Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10020 |
| ensemblid | ENSG00000159921.20 |
| hgncid | 23657 |
| symbol | GNE |
| name | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase |
| refseq_nuc | NM_001128227.3 |
| refseq_prot | NP_001121699.1 |
| ensembl_nuc | ENST00000396594.8 |
| ensembl_prot | ENSP00000379839.3 |
| mane_status | MANE Plus Clinical |
| chr | chr9 |
| start | 36214441 |
| end | 36276978 |
| strand | - |
| ver | v1.2 |
| region | chr9:36214441-36276978 |
| region5000 | chr9:36209441-36281978 |
| regionname0 | GNE_chr9_36214441_36276978 |
| regionname5000 | GNE_chr9_36209441_36281978 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 753 | 354 | 84 | 72 | 138 | 16 | 42 | 102 | GNE_chr9_36209441_36281978 | GNE | METYG others(748): Show |
chr9 | 36209441 | 36281978 |
| a0002 | 0/0 | 753 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | METYG others(748): Show |
chr9 | 36209441 | 36281978 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2259 | 346 | 78 | 72 | 138 | 16 | 40 | GNE_chr9_36209441_36281978 | GNE | ATGGA others(2254): Show |
chr9 | 36209441 | 36281978 | ||
| a0001c0002 | 0/0 | 2259 | 8 | 6 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | ATGGA others(2254): Show |
chr9 | 36209441 | 36281978 | ||
| a0002c0003 | 0/0 | 2259 | 2 | 0 | 0 | 2 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | ATGGA others(2254): Show |
chr9 | 36209441 | 36281978 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5220 | 80 | 11 | 9 | 46 | 4 | 9 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5215): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0002 | 0/0 | 5252 | 33 | 5 | 5 | 21 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5247): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0003 | 0/0 | 5246 | 16 | 1 | 1 | 13 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5241): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0004 | 0/0 | 5221 | 15 | 0 | 4 | 11 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5216): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0005 | 0/0 | 5238 | 14 | 1 | 4 | 6 | 1 | 2 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5233): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0006 | 0/0 | 5240 | 13 | 1 | 5 | 5 | 1 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5235): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0007 | 0/0 | 5244 | 11 | 0 | 5 | 4 | 1 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5239): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0008 | 0/0 | 5242 | 10 | 3 | 2 | 4 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5237): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0009 | 0/0 | 5248 | 8 | 0 | 0 | 6 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5243): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0010 | 0/1 | 5223 | 9 | 0 | 3 | 4 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5218): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0011 | 0/0 | 5242 | 7 | 1 | 4 | 1 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5237): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0012 | 0/0 | 5238 | 5 | 5 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5233): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0013 | 0/0 | 5245 | 5 | 4 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5240): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0014 | 0/0 | 5231 | 5 | 4 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5226): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0015 | 0/0 | 5257 | 3 | 0 | 0 | 0 | 0 | 3 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5252): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0016 | 0/0 | 5255 | 2 | 1 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5250): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0017 | 0/0 | 5244 | 3 | 0 | 3 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5239): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0018 | 0/0 | 5242 | 3 | 0 | 0 | 1 | 2 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5237): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0019 | 0/0 | 5222 | 3 | 0 | 3 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5217): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0020 | 0/0 | 5252 | 3 | 0 | 2 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5247): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0021 | 0/0 | 5248 | 3 | 0 | 0 | 1 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5243): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0022 | 0/0 | 5236 | 3 | 0 | 2 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5231): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0023 | 0/0 | 5241 | 3 | 0 | 1 | 0 | 1 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5236): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0024 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5245): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0026 | 0/0 | 5251 | 2 | 1 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5246): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0027 | 0/0 | 5245 | 2 | 0 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5240): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0028 | 0/0 | 5254 | 2 | 0 | 1 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5249): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0029 | 0/0 | 5252 | 2 | 0 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5247): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0030 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5245): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0031 | 0/0 | 5246 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5241): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0032 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5239): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0033 | 0/0 | 5256 | 2 | 0 | 0 | 2 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5251): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0034 | 0/0 | 5226 | 2 | 0 | 2 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5221): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0035 | 0/0 | 5249 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5244): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0036 | 0/0 | 5249 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5244): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0037 | 0/0 | 5248 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5243): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0038 | 0/0 | 5246 | 2 | 0 | 0 | 1 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5241): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0039 | 0/0 | 5240 | 2 | 0 | 0 | 1 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5235): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0040 | 0/0 | 5238 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5233): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0041 | 0/0 | 5234 | 2 | 1 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5229): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0042 | 0/0 | 5228 | 2 | 0 | 2 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5223): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0043 | 0/0 | 5217 | 2 | 0 | 1 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5212): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0044 | 0/0 | 5235 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5230): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0045 | 0/0 | 5211 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5206): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0046 | 0/0 | 5249 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5244): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0047 | 0/0 | 5246 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5241): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0048 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5227): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0049 | 0/0 | 5254 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5249): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0051 | 0/0 | 5239 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5234): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0053 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5233): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0054 | 0/0 | 5252 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5247): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0055 | 0/0 | 5243 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5238): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0056 | 0/0 | 5242 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5237): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0057 | 0/0 | 5230 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5225): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0058 | 0/0 | 5228 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5223): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0059 | 0/0 | 5252 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5247): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0061 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5227): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0062 | 0/0 | 5253 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5248): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0063 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5242): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0064 | 0/0 | 5256 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5251): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0065 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5245): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0066 | 0/0 | 5248 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5243): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0067 | 0/0 | 5246 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5241): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0068 | 0/0 | 5242 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5237): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0069 | 0/0 | 5254 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5249): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0070 | 0/0 | 5252 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5247): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0071 | 0/0 | 5245 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5240): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0072 | 0/0 | 5249 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5244): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0073 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5233): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0074 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5239): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0075 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5235): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0076 | 0/0 | 5222 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5217): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0077 | 0/0 | 5220 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5215): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0078 | 0/0 | 5220 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5215): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0079 | 0/0 | 5264 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5259): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0080 | 0/0 | 5254 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5249): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0081 | 0/0 | 5244 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5239): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0082 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5239): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0083 | 0/0 | 5240 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5235): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0084 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5233): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0085 | 0/0 | 5238 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5233): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0086 | 0/0 | 5238 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5233): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0087 | 0/0 | 5249 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5244): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0088 | 0/0 | 5243 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5238): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0089 | 0/0 | 5241 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5236): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0090 | 0/0 | 5233 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5228): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0091 | 0/0 | 5249 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5244): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0092 | 0/0 | 5255 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5250): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0093 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5243): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0094 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5239): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0095 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5237): Show |
chr9 | 36209441 | 36281978 |
| a0001c0001t0096 | 0/0 | 5234 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5229): Show |
chr9 | 36209441 | 36281978 |
| a0001c0002t0016 | 0/0 | 5255 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5250): Show |
chr9 | 36209441 | 36281978 |
| a0001c0002t0024 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5245): Show |
chr9 | 36209441 | 36281978 |
| a0001c0002t0025 | 0/0 | 5240 | 2 | 2 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5235): Show |
chr9 | 36209441 | 36281978 |
| a0001c0002t0032 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5239): Show |
chr9 | 36209441 | 36281978 |
| a0001c0002t0050 | 0/0 | 5246 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5241): Show |
chr9 | 36209441 | 36281978 |
| a0001c0002t0052 | 0/0 | 5255 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5250): Show |
chr9 | 36209441 | 36281978 |
| a0001c0002t0060 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5253): Show |
chr9 | 36209441 | 36281978 |
