 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0035 others(37): Show |
40 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.542-972T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486691 | |||||||
| chr4:82486889 | C | A | 1 | a0001c0001t0020g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.542-1170G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486889 | |||||||
| chr4:82487129 | A | G | 2 | a0001c0001t0002g0168 a0001c0001t0002g0240 |
2 | HG00735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.542-1410T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487129 | |||||||
| chr4:82487173 | A | G | 173 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0002g0014 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.542-1454T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487173 | |||||||
| chr4:82487224 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0002g0130 |
2 | NA18948.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.542-1505C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487224 | |||||||
| chr4:82487241 | TAG | T | 12 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0041 others(9): Show |
12 | HG00642.hp2 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.542-1524_542-1523d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487241 | |||||||
| chr4:82487265 | A | G | 1 | a0001c0001t0030g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.542-1546T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487265 | |||||||
| chr4:82487284 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.542-1565T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487284 | |||||||
| chr4:82487305 | C | T | 65 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0035 others(62): Show |
65 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.542-1586G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487305 | |||||||
| chr4:82487805 | A | C | 1 | a0001c0001t0003g0233 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.542-2086T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487805 | |||||||
| chr4:82487815 | C | A | 65 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0035 others(62): Show |
65 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.542-2096G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487815 | |||||||
| chr4:82487819 | C | A | 2 | a0001c0001t0007g0140 a0001c0001t0007g0141 |
2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.542-2100G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487819 | |||||||
| chr4:82487836 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.542-2117C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487836 | |||||||
| chr4:82488027 | T | C | 4 | a0001c0001t0010g0001 a0001c0001t0010g0095 a0001c0001t0010g0097 others(1): Show |
6 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.541+2034A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488027 | |||||||
| chr4:82488051 | T | C | 22 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0081 others(19): Show |
22 | HG00140.hp2 HG00323.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.541+2010A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488051 | |||||||
| chr4:82488178 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.541+1883T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488178 | |||||||
| chr4:82488315 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0206 |
3 | NA18944.hp2 NA18995.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.541+1746C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488315 | |||||||
| chr4:82488354 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.541+1707C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488354 | |||||||
| chr4:82488392 | A | G | 119 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(116): Show |
121 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.541+1669T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488392 | |||||||
| chr4:82488499 | T | C | 7 | a0001c0001t0005g0038 a0001c0001t0005g0084 a0001c0001t0005g0101 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+1562A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488499 | |||||||
| chr4:82488954 | G | A | 3 | a0001c0001t0003g0132 a0001c0001t0003g0138 a0001c0001t0003g0175 |
3 | HG00609.hp1 HG01943.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.541+1107C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488954 | |||||||
| chr4:82489037 | G | A | 51 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0043 others(48): Show |
51 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.541+1024C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489037 | |||||||
| chr4:82489062 | A | AT | 45 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0046 others(42): Show |
45 | HG00738.hp2 HG01106.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.541+998dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489062 | |||||||
| chr4:82489062 | A | ATT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0052 others(6): Show |
9 | HG00544.hp2 HG02486.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.541+997_541+998dup others(2): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489062 | |||||||
| chr4:82489325 | G | A | 12 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0234 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.541+736C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489325 | |||||||
| chr4:82489411 | ACCT | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(4): Show |
7 | HG02165.hp1 HG03098.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+647_541+649del others(3): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489411 | |||||||
| chr4:82489469 | C | T | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.541+592G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489469 | |||||||
| chr4:82489597 | T | C | 1 | a0001c0001t0033g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.541+464A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489597 | |||||||
| chr4:82489611 | T | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(4): Show |
7 | HG02165.hp1 HG03098.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+450A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489611 | |||||||
| chr4:82489715 | A | C | 17 | a0001c0001t0009g0019 a0001c0001t0009g0030 a0001c0001t0009g0085 others(14): Show |
17 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.541+346T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489715 | |||||||
| chr4:82489893 | T | C | 24 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0234 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.541+168A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489893 | |||||||
| chr4:82490044 | T | C | 46 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0232 others(43): Show |
46 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.541+17A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82490044 | |||||||
| chr4:82490048 | G | A | 42 | a0001c0001t0002g0117 a0001c0001t0004g0017 a0001c0001t0004g0111 others(39): Show |
44 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.541+13C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82490048 | |||||||
| chr4:82490309 | AT | A | 3 | a0001c0001t0012g0058 a0001c0001t0012g0069 a0001c0001t0012g0070 |
3 | HG01167.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.364-72delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490309 | |||||||
| chr4:82490311 | A | C | 3 | a0001c0001t0012g0058 a0001c0001t0012g0069 a0001c0001t0012g0070 |
3 | HG01167.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.364-73T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490311 | |||||||
| chr4:82490482 | A | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.364-244T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490482 | |||||||
| chr4:82490508 | T | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG00738.hp2 HG01192.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-270A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490508 | |||||||
| chr4:82490593 | T | G | 20 | a0001c0001t0002g0117 a0001c0001t0004g0017 a0001c0001t0004g0111 others(17): Show |
20 | HG00544.hp2 HG01106.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.364-355A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490593 | |||||||
| chr4:82490754 | G | T | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.364-516C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490754 | |||||||
| chr4:82490798 | G | A | 1 | a0001c0001t0031g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.364-560C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490798 | |||||||
| chr4:82490838 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.364-600C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490838 | |||||||
| chr4:82490934 | G | A | 4 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0031g0153 others(1): Show |
4 | HG02486.hp1 HG03130.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-696C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490934 | |||||||
| chr4:82491049 | C | T | 2 | a0001c0001t0009g0211 a0001c0001t0028g0029 |
2 | HG02145.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.364-811G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491049 | |||||||
| chr4:82491209 | C | T | 17 | a0001c0001t0009g0019 a0001c0001t0009g0030 a0001c0001t0009g0085 others(14): Show |
17 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.364-971G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491209 | |||||||
| chr4:82491237 | G | A | 2 | a0001c0001t0005g0038 a0001c0001t0005g0202 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.364-999C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491237 | |||||||
| chr4:82491446 | G | A | 1 | a0001c0001t0007g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.364-1208C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491446 | |||||||
| chr4:82491595 | G | A | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.364-1357C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491595 | |||||||
| chr4:82491702 | A | G | 23 | a0001c0001t0009g0019 a0001c0001t0009g0030 a0001c0001t0009g0085 others(20): Show |
25 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-1464T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491702 | |||||||
| chr4:82491895 | G | T | 46 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0002g0117 others(43): Show |
48 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.364-1657C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491895 | |||||||
| chr4:82491924 | T | A | 1 | a0001c0001t0003g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.364-1686A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491924 | |||||||
| chr4:82491936 | GT | G | 77 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(74): Show |
79 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.364-1699delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491936 | |||||||
| chr4:82491949 | G | T | 24 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0234 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.364-1711C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491949 | |||||||
| chr4:82491991 | GTGCAGTG others(19): Show |
G | 4 | a0001c0001t0005g0007 a0001c0001t0005g0023 a0001c0001t0005g0031 others(1): Show |
4 | HG02055.hp1 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1779_364-1754d others(28): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491991 | |||||||
| chr4:82492047 | TG | T | 17 | a0001c0001t0009g0019 a0001c0001t0009g0030 a0001c0001t0009g0085 others(14): Show |
17 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.364-1810delC | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492047 | |||||||
| chr4:82492117 | TTTG | T | 133 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(130): Show |
135 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.364-1882_364-1880d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492117 | |||||||
| chr4:82492120 | G | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG00735.hp2 HG00738.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.364-1882C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492120 | |||||||
| chr4:82492152 | A | C | 1 | a0001c0001t0002g0197 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.364-1914T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492152 | |||||||
| chr4:82492238 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.364-2000G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492238 | |||||||
| chr4:82492344 | T | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(4): Show |
7 | HG02165.hp1 HG03098.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-2106A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492344 | |||||||
| chr4:82492391 | G | A | 1 | a0001c0001t0004g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.364-2153C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492391 | |||||||
| chr4:82492448 | A | AT | 56 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(53): Show |
58 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.364-2211dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492448 | |||||||
| chr4:82492792 | C | CA | 19 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0164 others(16): Show |
19 | HG01243.hp2 HG01261.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.364-2555dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492792 | |||||||
| chr4:82492792 | C | CAA | 5 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0052 others(2): Show |
5 | HG02165.hp1 HG03098.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-2556_364-2555d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492792 | |||||||
| chr4:82492805 | AAAAAAC | A | 10 | a0001c0001t0005g0101 a0001c0001t0006g0006 a0001c0001t0006g0026 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.364-2573_364-2568d others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492805 | |||||||
| chr4:82492806 | AAAAAC | A | 14 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0234 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.364-2573_364-2569d others(7): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492806 | |||||||
| chr4:82492809 | AAC | A | 12 | a0001c0001t0002g0117 a0001c0001t0004g0017 a0001c0001t0004g0111 others(9): Show |
12 | HG01168.hp2 HG01192.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.364-2573_364-2572d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492809 | |||||||
| chr4:82492810 | AC | A | 5 | a0001c0001t0004g0195 a0001c0001t0004g0207 a0001c0001t0004g0235 others(2): Show |
5 | HG00544.hp2 HG01515.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-2573delG | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492810 | |||||||
| chr4:82492811 | C | A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(82): Show |
87 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.364-2573G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492811 | |||||||
| chr4:82492858 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.364-2620C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492858 | |||||||
| chr4:82492864 | G | GTA | 40 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0045 others(37): Show |
40 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.364-2628_364-2627d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTATA | 20 | a0001c0001t0001g0062 a0001c0001t0001g0119 a0001c0001t0001g0123 others(17): Show |
20 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.364-2630_364-2627d others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTATATA | 15 | a0001c0001t0001g0187 a0001c0001t0002g0224 a0001c0001t0003g0064 others(12): Show |
15 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.364-2632_364-2627d others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTATATAT others(1): Show |
12 | a0001c0001t0002g0126 a0001c0001t0003g0042 a0001c0001t0003g0107 others(9): Show |
12 | HG00558.hp1 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.364-2634_364-2627d others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTATATAT others(3): Show |
7 | a0001c0001t0001g0181 a0001c0001t0003g0035 a0001c0001t0003g0139 others(4): Show |
7 | HG00423.hp2 HG01884.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-2636_364-2627d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTATATAT others(5): Show |
12 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0002g0127 others(9): Show |
12 | HG01891.hp1 HG01981.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.364-2638_364-2627d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTATATAT others(7): Show |
4 | a0001c0001t0002g0222 a0001c0001t0003g0005 a0001c0001t0003g0020 others(1): Show |
4 | HG01106.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-2640_364-2627d others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTATATAT others(9): Show |
3 | a0001c0001t0001g0060 a0001c0001t0003g0213 a0001c0001t0003g0239 |
3 | HG01109.hp1 HG02027.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.364-2642_364-2627d others(18): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTATATAT others(11): Show |
1 | a0001c0001t0003g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.364-2644_364-2627d others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTATATAT others(23): Show |
1 | a0001c0001t0001g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.364-2627_364-2626i others(32): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTGTATA | 3 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0143 |
3 | NA18961.hp1 NA18969.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.364-2627_364-2626i others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTGTATAT others(3): Show |
1 | a0001c0001t0031g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.364-2627_364-2626i others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTGTATAT others(5): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0122 |
3 | HG02165.hp1 NA18972.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.364-2627_364-2626i others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | G | GTGTATAT others(9): Show |
1 | a0001c0001t0001g0018 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364-2627_364-2626i others(18): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | GTA | G | 17 | a0001c0001t0001g0148 a0001c0001t0002g0071 a0001c0001t0002g0117 others(14): Show |
17 | HG01071.hp1 HG01261.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.364-2628_364-2627d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | GTATA | G | 15 | a0001c0001t0001g0078 a0001c0001t0007g0141 a0001c0001t0009g0085 others(12): Show |
15 | HG00323.hp2 HG01167.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.364-2630_364-2627d others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | GTATATA | G | 7 | a0001c0001t0002g0067 a0001c0001t0005g0084 a0001c0001t0005g0147 others(4): Show |
7 | HG00140.hp2 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-2632_364-2627d others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | GTATATAT others(1): Show |
G | 19 | a0001c0001t0002g0014 a0001c0001t0002g0234 a0001c0001t0003g0041 others(16): Show |
21 | HG00544.hp1 HG01884.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.364-2634_364-2627d others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | GTATATAT others(3): Show |
G | 3 | a0001c0001t0007g0102 a0001c0001t0016g0144 a0001c0001t0016g0146 |
3 | HG02886.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.364-2636_364-2627d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0018g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.364-2638_364-2627d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492864 | GTATATAT others(7): Show |
G | 3 | a0001c0001t0001g0120 a0001c0001t0004g0131 a0001c0001t0004g0231 |
3 | HG01106.hp1 HG01975.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.364-2640_364-2627d others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | |||||||
| chr4:82492866 | A | G | 10 | a0001c0001t0004g0125 a0001c0001t0004g0189 a0001c0001t0004g0192 others(7): Show |
10 | HG00544.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-2628T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492866 | |||||||
| chr4:82492868 | A | G | 21 | a0001c0001t0001g0148 a0001c0001t0002g0117 a0001c0001t0004g0017 others(18): Show |
21 | HG00544.hp2 HG01168.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.364-2630T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492868 | |||||||
| chr4:82492870 | A | G | 25 | a0001c0001t0001g0078 a0001c0001t0002g0117 a0001c0001t0004g0017 others(22): Show |
25 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-2632T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492870 | |||||||
| chr4:82492872 | A | G | 13 | a0001c0001t0009g0085 a0001c0001t0009g0086 a0001c0001t0009g0169 others(10): Show |
13 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.364-2634T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492872 | |||||||
| chr4:82492874 | A | G | 5 | a0001c0001t0010g0001 a0001c0001t0010g0095 a0001c0001t0010g0097 others(2): Show |
7 | HG02886.hp2 HG02970.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-2636T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492874 | |||||||
| chr4:82492880 | A | G | 2 | a0001c0001t0004g0131 a0001c0001t0004g0231 |
2 | HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.364-2642T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492880 | |||||||
| chr4:82492882 | A | G | 2 | a0001c0001t0004g0131 a0001c0001t0004g0231 |
2 | HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.364-2644T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492882 | |||||||
| chr4:82492896 | A | ATATATAT others(3): Show |
1 | a0001c0001t0035g0016 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.364-2659_364-2658i others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492896 | |||||||
| chr4:82492898 | A | G | 7 | a0001c0001t0005g0084 a0001c0001t0005g0147 a0001c0001t0005g0171 others(4): Show |