| a0002c0003t0009 | 0/0 | 5248 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5243): Show |
chr9 | 36209441 | 36281978 |
| a0002c0003t0030 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | AAACC others(5245): Show |
chr9 | 36209441 | 36281978 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0239 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0008g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0009g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0009g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0009g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0010g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0010g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0010g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0010g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0010g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0010g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0010g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0010g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0010g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0011g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0011g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0011g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0011g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0011g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0011g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0011g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0012g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0012g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0012g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0013g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0014g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0014g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0014g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0015g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0015g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0015g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0016g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0016g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0017g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0017g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0017g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0018g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0018g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0018g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0019g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0019g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0019g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0020g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0020g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0020g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0021g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0021g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0021g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0022g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0022g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0022g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0023g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0023g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0023g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0024g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0026g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0026g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0027g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0027g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0028g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0028g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0029g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0030g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0031g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0031g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0032g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0033g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0033g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0034g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0034g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0035g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0035g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0036g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0036g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0037g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0037g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0038g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0038g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0039g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0039g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0040g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0040g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0041g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0041g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0042g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0042g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0043g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0043g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0044g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0044g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0045g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0045g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0046g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0046g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0047g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0047g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0048g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0049g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0051g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0053g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0054g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0055g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0056g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0057g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0058g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0059g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0061g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0062g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0063g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0064g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0065g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0066g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0067g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0068g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0069g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0070g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0071g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0072g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0073g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0074g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0075g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0076g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0077g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0078g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0079g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0080g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0081g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0082g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0083g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0084g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0085g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0086g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0087g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0088g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0089g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0090g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0091g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0092g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0093g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0094g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0095g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0001t0096g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0002t0016g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0002t0024g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0002t0025g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0002t0025g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0002t0032g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0002t0050g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0002t0052g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0001c0002t0060g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0002c0003t0009g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| a0002c0003t0030g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0010 | g0289 | EUR | GBR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00099 | hp2 | a0001 | c0001 | t0023 | g0163 | EUR | GBR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | GBR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0198 | EUR | GBR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0177 | EUR | FIN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00280 | hp2 | a0001 | c0001 | t0028 | g0225 | EUR | FIN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00408 | hp2 | a0001 | c0001 | t0009 | g0002 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00544 | hp1 | a0001 | c0001 | t0067 | g0053 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00609 | hp1 | a0001 | c0001 | t0010 | g0267 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00639 | hp1 | a0001 | c0001 | t0010 | g0287 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0275 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00738 | hp1 | a0001 | c0001 | t0020 | g0171 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0292 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00741 | hp1 | a0001 | c0001 | t0020 | g0149 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0211 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01069 | hp1 | a0001 | c0001 | t0011 | g0209 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01071 | hp1 | a0001 | c0001 | t0011 | g0208 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01071 | hp2 | a0001 | c0001 | t0041 | g0213 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01074 | hp1 | a0001 | c0001 | t0028 | g0133 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01074 | hp2 | a0001 | c0001 | t0014 | g0083 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0223 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0274 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01099 | hp1 | a0001 | c0001 | t0023 | g0147 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01106 | hp2 | a0001 | c0001 | t0022 | g0217 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01109 | hp1 | a0001 | c0001 | t0092 | g0012 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01109 | hp2 | a0001 | c0001 | t0043 | g0259 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0168 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0193 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0194 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0174 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01175 | hp2 | a0001 | c0001 | t0054 | g0032 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0197 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0224 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0074 | AMR | PUR | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01255 | hp1 | a0001 | c0001 | t0037 | g0349 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01255 | hp2 | a0001 | c0001 | t0079 | g0150 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01256 | hp1 | a0001 | c0001 | t0042 | g0144 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01256 | hp2 | a0001 | c0001 | t0034 | g0290 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0173 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01257 | hp2 | a0001 | c0001 | t0031 | g0091 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0175 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01258 | hp2 | a0001 | c0001 | t0034 | g0293 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0308 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01261 | hp2 | a0001 | c0001 | t0011 | g0181 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01346 | hp2 | a0001 | c0001 | t0042 | g0178 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01361 | hp1 | a0001 | c0001 | t0085 | g0200 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0167 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01515 | hp1 | a0001 | c0001 | t0083 | g0210 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01515 | hp2 | a0001 | c0001 | t0018 | g0060 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0176 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01517 | hp1 | a0001 | c0001 | t0018 | g0061 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0323 | EUR | IBS | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01884 | hp1 | a0001 | c0001 | t0096 | g0273 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01884 | hp2 | a0001 | c0002 | t0050 | g0028 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01891 | hp2 | a0001 | c0002 | t0052 | g0340 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0205 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0261 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01934 | hp2 | a0001 | c0001 | t0086 | g0221 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0160 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0199 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01952 | hp1 | a0001 | c0001 | t0019 | g0296 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01952 | hp2 | a0001 | c0001 | t0022 | g0195 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01975 | hp1 | a0001 | c0001 | t0007 | g0139 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01978 | hp1 | a0001 | c0001 | t0017 | g0034 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01978 | hp2 | a0001 | c0001 | t0081 | g0219 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0214 