7 | HG02145.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-2660T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492898 | |||||||
| chr4:82493249 | T | G | 2 | a0001c0001t0016g0144 a0001c0001t0016g0146 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.363+2819A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493249 | |||||||
| chr4:82493266 | CAT | C | 3 | a0001c0001t0012g0058 a0001c0001t0012g0069 a0001c0001t0012g0070 |
3 | HG01167.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.363+2800_363+2801d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493266 | |||||||
| chr4:82493293 | G | A | 1 | a0001c0001t0020g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.363+2775C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493293 | |||||||
| chr4:82493342 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.363+2726T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493342 | |||||||
| chr4:82493417 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.363+2651C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493417 | |||||||
| chr4:82493512 | T | C | 1 | a0001c0001t0029g0170 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.363+2556A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493512 | |||||||
| chr4:82493667 | A | C | 14 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0234 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.363+2401T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493667 | |||||||
| chr4:82494388 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(2): Show |
5 | HG02165.hp1 HG03098.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1680C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494388 | |||||||
| chr4:82494662 | C | A | 1 | a0001c0001t0003g0178 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.363+1406G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494662 | |||||||
| chr4:82494696 | A | G | 183 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(180): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.363+1372T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494696 | |||||||
| chr4:82494783 | A | AT | 66 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0078 others(63): Show |
66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.363+1284dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494783 | |||||||
| chr4:82494783 | A | ATT | 70 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0002g0014 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.363+1283_363+1284d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494783 | |||||||
| chr4:82494783 | A | ATTT | 10 | a0001c0001t0001g0018 a0001c0001t0001g0232 a0001c0001t0003g0035 others(7): Show |
10 | HG00609.hp1 HG00639.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+1282_363+1284d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494783 | |||||||
| chr4:82494783 | ATTTTTT | A | 19 | a0001c0001t0009g0019 a0001c0001t0009g0030 a0001c0001t0009g0085 others(16): Show |
21 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.363+1279_363+1284d others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494783 | |||||||
| chr4:82494954 | T | A | 45 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0148 others(42): Show |
47 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.363+1114A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494954 | |||||||
| chr4:82494974 | C | T | 1 | a0001c0001t0030g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.363+1094G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494974 | |||||||
| chr4:82495106 | G | C | 4 | a0001c0001t0010g0001 a0001c0001t0010g0095 a0001c0001t0010g0097 others(1): Show |
6 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+962C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495106 | |||||||
| chr4:82495145 | A | G | 1 | a0001c0001t0005g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.363+923T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495145 | |||||||
| chr4:82495201 | G | A | 1 | a0001c0001t0012g0058 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.363+867C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495201 | |||||||
| chr4:82495214 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.363+854C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495214 | |||||||
| chr4:82495397 | C | T | 8 | a0001c0001t0002g0117 a0001c0001t0004g0125 a0001c0001t0004g0189 others(5): Show |
8 | HG01168.hp2 HG01192.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.363+671G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495397 | |||||||
| chr4:82495605 | T | C | 2 | a0001c0001t0019g0182 a0001c0001t0019g0196 |
2 | HG00735.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.363+463A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495605 | |||||||
| chr4:82495636 | T | A | 1 | a0001c0001t0007g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.363+432A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495636 | |||||||
| chr4:82495872 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.363+196C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495872 | |||||||
| chr4:82496324 | C | T | 2 | a0001c0001t0005g0038 a0001c0001t0005g0202 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.236-129G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82496324 | |||||||
| chr4:82496396 | A | G | 1 | a0001c0001t0004g0131 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.236-201T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82496396 | |||||||
| chr4:82496635 | C | A | 2 | a0001c0001t0003g0139 a0001c0001t0015g0225 |
2 | HG00423.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.236-440G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82496635 | |||||||
| chr4:82496680 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.236-485T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82496680 | |||||||
| chr4:82496829 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0251 |
2 | NA18948.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.236-634C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82496829 | |||||||
| chr4:82497045 | T | G | 26 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0234 others(23): Show |
26 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.236-850A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497045 | |||||||
| chr4:82497100 | G | A | 1 | a0002c0003t0003g0190 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.236-905C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497100 | |||||||
| chr4:82497306 | C | T | 1 | a0001c0001t0003g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.236-1111G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497306 | |||||||
| chr4:82497357 | G | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.236-1162C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497357 | |||||||
| chr4:82497360 | C | T | 13 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0005 others(10): Show |
13 | HG00642.hp2 HG01109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.236-1165G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497360 | |||||||
| chr4:82497432 | A | C | 5 | a0001c0001t0006g0081 a0001c0001t0006g0089 a0001c0001t0006g0212 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-1237T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497432 | |||||||
| chr4:82497512 | T | C | 2 | a0001c0001t0005g0084 a0001c0001t0005g0171 |
2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.236-1317A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497512 | |||||||
| chr4:82497588 | T | C | 3 | a0001c0001t0013g0032 a0001c0001t0013g0033 a0001c0001t0029g0170 |
3 | HG01243.hp2 HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.236-1393A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497588 | |||||||
| chr4:82497648 | A | G | 1 | a0001c0001t0003g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.236-1453T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497648 | |||||||
| chr4:82497777 | A | G | 50 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0002g0117 others(47): Show |
52 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.236-1582T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497777 | |||||||
| chr4:82497887 | G | A | 49 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0148 others(46): Show |
51 | HG00544.hp2 HG01167.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.236-1692C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497887 | |||||||
| chr4:82498018 | AT | A | 182 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0037 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.236-1824delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82498018 | |||||||
| chr4:82498384 | G | A | 44 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0232 others(41): Show |
44 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.236-2189C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82498384 | |||||||
| chr4:82498759 | G | T | 2 | a0001c0001t0009g0086 a0001c0001t0009g0169 |
2 | HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.236-2564C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82498759 | |||||||
| chr4:82499028 | G | C | 4 | a0001c0001t0005g0038 a0001c0001t0005g0084 a0001c0001t0005g0171 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-2833C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499028 | |||||||
| chr4:82499248 | C | T | 1 | a0001c0001t0007g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.236-3053G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499248 | |||||||
| chr4:82499375 | G | A | 1 | a0001c0001t0004g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.236-3180C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499375 | |||||||
| chr4:82499391 | G | A | 24 | a0001c0001t0005g0147 a0001c0001t0005g0172 a0001c0001t0009g0019 others(21): Show |
26 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.236-3196C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499391 | |||||||
| chr4:82499424 | AAAG | A | 4 | a0001c0001t0004g0113 a0001c0001t0016g0144 a0001c0001t0016g0146 others(1): Show |
4 | HG02818.hp1 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-3232_236-3230d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499424 | |||||||
| chr4:82499487 | C | T | 4 | a0001c0001t0004g0113 a0001c0001t0016g0144 a0001c0001t0016g0146 others(1): Show |
4 | HG02818.hp1 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+3240G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499487 | |||||||
| chr4:82499488 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0033g0080 |
2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.235+3239C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499488 | |||||||
| chr4:82499503 | C | T | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | NA19068.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.235+3224G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499503 | |||||||
| chr4:82499616 | G | A | 4 | a0001c0001t0010g0001 a0001c0001t0010g0095 a0001c0001t0010g0097 others(1): Show |
6 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+3111C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499616 | |||||||
| chr4:82499685 | T | G | 5 | a0001c0001t0009g0019 a0001c0001t0009g0030 a0001c0001t0009g0087 others(2): Show |
5 | HG02622.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+3042A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499685 | |||||||
| chr4:82499713 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.235+3014G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499713 | |||||||
| chr4:82499719 | C | CA | 61 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0123 others(58): Show |
61 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.235+3007dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | |||||||
| chr4:82499719 | C | CAA | 38 | a0001c0001t0001g0018 a0001c0001t0001g0148 a0001c0001t0001g0164 others(35): Show |
38 | HG00544.hp2 HG01106.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.235+3006_235+3007d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | |||||||
| chr4:82499719 | C | CAAA | 23 | a0001c0001t0001g0078 a0001c0001t0003g0199 a0001c0001t0004g0112 others(20): Show |
25 | HG00140.hp2 HG00323.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.235+3005_235+3007d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | |||||||
| chr4:82499719 | C | CAAAA | 10 | a0001c0001t0002g0067 a0001c0001t0002g0234 a0001c0001t0005g0038 others(7): Show |
10 | HG00544.hp1 HG01167.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+3004_235+3007d others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | |||||||
| chr4:82499719 | C | CAAAAA | 10 | a0001c0001t0002g0014 a0001c0001t0009g0019 a0001c0001t0009g0030 others(7): Show |
10 | HG01515.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+3003_235+3007d others(7): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | |||||||
| chr4:82499719 | C | CAAAAAA | 6 | a0001c0001t0005g0172 a0001c0001t0009g0087 a0001c0001t0009g0103 others(3): Show |
6 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+3002_235+3007d others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | |||||||
| chr4:82499862 | G | A | 4 | a0001c0001t0005g0038 a0001c0001t0005g0084 a0001c0001t0005g0171 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+2865C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499862 | |||||||
| chr4:82499984 | G | A | 3 | a0001c0001t0007g0028 a0001c0001t0007g0102 a0001c0001t0027g0096 |
3 | HG01884.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.235+2743C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499984 | |||||||
| chr4:82500011 | A | T | 3 | a0001c0001t0013g0032 a0001c0001t0013g0033 a0001c0001t0029g0170 |
3 | HG01243.hp2 HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.235+2716T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500011 | |||||||
| chr4:82500066 | A | C | 1 | a0001c0001t0003g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.235+2661T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500066 | |||||||
| chr4:82500082 | T | C | 1 | a0001c0001t0016g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.235+2645A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500082 | |||||||
| chr4:82500127 | A | G | 1 | a0001c0001t0003g0233 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.235+2600T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500127 | |||||||
| chr4:82500287 | G | T | 26 | a0001c0001t0001g0232 a0001c0001t0003g0040 a0001c0001t0003g0042 others(23): Show |
26 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.235+2440C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500287 | |||||||
| chr4:82500583 | G | A | 53 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0148 others(50): Show |
55 | HG00544.hp2 HG01167.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.235+2144C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500583 | |||||||
| chr4:82500743 | T | C | 26 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0234 others(23): Show |
26 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.235+1984A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500743 | |||||||
| chr4:82500991 | C | T | 3 | a0001c0001t0004g0017 a0001c0001t0004g0111 a0001c0001t0004g0112 |
3 | HG02723.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.235+1736G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500991 | |||||||
| chr4:82501096 | TAAATGCA others(5): Show |
T | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.235+1619_235+1630d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82501096 | |||||||
| chr4:82501145 | G | A | 2 | a0001c0001t0012g0069 a0001c0001t0012g0070 |
2 | HG01167.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.235+1582C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82501145 | |||||||
| chr4:82501475 | C | A | 12 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0234 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.235+1252G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82501475 | |||||||
| chr4:82501861 | A | AAT | 5 | a0001c0001t0010g0001 a0001c0001t0010g0095 a0001c0001t0010g0097 others(2): Show |
7 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+864_235+865dup others(2): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82501861 | |||||||
| chr4:82502070 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.235+657A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502070 | |||||||
| chr4:82502262 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.235+465T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502262 | |||||||
| chr4:82502447 | T | C | 19 | a0001c0001t0005g0147 a0001c0001t0005g0172 a0001c0001t0009g0019 others(16): Show |
19 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.235+280A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502447 | |||||||
| chr4:82502584 | A | G | 15 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0035 others(12): Show |
15 | HG00642.hp2 HG01109.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.235+143T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502584 | |||||||
| chr4:82502691 | C | T | 26 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0234 others(23): Show |
26 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.235+36G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502691 | |||||||
| chr4:82502707 | G | A | 2 | a0001c0001t0005g0079 a0001c0001t0005g0201 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.235+20C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502707 | |||||||
| chr4:82502936 | T | TA | 19 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.135-10dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 3/7 | chr4 | 82502936 | |||||||
| chr4:82503049 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.134+10A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 3/7 | chr4 | 82503049 | |||||||
| chr4:82503195 | C | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.81-83G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503195 | |||||||
| chr4:82503283 | A | G | 1 | a0001c0001t0005g0023 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.81-171T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503283 | |||||||
| chr4:82503285 | T | C | 25 | a0001c0001t0001g0018 a0001c0001t0001g0148 a0001c0001t0002g0117 others(22): Show |
25 | HG00544.hp2 HG01168.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.81-173A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503285 | |||||||
| chr4:82503420 | G | A | 4 | a0001c0001t0005g0038 a0001c0001t0005g0084 a0001c0001t0005g0171 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-308C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503420 | |||||||
| chr4:82503577 | G | A | 1 | a0001c0001t0010g0001 | 3 | NA18906.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.81-465C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503577 | |||||||
| chr4:82503597 | T | C | 5 | a0001c0001t0009g0019 a0001c0001t0009g0030 a0001c0001t0009g0087 others(2): Show |
5 | HG02622.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-485A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503597 | |||||||
| chr4:82503633 | G | A | 1 | a0001c0001t0006g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81-521C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503633 | |||||||
| chr4:82503653 | A | G | 1 | a0001c0001t0002g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.81-541T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503653 | |||||||
| chr4:82503723 | G | A | 4 | a0001c0001t0010g0001 a0001c0001t0010g0095 a0001c0001t0010g0097 others(1): Show |
6 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-611C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503723 | |||||||
| chr4:82503755 | C | T | 1 | a0001c0001t0006g0026 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81-643G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503755 | |||||||
| chr4:82503897 | A | G | 4 | a0001c0001t0005g0038 a0001c0001t0005g0084 a0001c0001t0005g0171 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+681T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503897 | |||||||
| chr4:82503973 | C | T | 26 | a0001c0001t0001g0232 a0001c0001t0003g0040 a0001c0001t0003g0042 others(23): Show |
26 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.80+605G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503973 | |||||||
| chr4:82504106 | T | C | 1 | a0001c0001t0001g0003 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.80+472A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82504106 | |||||||
| chr4:82504213 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.80+365A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82504213 | |||||||
| chr4:82504214 | T | G | 2 | a0001c0001t0005g0038 a0001c0001t0005g0202 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.80+364A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82504214 | |||||||
| chr4:82504550 | T | C | 1 | a0001c0001t0003g0247 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.80+28A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82504550 | |||||||
| chr4:82504826 | C | A | 1 | a0001c0001t0033g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-10-159G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82504826 | |||||||
| chr4:82504826 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0119 others(10): Show |
14 | HG00673.hp2 HG01109.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10-159G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82504826 | |||||||
| chr4:82505108 | A | G | 41 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0232 others(38): Show |
41 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.-10-441T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82505108 | |||||||
| chr4:82505128 | G | C | 1 | a0001c0001t0030g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-10-461C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82505128 | |||||||