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01981 | hp2 | a0001 | c0001 | t0035 | g0135 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01993 | hp1 | a0001 | c0001 | t0019 | g0263 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01993 | hp2 | a0001 | c0001 | t0017 | g0063 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02040 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0202 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0071 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02056 | hp1 | a0001 | c0001 | t0071 | g0022 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02071 | hp2 | a0001 | c0001 | t0008 | g0152 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02074 | hp1 | a0001 | c0001 | t0075 | g0021 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0182 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0049 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0207 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02135 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | KHV | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02148 | hp1 | a0001 | c0001 | t0017 | g0064 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02148 | hp2 | a0001 | c0001 | t0019 | g0318 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | CDX | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02257 | hp1 | a0001 | c0001 | t0035 | g0350 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02258 | hp1 | a0001 | c0001 | t0041 | g0220 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0351 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02280 | hp1 | a0001 | c0001 | t0045 | g0341 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0204 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | PEL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02451 | hp2 | a0001 | c0001 | t0048 | g0006 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02572 | hp1 | a0001 | c0001 | t0087 | g0354 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02572 | hp2 | a0001 | c0001 | t0036 | g0137 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02615 | hp1 | a0001 | c0001 | t0076 | g0231 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02615 | hp2 | a0001 | c0001 | t0069 | g0129 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02622 | hp1 | a0001 | c0001 | t0046 | g0015 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0151 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02647 | hp1 | a0001 | c0001 | t0089 | g0352 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02647 | hp2 | a0001 | c0002 | t0032 | g0062 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02683 | hp1 | a0001 | c0001 | t0015 | g0077 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02683 | hp2 | a0001 | c0001 | t0043 | g0258 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0216 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02717 | hp2 | a0001 | c0001 | t0072 | g0124 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0142 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02723 | hp2 | a0001 | c0001 | t0044 | g0089 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02735 | hp1 | a0001 | c0001 | t0064 | g0041 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0153 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02738 | hp2 | a0001 | c0001 | t0066 | g0130 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02809 | hp2 | a0001 | c0001 | t0049 | g0072 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02818 | hp1 | a0001 | c0001 | t0094 | g0018 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02818 | hp2 | a0001 | c0002 | t0024 | g0027 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02896 | hp1 | a0001 | c0001 | t0012 | g0008 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02896 | hp2 | a0001 | c0001 | t0088 | g0353 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0007 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02897 | hp2 | a0001 | c0001 | t0095 | g0013 | AFR | GWD | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02922 | hp2 | a0001 | c0001 | t0014 | g0087 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02965 | hp1 | a0001 | c0002 | t0025 | g0026 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02965 | hp2 | a0001 | c0001 | t0044 | g0233 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02976 | hp2 | a0001 | c0001 | t0084 | g0179 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03098 | hp1 | a0001 | c0001 | t0046 | g0011 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03098 | hp2 | a0001 | c0001 | t0036 | g0138 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03130 | hp1 | a0001 | c0001 | t0090 | g0234 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0084 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03195 | hp1 | a0001 | c0001 | t0082 | g0343 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0232 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03225 | hp1 | a0001 | c0001 | t0073 | g0082 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0005 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03239 | hp1 | a0001 | c0001 | t0057 | g0172 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03239 | hp2 | a0001 | c0001 | t0011 | g0196 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03453 | hp1 | a0001 | c0001 | t0032 | g0066 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03453 | hp2 | a0001 | c0001 | t0037 | g0347 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03486 | hp1 | a0001 | c0001 | t0091 | g0019 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03486 | hp2 | a0001 | c0001 | t0031 | g0088 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03490 | hp1 | a0001 | c0001 | t0029 | g0001 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03490 | hp2 | a0001 | c0001 | t0058 | g0155 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03491 | hp2 | a0001 | c0001 | t0020 | g0166 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03492 | hp2 | a0001 | c0001 | t0029 | g0001 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0236 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03516 | hp2 | a0001 | c0002 | t0025 | g0029 | AFR | ESN | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03579 | hp1 | a0001 | c0001 | t0074 | g0348 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0067 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0109 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03669 | hp2 | a0001 | c0001 | t0068 | g0128 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03688 | hp1 | a0001 | c0001 | t0027 | g0316 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0040 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0038 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03704 | hp2 | a0001 | c0001 | t0065 | g0108 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03710 | hp1 | a0001 | c0002 | t0016 | g0024 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03834 | hp2 | a0001 | c0001 | t0059 | g0052 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03927 | hp1 | a0001 | c0001 | t0021 | g0154 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0215 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03942 | hp1 | a0001 | c0002 | t0060 | g0025 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03942 | hp2 | a0001 | c0001 | t0023 | g0140 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG04115 | hp2 | a0001 | c0001 | t0038 | g0099 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG04184 | hp1 | a0001 | c0001 | t0015 | g0055 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG04199 | hp1 | a0001 | c0001 | t0027 | g0317 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG04204 | hp1 | a0001 | c0001 | t0021 | g0164 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG04204 | hp2 | a0001 | c0001 | t0015 | g0039 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG04228 | hp1 | a0001 | c0001 | t0039 | g0203 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18522 | hp1 | a0001 | c0001 | t0055 | g0070 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18612 | hp1 | a0001 | c0001 | t0011 | g0192 | EAS | CHB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18747 | hp1 | a0001 | c0001 | t0039 | g0146 | EAS | CHB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18747 | hp2 | a0001 | c0001 | t0078 | g0284 | EAS | CHB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18906 | hp2 | a0001 | c0001 | t0047 | g0017 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18943 | hp1 | a0001 | c0001 | t0009 | g0057 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0169 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18945 | hp1 | a0001 | c0001 | t0009 | g0037 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18946 | hp1 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18951 | hp2 | a0002 | c0003 | t0030 | g0189 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18952 | hp1 | a0001 | c0001 | t0018 | g0045 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18954 | hp1 | a0001 | c0001 | t0077 | g0320 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18954 | hp2 | a0001 | c0001 | t0010 | g0282 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18956 | hp1 | a0001 | c0001 | t0063 | g0031 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18959 | hp1 | a0001 | c0001 | t0016 | g0114 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18959 | hp2 | a0001 | c0001 | t0008 | g0156 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18984 | hp1 | a0001 | c0001 | t0033 | g0131 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18986 | hp2 | a0001 | c0001 | t0070 | g0118 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18990 | hp2 | a0001 | c0001 | t0008 | g0116 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18993 | hp2 | a0001 | c0001 | t0030 | g0042 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0145 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19030 | hp2 | a0001 | c0001 | t0040 | g0342 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19043 | hp1 | a0001 | c0001 | t0045 | g0345 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19062 | hp1 | a0001 | c0001 | t0010 | g0272 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19063 | hp2 | a0002 | c0003 | t0009 | g0185 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19066 | hp2 | a0001 | c0001 | t0010 | g0281 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19079 | hp1 | a0001 | c0001 | t0080 | g0148 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0170 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19084 | hp1 | a0001 | c0001 | t0009 | g0056 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19084 | hp2 | a0001 | c0001 | t0021 | g0161 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19086 | hp1 | a0001 | c0001 | t0038 | g0110 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19089 | hp1 | a0001 | c0001 | t0061 | g0111 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19091 | hp1 | a0001 | c0001 | t0033 | g0132 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19240 | hp1 | a0001 | c0001 | t0047 | g0016 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0004 | AFR | YRI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ASW | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0069 | AFR | ASW | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0335 | EUR | TSI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA20752 | hp2 | a0001 | c0001 | t0022 | g0190 | EUR | TSI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0212 | EUR | TSI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA20805 | hp2 | a0001 | c0001 | t0026 | g0123 | EUR | TSI | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG01123 | hp2 | a0001 | c0001 | t0056 | g0143 | AMR | CLM | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02109 | hp1 | a0001 | c0001 | t0062 | g0301 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0068 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02486 | hp2 | a0001 | c0001 | t0053 | g0346 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02559 | hp1 | a0001 | c0001 | t0051 | g0073 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG02559 | hp2 | a0001 | c0001 | t0026 | g0090 | AFR | ACB | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG03471 | hp2 | a0001 | c0001 | t0093 | g0014 | AFR | MSL | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG06807 | hp1 | a0001 | c0001 | t0040 | g0344 | AFR | USA | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| HG06807 | hp2 | a0001 | c0001 | t0024 | g0235 | AFR | USA | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA18955 | hp2 | a0001 | c0001 | t0007 | g0180 | EAS | JPT | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | USA | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0201 | AFR | USA | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0098 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0286 | REF | REF | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0239 | REF | REF | GNE_chr9_36209441_36281978 | GNE | chr9 | 36209441 | 36281978 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:36246120 | T | A | 1 | a0002 | 2 | NA18951.hp2 NA19063.hp2 |
missense_variant | MODERATE | c.620A>T | p.Asp207Val | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/12 | 654/5220 | 620/2262 | 207/753 | chr9 | 36246120 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:36246047 | G | A | 1 | a0001c0002 | 8 | HG01884.hp2 HG01891.hp2 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.693C>T | p.Ile231Ile | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/12 | 727/5220 | 693/2262 | 231/753 | chr9 | 36246047 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:36214576 | C | T | 1 | a0001c0001t0033 | 2 | NA18984.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2789G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2789 | chr9 | 36214576 | ||||||
| chr9:36214638 | G | T | 1 | a0001c0001t0067 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2727C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2727 | chr9 | 36214638 | ||||||
| chr9:36214653 | G | A | 1 | a0001c0001t0083 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2712C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2712 | chr9 | 36214653 | ||||||
| chr9:36214654 | C | T | 1 | a0001c0001t0083 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2711G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2711 | chr9 | 36214654 | ||||||
| chr9:36214815 | C | T | 1 | a0001c0001t0070 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2550G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2550 | chr9 | 36214815 | ||||||
| chr9:36214974 | G | A | 69 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(66): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*2391C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2391 | chr9 | 36214974 | ||||||
| chr9:36215099 | C | T | 1 | a0001c0001t0077 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2266G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2266 | chr9 | 36215099 | ||||||
| chr9:36215154 | G | C | 1 | a0001c0001t0085 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2211C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2211 | chr9 | 36215154 | ||||||
| chr9:36215168 | C | CA | 1 | a0001c0001t0004 | 15 | HG00609.hp2 HG00735.hp2 HG01261.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2196dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2196 | chr9 | 36215168 | ||||||
| chr9:36215209 | C | G | 2 | a0001c0001t0013 a0001c0001t0055 |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2156G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2156 | chr9 | 36215209 | ||||||
| chr9:36215309 | G | A | 2 | a0001c0001t0019 a0001c0001t0078 |
4 | HG01952.hp1 HG01993.hp1 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2056C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 2056 | chr9 | 36215309 | ||||||
| chr9:36215539 | C | G | 12 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0016 others(9): Show |
49 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1826G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1826 | chr9 | 36215539 | ||||||
| chr9:36215584 | C | T | 15 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0012 others(12): Show |
46 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1781G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1781 | chr9 | 36215584 | ||||||
| chr9:36216297 | T | A | 2 | a0001c0001t0040 a0001c0001t0082 |
3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1068A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1068 | chr9 | 36216297 | ||||||
| chr9:36216311 | G | T | 2 | a0001c0001t0013 a0001c0001t0055 |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1054C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1054 | chr9 | 36216311 | ||||||
| chr9:36216327 | A | ATG | 2 | a0001c0001t0019 a0001c0001t0076 |
4 | HG01952.hp1 HG01993.hp1 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1036_*1037dupCA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(1): Show |
2 | a0001c0001t0042 a0001c0001t0096 |
3 | HG01256.hp1 HG01346.hp2 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1030_*1037dupCACA others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0048 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1026_*1037dupCACA others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(7): Show |
2 | a0001c0001t0041 a0001c0002t0025 |
4 | HG01071.hp2 HG02258.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1024_*1037dupCACA others(10): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(9): Show |
5 | a0001c0001t0018 a0001c0001t0022 a0001c0001t0027 others(2): Show |
10 | HG01106.hp2 HG01515.hp2 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1022_*1037dupCACA others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(19): Show |
9 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0036 others(6): Show |
44 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(22): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(21): Show |
2 | a0001c0001t0015 a0001c0001t0069 |
4 | HG02615.hp2 HG02683.hp1 HG04184.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(24): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(23): Show |
1 | a0001c0001t0033 | 2 | NA18984.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(26): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(11): Show |
13 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0017 others(10): Show |
33 | HG00140.hp2 HG00438.hp1 HG01361.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1020_*1037dupCACA others(14): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(13): Show |
15 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0014 others(12): Show |
50 | HG00544.hp1 HG01074.hp2 HG01081.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1018_*1037dupCACA others(16): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(15): Show |
12 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0011 others(9): Show |
35 | HG00408.hp2 HG00741.hp2 HG01069.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1016_*1037dupCACA others(18): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(17): Show |
14 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0023 others(11): Show |
31 | HG00099.hp2 HG00280.hp1 HG01099.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1014_*1037dupCACA others(20): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(19): Show |
4 | a0001c0001t0029 a0001c0001t0035 a0001c0001t0088 others(1): Show |
6 | HG01109.hp1 HG01981.hp2 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1012_*1037dupCACA others(22): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(21): Show |
4 | a0001c0001t0021 a0001c0001t0028 a0001c0001t0037 others(1): Show |
8 | HG00280.hp2 HG01074.hp1 HG01255.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(24): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(23): Show |
1 | a0001c0001t0064 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(26): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(25): Show |
2 | a0001c0001t0020 a0001c0001t0087 |
4 | HG00738.hp1 HG00741.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(28): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(27): Show |
2 | a0001c0001t0056 a0001c0001t0080 |
2 | HG01123.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(30): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216327 | A | ATGTGTGT others(37): Show |
1 | a0001c0001t0079 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1037_*1038insCACA others(40): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 1037 | chr9 | 36216327 | ||||||
| chr9:36216367 | G | A | 1 | a0001c0001t0086 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 998 | chr9 | 36216367 | ||||||
| chr9:36216428 | C | G | 1 | a0001c0001t0091 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 937 | chr9 | 36216428 | ||||||
| chr9:36216428 | C | T | 4 | a0001c0001t0073 a0001c0001t0087 a0001c0001t0088 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 937 | chr9 | 36216428 | ||||||
| chr9:36216429 | G | A | 29 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(26): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*936C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 936 | chr9 | 36216429 | ||||||
| chr9:36216640 | G | GATT | 5 | a0001c0001t0010 a0001c0001t0035 a0001c0001t0036 others(2): Show |
14 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*722_*724dupAAT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 724 | chr9 | 36216640 | ||||||
| chr9:36216640 | G | GATTATT | 32 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(29): Show |
97 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*719_*724dupAATAAT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 724 | chr9 | 36216640 | ||||||
| chr9:36216640 | G | GATTATTA others(2): Show |
11 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0026 others(8): Show |
17 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*716_*724dupAATAAT others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 724 | chr9 | 36216640 | ||||||
| chr9:36216640 | G | GATTATTA others(5): Show |
4 | a0001c0001t0054 a0001c0001t0059 a0001c0001t0061 others(1): Show |
4 | HG01175.hp2 HG03834.hp2 HG03942.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*713_*724dupAATAAT others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 724 | chr9 | 36216640 | ||||||
| chr9:36216640 | GATT | G | 5 | a0001c0001t0043 a0001c0001t0051 a0001c0001t0087 others(2): Show |
6 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*722_*724delAAT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 722 | chr9 | 36216640 | ||||||
| chr9:36216640 | GATTATTA others(2): Show |
G | 4 | a0001c0001t0014 a0001c0001t0044 a0001c0001t0045 others(1): Show |
10 | HG01074.hp2 HG02280.hp1 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*716_*724delAATAAT others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 716 | chr9 | 36216640 | ||||||
| chr9:36216663 | TTATTATT others(5): Show |
T | 3 | a0001c0001t0056 a0001c0001t0057 a0001c0001t0058 |
3 | HG01123.hp2 HG03239.hp1 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690_*701delTAAATA others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 690 | chr9 | 36216663 | ||||||
| chr9:36216669 | TTATTTA | T | 11 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0012 others(8): Show |
42 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*690_*695delTAAATA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 690 | chr9 | 36216669 | ||||||
| chr9:36216672 | T | TTA | 3 | a0001c0001t0013 a0001c0001t0055 a0001c0001t0082 |
7 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*692_*693insTA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 692 | chr9 | 36216672 | ||||||
| chr9:36216672 | TTTA | T | 9 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0011 others(6): Show |
40 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*690_*692delTAA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 690 | chr9 | 36216672 | ||||||
| chr9:36216674 | T | A | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0022 others(1): Show |
4 | HG01928.hp1 NA19030.hp2 NA20752.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*691A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 691 | chr9 | 36216674 | ||||||
| chr9:36216675 | A | AT | 3 | a0001c0001t0040 a0001c0001t0053 a0001c0001t0082 |
3 | HG02486.hp2 HG03195.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*689dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 689 | chr9 | 36216675 | ||||||
| chr9:36216675 | A | T | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0022 others(1): Show |
4 | HG01928.hp1 NA19030.hp2 NA20752.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*690T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 690 | chr9 | 36216675 | ||||||
| chr9:36216678 | A | AT | 2 | a0001c0001t0013 a0001c0001t0055 |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*686dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 686 | chr9 | 36216678 | ||||||
| chr9:36216735 | G | A | 8 | a0001c0001t0046 a0001c0001t0047 a0001c0001t0091 others(5): Show |
10 | HG01109.hp1 HG01884.hp1 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*630C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 630 | chr9 | 36216735 | ||||||
| chr9:36216782 | C | T | 1 | a0001c0001t0054 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*583G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 583 | chr9 | 36216782 | ||||||
| chr9:36216914 | C | T | 1 | a0001c0001t0053 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*451G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 451 | chr9 | 36216914 | ||||||
| chr9:36217012 | C | T | 1 | a0001c0002t0052 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*353G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 353 | chr9 | 36217012 | ||||||
| chr9:36217082 | CTAT | C | 1 | a0001c0001t0023 | 3 | HG00099.hp2 HG01099.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*280_*282delATA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 280 | chr9 | 36217082 | ||||||
| chr9:36217291 | C | T | 6 | a0001c0001t0024 a0001c0001t0049 a0001c0001t0051 others(3): Show |
7 | HG01884.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*74G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 12/12 | 74 | chr9 | 36217291 | ||||||
| chr9:36276954 | C | T | 2 | a0001c0001t0012 a0001c0001t0048 |
6 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/12 | chr9 | 36276954 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:36217801 | G | A | 99 | a0001c0001t0005g0009 a0001c0001t0005g0109 a0001c0001t0005g0186 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2027-201C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36217801 | |||||||
| chr9:36217819 | C | T | 1 | a0001c0001t0022g0217 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2027-219G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36217819 | |||||||
| chr9:36217893 | G | T | 1 | a0001c0001t0011g0192 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2026+290C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36217893 | |||||||
| chr9:36218015 | T | C | 1 | a0001c0001t0015g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2026+168A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218015 | |||||||
| chr9:36218021 | C | G | 240 | a0001c0001t0002g0075 a0001c0001t0002g0078 a0001c0001t0002g0079 others(237): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.2026+162G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218021 | |||||||
| chr9:36218043 | G | A | 1 | a0001c0001t0001g0334 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2026+140C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218043 | |||||||
| chr9:36218084 | CT | C | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2026+98delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218084 | |||||||
| chr9:36218142 | G | A | 1 | a0001c0001t0037g0347 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2026+41C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218142 | |||||||
| chr9:36218153 | C | G | 1 | a0001c0001t0022g0195 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2026+30G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 11/11 | chr9 | 36218153 | |||||||
| chr9:36218380 | C | G | 44 | a0001c0001t0007g0139 a0001c0001t0007g0141 a0001c0001t0007g0153 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1910-81G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218380 | |||||||
| chr9:36218400 | G | A | 1 | a0001c0001t0057g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1910-101C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218400 | |||||||
| chr9:36218473 | C | T | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1910-174G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218473 | |||||||
| chr9:36218525 | C | T | 2 | a0001c0001t0034g0290 a0001c0001t0034g0293 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1910-226G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218525 | |||||||