| chr4:82505219 | A | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0148 a0001c0001t0003g0199 |
3 | HG02622.hp1 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-10-552T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82505219 | |||||||
| chr4:82505872 | T | C | 3 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0029g0170 |
3 | HG01243.hp2 HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-10-1205A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82505872 | |||||||
| chr4:82505955 | A | G | 2 | a0001c0001t0005g0147 a0001c0001t0005g0172 |
2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-10-1288T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82505955 | |||||||
| chr4:82506023 | G | A | 1 | a0001c0001t0030g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-10-1356C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506023 | |||||||
| chr4:82506084 | T | G | 1 | a0001c0001t0003g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-10-1417A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506084 | |||||||
| chr4:82506311 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(91): Show |
95 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-10-1644A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506311 | |||||||
| chr4:82506320 | A | G | 4 | a0001c0001t0006g0026 a0001c0001t0007g0028 a0001c0001t0017g0094 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-1653T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506320 | |||||||
| chr4:82506423 | C | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0052 others(3): Show |
6 | HG02165.hp1 NA18961.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-1756G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506423 | |||||||
| chr4:82506612 | T | C | 19 | a0001c0001t0001g0018 a0001c0001t0003g0173 a0001c0001t0003g0174 others(16): Show |
19 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10-1945A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506612 | |||||||
| chr4:82506614 | C | T | 4 | a0001c0001t0003g0132 a0001c0001t0003g0138 a0001c0001t0003g0175 others(1): Show |
4 | HG00609.hp1 HG01106.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-1947G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506614 | |||||||
| chr4:82506817 | C | T | 1 | a0001c0001t0005g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10-2150G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506817 | |||||||
| chr4:82506868 | C | T | 1 | a0001c0001t0031g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10-2201G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506868 | |||||||
| chr4:82506905 | A | G | 2 | a0001c0001t0007g0015 a0001c0001t0007g0077 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-2238T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506905 | |||||||
| chr4:82506954 | G | A | 1 | a0001c0001t0004g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-10-2287C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506954 | |||||||
| chr4:82506976 | T | A | 3 | a0001c0001t0012g0058 a0001c0001t0012g0069 a0001c0001t0012g0070 |
3 | HG01167.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-10-2309A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506976 | |||||||
| chr4:82507030 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-10-2363T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507030 | |||||||
| chr4:82507066 | T | G | 1 | a0001c0001t0007g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-2399A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507066 | |||||||
| chr4:82507270 | T | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(110): Show |
115 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.-10-2603A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507270 | |||||||
| chr4:82507325 | A | G | 4 | a0001c0001t0012g0106 a0001c0001t0013g0025 a0001c0001t0013g0027 others(1): Show |
4 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-2658T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507325 | |||||||
| chr4:82507346 | G | T | 1 | a0001c0001t0020g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10-2679C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507346 | |||||||
| chr4:82507362 | G | T | 1 | a0001c0001t0002g0022 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-10-2695C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507362 | |||||||
| chr4:82507364 | G | A | 3 | a0001c0001t0004g0113 a0001c0001t0005g0084 a0001c0001t0005g0202 |
3 | HG02258.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-10-2697C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507364 | |||||||
| chr4:82507444 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(149): Show |
154 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-10-2777A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507444 | |||||||
| chr4:82507570 | A | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(110): Show |
115 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.-10-2903T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507570 | |||||||
| chr4:82507719 | CTCTCTCT others(19): Show |
C | 6 | a0001c0001t0001g0018 a0001c0001t0003g0173 a0001c0001t0003g0174 others(3): Show |
6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-3078_-10-3053d others(28): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507719 | |||||||
| chr4:82507719 | CTCTCTCT others(21): Show |
C | 6 | a0001c0001t0005g0147 a0001c0001t0005g0172 a0001c0001t0012g0058 others(3): Show |
6 | HG01167.hp1 HG01515.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-3080_-10-3053d others(30): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507719 | |||||||
| chr4:82507719 | CTCTCTCT others(22): Show |
C | 1 | a0001c0001t0009g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-10-3081_-10-3053d others(31): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507719 | |||||||
| chr4:82507723 | CTCTCTTT others(3): Show |
C | 2 | a0001c0001t0007g0140 a0001c0001t0007g0141 |
2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-10-3066_-10-3057d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | |||||||
| chr4:82507723 | CTCTCTTT others(4): Show |
C | 6 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0234 others(3): Show |
6 | HG00544.hp1 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-3067_-10-3057d others(13): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | |||||||
| chr4:82507723 | CTCTCTTT others(5): Show |
C | 1 | a0001c0001t0002g0043 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-10-3068_-10-3057d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | |||||||
| chr4:82507723 | CTCTCTTT others(7): Show |
C | 3 | a0001c0001t0003g0064 a0001c0001t0020g0088 a0001c0001t0020g0090 |
3 | HG02922.hp1 HG03139.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-10-3070_-10-3057d others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | |||||||
| chr4:82507723 | CTCTCTTT others(11): Show |
C | 2 | a0001c0001t0004g0149 a0001c0001t0005g0031 |
2 | HG02572.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-10-3074_-10-3057d others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | |||||||
| chr4:82507723 | CTCTCTTT others(12): Show |
C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0066 others(16): Show |
19 | HG00544.hp2 HG00738.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-3075_-10-3057d others(21): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | |||||||
| chr4:82507723 | CTCTCTTT others(13): Show |
C | 73 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0054 others(70): Show |
75 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.-10-3076_-10-3057d others(22): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | |||||||
| chr4:82507723 | CTCTCTTT others(14): Show |
C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0176 a0001c0001t0001g0226 others(2): Show |
5 | HG02615.hp2 HG03041.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-3077_-10-3057d others(23): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | |||||||
| chr4:82507723 | CTCTCTTT others(19): Show |
C | 1 | a0001c0001t0004g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-10-3082_-10-3057d others(28): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | |||||||
| chr4:82507725 | CTCTTTTT others(4): Show |
C | 3 | a0001c0001t0003g0139 a0001c0001t0005g0171 a0001c0001t0015g0225 |
3 | HG00423.hp2 HG03098.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-10-3069_-10-3059d others(13): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507725 | |||||||
| chr4:82507725 | CTCTTTTT others(5): Show |
C | 1 | a0001c0001t0009g0030 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-10-3070_-10-3059d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507725 | |||||||
| chr4:82507725 | CTCTTTTT others(11): Show |
C | 2 | a0001c0001t0003g0005 a0001c0001t0005g0101 |
2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-10-3076_-10-3059d others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507725 | |||||||
| chr4:82507727 | C | CT | 10 | a0001c0001t0001g0072 a0001c0001t0001g0180 a0001c0001t0001g0183 others(7): Show |
10 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-3061dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0002g0197 a0001c0001t0008g0161 |
2 | HG00099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-10-3070_-10-3061d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | C | CTTTTTTT others(4): Show |
5 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0156 others(2): Show |
5 | HG00735.hp1 HG01257.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-3071_-10-3061d others(13): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0071 a0001c0001t0002g0073 |
2 | HG00099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-10-3072_-10-3061d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0002 a0001c0001t0002g0048 a0001c0001t0008g0217 |
3 | HG01256.hp1 HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-10-3073_-10-3061d others(15): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0002 a0001c0001t0002g0076 a0001c0001t0002g0223 |
3 | HG02027.hp2 NA18990.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-10-3074_-10-3061d others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0002g0194 a0001c0001t0008g0220 |
2 | HG01515.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-10-3077_-10-3061d others(19): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0008g0218 a0001c0001t0008g0219 a0001c0001t0008g0221 |
3 | HG01123.hp2 HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-10-3078_-10-3061d others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | C | T | 1 | a0001c0001t0007g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-3060G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | CT | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0062 others(12): Show |
15 | HG00140.hp1 HG01167.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-3061delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0002g0151 a0001c0001t0002g0168 a0001c0001t0002g0210 others(4): Show |
7 | HG02109.hp2 HG02486.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-3068_-10-3061d others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | CTTTTTTT others(2): Show |
C | 19 | a0001c0001t0001g0052 a0001c0001t0001g0122 a0001c0001t0001g0164 others(16): Show |
19 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10-3069_-10-3061d others(11): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0165 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-10-3070_-10-3061d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0251 a0001c0001t0002g0126 a0001c0001t0002g0127 others(2): Show |
5 | HG00438.hp2 HG00673.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-3073_-10-3061d others(15): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0078 a0001c0001t0002g0155 |
2 | HG01993.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-10-3074_-10-3061d others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507727 | CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0002g0115 a0001c0001t0002g0130 a0001c0001t0002g0154 |
3 | HG01975.hp2 NA18948.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-10-3075_-10-3061d others(17): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | |||||||
| chr4:82507729 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-10-3062A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507729 | |||||||
| chr4:82507737 | T | C | 1 | a0001c0001t0006g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10-3070A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507737 | |||||||
| chr4:82507744 | T | C | 2 | a0001c0001t0002g0115 a0001c0001t0002g0130 |
2 | NA18948.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-10-3077A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507744 | |||||||
| chr4:82507789 | C | A | 2 | a0001c0001t0007g0140 a0001c0001t0007g0141 |
2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-10-3122G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507789 | |||||||
| chr4:82507921 | TATTTTTT others(46): Show |
T | 1 | a0001c0001t0011g0252 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-10-3307_-10-3255d others(55): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507921 | |||||||
| chr4:82507950 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-10-3283C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507950 | |||||||
| chr4:82507972 | T | C | 1 | a0001c0004t0001g0055 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-10-3305A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507972 | |||||||
| chr4:82508005 | C | CTGCCCAG others(44): Show |
1 | a0001c0001t0011g0252 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-10-3339_-10-3338i others(53): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508005 | |||||||
| chr4:82508320 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(85): Show |
90 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-10-3653G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508320 | |||||||
| chr4:82508434 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0003g0199 a0001c0001t0031g0153 |
3 | HG02622.hp1 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-10-3767G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508434 | |||||||
| chr4:82508470 | C | CT | 7 | a0001c0001t0005g0147 a0001c0001t0005g0172 a0001c0001t0009g0086 others(4): Show |
7 | HG01167.hp1 HG01515.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-3804dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508470 | |||||||
| chr4:82508504 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-10-3837G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508504 | |||||||
| chr4:82508700 | A | T | 2 | a0001c0001t0020g0088 a0001c0001t0020g0090 |
2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-10-4033T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508700 | |||||||
| chr4:82508853 | C | T | 5 | a0001c0001t0007g0102 a0001c0001t0012g0106 a0001c0001t0013g0025 others(2): Show |
5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-4186G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508853 | |||||||
| chr4:82508869 | T | C | 20 | a0001c0001t0001g0018 a0001c0001t0003g0173 a0001c0001t0003g0174 others(17): Show |
20 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10-4202A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508869 | |||||||
| chr4:82509044 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-10-4377G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509044 | |||||||
| chr4:82509137 | T | A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0054 others(36): Show |
39 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.-10-4470A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509137 | |||||||
| chr4:82509359 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | NA18944.hp2 NA18995.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-4692G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509359 | |||||||
| chr4:82509430 | A | G | 3 | a0001c0001t0004g0113 a0001c0001t0005g0084 a0001c0001t0005g0202 |
3 | HG02258.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-10-4763T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509430 | |||||||
| chr4:82509513 | C | T | 1 | a0001c0001t0009g0211 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10-4846G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509513 | |||||||
| chr4:82509550 | C | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(85): Show |
90 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-10-4883G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509550 | |||||||
| chr4:82509607 | C | A | 2 | a0001c0001t0003g0139 a0001c0001t0015g0225 |
2 | HG00423.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-10-4940G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509607 | |||||||
| chr4:82509613 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(85): Show |
90 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-10-4946A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509613 | |||||||
| chr4:82509884 | G | C | 5 | a0001c0001t0007g0102 a0001c0001t0012g0106 a0001c0001t0013g0025 others(2): Show |
5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-5217C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509884 | |||||||
| chr4:82509895 | G | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(85): Show |
90 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-10-5228C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509895 | |||||||
| chr4:82509905 | G | A | 2 | a0001c0001t0004g0125 a0001c0001t0004g0249 |
2 | HG01192.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-10-5238C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509905 | |||||||
| chr4:82509960 | C | G | 1 | a0001c0001t0002g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-10-5293G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509960 | |||||||
| chr4:82510150 | G | A | 26 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0041 others(23): Show |
26 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-10-5483C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510150 | |||||||
| chr4:82510193 | C | T | 2 | a0001c0001t0005g0171 a0001c0001t0009g0030 |
2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10-5526G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510193 | |||||||
| chr4:82510204 | G | A | 1 | a0001c0001t0014g0109 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-10-5537C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510204 | |||||||
| chr4:82510205 | G | C | 6 | a0001c0001t0003g0040 a0001c0001t0006g0006 a0001c0001t0009g0087 others(3): Show |
6 | HG02886.hp1 HG02896.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5538C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510205 | |||||||
| chr4:82510339 | G | C | 6 | a0001c0001t0001g0018 a0001c0001t0003g0173 a0001c0001t0003g0174 others(3): Show |
6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5672C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510339 | |||||||
| chr4:82510637 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(149): Show |
154 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-10-5970A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510637 | |||||||
| chr4:82510798 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-10-6131C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510798 | |||||||
| chr4:82510806 | C | T | 1 | a0001c0001t0009g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-6139G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510806 | |||||||
| chr4:82511125 | G | A | 5 | a0001c0001t0007g0102 a0001c0001t0012g0106 a0001c0001t0013g0025 others(2): Show |
5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-6458C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511125 | |||||||
| chr4:82511472 | A | AT | 10 | a0001c0001t0002g0021 a0001c0001t0002g0117 a0001c0001t0002g0222 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-6806dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | |||||||
| chr4:82511472 | A | ATTT | 9 | a0001c0001t0001g0018 a0001c0001t0003g0139 a0001c0001t0003g0173 others(6): Show |
9 | HG00423.hp2 HG01243.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-6808_-10-6806d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | |||||||
| chr4:82511472 | A | ATTTT | 20 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0041 others(17): Show |
20 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10-6809_-10-6806d others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | |||||||
| chr4:82511472 | A | ATTTTT | 16 | a0001c0001t0003g0175 a0001c0001t0003g0228 a0001c0001t0005g0147 others(13): Show |
16 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-6810_-10-6806d others(7): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | |||||||
| chr4:82511472 | A | ATTTTTTT | 56 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0054 others(53): Show |
58 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10-6812_-10-6806d others(9): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | |||||||
| chr4:82511472 | A | ATTTTTTT others(1): Show |
19 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0177 others(16): Show |
19 | HG00140.hp2 HG00544.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-6813_-10-6806d others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | |||||||
| chr4:82511472 | A | ATTTTTTT others(2): Show |
20 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0046 others(17): Show |
20 | HG00544.hp2 HG00738.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10-6814_-10-6806d others(11): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | |||||||
| chr4:82511472 | A | ATTTTTTT others(3): Show |
8 | a0001c0001t0004g0114 a0001c0001t0004g0149 a0001c0001t0004g0192 others(5): Show |
8 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-6815_-10-6806d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | |||||||
| chr4:82511819 | A | C | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-7152T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511819 | |||||||
| chr4:82511845 | A | C | 13 | a0001c0001t0001g0018 a0001c0001t0003g0173 a0001c0001t0003g0174 others(10): Show |
13 | HG01167.hp1 HG01243.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-7178T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511845 | |||||||
| chr4:82511994 | C | T | 7 | a0001c0001t0002g0067 a0001c0001t0002g0234 a0001c0001t0007g0093 others(4): Show |
7 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-7327G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511994 | |||||||
| chr4:82512079 | A | G | 1 | a0001c0001t0008g0214 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-10-7412T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512079 | |||||||
| chr4:82512253 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(78): Show |
83 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-10-7586G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512253 | |||||||
| chr4:82512254 | G | A | 1 | a0001c0001t0005g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10-7587C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512254 | |||||||
| chr4:82512273 | AC | A | 7 | a0001c0001t0005g0147 a0001c0001t0005g0172 a0001c0001t0009g0086 others(4): Show |
7 | HG01167.hp1 HG01515.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-7607delG | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512273 | |||||||
| chr4:82512309 | G | A | 2 | a0001c0001t0011g0010 a0001c0001t0011g0057 |
2 | HG00673.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-10-7642C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512309 | |||||||
| chr4:82512581 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0003g0199 a0001c0001t0031g0153 |
3 | HG02622.hp1 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-10-7914G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512581 | |||||||
| chr4:82512760 | C | A | 13 | a0001c0001t0001g0018 a0001c0001t0003g0173 a0001c0001t0003g0174 others(10): Show |
13 | HG01167.hp1 HG01243.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-8093G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512760 | |||||||
| chr4:82512796 | T | C | 1 | a0001c0001t0002g0073 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-10-8129A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512796 | |||||||
| chr4:82512932 | G | A | 1 | a0001c0001t0011g0252 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-10-8265C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512932 | |||||||
| chr4:82513034 | G | C | 42 | a0001c0001t0001g0078 a0001c0001t0001g0164 a0001c0001t0001g0165 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.-10-8367C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513034 | |||||||
| chr4:82513075 | C | T | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-8408G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513075 | |||||||
| chr4:82513136 | C | T | 13 | a0001c0001t0001g0018 a0001c0001t0003g0173 a0001c0001t0003g0174 others(10): Show |
13 | HG01167.hp1 HG01243.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-8469G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513136 | |||||||
| chr4:82513168 | G | C | 35 | a0001c0001t0001g0078 a0001c0001t0001g0164 a0001c0001t0001g0165 others(32): Show |
35 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.-10-8501C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513168 | |||||||
| chr4:82513248 | C | T | 2 | a0001c0001t0005g0171 a0001c0001t0009g0030 |
2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10-8581G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513248 | |||||||
| chr4:82513249 | A | C | 5 | a0001c0001t0007g0102 a0001c0001t0012g0106 a0001c0001t0013g0025 others(2): Show |
5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-8582T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513249 | |||||||
| chr4:82513402 | G | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(150): Show |
155 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.-10-8735C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513402 | |||||||
| chr4:82513458 | A | C | 1 | a0001c0001t0011g0011 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-10-8791T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513458 | |||||||
| chr4:82513494 | A | T | 4 | a0001c0001t0003g0020 a0001c0001t0005g0023 a0001c0001t0006g0104 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-8827T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513494 | |||||||
| chr4:82513559 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10-8892A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513559 | |||||||
| chr4:82513608 | T | C | 36 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0137 others(33): Show |
36 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-10-8941A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513608 | |||||||
| chr4:82513834 | G | C | 1 | a0001c0001t0009g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-9167C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513834 | |||||||
| chr4:82514220 | G | A | 33 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0137 others(30): Show |
33 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-10-9553C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514220 | |||||||
| chr4:82514363 | T | C | 2 | a0001c0001t0002g0056 a0001c0001t0002g0065 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-10-9696A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514363 | |||||||
| chr4:82514437 | C | T | 1 | a0001c0001t0009g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-9770G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514437 | |||||||
| chr4:82514457 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0003g0173 a0001c0001t0003g0174 others(3): Show |
6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-9790G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514457 | |||||||
| chr4:82514471 | C | A | 1 | a0001c0001t0005g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10-9804G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514471 | |||||||
| chr4:82514607 | C | T | 5 | a0001c0001t0007g0102 a0001c0001t0012g0106 a0001c0001t0013g0025 others(2): Show |
5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-9940G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514607 | |||||||
| chr4:82514738 | T | C | 7 | a0001c0001t0005g0147 a0001c0001t0005g0172 a0001c0001t0009g0086 others(4): Show |
7 | HG01167.hp1 HG01515.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-10071A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514738 | |||||||
| chr4:82514796 | C | T | 1 | a0001c0001t0007g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-10129G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514796 | |||||||
| chr4:82514797 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-10-10130C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514797 | |||||||
| chr4:82514842 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-10-10175A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514842 | |||||||
| chr4:82514853 | G | T | 39 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0137 others(36): Show |
39 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.-10-10186C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514853 | |||||||
| chr4:82515133 | CT | C | 6 | a0001c0001t0004g0017 a0001c0001t0006g0081 a0001c0001t0006g0089 others(3): Show |
6 | HG02572.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-10467delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515133 | |||||||
| chr4:82515267 | T | C | 38 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0137 others(35): Show |
38 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.-10-10600A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515267 | |||||||
| chr4:82515298 | G | A | 1 | a0001c0001t0014g0109 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-10-10631C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515298 | |||||||
| chr4:82515459 | C | T | 38 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0137 others(35): Show |
38 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.-10-10792G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515459 | |||||||
| chr4:82515504 | C | T | 1 | a0001c0001t0005g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10-10837G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515504 | |||||||
| chr4:82515524 | G | T | 1 | a0001c0001t0005g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10-10857C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515524 | |||||||
| chr4:82515554 | T | C | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-10887A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515554 | |||||||
| chr4:82515594 | G | T | 38 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0137 others(35): Show |
38 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.-10-10927C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515594 | |||||||
| chr4:82515607 | C | T | 34 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0137 others(31): Show |
34 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.-10-10940G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515607 | |||||||
| chr4:82515610 | G | A | 34 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0137 others(31): Show |
34 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.-10-10943C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515610 | |||||||
| chr4:82515637 | T | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0037 others(50): Show |
54 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10-10970A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515637 | |||||||
| chr4:82515652 | G | A | 1 | a0001c0001t0004g0253 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-10-10985C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515652 | |||||||
| chr4:82515715 | C | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0045 others(83): Show |
88 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.-10-11048G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515715 | |||||||
| chr4:82515736 | CA | C | 40 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0137 others(37): Show |
40 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.-10-11070delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515736 | |||||||
| chr4:82515847 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-10-11180C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515847 | |||||||
| chr4:82515876 | G | A | 1 | a0001c0001t0005g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-11209C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515876 | |||||||
| chr4:82516030 | A | G | 1 | a0001c0001t0007g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-11363T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516030 | |||||||
| chr4:82516031 | C | T | 5 | a0001c0001t0007g0102 a0001c0001t0012g0106 a0001c0001t0013g0025 others(2): Show |
5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-11364G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516031 | |||||||
| chr4:82516286 | G | A | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-11619C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516286 | |||||||
| chr4:82516614 | T | C | 1 | a0001c0001t0017g0094 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10-11947A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516614 | |||||||
| chr4:82516825 | G | A | 32 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0137 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-10-12158C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516825 | |||||||
| chr4:82516856 | T | C | 29 | a0001c0001t0001g0110 a0001c0001t0001g0137 a0001c0001t0001g0164 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.-10-12189A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516856 | |||||||
| chr4:82516895 | A | G | 1 | a0001c0001t0007g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-10-12228T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516895 | |||||||
| chr4:82516959 | C | T | 5 | a0001c0001t0004g0189 a0001c0001t0004g0192 a0001c0001t0004g0193 others(2): Show |
5 | HG01168.hp2 HG01496.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-12292G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516959 | |||||||
| chr4:82517277 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-10-12610T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82517277 | |||||||
| chr4:82517492 | T | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0074 a0001c0001t0001g0128 others(17): Show |
20 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-12825A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82517492 | |||||||
| chr4:82517496 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0003g0173 a0001c0001t0003g0174 others(3): Show |
6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-12829A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82517496 | |||||||
| chr4:82517623 | T | A | 7 | a0001c0001t0004g0017 a0001c0001t0006g0081 a0001c0001t0006g0089 others(4): Show |
7 | HG02572.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-12956A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82517623 | |||||||
| chr4:82517890 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-10-13223C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82517890 | |||||||
| chr4:82518007 | A | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0052 others(60): Show |
63 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-10-13340T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518007 | |||||||
| chr4:82518008 | A | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0052 others(60): Show |
63 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-10-13341T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518008 | |||||||
| chr4:82518086 | C | T | 1 | a0001c0001t0007g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-10-13419G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518086 | |||||||
| chr4:82518090 | C | T | 1 | a0001c0001t0008g0216 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-10-13423G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518090 | |||||||
| chr4:82518132 | A | G | 3 | a0001c0001t0005g0171 a0001c0001t0007g0015 a0001c0001t0009g0030 |
3 | HG02647.hp2 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-13465T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518132 | |||||||
| chr4:82518171 | G | A | 6 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0213 others(3): Show |
6 | HG00735.hp2 HG01109.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-13504C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518171 | |||||||
| chr4:82518190 | C | A | 2 | a0001c0001t0006g0026 a0001c0001t0007g0028 |
2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-10-13523G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518190 | |||||||
| chr4:82518241 | G | A | 1 | a0001c0001t0004g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-10-13574C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518241 | |||||||
| chr4:82518303 | G | A | 3 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0029g0170 |
3 | HG01243.hp2 HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-10-13636C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518303 | |||||||
| chr4:82518393 | C | T | 1 | a0001c0001t0003g0228 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-10-13726G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518393 | |||||||
| chr4:82518422 | C | G | 25 | a0001c0001t0001g0129 a0001c0001t0001g0162 a0001c0001t0001g0183 others(22): Show |
25 | HG00099.hp2 HG00438.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.-10-13755G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518422 | |||||||
| chr4:82518812 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-10-14145C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518812 | |||||||
| chr4:82519095 | T | C | 1 | a0001c0001t0002g0234 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-10-14428A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519095 | |||||||
| chr4:82519302 | G | A | 11 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0165 others(8): Show |
11 | HG02055.hp1 HG02486.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-14635C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519302 | |||||||
| chr4:82519392 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-10-14725C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519392 | |||||||
| chr4:82519398 | C | G | 1 | a0001c0001t0005g0023 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-14731G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519398 | |||||||
| chr4:82519410 | TTTTC | T | 15 | a0001c0001t0001g0078 a0001c0001t0001g0164 a0001c0001t0001g0165 others(12): Show |
15 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-14747_-10-1474 others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519410 | |||||||
| chr4:82519422 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-10-14755G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519422 | |||||||
| chr4:82519429 | T | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(137): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-10-14762A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519429 | |||||||
| chr4:82519574 | G | A | 3 | a0001c0001t0003g0213 a0001c0001t0003g0239 a0001c0001t0017g0246 |
3 | HG01109.hp1 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-10-14907C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519574 | |||||||
| chr4:82519818 | A | T | 1 | a0001c0001t0013g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-10-15151T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519818 | |||||||
| chr4:82519877 | T | A | 1 | a0001c0001t0005g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-15210A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519877 | |||||||
| chr4:82520422 | T | G | 10 | a0001c0001t0001g0078 a0001c0001t0001g0164 a0001c0001t0001g0165 others(7): Show |
10 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-15755A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82520422 | |||||||
| chr4:82520491 | T | C | 2 | a0001c0001t0005g0147 a0001c0001t0009g0030 |
2 | HG02145.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-10-15824A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82520491 | |||||||
| chr4:82520714 | G | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(198): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-10-16047C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82520714 | |||||||
| chr4:82521007 | C | T | 10 | a0001c0001t0001g0078 a0001c0001t0001g0164 a0001c0001t0001g0165 others(7): Show |
10 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-16340G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521007 | |||||||
| chr4:82521140 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-10-16473T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521140 | |||||||
| chr4:82521264 | G | A | 2 | a0001c0001t0003g0174 a0001c0001t0029g0170 |
2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-10-16597C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521264 | |||||||
| chr4:82521438 | G | C | 1 | a0001c0001t0001g0236 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-10-16771C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521438 | |||||||
| chr4:82521479 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(158): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-10-16812C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521479 | |||||||
| chr4:82521538 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00738.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-10-16871G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521538 | |||||||
| chr4:82521754 | C | T | 4 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0007g0102 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-17087G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521754 | |||||||
| chr4:82521755 | G | A | 44 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0142 others(41): Show |
46 | HG00140.hp2 HG00323.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.-10-17088C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521755 | |||||||
| chr4:82521884 | G | T | 1 | a0001c0001t0003g0042 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-10-17217C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521884 | |||||||
| chr4:82521901 | G | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(29): Show |
32 | HG00642.hp2 HG01167.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.-10-17234C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521901 | |||||||
| chr4:82522166 | C | G | 1 | a0001c0001t0003g0228 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-10-17499G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82522166 | |||||||
| chr4:82522169 | C | T | 1 | a0001c0001t0007g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-10-17502G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82522169 | |||||||
| chr4:82522196 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0007g0140 a0001c0001t0007g0141 |
3 | HG00140.hp2 HG00323.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-10-17529G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82522196 | |||||||
| chr4:82522355 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-10-17688G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82522355 | |||||||
| chr4:82522771 | G | A | 1 | a0001c0001t0005g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-18104C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82522771 | |||||||
| chr4:82523032 | A | T | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-18365T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523032 | |||||||
| chr4:82523100 | T | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(141): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-10-18433A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523100 | |||||||