| chr9:36218575 | C | T | 2 | a0001c0001t0007g0169 a0001c0001t0007g0180 |
2 | NA18944.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1910-276G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218575 | |||||||
| chr9:36218967 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1910-668C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36218967 | |||||||
| chr9:36219011 | A | G | 7 | a0001c0001t0024g0235 a0001c0001t0049g0072 a0001c0001t0051g0073 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1910-712T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36219011 | |||||||
| chr9:36219089 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1909+749A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36219089 | |||||||
| chr9:36219343 | T | G | 1 | a0001c0001t0032g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1909+495A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36219343 | |||||||
| chr9:36219508 | C | T | 2 | a0001c0001t0011g0211 a0001c0001t0083g0210 |
2 | HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1909+330G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36219508 | |||||||
| chr9:36219820 | C | T | 1 | a0001c0002t0025g0029 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1909+18G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 10/11 | chr9 | 36219820 | |||||||
| chr9:36220027 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18951.hp1 | splice_region_variant&intron_variant | LOW | c.1727-7G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36220027 | |||||||
| chr9:36220137 | T | C | 50 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0023 others(47): Show |
52 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1727-117A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36220137 | |||||||
| chr9:36220208 | A | C | 1 | a0001c0001t0002g0127 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1727-188T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36220208 | |||||||
| chr9:36220439 | G | A | 251 | a0001c0001t0001g0119 a0001c0001t0002g0075 a0001c0001t0002g0078 others(248): Show |
253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1727-419C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36220439 | |||||||
| chr9:36220848 | T | C | 22 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0242 others(19): Show |
22 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1727-828A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36220848 | |||||||
| chr9:36221039 | G | A | 1 | a0001c0001t0004g0308 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1727-1019C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221039 | |||||||
| chr9:36221137 | G | A | 241 | a0001c0001t0001g0119 a0001c0001t0002g0075 a0001c0001t0002g0078 others(238): Show |
243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1727-1117C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221137 | |||||||
| chr9:36221148 | T | G | 5 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1727-1128A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221148 | |||||||
| chr9:36221178 | G | A | 51 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0023 others(48): Show |
53 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.1727-1158C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221178 | |||||||
| chr9:36221337 | G | T | 1 | a0001c0001t0014g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1727-1317C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221337 | |||||||
| chr9:36221338 | A | G | 1 | a0001c0001t0014g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1727-1318T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221338 | |||||||
| chr9:36221974 | C | T | 3 | a0001c0001t0012g0003 a0001c0001t0012g0004 a0001c0001t0012g0005 |
3 | HG02922.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1726+803G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36221974 | |||||||
| chr9:36222144 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1726+633G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222144 | |||||||
| chr9:36222146 | C | T | 10 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0014g0083 others(7): Show |
10 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1726+631G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222146 | |||||||
| chr9:36222190 | G | A | 3 | a0001c0001t0005g0191 a0001c0001t0005g0206 a0001c0001t0006g0215 |
3 | HG03927.hp2 NA19007.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1726+587C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222190 | |||||||
| chr9:36222215 | G | A | 2 | a0001c0001t0010g0287 a0001c0001t0010g0292 |
2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1726+562C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222215 | |||||||
| chr9:36222234 | C | T | 1 | a0001c0001t0004g0339 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1726+543G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222234 | |||||||
| chr9:36222235 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1726+542C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222235 | |||||||
| chr9:36222262 | A | G | 3 | a0001c0001t0012g0003 a0001c0001t0012g0004 a0001c0001t0012g0005 |
3 | HG02922.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1726+515T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222262 | |||||||
| chr9:36222292 | G | A | 135 | a0001c0001t0001g0119 a0001c0001t0002g0080 a0001c0001t0002g0092 others(132): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1726+485C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222292 | |||||||
| chr9:36222346 | G | A | 2 | a0001c0001t0011g0208 a0001c0001t0011g0209 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1726+431C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222346 | |||||||
| chr9:36222418 | C | CA | 129 | a0001c0001t0001g0159 a0001c0001t0001g0227 a0001c0001t0001g0249 others(126): Show |
129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1726+358dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222418 | |||||||
| chr9:36222418 | C | CAA | 19 | a0001c0001t0001g0119 a0001c0001t0002g0080 a0001c0001t0002g0094 others(16): Show |
19 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1726+357_1726+358d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222418 | |||||||
| chr9:36222418 | CA | C | 59 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0023 others(56): Show |
61 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1726+358delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222418 | |||||||
| chr9:36222436 | C | A | 2 | a0001c0001t0002g0122 a0001c0001t0072g0124 |
2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1726+341G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222436 | |||||||
| chr9:36222501 | C | G | 1 | a0001c0001t0073g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1726+276G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222501 | |||||||
| chr9:36222540 | G | A | 39 | a0001c0001t0001g0119 a0001c0001t0002g0080 a0001c0001t0002g0092 others(36): Show |
39 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1726+237C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222540 | |||||||
| chr9:36222625 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | NA18960.hp1 NA19086.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1726+152G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222625 | |||||||
| chr9:36222652 | C | G | 52 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0023 others(49): Show |
54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1726+125G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222652 | |||||||
| chr9:36222659 | A | G | 6 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1726+118T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 9/11 | chr9 | 36222659 | |||||||
| chr9:36223002 | C | T | 2 | a0001c0001t0008g0156 a0001c0001t0021g0161 |
2 | NA18959.hp2 NA19084.hp2 |
splice_region_variant&intron_variant | LOW | c.1505-4G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 8/11 | chr9 | 36223002 | |||||||
| chr9:36223269 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1504+104T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 8/11 | chr9 | 36223269 | |||||||
| chr9:36223350 | G | A | 1 | a0001c0001t0038g0099 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1504+23C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 8/11 | chr9 | 36223350 | |||||||
| chr9:36223657 | G | A | 81 | a0001c0001t0001g0119 a0001c0001t0002g0080 a0001c0001t0002g0092 others(78): Show |
81 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1375-155C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223657 | |||||||
| chr9:36223755 | C | CT | 7 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(4): Show |
7 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1375-254dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223755 | |||||||
| chr9:36223783 | G | A | 50 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0023 others(47): Show |
52 | HG00408.hp2 HG00544.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.1375-281C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223783 | |||||||
| chr9:36223804 | C | T | 212 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(209): Show |
214 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1375-302G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223804 | |||||||
| chr9:36223854 | C | T | 11 | a0001c0001t0024g0235 a0001c0001t0049g0072 a0001c0001t0051g0073 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1375-352G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223854 | |||||||
| chr9:36223855 | G | A | 7 | a0001c0001t0001g0081 a0001c0001t0001g0314 a0001c0001t0013g0067 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.1375-353C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36223855 | |||||||
| chr9:36224048 | G | A | 1 | a0001c0001t0003g0054 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1375-546C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224048 | |||||||
| chr9:36224084 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0300 |
2 | HG00140.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1375-582C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224084 | |||||||
| chr9:36224165 | G | A | 10 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0014g0083 others(7): Show |
10 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-663C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224165 | |||||||
| chr9:36224374 | C | T | 45 | a0001c0001t0007g0139 a0001c0001t0007g0141 a0001c0001t0007g0153 others(42): Show |
45 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1375-872G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224374 | |||||||
| chr9:36224591 | G | A | 2 | a0001c0001t0043g0258 a0001c0001t0043g0259 |
2 | HG01109.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1375-1089C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224591 | |||||||
| chr9:36224609 | C | T | 1 | a0001c0001t0074g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1375-1107G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224609 | |||||||
| chr9:36224681 | G | A | 1 | a0001c0002t0050g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1375-1179C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224681 | |||||||
| chr9:36224681 | G | T | 1 | a0001c0001t0006g0188 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1375-1179C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224681 | |||||||
| chr9:36224715 | C | A | 1 | a0001c0002t0032g0062 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1375-1213G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224715 | |||||||
| chr9:36224724 | G | T | 1 | a0001c0002t0032g0062 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1375-1222C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224724 | |||||||
| chr9:36224914 | C | A | 3 | a0001c0001t0002g0107 a0001c0001t0002g0121 a0001c0001t0002g0270 |
3 | HG00639.hp2 HG00735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1375-1412G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36224914 | |||||||
| chr9:36225592 | G | A | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1374+1656C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36225592 | |||||||
| chr9:36225745 | C | T | 1 | a0001c0001t0007g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1374+1503G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36225745 | |||||||
| chr9:36225785 | A | T | 6 | a0001c0001t0012g0003 a0001c0001t0012g0004 a0001c0001t0012g0005 others(3): Show |
6 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1374+1463T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36225785 | |||||||
| chr9:36225902 | ACT | A | 21 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0253 others(18): Show |
21 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1374+1344_1374+134 others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36225902 | |||||||
| chr9:36226116 | T | C | 3 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0082g0343 |
3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1374+1132A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36226116 | |||||||
| chr9:36226265 | T | C | 4 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0319 others(1): Show |
4 | HG02109.hp1 HG02717.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1374+983A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36226265 | |||||||
| chr9:36226339 | A | AT | 95 | a0001c0001t0001g0119 a0001c0001t0001g0227 a0001c0001t0001g0249 others(92): Show |
96 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1374+908dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36226339 | |||||||
| chr9:36226339 | A | ATT | 46 | a0001c0001t0002g0107 a0001c0001t0002g0112 a0001c0001t0005g0214 others(43): Show |
46 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1374+907_1374+908d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36226339 | |||||||
| chr9:36226431 | A | T | 1 | a0001c0001t0032g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1374+817T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36226431 | |||||||
| chr9:36227188 | T | TA | 8 | a0001c0001t0036g0137 a0001c0001t0036g0138 a0001c0001t0040g0342 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1374+59dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36227188 | |||||||
| chr9:36227204 | C | T | 11 | a0001c0001t0024g0235 a0001c0001t0049g0072 a0001c0001t0051g0073 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1374+44G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36227204 | |||||||