| chr4:82523204 | C | T | 2 | a0001c0001t0005g0007 a0001c0001t0006g0006 |
2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-10-18537G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523204 | |||||||
| chr4:82523210 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00738.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-10-18543G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523210 | |||||||
| chr4:82523338 | C | CATGTTTG others(10): Show |
1 | a0001c0001t0001g0045 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-10-18672_-10-1867 others(21): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523338 | |||||||
| chr4:82523339 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-10-18672A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523339 | |||||||
| chr4:82523340 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-10-18673G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523340 | |||||||
| chr4:82523449 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0251 |
2 | NA18948.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.-10-18782C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523449 | |||||||
| chr4:82523531 | G | C | 12 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(9): Show |
12 | HG00642.hp2 HG01243.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-18864C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523531 | |||||||
| chr4:82523697 | CT | C | 28 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0001c0001t0001g0164 others(25): Show |
28 | HG00642.hp2 HG01168.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-10-19031delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523697 | |||||||
| chr4:82523711 | T | A | 26 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0164 others(23): Show |
26 | HG00642.hp2 HG01243.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-10-19044A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523711 | |||||||
| chr4:82523829 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-10-19162G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523829 | |||||||
| chr4:82524102 | C | CA | 66 | a0001c0001t0001g0046 a0001c0001t0001g0110 a0001c0001t0001g0116 others(63): Show |
66 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.-10-19436dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524102 | |||||||
| chr4:82524102 | C | CAA | 27 | a0001c0001t0001g0018 a0001c0001t0001g0123 a0001c0001t0001g0142 others(24): Show |
29 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.-10-19437_-10-1943 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524102 | |||||||
| chr4:82524203 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-10-19536C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524203 | |||||||
| chr4:82524430 | C | A | 2 | a0001c0001t0005g0202 a0001c0001t0009g0086 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-10-19763G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524430 | |||||||
| chr4:82524513 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-19846G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524513 | |||||||
| chr4:82524516 | T | C | 6 | a0001c0001t0001g0226 a0001c0001t0002g0227 a0001c0001t0002g0229 others(3): Show |
6 | HG00323.hp1 HG00609.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-19849A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524516 | |||||||
| chr4:82524534 | T | C | 1 | a0003c0002t0032g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-10-19867A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524534 | |||||||
| chr4:82524746 | C | T | 2 | a0001c0001t0007g0077 a0001c0001t0028g0029 |
2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-10-20079G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524746 | |||||||
| chr4:82524751 | T | C | 7 | a0001c0001t0008g0214 a0001c0001t0008g0216 a0001c0001t0008g0217 others(4): Show |
7 | HG01071.hp2 HG01123.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-20084A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524751 | |||||||
| chr4:82525106 | A | G | 2 | a0001c0001t0002g0197 a0001c0001t0002g0222 |
2 | HG01168.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-10-20439T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525106 | |||||||
| chr4:82525142 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-20475G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525142 | |||||||
| chr4:82525247 | G | C | 4 | a0001c0001t0003g0005 a0001c0001t0005g0202 a0001c0001t0009g0086 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-20580C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525247 | |||||||
| chr4:82525297 | T | C | 1 | a0001c0004t0001g0055 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-10-20630A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525297 | |||||||
| chr4:82525352 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(120): Show |
125 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-10-20685G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525352 | |||||||
| chr4:82525802 | G | A | 47 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0142 others(44): Show |
49 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-10-21135C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525802 | |||||||
| chr4:82525814 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(8): Show |
11 | HG01168.hp1 HG01433.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-21147C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525814 | |||||||
| chr4:82525919 | T | A | 2 | a0001c0001t0001g0060 a0001c0001t0003g0061 |
2 | HG02027.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-10-21252A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525919 | |||||||
| chr4:82525966 | A | C | 3 | a0001c0001t0003g0213 a0001c0001t0006g0212 a0001c0001t0024g0008 |
3 | HG01109.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-10-21299T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525966 | |||||||
| chr4:82525971 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0002g0073 |
2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.-10-21304G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525971 | |||||||
| chr4:82525983 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-10-21316G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525983 | |||||||
| chr4:82526308 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-10-21641A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526308 | |||||||
| chr4:82526379 | A | G | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-21712T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526379 | |||||||
| chr4:82526488 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(64): Show |
69 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.-10-21821G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526488 | |||||||
| chr4:82526584 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-10-21917G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526584 | |||||||
| chr4:82526675 | A | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(15): Show |
20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-22008T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526675 | |||||||
| chr4:82526680 | C | A | 1 | a0001c0001t0003g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-10-22013G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526680 | |||||||
| chr4:82526788 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(133): Show |
138 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-10-22121G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526788 | |||||||
| chr4:82526890 | G | A | 1 | a0001c0001t0002g0115 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-10-22223C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526890 | |||||||
| chr4:82526910 | T | A | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-22243A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526910 | |||||||
| chr4:82527019 | C | CT | 18 | a0001c0001t0001g0018 a0001c0001t0001g0072 a0001c0001t0001g0186 others(15): Show |
18 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.-10-22353dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527019 | |||||||
| chr4:82527019 | C | CTT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(5): Show |
8 | HG01168.hp1 HG01433.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-22354_-10-2235 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527019 | |||||||
| chr4:82527019 | CT | C | 70 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(67): Show |
72 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-10-22353delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527019 | |||||||
| chr4:82527019 | CTT | C | 8 | a0001c0001t0003g0035 a0001c0001t0004g0017 a0001c0001t0005g0031 others(5): Show |
8 | HG01515.hp1 HG01884.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-22354_-10-2235 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527019 | |||||||
| chr4:82527019 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0066 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-10-22364_-10-2235 others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527019 | |||||||
| chr4:82527102 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-22435C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527102 | |||||||
| chr4:82527165 | T | C | 1 | a0001c0001t0034g0241 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-10-22498A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527165 | |||||||
| chr4:82527187 | T | C | 7 | a0001c0001t0003g0035 a0001c0001t0004g0017 a0001c0001t0005g0031 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-22520A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527187 | |||||||
| chr4:82527196 | G | A | 18 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(15): Show |
20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-22529C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527196 | |||||||
| chr4:82527210 | C | T | 59 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(56): Show |
59 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.-10-22543G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527210 | |||||||
| chr4:82527210 | CAA | C | 5 | a0001c0001t0003g0005 a0001c0001t0004g0017 a0001c0001t0005g0101 others(2): Show |
5 | HG02258.hp1 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-22545_-10-2254 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527210 | |||||||
| chr4:82527227 | C | T | 1 | a0001c0001t0005g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-10-22560G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527227 | |||||||
| chr4:82527228 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-10-22561C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527228 | |||||||
| chr4:82527324 | T | A | 3 | a0001c0001t0003g0005 a0001c0001t0005g0202 a0001c0001t0009g0086 |
3 | HG02258.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-10-22657A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527324 | |||||||
| chr4:82527354 | A | G | 104 | a0001c0001t0001g0018 a0001c0001t0001g0110 a0001c0001t0001g0116 others(101): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-10-22687T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527354 | |||||||
| chr4:82527386 | C | T | 1 | a0001c0001t0018g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-10-22719G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527386 | |||||||
| chr4:82527540 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-22873C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527540 | |||||||
| chr4:82527611 | A | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(98): Show |
103 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-10-22944T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527611 | |||||||
| chr4:82527623 | T | C | 2 | a0001c0001t0004g0192 a0001c0001t0004g0193 |
2 | HG01168.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-10-22956A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527623 | |||||||
| chr4:82527640 | C | A | 4 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0206 others(1): Show |
4 | NA18944.hp2 NA18995.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-22973G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527640 | |||||||
| chr4:82527643 | T | C | 33 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0142 others(30): Show |
35 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10-22976A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527643 | |||||||
| chr4:82527752 | T | A | 15 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(12): Show |
15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23085A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527752 | |||||||
| chr4:82527757 | T | C | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-23090A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527757 | |||||||
| chr4:82527833 | A | G | 15 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(12): Show |
15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23166T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527833 | |||||||
| chr4:82527836 | C | A | 15 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(12): Show |
15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23169G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527836 | |||||||
| chr4:82527954 | A | AAGGAGAG others(16): Show |
15 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(12): Show |
15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23288_-10-2328 others(27): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527954 | |||||||
| chr4:82528034 | T | C | 5 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-23367A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528034 | |||||||
| chr4:82528084 | T | C | 15 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(12): Show |
15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23417A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528084 | |||||||
| chr4:82528238 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-10-23571T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528238 | |||||||
| chr4:82528239 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-10-23572C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528239 | |||||||
| chr4:82528294 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-10-23627G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528294 | |||||||
| chr4:82528334 | G | A | 15 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(12): Show |
15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23667C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528334 | |||||||
| chr4:82528488 | G | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(15): Show |
20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-23821C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528488 | |||||||
| chr4:82528570 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(7): Show |
10 | HG01168.hp1 HG01433.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-23903A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528570 | |||||||
| chr4:82528601 | G | A | 14 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(11): Show |
14 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10-23934C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528601 | |||||||
| chr4:82528601 | G | T | 1 | a0001c0001t0002g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-10-23934C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528601 | |||||||
| chr4:82528605 | C | CT | 15 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(12): Show |
15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23939dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528605 | |||||||
| chr4:82528605 | C | CTT | 16 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(13): Show |
16 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-23940_-10-2393 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528605 | |||||||
| chr4:82528638 | A | G | 15 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(12): Show |
15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23971T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528638 | |||||||
| chr4:82528780 | A | G | 15 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(12): Show |
15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-24113T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528780 | |||||||
| chr4:82528894 | C | T | 11 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(8): Show |
11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-24227G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528894 | |||||||
| chr4:82529055 | AC | A | 14 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(11): Show |
14 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10-24389delG | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529055 | |||||||
| chr4:82529065 | T | G | 1 | a0001c0001t0003g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-10-24398A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529065 | |||||||
| chr4:82529099 | G | A | 13 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(10): Show |
13 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-10-24432C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529099 | |||||||
| chr4:82529224 | T | G | 15 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(12): Show |
15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-24557A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529224 | |||||||
| chr4:82529297 | CT | C | 18 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(15): Show |
18 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-10-24631delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529297 | |||||||
| chr4:82529363 | A | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(15): Show |
20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-24696T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529363 | |||||||
| chr4:82529435 | T | C | 18 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0003g0020 others(15): Show |
18 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-10-24768A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529435 | |||||||
| chr4:82529619 | G | C | 1 | a0001c0001t0007g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-10-24952C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529619 | |||||||
| chr4:82529918 | A | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(15): Show |
20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-25251T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529918 | |||||||
| chr4:82529975 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(7): Show |
10 | HG01168.hp1 HG01433.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-25308C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529975 | |||||||
| chr4:82530084 | A | ATCTC | 4 | a0001c0001t0001g0148 a0001c0001t0003g0005 a0001c0001t0005g0202 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-25421_-10-2541 others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530084 | |||||||
| chr4:82530084 | ATCTC | A | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-25421_-10-2541 others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530084 | |||||||
| chr4:82530104 | C | A | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-25437G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530104 | |||||||
| chr4:82530105 | T | G | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-25438A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530105 | |||||||
| chr4:82530198 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-10-25531T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530198 | |||||||
| chr4:82530417 | T | C | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-25750A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530417 | |||||||
| chr4:82530513 | C | T | 3 | a0001c0001t0004g0017 a0001c0001t0005g0007 a0001c0001t0006g0006 |
3 | HG02818.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-10-25846G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530513 | |||||||
| chr4:82530630 | A | T | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-25963T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530630 | |||||||
| chr4:82530735 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(130): Show |
135 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-10-26068T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530735 | |||||||
| chr4:82530832 | T | C | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-26165A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530832 | |||||||
| chr4:82530861 | C | A | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-26194G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530861 | |||||||
| chr4:82530862 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0003g0005 a0001c0001t0005g0202 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-26195C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530862 | |||||||
| chr4:82530944 | C | A | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-26277G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530944 | |||||||
| chr4:82530994 | C | T | 2 | a0001c0001t0005g0202 a0001c0001t0009g0086 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-10-26327G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530994 | |||||||
| chr4:82531115 | T | C | 5 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-26448A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531115 | |||||||
| chr4:82531219 | C | T | 63 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0116 others(60): Show |
63 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-10-26552G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531219 | |||||||
| chr4:82531230 | G | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-10-26563C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531230 | |||||||
| chr4:82531311 | A | T | 1 | a0001c0001t0002g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-10-26644T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531311 | |||||||
| chr4:82531417 | G | A | 1 | a0001c0001t0003g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-10-26750C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531417 | |||||||
| chr4:82531616 | G | A | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-26949C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531616 | |||||||
| chr4:82531626 | A | G | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-26959T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531626 | |||||||
| chr4:82531703 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-10-27036G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531703 | |||||||
| chr4:82531704 | G | A | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-27037C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531704 | |||||||
| chr4:82531754 | C | CA | 42 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(39): Show |
42 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.-10-27088dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531754 | |||||||
| chr4:82531754 | C | CAA | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0002g0194 others(2): Show |
5 | HG01361.hp1 HG02280.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-27089_-10-2708 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531754 | |||||||
| chr4:82531754 | CA | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0116 others(55): Show |
58 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-10-27088delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531754 | |||||||
| chr4:82531754 | CAA | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0037 others(27): Show |
30 | HG01168.hp1 HG01257.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.-10-27089_-10-2708 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531754 | |||||||
| chr4:82531754 | CAAAAAAA others(5): Show |
C | 22 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(19): Show |
24 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.-10-27099_-10-2708 others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531754 | |||||||
| chr4:82531839 | G | A | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-27172C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531839 | |||||||
| chr4:82531902 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0003g0005 a0001c0001t0005g0202 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-27235C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531902 | |||||||
| chr4:82531920 | T | C | 22 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(19): Show |
24 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.-10-27253A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531920 | |||||||
| chr4:82531996 | T | C | 16 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(13): Show |
16 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-27329A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531996 | |||||||
| chr4:82532593 | T | C | 5 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-27926A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532593 | |||||||
| chr4:82532606 | G | A | 52 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(49): Show |
52 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-10-27939C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532606 | |||||||
| chr4:82532608 | G | A | 4 | a0001c0001t0004g0017 a0001c0001t0004g0111 a0001c0001t0004g0112 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-27941C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532608 | |||||||
| chr4:82532885 | C | A | 1 | a0001c0001t0002g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-10-28218G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532885 | |||||||
| chr4:82532885 | C | T | 14 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(11): Show |
14 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10-28218G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532885 | |||||||
| chr4:82532886 | G | A | 1 | a0001c0001t0028g0029 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-10-28219C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532886 | |||||||
| chr4:82532889 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-10-28222G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532889 | |||||||
| chr4:82532964 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0007g0140 a0001c0001t0007g0141 |
3 | HG00140.hp2 HG00323.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-10-28297C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532964 | |||||||
| chr4:82533020 | G | A | 50 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(47): Show |
50 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-10-28353C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533020 | |||||||
| chr4:82533176 | TTATAAC | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(105): Show |
108 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-10-28515_-10-2851 others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533176 | |||||||
| chr4:82533216 | G | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0197 others(1): Show |
4 | HG01168.hp1 HG03688.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-28549C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533216 | |||||||
| chr4:82533232 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(10): Show |
13 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-28565G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533232 | |||||||
| chr4:82533261 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-10-28594G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533261 | |||||||
| chr4:82533306 | CTT | C | 3 | a0001c0001t0005g0038 a0001c0001t0007g0039 a0001c0001t0010g0001 |
5 | HG03486.hp1 NA18906.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+28598_-11+2859 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533306 | |||||||
| chr4:82533369 | A | G | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+28537T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533369 | |||||||
| chr4:82533491 | A | C | 1 | a0001c0001t0002g0248 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-11+28415T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533491 | |||||||
| chr4:82533641 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+28265G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533641 | |||||||
| chr4:82533824 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0009g0103 |
2 | HG02602.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-11+28082G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533824 | |||||||
| chr4:82533953 | C | T | 53 | a0001c0001t0001g0062 a0001c0001t0001g0110 a0001c0001t0001g0116 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-11+27953G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533953 | |||||||
| chr4:82533970 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-11+27936C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533970 | |||||||
| chr4:82534115 | C | CCA | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(133): Show |
138 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11+27789_-11+2779 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534115 | |||||||
| chr4:82534178 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(10): Show |
13 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+27728G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534178 | |||||||
| chr4:82534207 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0003g0061 |
2 | HG02027.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-11+27699C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534207 | |||||||
| chr4:82534244 | T | C | 1 | a0003c0002t0032g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11+27662A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534244 | |||||||
| chr4:82534390 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-11+27516T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534390 | |||||||
| chr4:82534671 | T | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(10): Show |
13 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+27235A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534671 | |||||||
| chr4:82534743 | T | C | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11+27163A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534743 | |||||||
| chr4:82534834 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+27072C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534834 | |||||||
| chr4:82534979 | G | T | 3 | a0001c0001t0006g0026 a0001c0001t0007g0028 a0001c0001t0013g0027 |
3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+26927C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534979 | |||||||
| chr4:82535230 | G | C | 3 | a0001c0001t0005g0147 a0001c0001t0005g0201 a0001c0001t0009g0030 |
3 | HG02145.hp1 HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-11+26676C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82535230 | |||||||
| chr4:82535541 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(10): Show |
13 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+26365C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82535541 | |||||||
| chr4:82535733 | T | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(67): Show |
70 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11+26173A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82535733 | |||||||
| chr4:82535742 | T | C | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(67): Show |
70 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11+26164A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82535742 | |||||||
| chr4:82536013 | C | T | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+25893G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536013 | |||||||
| chr4:82536050 | C | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(104): Show |
107 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.-11+25856G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536050 | |||||||
| chr4:82536066 | T | C | 4 | a0001c0001t0006g0092 a0001c0001t0007g0093 a0001c0001t0007g0102 others(1): Show |
4 | HG02717.hp1 HG02965.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+25840A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536066 | |||||||
| chr4:82536095 | T | G | 1 | a0001c0001t0007g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+25811A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536095 | |||||||
| chr4:82536356 | C | CA | 34 | a0001c0001t0001g0059 a0001c0001t0001g0148 a0001c0001t0001g0152 others(31): Show |
34 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+25549dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536356 | |||||||
| chr4:82536356 | CA | C | 50 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(47): Show |
50 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-11+25549delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536356 | |||||||
| chr4:82536356 | CAAAAAAA others(6): Show |
C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(53): Show |
58 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11+25537_-11+2554 others(17): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536356 | |||||||
| chr4:82536395 | G | A | 2 | a0001c0001t0002g0197 a0001c0001t0002g0222 |
2 | HG01168.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-11+25511C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536395 | |||||||
| chr4:82536419 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(117): Show |
122 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-11+25487G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536419 | |||||||
| chr4:82536734 | G | T | 1 | a0001c0001t0003g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-11+25172C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536734 | |||||||
| chr4:82536865 | A | G | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+25041T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536865 | |||||||
| chr4:82536877 | C | T | 5 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+25029G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536877 | |||||||
| chr4:82536967 | C | T | 4 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0206 others(1): Show |
4 | NA18944.hp2 NA18995.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+24939G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536967 | |||||||
| chr4:82537019 | C | T | 1 | a0001c0001t0006g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+24887G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537019 | |||||||
| chr4:82537143 | G | A | 3 | a0001c0001t0006g0026 a0001c0001t0007g0028 a0001c0001t0013g0027 |
3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+24763C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537143 | |||||||
| chr4:82537175 | T | C | 6 | a0001c0001t0001g0180 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | HG01123.hp1 HG01361.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+24731A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537175 | |||||||
| chr4:82537192 | A | G | 3 | a0001c0001t0006g0026 a0001c0001t0007g0028 a0001c0001t0013g0027 |
3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+24714T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537192 | |||||||
| chr4:82537280 | C | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(47): Show |
52 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.-11+24626G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537280 | |||||||
| chr4:82537415 | A | G | 13 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(10): Show |
13 | HG00642.hp2 HG01243.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+24491T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537415 | |||||||
| chr4:82537468 | G | T | 1 | a0001c0001t0020g0088 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+24438C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537468 | |||||||
| chr4:82537477 | T | A | 1 | a0001c0001t0003g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+24429A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537477 | |||||||
| chr4:82537514 | C | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(113): Show |
118 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-11+24392G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537514 | |||||||
| chr4:82537782 | A | G | 1 | a0001c0001t0015g0157 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-11+24124T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537782 | |||||||
| chr4:82537942 | T | C | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+23964A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537942 | |||||||
| chr4:82537978 | C | A | 11 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(8): Show |
11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+23928G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537978 | |||||||
| chr4:82538000 | GA | G | 7 | a0001c0001t0001g0018 a0001c0001t0007g0015 a0001c0001t0010g0095 others(4): Show |
7 | HG02451.hp2 HG02615.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+23905delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538000 | |||||||
| chr4:82538099 | C | G | 3 | a0001c0001t0004g0113 a0001c0001t0005g0084 a0001c0001t0009g0085 |
3 | HG03209.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+23807G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538099 | |||||||
| chr4:82538100 | C | T | 11 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(8): Show |
11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+23806G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538100 | |||||||
| chr4:82538344 | C | T | 3 | a0001c0001t0006g0026 a0001c0001t0007g0028 a0001c0001t0013g0027 |
3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+23562G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538344 | |||||||
| chr4:82538357 | C | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(15): Show |
20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+23549G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538357 | |||||||
| chr4:82538507 | T | C | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+23399A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538507 | |||||||
| chr4:82538529 | TAA | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(15): Show |
20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+23375_-11+2337 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538529 | |||||||
| chr4:82538603 | G | A | 11 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(8): Show |
11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+23303C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538603 | |||||||
| chr4:82538665 | A | G | 1 | a0001c0001t0024g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-11+23241T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538665 | |||||||
| chr4:82538673 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0007g0140 a0001c0001t0007g0141 |
3 | HG00140.hp2 HG00323.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-11+23233C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538673 | |||||||
| chr4:82538686 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0181 |
2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-11+23220G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538686 | |||||||
| chr4:82538863 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(7): Show |
10 | HG01168.hp1 HG01433.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+23043G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538863 | |||||||
| chr4:82538869 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-11+23037A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538869 | |||||||
| chr4:82538882 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(48): Show |
53 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11+23024C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538882 | |||||||
| chr4:82538935 | G | C | 2 | a0001c0001t0001g0232 a0001c0001t0003g0068 |
2 | HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-11+22971C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538935 | |||||||
| chr4:82539357 | AATT | A | 2 | a0001c0001t0007g0077 a0001c0001t0028g0029 |
2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-11+22546_-11+2254 others(7): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539357 | |||||||
| chr4:82539385 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0003g0061 |
2 | HG02027.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-11+22521C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539385 | |||||||
| chr4:82539414 | G | A | 2 | a0001c0001t0005g0202 a0001c0001t0009g0086 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-11+22492C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539414 | |||||||
| chr4:82539432 | T | A | 1 | a0001c0001t0003g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+22474A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539432 | |||||||
| chr4:82539459 | C | CTTTTT | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(48): Show |
53 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11+22442_-11+2244 others(9): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539459 | |||||||
| chr4:82539459 | C | CTTTTTT | 67 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0116 others(64): Show |
67 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-11+22441_-11+2244 others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539459 | |||||||
| chr4:82539539 | G | A | 1 | a0001c0001t0003g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-11+22367C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539539 | |||||||
| chr4:82539546 | G | A | 3 | a0001c0001t0006g0026 a0001c0001t0007g0028 a0001c0001t0013g0027 |
3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+22360C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539546 | |||||||
| chr4:82539625 | T | G | 1 | a0001c0001t0001g0037 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-11+22281A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539625 | |||||||
| chr4:82539970 | T | C | 3 | a0001c0001t0004g0113 a0001c0001t0005g0084 a0001c0001t0009g0085 |
3 | HG03209.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+21936A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539970 | |||||||
| chr4:82540114 | C | CT | 51 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(48): Show |
51 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+21791dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | C | CTT | 5 | a0001c0001t0001g0074 a0001c0001t0001g0177 a0001c0001t0001g0236 others(2): Show |
5 | HG02074.hp2 NA18967.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+21790_-11+2179 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0003g0199 others(4): Show |
7 | HG00140.hp2 HG00323.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+21782_-11+2179 others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | CTTTTTTT others(4): Show |
C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(16): Show |
21 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11+21781_-11+2179 others(15): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | CTTTTTTT others(5): Show |
C | 23 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0107 others(20): Show |
23 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.-11+21780_-11+2179 others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0004g0112 a0001c0001t0005g0201 a0001c0001t0009g0019 others(1): Show |
4 | HG00642.hp2 HG02622.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+21779_-11+2179 others(17): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | CTTTTTTT others(7): Show |
C | 56 | a0001c0001t0001g0078 a0001c0001t0001g0116 a0001c0001t0001g0119 others(53): Show |
56 | HG00438.hp2 HG00673.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.-11+21778_-11+2179 others(18): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | CTTTTTTT others(8): Show |