| chr9:36227221 | A | G | 1 | a0001c0001t0069g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1374+27T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 7/11 | chr9 | 36227221 | |||||||
| chr9:36227633 | G | T | 3 | a0001c0001t0036g0137 a0001c0001t0036g0138 a0001c0001t0059g0052 |
3 | HG02572.hp2 HG03098.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1164-175C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36227633 | |||||||
| chr9:36227811 | G | A | 1 | a0001c0001t0020g0166 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1164-353C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36227811 | |||||||
| chr9:36228032 | C | CA | 23 | a0001c0001t0001g0050 a0001c0001t0001g0240 a0001c0001t0001g0251 others(20): Show |
23 | HG00735.hp1 HG01069.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164-575dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228032 | |||||||
| chr9:36228051 | AC | A | 9 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(6): Show |
9 | HG01255.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164-594delG | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228051 | |||||||
| chr9:36228052 | C | A | 3 | a0001c0001t0036g0137 a0001c0001t0036g0138 a0001c0001t0082g0343 |
3 | HG02572.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1164-594G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228052 | |||||||
| chr9:36228283 | CTT | C | 6 | a0001c0001t0012g0003 a0001c0001t0012g0004 a0001c0001t0012g0005 others(3): Show |
6 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1163+736_1163+737d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228283 | |||||||
| chr9:36228425 | T | G | 2 | a0001c0001t0034g0290 a0001c0001t0034g0293 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1163+596A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228425 | |||||||
| chr9:36228567 | C | A | 45 | a0001c0001t0007g0139 a0001c0001t0007g0141 a0001c0001t0007g0153 others(42): Show |
45 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1163+454G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228567 | |||||||
| chr9:36228716 | C | T | 3 | a0001c0001t0002g0113 a0001c0001t0002g0126 a0001c0001t0002g0127 |
3 | NA19060.hp2 NA19064.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1163+305G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228716 | |||||||
| chr9:36228750 | C | T | 1 | a0001c0001t0007g0169 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1163+271G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228750 | |||||||
| chr9:36228759 | A | G | 1 | a0001c0001t0014g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1163+262T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228759 | |||||||
| chr9:36228793 | C | CA | 41 | a0001c0001t0001g0249 a0001c0001t0002g0100 a0001c0001t0007g0139 others(38): Show |
41 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1163+227dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228793 | |||||||
| chr9:36228793 | CA | C | 43 | a0001c0001t0001g0158 a0001c0001t0001g0162 a0001c0001t0001g0325 others(40): Show |
43 | HG00544.hp2 HG01074.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1163+227delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228793 | |||||||
| chr9:36228793 | CAA | C | 39 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0023 others(36): Show |
41 | HG00408.hp2 HG00544.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.1163+226_1163+227d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 6/11 | chr9 | 36228793 | |||||||
| chr9:36229260 | T | C | 2 | a0002c0003t0009g0185 a0002c0003t0030g0189 |
2 | NA18951.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1076-152A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229260 | |||||||
| chr9:36229381 | C | T | 22 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0014g0083 others(19): Show |
22 | HG01074.hp2 HG01255.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1076-273G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229381 | |||||||
| chr9:36229599 | T | G | 240 | a0001c0001t0001g0119 a0001c0001t0002g0075 a0001c0001t0002g0078 others(237): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1076-491A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229599 | |||||||
| chr9:36229712 | A | G | 10 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0014g0083 others(7): Show |
10 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1076-604T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229712 | |||||||
| chr9:36229821 | A | G | 3 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0082g0343 |
3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1076-713T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229821 | |||||||
| chr9:36229885 | C | T | 1 | a0001c0001t0056g0143 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1076-777G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229885 | |||||||
| chr9:36229920 | C | T | 1 | a0001c0001t0023g0163 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1076-812G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229920 | |||||||
| chr9:36229952 | C | CT | 8 | a0001c0001t0001g0315 a0001c0001t0002g0122 a0001c0001t0013g0067 others(5): Show |
8 | HG00621.hp1 HG01243.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1076-845dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36229952 | |||||||
| chr9:36230011 | A | G | 1 | a0001c0001t0062g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1076-903T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230011 | |||||||
| chr9:36230082 | G | A | 3 | a0001c0001t0007g0139 a0001c0001t0007g0160 a0001c0001t0008g0201 |
3 | HG01943.hp1 HG01975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1076-974C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230082 | |||||||
| chr9:36230371 | C | A | 1 | a0001c0001t0002g0117 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1076-1263G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230371 | |||||||
| chr9:36230483 | G | T | 4 | a0001c0001t0005g0199 a0001c0001t0005g0205 a0001c0001t0006g0197 others(1): Show |
4 | HG01192.hp1 HG01928.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-1375C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230483 | |||||||
| chr9:36230619 | C | A | 1 | a0001c0001t0024g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1076-1511G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230619 | |||||||
| chr9:36230660 | CT | C | 6 | a0001c0001t0001g0304 a0001c0001t0002g0092 a0001c0001t0002g0112 others(3): Show |
6 | HG01099.hp2 HG01167.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1076-1553delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230660 | |||||||
| chr9:36230682 | C | T | 2 | a0001c0001t0006g0065 a0001c0001t0011g0351 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1076-1574G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36230682 | |||||||
| chr9:36231066 | T | TAAAA | 46 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0030 others(43): Show |
48 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1076-1962_1076-195 others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231066 | |||||||
| chr9:36231066 | T | TAAAAA | 12 | a0001c0001t0024g0235 a0001c0001t0046g0011 a0001c0001t0049g0072 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1076-1963_1076-195 others(9): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231066 | |||||||
| chr9:36231066 | TA | T | 14 | a0001c0001t0001g0245 a0001c0001t0001g0268 a0001c0001t0001g0302 others(11): Show |
14 | HG01943.hp2 HG01975.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.1076-1959delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231066 | |||||||
| chr9:36231081 | A | AAAG | 15 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0014g0083 others(12): Show |
15 | HG01074.hp2 HG01255.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1076-1974_1076-197 others(7): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231081 | |||||||
| chr9:36231081 | A | G | 2 | a0001c0001t0045g0341 a0001c0001t0045g0345 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1076-1973T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231081 | |||||||
| chr9:36231084 | AG | A | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1076-1977delC | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231084 | |||||||
| chr9:36231085 | G | A | 15 | a0001c0001t0002g0075 a0001c0001t0002g0078 a0001c0001t0002g0079 others(12): Show |
15 | HG00280.hp2 HG01074.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.1076-1977C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231085 | |||||||
| chr9:36231089 | G | A | 4 | a0001c0001t0027g0316 a0001c0001t0027g0317 a0001c0001t0031g0091 others(1): Show |
4 | HG01257.hp2 HG03669.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076-1981C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231089 | |||||||
| chr9:36231089 | GAA | G | 3 | a0001c0001t0001g0299 a0001c0001t0007g0173 a0001c0001t0007g0175 |
3 | HG01257.hp1 HG01258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1076-1983_1076-198 others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231089 | |||||||
| chr9:36231091 | AAGAG | A | 13 | a0001c0001t0002g0075 a0001c0001t0002g0078 a0001c0001t0002g0079 others(10): Show |
13 | HG00280.hp2 HG01074.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1076-1987_1076-198 others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231091 | |||||||
| chr9:36231095 | G | A | 4 | a0001c0001t0027g0316 a0001c0001t0027g0317 a0001c0001t0031g0091 others(1): Show |
4 | HG01257.hp2 HG03669.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076-1987C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231095 | |||||||
| chr9:36231123 | CAATG | C | 240 | a0001c0001t0001g0119 a0001c0001t0002g0075 a0001c0001t0002g0078 others(237): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1076-2019_1076-201 others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231123 | |||||||
| chr9:36231134 | G | A | 240 | a0001c0001t0001g0119 a0001c0001t0002g0075 a0001c0001t0002g0078 others(237): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1076-2026C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231134 | |||||||
| chr9:36231274 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1076-2166C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231274 | |||||||
| chr9:36231414 | C | T | 1 | a0001c0001t0087g0354 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1076-2306G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231414 | |||||||
| chr9:36231486 | T | C | 240 | a0001c0001t0001g0119 a0001c0001t0002g0075 a0001c0001t0002g0078 others(237): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1076-2378A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231486 | |||||||
| chr9:36231488 | C | T | 1 | a0001c0001t0031g0091 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1076-2380G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231488 | |||||||
| chr9:36231801 | A | G | 10 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0014g0083 others(7): Show |
10 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075+2119T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231801 | |||||||
| chr9:36231930 | A | G | 1 | a0001c0001t0008g0151 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1075+1990T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231930 | |||||||
| chr9:36231970 | C | T | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1075+1950G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36231970 | |||||||
| chr9:36232196 | A | T | 1 | a0001c0001t0015g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1075+1724T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232196 | |||||||
| chr9:36232222 | C | T | 5 | a0001c0001t0010g0289 a0001c0001t0035g0350 a0001c0001t0037g0347 others(2): Show |
5 | HG00099.hp1 HG01255.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075+1698G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232222 | |||||||
| chr9:36232328 | G | GC | 12 | a0001c0001t0001g0254 a0001c0001t0001g0276 a0001c0001t0001g0338 others(9): Show |
12 | HG00735.hp2 HG01928.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+1591dupG | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232328 | |||||||
| chr9:36232328 | GC | G | 14 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0244 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1075+1591delG | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232328 | |||||||
| chr9:36232331 | C | G | 147 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(144): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1075+1589G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232331 | |||||||
| chr9:36232332 | C | G | 15 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0244 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1075+1588G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232332 | |||||||
| chr9:36232332 | CCCCGCCC others(5): Show |
C | 55 | a0001c0001t0001g0050 a0001c0001t0001g0310 a0001c0001t0001g0311 others(52): Show |
57 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+1576_1075+158 others(16): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232332 | |||||||
| chr9:36232334 | CCGCCCCC others(3): Show |
C | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1075+1576_1075+158 others(14): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232334 | |||||||
| chr9:36232335 | C | A | 2 | a0001c0001t0008g0151 a0001c0001t0084g0179 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1075+1585G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232335 | |||||||
| chr9:36232336 | G | A | 14 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0244 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1075+1584C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232336 | |||||||
| chr9:36232336 | G | C | 2 | a0001c0001t0008g0151 a0001c0001t0084g0179 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1075+1584C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232336 | |||||||
| chr9:36232338 | C | G | 2 | a0001c0001t0043g0258 a0001c0001t0043g0259 |
2 | HG01109.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1075+1582G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232338 | |||||||
| chr9:36232340 | C | A | 5 | a0001c0001t0036g0137 a0001c0001t0036g0138 a0001c0001t0040g0342 others(2): Show |
5 | HG02572.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075+1580G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232340 | |||||||
| chr9:36232341 | C | G | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+1579G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232341 | |||||||
| chr9:36232343 | CT | C | 5 | a0001c0001t0036g0137 a0001c0001t0036g0138 a0001c0001t0040g0342 others(2): Show |
5 | HG02572.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075+1576delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232343 | |||||||
| chr9:36232344 | T | C | 146 | a0001c0001t0001g0081 a0001c0001t0001g0106 a0001c0001t0001g0226 others(143): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1075+1576A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232344 | |||||||
| chr9:36232345 | C | A | 105 | a0001c0001t0001g0081 a0001c0001t0001g0106 a0001c0001t0001g0226 others(102): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.1075+1575G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232345 | |||||||
| chr9:36232345 | C | CA | 35 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0276 others(32): Show |
35 | HG00544.hp2 HG00609.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1075+1574_1075+157 others(5): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232345 | |||||||
| chr9:36232416 | T | C | 178 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1075+1504A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232416 | |||||||
| chr9:36232548 | C | T | 7 | a0001c0001t0049g0072 a0001c0001t0051g0073 a0001c0002t0024g0027 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075+1372G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232548 | |||||||
| chr9:36232700 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+1220G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232700 | |||||||
| chr9:36232723 | C | G | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+1197G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232723 | |||||||
| chr9:36232869 | A | T | 1 | a0001c0001t0001g0303 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1075+1051T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232869 | |||||||
| chr9:36232997 | C | G | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+923G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36232997 | |||||||
| chr9:36233061 | C | T | 52 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(49): Show |
54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1075+859G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233061 | |||||||
| chr9:36233241 | G | A | 3 | a0001c0001t0012g0003 a0001c0001t0012g0004 a0001c0001t0012g0005 |
3 | HG02922.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1075+679C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233241 | |||||||
| chr9:36233260 | T | C | 1 | a0001c0001t0076g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1075+660A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233260 | |||||||
| chr9:36233289 | C | T | 13 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(10): Show |
13 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1075+631G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233289 | |||||||
| chr9:36233392 | C | T | 1 | a0001c0001t0032g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1075+528G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233392 | |||||||
| chr9:36233432 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+488G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233432 | |||||||
| chr9:36233441 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+479G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233441 | |||||||
| chr9:36233484 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1075+436C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233484 | |||||||
| chr9:36233552 | A | G | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1075+368T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233552 | |||||||
| chr9:36233666 | CA | C | 237 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(234): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1075+253delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233666 | |||||||
| chr9:36233673 | A | C | 22 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(19): Show |
22 | HG00280.hp2 HG01074.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1075+247T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 5/11 | chr9 | 36233673 | |||||||
| chr9:36234247 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.863-115A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36234247 | |||||||
| chr9:36234442 | G | T | 52 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(49): Show |
54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.863-310C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36234442 | |||||||
| chr9:36234611 | A | G | 1 | a0001c0001t0072g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.863-479T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36234611 | |||||||
| chr9:36234700 | C | T | 1 | a0001c0001t0049g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.863-568G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36234700 | |||||||
| chr9:36234939 | C | T | 5 | a0001c0001t0005g0202 a0001c0001t0005g0204 a0001c0001t0005g0207 others(2): Show |
5 | HG00438.hp1 HG01981.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.863-807G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36234939 | |||||||
| chr9:36235077 | A | C | 9 | a0001c0001t0046g0011 a0001c0001t0046g0015 a0001c0001t0047g0016 others(6): Show |
9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.863-945T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235077 | |||||||
| chr9:36235129 | C | T | 3 | a0001c0001t0002g0113 a0001c0001t0002g0126 a0001c0001t0002g0127 |
3 | NA19060.hp2 NA19064.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.863-997G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235129 | |||||||
| chr9:36235151 | G | T | 1 | a0001c0001t0020g0166 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.863-1019C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235151 | |||||||
| chr9:36235190 | C | T | 231 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(228): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.863-1058G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235190 | |||||||
| chr9:36235308 | G | A | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.863-1176C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235308 | |||||||
| chr9:36235506 | T | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0276 others(3): Show |
6 | HG02056.hp2 NA18946.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.862+1326A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235506 | |||||||
| chr9:36235541 | T | C | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+1291A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235541 | |||||||
| chr9:36235624 | A | C | 139 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(136): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.862+1208T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235624 | |||||||
| chr9:36235769 | G | A | 1 | a0001c0001t0022g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.862+1063C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235769 | |||||||
| chr9:36235779 | C | G | 4 | a0001c0001t0073g0082 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+1053G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235779 | |||||||
| chr9:36235791 | G | A | 10 | a0001c0001t0049g0072 a0001c0001t0051g0073 a0001c0002t0016g0024 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.862+1041C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235791 | |||||||
| chr9:36235884 | T | C | 4 | a0001c0001t0007g0173 a0001c0001t0007g0175 a0001c0001t0008g0174 others(1): Show |
4 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.862+948A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36235884 | |||||||
| chr9:36236070 | G | A | 2 | a0001c0001t0027g0316 a0001c0001t0027g0317 |
2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.862+762C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36236070 | |||||||
| chr9:36236200 | C | A | 4 | a0001c0001t0073g0082 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+632G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36236200 | |||||||
| chr9:36236206 | C | CT | 11 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0246 others(8): Show |
11 | HG02027.hp1 HG02027.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.862+625dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36236206 | |||||||
| chr9:36236497 | A | G | 231 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(228): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.862+335T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36236497 | |||||||
| chr9:36236636 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.862+196A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 4/11 | chr9 | 36236636 | |||||||
| chr9:36237244 | T | G | 5 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(2): Show |
5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-260A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237244 | |||||||
| chr9:36237282 | A | G | 10 | a0001c0001t0049g0072 a0001c0001t0051g0073 a0001c0002t0016g0024 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.710-298T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237282 | |||||||
| chr9:36237489 | AG | A | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.710-506delC | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237489 | |||||||
| chr9:36237525 | G | A | 2 | a0001c0001t0027g0316 a0001c0001t0027g0317 |
2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.710-541C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237525 | |||||||
| chr9:36237525 | G | C | 1 | a0001c0001t0073g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.710-541C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237525 | |||||||
| chr9:36237645 | C | CT | 44 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0162 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.710-662dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237645 | |||||||
| chr9:36237654 | T | TA | 26 | a0001c0001t0001g0119 a0001c0001t0002g0092 a0001c0001t0002g0093 others(23): Show |
26 | HG00621.hp2 HG01106.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-671_710-670ins others(1): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237654 | |||||||
| chr9:36237655 | T | A | 30 | a0001c0001t0001g0119 a0001c0001t0002g0092 a0001c0001t0002g0093 others(27): Show |
30 | HG00621.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.710-671A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237655 | |||||||
| chr9:36237655 | T | TA | 64 | a0001c0001t0002g0097 a0001c0001t0002g0105 a0001c0001t0002g0107 others(61): Show |
64 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.710-672dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237655 | |||||||
| chr9:36237806 | C | T | 1 | a0001c0001t0015g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.710-822G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237806 | |||||||
| chr9:36237861 | C | A | 13 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(10): Show |
13 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.710-877G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237861 | |||||||
| chr9:36237997 | CT | C | 3 | a0001c0001t0033g0131 a0001c0001t0045g0341 a0001c0001t0045g0345 |
3 | HG02280.hp1 NA18984.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.710-1014delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36237997 | |||||||
| chr9:36238071 | TAC | T | 51 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(48): Show |
53 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.710-1089_710-1088d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238071 | |||||||
| chr9:36238123 | T | TAC | 16 | a0001c0001t0001g0277 a0001c0001t0003g0048 a0001c0001t0027g0317 others(13): Show |
16 | HG00438.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.710-1141_710-1140d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238123 | |||||||
| chr9:36238123 | T | TACAC | 5 | a0001c0001t0003g0044 a0001c0001t0035g0350 a0001c0001t0037g0347 others(2): Show |
5 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-1143_710-1140d others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238123 | |||||||
| chr9:36238123 | T | TACACAC | 51 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(48): Show |
53 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.710-1145_710-1140d others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238123 | |||||||
| chr9:36238123 | TAC | T | 26 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(23): Show |
26 | HG00280.hp2 HG01074.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-1141_710-1140d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238123 | |||||||
| chr9:36238145 | C | CAT | 138 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(135): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.710-1163_710-1162d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238145 | |||||||
| chr9:36238145 | C | T | 2 | a0001c0001t0006g0223 a0001c0001t0006g0224 |
2 | HG01081.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.710-1161G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238145 | |||||||
| chr9:36238219 | A | G | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-1235T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238219 | |||||||
| chr9:36238227 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.710-1243A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238227 | |||||||
| chr9:36238246 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-1262G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238246 | |||||||
| chr9:36238247 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.710-1263C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238247 | |||||||
| chr9:36238327 | A | AGTTCTAC others(27): Show |
4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-1344_710-1343i others(36): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238327 | |||||||
| chr9:36238521 | A | G | 1 | a0001c0001t0005g0009 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.710-1537T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238521 | |||||||
| chr9:36238529 | T | G | 2 | a0001c0001t0006g0223 a0001c0001t0006g0224 |
2 | HG01081.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.710-1545A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238529 | |||||||