C | 11 | a0001c0001t0001g0110 a0001c0001t0001g0136 a0001c0001t0001g0137 others(8): Show |
11 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+21777_-11+2179 others(19): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | CTTTTTTT others(9): Show |
C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0209 a0001c0001t0002g0210 others(7): Show |
11 | HG01256.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+21776_-11+2179 others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | CTTTTTTT others(11): Show |
C | 3 | a0001c0001t0004g0114 a0001c0001t0012g0069 a0001c0001t0012g0070 |
3 | HG01167.hp1 HG01515.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-11+21774_-11+2179 others(22): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0003g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+21771_-11+2179 others(25): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540114 | CTTTTTTT others(15): Show |
C | 1 | a0001c0001t0003g0174 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11+21770_-11+2179 others(26): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | |||||||
| chr4:82540129 | T | C | 3 | a0001c0001t0005g0007 a0001c0001t0006g0006 a0001c0001t0014g0109 |
3 | HG01167.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+21777A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540129 | |||||||
| chr4:82540130 | T | C | 2 | a0001c0001t0009g0019 a0001c0001t0035g0016 |
2 | HG00642.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-11+21776A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540130 | |||||||
| chr4:82540131 | T | C | 51 | a0001c0001t0001g0078 a0001c0001t0001g0116 a0001c0001t0001g0119 others(48): Show |
51 | HG00438.hp2 HG00673.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-11+21775A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540131 | |||||||
| chr4:82540132 | T | C | 9 | a0001c0001t0001g0110 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+21774A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540132 | |||||||
| chr4:82540133 | T | C | 2 | a0001c0001t0007g0028 a0001c0001t0013g0027 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-11+21773A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540133 | |||||||
| chr4:82540468 | G | T | 1 | a0001c0001t0028g0029 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11+21438C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540468 | |||||||
| chr4:82540515 | TTATTAA | T | 2 | a0001c0001t0007g0077 a0001c0001t0028g0029 |
2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-11+21385_-11+2139 others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540515 | |||||||
| chr4:82540658 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-11+21248T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540658 | |||||||
| chr4:82541238 | T | A | 1 | a0001c0001t0002g0194 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-11+20668A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541238 | |||||||
| chr4:82541292 | T | G | 7 | a0001c0001t0001g0148 a0001c0001t0004g0017 a0001c0001t0004g0111 others(4): Show |
7 | HG02258.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+20614A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541292 | |||||||
| chr4:82541606 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(129): Show |
134 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+20300C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541606 | |||||||
| chr4:82541782 | T | C | 51 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(48): Show |
51 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-11+20124A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541782 | |||||||
| chr4:82541891 | C | A | 1 | a0001c0001t0003g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+20015G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541891 | |||||||
| chr4:82541979 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11+19927T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541979 | |||||||
| chr4:82542024 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-11+19882C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542024 | |||||||
| chr4:82542164 | A | C | 1 | a0001c0001t0002g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-11+19742T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542164 | |||||||
| chr4:82542428 | G | A | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+19478C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542428 | |||||||
| chr4:82542728 | G | C | 1 | a0001c0001t0002g0151 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-11+19178C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542728 | |||||||
| chr4:82542865 | C | T | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+19041G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542865 | |||||||
| chr4:82542896 | G | A | 5 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+19010C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542896 | |||||||
| chr4:82542931 | A | T | 1 | a0001c0001t0006g0006 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-11+18975T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542931 | |||||||
| chr4:82543069 | T | C | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+18837A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82543069 | |||||||
| chr4:82543517 | A | T | 1 | a0001c0001t0001g0176 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-11+18389T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82543517 | |||||||
| chr4:82543660 | A | C | 1 | a0001c0001t0003g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-11+18246T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82543660 | |||||||
| chr4:82544023 | G | A | 19 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0035 others(16): Show |
19 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-11+17883C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544023 | |||||||
| chr4:82544049 | C | T | 1 | a0001c0001t0003g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+17857G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544049 | |||||||
| chr4:82544161 | C | T | 3 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0009g0103 |
3 | HG01891.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-11+17745G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544161 | |||||||
| chr4:82544252 | C | T | 3 | a0001c0001t0003g0213 a0001c0001t0006g0212 a0001c0001t0024g0008 |
3 | HG01109.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-11+17654G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544252 | |||||||
| chr4:82544257 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0002g0071 |
3 | HG01256.hp1 HG01261.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-11+17649C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544257 | |||||||
| chr4:82544309 | G | A | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+17597C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544309 | |||||||
| chr4:82544345 | G | A | 5 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+17561C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544345 | |||||||
| chr4:82544409 | C | A | 1 | a0001c0001t0017g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-11+17497G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544409 | |||||||
| chr4:82544473 | A | G | 3 | a0001c0001t0004g0113 a0001c0001t0005g0084 a0001c0001t0009g0085 |
3 | HG03209.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+17433T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544473 | |||||||
| chr4:82544569 | A | G | 1 | a0001c0001t0003g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+17337T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544569 | |||||||
| chr4:82544569 | AG | A | 3 | a0001c0001t0001g0148 a0001c0001t0005g0202 a0001c0001t0009g0086 |
3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+17336delC | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544569 | |||||||
| chr4:82544580 | A | C | 1 | a0001c0001t0003g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-11+17326T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544580 | |||||||
| chr4:82544610 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(129): Show |
134 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+17296A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544610 | |||||||
| chr4:82544711 | A | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(129): Show |
134 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+17195T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544711 | |||||||
| chr4:82544775 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0002g0021 a0001c0001t0003g0107 |
2 | HG02922.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(15): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | |||||||
| chr4:82544775 | C | CAAAAAAA others(5): Show |
28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(25): Show |
30 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | |||||||
| chr4:82544775 | C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0142 a0001c0001t0003g0005 a0001c0001t0004g0113 others(2): Show |
5 | HG02602.hp1 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(17): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | |||||||
| chr4:82544775 | C | CAAAAAAA others(7): Show |
13 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0199 others(10): Show |
13 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(18): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | |||||||
| chr4:82544775 | C | CAAAAAAA others(8): Show |
7 | a0001c0001t0004g0111 a0001c0001t0004g0112 a0001c0001t0006g0026 others(4): Show |
7 | HG01884.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(19): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | |||||||
| chr4:82544775 | C | CAAAAAAA others(9): Show |
6 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | |||||||
| chr4:82544827 | A | C | 1 | a0001c0001t0001g0018 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-11+17079T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544827 | |||||||
| chr4:82545405 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(28): Show |
33 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.-11+16501C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545405 | |||||||
| chr4:82545434 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-11+16472T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545434 | |||||||
| chr4:82545439 | A | G | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG01975.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-11+16467T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545439 | |||||||
| chr4:82545586 | A | G | 1 | a0001c0001t0003g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+16320T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545586 | |||||||
| chr4:82545889 | C | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(15): Show |
20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+16017G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545889 | |||||||
| chr4:82545932 | CA | C | 100 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0116 others(97): Show |
100 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.-11+15973delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545932 | |||||||
| chr4:82546050 | A | G | 4 | a0001c0001t0004g0017 a0001c0001t0004g0111 a0001c0001t0004g0112 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+15856T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546050 | |||||||
| chr4:82546255 | T | G | 30 | a0001c0001t0001g0078 a0001c0001t0003g0005 a0001c0001t0003g0020 others(27): Show |
30 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-11+15651A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546255 | |||||||
| chr4:82546594 | C | T | 7 | a0001c0001t0003g0005 a0001c0001t0003g0199 a0001c0001t0006g0026 others(4): Show |
7 | HG01884.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+15312G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546594 | |||||||
| chr4:82546610 | C | T | 50 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(47): Show |
50 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-11+15296G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546610 | |||||||
| chr4:82546656 | G | A | 1 | a0001c0001t0003g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-11+15250C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546656 | |||||||
| chr4:82546783 | C | T | 1 | a0001c0001t0005g0023 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11+15123G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546783 | |||||||
| chr4:82546797 | A | T | 1 | a0001c0001t0003g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+15109T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546797 | |||||||
| chr4:82547285 | G | GA | 8 | a0001c0001t0001g0018 a0001c0001t0003g0041 a0001c0001t0007g0015 others(5): Show |
8 | HG02451.hp2 HG02615.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+14620dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547285 | |||||||
| chr4:82547285 | GA | G | 17 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0035 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-11+14620delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547285 | |||||||
| chr4:82547326 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(128): Show |
133 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11+14580A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547326 | |||||||
| chr4:82547363 | C | T | 1 | a0001c0001t0002g0117 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-11+14543G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547363 | |||||||
| chr4:82547462 | G | A | 1 | a0001c0001t0004g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-11+14444C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547462 | |||||||
| chr4:82547592 | T | TA | 13 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+14313dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547592 | |||||||
| chr4:82547718 | G | T | 3 | a0001c0001t0005g0007 a0001c0001t0006g0006 a0001c0001t0014g0109 |
3 | HG01167.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+14188C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547718 | |||||||
| chr4:82548000 | C | T | 1 | a0001c0001t0003g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+13906G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548000 | |||||||
| chr4:82548125 | T | C | 1 | a0001c0001t0009g0211 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-11+13781A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548125 | |||||||
| chr4:82548451 | G | T | 3 | a0001c0001t0005g0007 a0001c0001t0006g0006 a0001c0001t0014g0109 |
3 | HG01167.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+13455C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548451 | |||||||
| chr4:82548471 | G | C | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+13435C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548471 | |||||||
| chr4:82548478 | G | A | 9 | a0001c0001t0003g0005 a0001c0001t0003g0199 a0001c0001t0004g0017 others(6): Show |
9 | HG01884.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+13428C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548478 | |||||||
| chr4:82548515 | T | C | 2 | a0001c0001t0004g0017 a0001c0001t0005g0101 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-11+13391A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548515 | |||||||
| chr4:82548723 | T | G | 6 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0005g0171 others(3): Show |
6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+13183A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548723 | |||||||
| chr4:82548771 | T | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0040 others(15): Show |
20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+13135A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548771 | |||||||
| chr4:82548842 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+13064C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548842 | |||||||
| chr4:82549141 | AAT | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(128): Show |
133 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11+12763_-11+1276 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549141 | |||||||
| chr4:82549227 | A | C | 5 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+12679T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549227 | |||||||
| chr4:82549305 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(128): Show |
133 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11+12601C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549305 | |||||||
| chr4:82549469 | G | T | 73 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(70): Show |
73 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-11+12437C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549469 | |||||||
| chr4:82549542 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-11+12364G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549542 | |||||||
| chr4:82549568 | C | T | 1 | a0001c0001t0031g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-11+12338G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549568 | |||||||
| chr4:82549645 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-11+12261A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549645 | |||||||
| chr4:82549745 | G | A | 3 | a0001c0001t0014g0145 a0001c0001t0016g0144 a0001c0001t0016g0146 |
3 | HG02886.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-11+12161C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549745 | |||||||
| chr4:82549788 | G | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(128): Show |
133 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11+12118C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549788 | |||||||
| chr4:82549840 | G | T | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+12066C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549840 | |||||||
| chr4:82549931 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG00639.hp2 HG00738.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+11975G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549931 | |||||||
| chr4:82550157 | G | A | 1 | a0001c0001t0007g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-11+11749C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550157 | |||||||
| chr4:82550444 | A | G | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-11+11462T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550444 | |||||||
| chr4:82550488 | T | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(29): Show |
34 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+11418A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550488 | |||||||
| chr4:82550489 | T | G | 3 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0009g0103 |
3 | HG01891.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-11+11417A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550489 | |||||||
| chr4:82550507 | A | G | 3 | a0001c0001t0004g0113 a0001c0001t0005g0084 a0001c0001t0009g0085 |
3 | HG03209.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+11399T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550507 | |||||||
| chr4:82550664 | C | A | 5 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+11242G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550664 | |||||||
| chr4:82550664 | C | T | 3 | a0001c0001t0006g0026 a0001c0001t0007g0028 a0001c0001t0013g0027 |
3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+11242G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550664 | |||||||
| chr4:82550799 | AAAAG | A | 11 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(8): Show |
11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+11103_-11+1110 others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550799 | |||||||
| chr4:82550967 | G | A | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+10939C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550967 | |||||||
| chr4:82551098 | G | A | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+10808C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551098 | |||||||
| chr4:82551268 | T | C | 4 | a0001c0001t0004g0017 a0001c0001t0004g0111 a0001c0001t0004g0112 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+10638A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551268 | |||||||
| chr4:82551328 | T | C | 19 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0003g0005 others(16): Show |
21 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11+10578A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551328 | |||||||
| chr4:82551375 | T | C | 1 | a0001c0001t0028g0029 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11+10531A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551375 | |||||||
| chr4:82551589 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0005g0202 a0001c0001t0009g0086 |
3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+10317T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551589 | |||||||
| chr4:82551686 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11+10220A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551686 | |||||||
| chr4:82551693 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(29): Show |
34 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+10213G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551693 | |||||||
| chr4:82551702 | T | G | 1 | a0001c0001t0007g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-11+10204A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551702 | |||||||
| chr4:82551761 | T | G | 1 | a0001c0001t0005g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11+10145A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551761 | |||||||
| chr4:82551804 | C | T | 1 | a0001c0001t0004g0017 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11+10102G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551804 | |||||||
| chr4:82551914 | C | T | 1 | a0001c0001t0005g0038 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-11+9992G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551914 | |||||||
| chr4:82552603 | T | C | 20 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0004g0113 others(17): Show |
20 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+9303A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82552603 | |||||||
| chr4:82552778 | C | T | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+9128G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82552778 | |||||||
| chr4:82552909 | G | T | 10 | a0001c0001t0001g0188 a0001c0001t0002g0168 a0001c0001t0002g0194 others(7): Show |
10 | HG01071.hp1 HG01109.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+8997C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82552909 | |||||||
| chr4:82553108 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-11+8798A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82553108 | |||||||
| chr4:82553384 | A | G | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0197 others(1): Show |
4 | HG01168.hp1 HG03688.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+8522T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82553384 | |||||||
| chr4:82553943 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(129): Show |
134 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+7963T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82553943 | |||||||
| chr4:82554159 | A | T | 46 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(43): Show |
46 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.-11+7747T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554159 | |||||||
| chr4:82554490 | T | C | 3 | a0001c0001t0001g0148 a0001c0001t0005g0202 a0001c0001t0009g0086 |
3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+7416A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554490 | |||||||
| chr4:82554578 | A | G | 1 | a0001c0001t0010g0095 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-11+7328T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554578 | |||||||
| chr4:82554635 | A | G | 3 | a0001c0001t0003g0213 a0001c0001t0006g0212 a0001c0001t0024g0008 |
3 | HG01109.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-11+7271T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554635 | |||||||
| chr4:82554657 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(129): Show |
134 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+7249T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554657 | |||||||
| chr4:82554948 | T | TC | 3 | a0001c0001t0004g0111 a0001c0001t0004g0112 a0001c0001t0005g0101 |
3 | HG02723.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+6957dupG | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554948 | |||||||
| chr4:82554970 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-11+6936T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554970 | |||||||
| chr4:82555199 | T | C | 3 | a0001c0001t0001g0148 a0001c0001t0005g0202 a0001c0001t0009g0086 |
3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+6707A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555199 | |||||||
| chr4:82555231 | C | T | 1 | a0001c0001t0004g0017 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11+6675G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555231 | |||||||
| chr4:82555375 | T | C | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+6531A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555375 | |||||||
| chr4:82555411 | A | T | 1 | a0001c0001t0009g0030 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-11+6495T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555411 | |||||||
| chr4:82555865 | C | T | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+6041G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555865 | |||||||
| chr4:82555878 | A | G | 56 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(53): Show |
56 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.-11+6028T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555878 | |||||||
| chr4:82555969 | T | A | 11 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(8): Show |
11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+5937A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555969 | |||||||
| chr4:82556028 | G | A | 11 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(8): Show |
11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+5878C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556028 | |||||||
| chr4:82556069 | G | A | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+5837C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556069 | |||||||
| chr4:82556071 | G | T | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+5835C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556071 | |||||||
| chr4:82556087 | T | G | 1 | a0001c0001t0007g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-11+5819A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556087 | |||||||
| chr4:82556109 | G | A | 7 | a0001c0001t0008g0214 a0001c0001t0008g0216 a0001c0001t0008g0217 others(4): Show |
7 | HG01071.hp2 HG01123.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+5797C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556109 | |||||||
| chr4:82556214 | G | C | 1 | a0001c0001t0017g0094 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-11+5692C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556214 | |||||||
| chr4:82556463 | A | T | 5 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+5443T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556463 | |||||||
| chr4:82556495 | T | A | 14 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0004g0113 others(11): Show |
14 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-11+5411A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556495 | |||||||
| chr4:82556541 | T | C | 3 | a0001c0001t0001g0148 a0001c0001t0005g0202 a0001c0001t0009g0086 |
3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+5365A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556541 | |||||||
| chr4:82556569 | C | T | 4 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0206 others(1): Show |
4 | NA18944.hp2 NA18995.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+5337G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556569 | |||||||
| chr4:82556859 | C | T | 3 | a0001c0001t0004g0113 a0001c0001t0005g0084 a0001c0001t0009g0085 |
3 | HG03209.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+5047G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556859 | |||||||
| chr4:82556932 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+4974A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556932 | |||||||
| chr4:82556998 | C | T | 16 | a0001c0001t0001g0188 a0001c0001t0002g0168 a0001c0001t0002g0194 others(13): Show |
16 | HG01071.hp1 HG01109.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11+4908G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556998 | |||||||
| chr4:82557235 | A | G | 1 | a0001c0001t0005g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11+4671T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557235 | |||||||
| chr4:82557238 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-11+4668G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557238 | |||||||
| chr4:82557477 | C | T | 2 | a0001c0001t0003g0005 a0001c0001t0004g0017 |
2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-11+4429G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557477 | |||||||
| chr4:82557531 | G | A | 94 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0116 others(91): Show |
94 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.-11+4375C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557531 | |||||||
| chr4:82557589 | C | A | 1 | a0001c0001t0028g0029 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11+4317G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557589 | |||||||
| chr4:82557734 | C | CT | 25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(22): Show |
25 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11+4171dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557734 | |||||||
| chr4:82557734 | CT | C | 91 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0116 others(88): Show |
91 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-11+4171delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557734 | |||||||
| chr4:82557734 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11+4162_-11+4171d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557734 | |||||||
| chr4:82557756 | T | C | 1 | a0001c0001t0003g0247 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-11+4150A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557756 | |||||||
| chr4:82557808 | A | G | 19 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0035 others(16): Show |
19 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-11+4098T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557808 | |||||||
| chr4:82557918 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0005g0202 a0001c0001t0009g0086 |
3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+3988T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557918 | |||||||
| chr4:82558267 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-11+3639A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558267 | |||||||
| chr4:82558289 | C | T | 16 | a0001c0001t0001g0078 a0001c0001t0003g0005 a0001c0001t0003g0020 others(13): Show |
16 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11+3617G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558289 | |||||||
| chr4:82558353 | T | C | 2 | a0001c0001t0003g0005 a0001c0001t0004g0017 |
2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-11+3553A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558353 | |||||||
| chr4:82558393 | T | G | 11 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(8): Show |
11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+3513A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558393 | |||||||
| chr4:82558637 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-11+3269A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558637 | |||||||
| chr4:82558765 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(22): Show |
27 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-11+3141C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558765 | |||||||
| chr4:82558889 | A | AAAG | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(126): Show |
131 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-11+3014_-11+3016d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558889 | |||||||
| chr4:82558971 | A | G | 5 | a0001c0001t0006g0026 a0001c0001t0007g0028 a0001c0001t0007g0077 others(2): Show |
5 | HG01884.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2935T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558971 | |||||||
| chr4:82559010 | A | ACCCCTAA others(13): Show |
1 | a0001c0001t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+2895_-11+2896i others(22): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559010 | |||||||
| chr4:82559040 | C | T | 3 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0003g0042 |
3 | NA18980.hp1 NA19011.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-11+2866G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559040 | |||||||
| chr4:82559053 | T | C | 8 | a0001c0001t0004g0113 a0001c0001t0005g0084 a0001c0001t0006g0026 others(5): Show |
8 | HG01884.hp2 HG02895.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+2853A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559053 | |||||||
| chr4:82559115 | A | G | 11 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0005g0079 others(8): Show |
11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+2791T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559115 | |||||||
| chr4:82559206 | T | C | 8 | a0001c0001t0001g0188 a0001c0001t0002g0194 a0001c0001t0003g0191 others(5): Show |
8 | HG01071.hp1 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+2700A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559206 | |||||||
| chr4:82559216 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-11+2690G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559216 | |||||||
| chr4:82559286 | T | C | 2 | a0001c0001t0005g0147 a0001c0001t0009g0030 |
2 | HG02145.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-11+2620A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559286 | |||||||
| chr4:82559302 | T | G | 1 | a0001c0001t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+2604A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559302 | |||||||
| chr4:82559316 | G | A | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0023 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+2590C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559316 | |||||||
| chr4:82559390 | C | CA | 33 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(30): Show |
35 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.-11+2515dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559390 | |||||||
| chr4:82559487 | G | A | 1 | a0001c0001t0007g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+2419C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559487 | |||||||
| chr4:82559658 | T | G | 5 | a0001c0001t0006g0026 a0001c0001t0007g0028 a0001c0001t0007g0077 others(2): Show |
5 | HG01884.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2248A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559658 | |||||||
| chr4:82559678 | A | G | 1 | a0001c0001t0005g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11+2228T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559678 | |||||||
| chr4:82559691 | T | C | 2 | a0001c0001t0003g0213 a0001c0001t0006g0212 |
2 | HG01109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-11+2215A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559691 | |||||||
| chr4:82559812 | G | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(30): Show |
35 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.-11+2094C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559812 | |||||||
| chr4:82559831 | A | T | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2075T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559831 | |||||||
| chr4:82559832 | A | C | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2074T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559832 | |||||||
| chr4:82559833 | T | A | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2073A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559833 | |||||||
| chr4:82559834 | G | C | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2072C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559834 | |||||||
| chr4:82559836 | C | T | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2070G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559836 | |||||||
| chr4:82559838 | A | T | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2068T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559838 | |||||||
| chr4:82559839 | G | C | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2067C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559839 | |||||||
| chr4:82559841 | T | C | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2065A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559841 | |||||||
| chr4:82559843 | G | A | 45 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0119 others(42): Show |
45 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.-11+2063C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559843 | |||||||
| chr4:82559844 | C | T | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2062G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559844 | |||||||
| chr4:82559845 | A | G | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2061T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559845 | |||||||
| chr4:82559846 | G | T | 1 | a0001c0001t0002g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2060C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559846 | |||||||
| chr4:82559869 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+2037G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559869 | |||||||
| chr4:82559892 | T | C | 2 | a0001c0001t0007g0077 a0001c0001t0028g0029 |
2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-11+2014A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559892 | |||||||
| chr4:82559955 | C | G | 54 | a0001c0001t0001g0148 a0001c0001t0001g0176 a0001c0001t0001g0177 others(51): Show |
54 | HG00438.hp1 HG00558.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.-11+1951G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559955 | |||||||
| chr4:82560002 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(71): Show |
76 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-11+1904A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560002 | |||||||
| chr4:82560078 | T | G | 3 | a0001c0001t0014g0145 a0001c0001t0016g0144 a0001c0001t0016g0146 |
3 | HG02886.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-11+1828A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560078 | |||||||
| chr4:82560117 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+1789G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560117 | |||||||
| chr4:82560119 | CA | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(91): Show |
96 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-11+1786delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560119 | |||||||
| chr4:82560352 | T | C | 14 | a0001c0001t0001g0078 a0001c0001t0003g0005 a0001c0001t0003g0020 others(11): Show |
14 | HG00642.hp2 HG01243.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-11+1554A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560352 | |||||||
| chr4:82560427 | C | T | 5 | a0001c0001t0003g0035 a0001c0001t0005g0031 a0001c0001t0005g0034 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+1479G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560427 | |||||||
| chr4:82560471 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(78): Show |
83 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-11+1435G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560471 | |||||||
| chr4:82560479 | C | T | 1 | a0001c0001t0004g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-11+1427G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560479 | |||||||
| chr4:82560571 | A | G | 3 | a0001c0001t0006g0026 a0001c0001t0007g0028 a0001c0001t0013g0027 |
3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+1335T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560571 | |||||||
| chr4:82560675 | A | G | 5 | a0001c0001t0004g0111 a0001c0001t0004g0112 a0001c0001t0004g0113 others(2): Show |
5 | HG02723.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+1231T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560675 | |||||||
| chr4:82560871 | A | G | 3 | a0001c0001t0007g0015 a0001c0001t0013g0025 a0001c0001t0035g0016 |
3 | HG00642.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-11+1035T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560871 | |||||||
| chr4:82561127 | TTAAAATG others(41): Show |
T | 1 | a0001c0001t0013g0025 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-11+731_-11+778del others(48): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561127 | |||||||
| chr4:82561157 | T | A | 1 | a0001c0001t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+749A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561157 | |||||||
| chr4:82561162 | T | A | 1 | a0001c0001t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+744A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561162 | |||||||
| chr4:82561218 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+688G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561218 | |||||||
| chr4:82561279 | G | A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | NA19068.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-11+627C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561279 | |||||||
| chr4:82561430 | C | G | 31 | a0001c0001t0001g0018 a0001c0001t0003g0020 a0001c0001t0003g0213 others(28): Show |
31 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.-11+476G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561430 | |||||||
| chr4:82561441 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-11+465C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561441 | |||||||
| chr4:82561446 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+460T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561446 | |||||||
| chr4:82561460 | C | T | 4 | a0001c0001t0005g0023 a0001c0001t0007g0108 a0001c0001t0014g0109 others(1): Show |
4 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+446G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561460 | |||||||
| chr4:82561529 | G | A | 1 | a0001c0001t0019g0196 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-11+377C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561529 | |||||||
| chr4:82561546 | A | ACGGGGC | 9 | a0001c0001t0001g0018 a0001c0001t0002g0021 a0001c0001t0002g0022 others(6): Show |
9 | HG00642.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+354_-11+359dup others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561546 | |||||||
| chr4:82561548 | G | A | 66 | a0001c0001t0001g0226 a0001c0001t0001g0232 a0001c0001t0001g0236 others(63): Show |
66 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+358C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561548 | |||||||
| chr4:82561594 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-11+312C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561594 | |||||||
| chr4:82561641 | G | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0036 others(145): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.-11+265C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561641 | |||||||
| chr4:82561838 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-11+68T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561838 |