| chr9:36238633 | G | T | 2 | a0001c0001t0036g0137 a0001c0001t0036g0138 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.710-1649C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238633 | |||||||
| chr9:36238719 | G | C | 1 | a0001c0001t0003g0033 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.710-1735C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238719 | |||||||
| chr9:36238989 | T | C | 10 | a0001c0001t0049g0072 a0001c0001t0051g0073 a0001c0002t0016g0024 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.710-2005A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36238989 | |||||||
| chr9:36239339 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.710-2355T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239339 | |||||||
| chr9:36239414 | T | C | 1 | a0001c0001t0068g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.710-2430A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239414 | |||||||
| chr9:36239448 | T | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0300 |
2 | HG00140.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.710-2464A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239448 | |||||||
| chr9:36239663 | G | C | 1 | a0001c0001t0046g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.710-2679C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239663 | |||||||
| chr9:36239720 | G | A | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.710-2736C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239720 | |||||||
| chr9:36239726 | G | A | 2 | a0001c0001t0008g0151 a0001c0001t0084g0179 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.710-2742C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239726 | |||||||
| chr9:36239730 | C | T | 1 | a0001c0001t0008g0168 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.710-2746G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239730 | |||||||
| chr9:36239754 | T | C | 1 | a0001c0001t0056g0143 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.710-2770A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36239754 | |||||||
| chr9:36240101 | T | C | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-3117A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240101 | |||||||
| chr9:36240120 | T | C | 1 | a0001c0002t0024g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.710-3136A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240120 | |||||||
| chr9:36240234 | G | C | 3 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0082g0343 |
3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.710-3250C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240234 | |||||||
| chr9:36240240 | A | G | 5 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(2): Show |
5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-3256T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240240 | |||||||
| chr9:36240448 | C | G | 239 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(236): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.710-3464G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240448 | |||||||
| chr9:36240519 | A | T | 231 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(228): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.710-3535T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240519 | |||||||
| chr9:36240732 | ATTC | A | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.710-3751_710-3749d others(5): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240732 | |||||||
| chr9:36240786 | T | C | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | NA18943.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.710-3802A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240786 | |||||||
| chr9:36240807 | A | T | 10 | a0001c0001t0049g0072 a0001c0001t0051g0073 a0001c0002t0016g0024 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.710-3823T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36240807 | |||||||
| chr9:36241119 | C | CT | 59 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(56): Show |
61 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.710-4136dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241119 | |||||||
| chr9:36241254 | T | C | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.710-4270A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241254 | |||||||
| chr9:36241272 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.710-4288G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241272 | |||||||
| chr9:36241438 | T | A | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-4454A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241438 | |||||||
| chr9:36241525 | G | T | 79 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(76): Show |
81 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.709+4506C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241525 | |||||||
| chr9:36241603 | A | G | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+4428T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241603 | |||||||
| chr9:36241714 | A | C | 1 | a0001c0001t0073g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.709+4317T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241714 | |||||||
| chr9:36241755 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.709+4276A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241755 | |||||||
| chr9:36241773 | A | G | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+4258T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241773 | |||||||
| chr9:36241857 | C | G | 2 | a0001c0001t0045g0341 a0001c0001t0045g0345 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.709+4174G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36241857 | |||||||
| chr9:36242046 | G | A | 2 | a0001c0001t0026g0123 a0001c0001t0066g0130 |
2 | HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.709+3985C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242046 | |||||||
| chr9:36242090 | T | C | 1 | a0001c0001t0076g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.709+3941A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242090 | |||||||
| chr9:36242164 | GA | G | 164 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0001g0157 others(161): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.709+3866delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242164 | |||||||
| chr9:36242281 | A | T | 1 | a0001c0001t0008g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.709+3750T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242281 | |||||||
| chr9:36242287 | C | CA | 145 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0001g0157 others(142): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.709+3743dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242287 | |||||||
| chr9:36242312 | T | C | 56 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(53): Show |
58 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.709+3719A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242312 | |||||||
| chr9:36242327 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0008g0156 a0001c0001t0021g0161 |
3 | NA18959.hp2 NA18988.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.709+3704G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242327 | |||||||
| chr9:36242400 | A | G | 1 | a0001c0002t0052g0340 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.709+3631T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242400 | |||||||
| chr9:36242514 | G | A | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.709+3517C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242514 | |||||||
| chr9:36242564 | T | C | 344 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(341): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.709+3467A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242564 | |||||||
| chr9:36242665 | G | A | 40 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.709+3366C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242665 | |||||||
| chr9:36242667 | C | T | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.709+3364G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242667 | |||||||
| chr9:36242684 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.709+3347G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242684 | |||||||
| chr9:36242730 | TTG | T | 7 | a0001c0001t0046g0015 a0001c0001t0047g0016 a0001c0001t0047g0017 others(4): Show |
7 | HG02622.hp1 HG02818.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.709+3299_709+3300d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242730 | |||||||
| chr9:36242732 | G | GC | 4 | a0001c0001t0007g0141 a0001c0001t0007g0153 a0001c0001t0008g0174 others(1): Show |
4 | HG01175.hp1 HG02135.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.709+3298_709+3299i others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | |||||||
| chr9:36242732 | G | GT | 13 | a0001c0001t0001g0249 a0001c0001t0001g0269 a0001c0001t0001g0291 others(10): Show |
13 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.709+3298dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | |||||||
| chr9:36242732 | G | GTTTTTTT others(40): Show |
1 | a0001c0001t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.709+3298_709+3299i others(49): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | |||||||
| chr9:36242732 | G | T | 1 | a0001c0001t0046g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.709+3299C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | |||||||
| chr9:36242732 | GT | G | 105 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0002g0080 others(102): Show |
105 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.709+3298delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | |||||||
| chr9:36242732 | GTT | G | 63 | a0001c0001t0001g0050 a0001c0001t0002g0075 a0001c0001t0002g0078 others(60): Show |
64 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.709+3297_709+3298d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242732 | |||||||
| chr9:36242733 | T | C | 53 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(50): Show |
53 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.709+3298A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242733 | |||||||
| chr9:36242734 | T | C | 82 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0002g0093 others(79): Show |
82 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.709+3297A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242734 | |||||||
| chr9:36242735 | T | C | 1 | a0001c0001t0083g0210 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.709+3296A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242735 | |||||||
| chr9:36242826 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+3205G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242826 | |||||||
| chr9:36242921 | C | G | 231 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(228): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.709+3110G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36242921 | |||||||
| chr9:36243029 | TG | T | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.709+3001delC | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243029 | |||||||
| chr9:36243336 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.709+2695G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243336 | |||||||
| chr9:36243449 | G | A | 2 | a0001c0001t0001g0297 a0001c0001t0004g0279 |
2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.709+2582C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243449 | |||||||
| chr9:36243708 | G | A | 1 | a0001c0001t0073g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.709+2323C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243708 | |||||||
| chr9:36243934 | G | GT | 57 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.709+2096dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243934 | |||||||
| chr9:36243958 | GT | G | 244 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(241): Show |
246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.709+2072delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243958 | |||||||
| chr9:36243967 | T | G | 1 | a0001c0001t0028g0133 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.709+2064A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36243967 | |||||||
| chr9:36244166 | G | A | 2 | a0001c0001t0036g0137 a0001c0001t0036g0138 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.709+1865C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244166 | |||||||
| chr9:36244246 | G | A | 224 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(221): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.709+1785C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244246 | |||||||
| chr9:36244399 | T | A | 139 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(136): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.709+1632A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244399 | |||||||
| chr9:36244582 | T | C | 84 | a0001c0001t0001g0119 a0001c0001t0002g0092 a0001c0001t0002g0093 others(81): Show |
84 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.709+1449A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244582 | |||||||
| chr9:36244703 | C | T | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.709+1328G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244703 | |||||||
| chr9:36244727 | G | A | 5 | a0001c0001t0002g0107 a0001c0001t0002g0120 a0001c0001t0002g0121 others(2): Show |
5 | HG00639.hp2 HG00735.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+1304C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244727 | |||||||
| chr9:36244781 | C | CA | 5 | a0001c0001t0002g0107 a0001c0001t0002g0120 a0001c0001t0002g0121 others(2): Show |
5 | HG00639.hp2 HG00735.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+1249dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244781 | |||||||
| chr9:36244864 | C | T | 1 | a0001c0001t0007g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.709+1167G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244864 | |||||||
| chr9:36244939 | C | CA | 9 | a0001c0001t0001g0246 a0001c0001t0001g0295 a0001c0001t0002g0104 others(6): Show |
9 | HG02071.hp2 HG02074.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.709+1091dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244939 | |||||||
| chr9:36244939 | CA | C | 16 | a0001c0001t0002g0080 a0001c0001t0014g0232 a0001c0001t0014g0236 others(13): Show |
16 | HG01255.hp1 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.709+1091delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244939 | |||||||
| chr9:36244939 | CAA | C | 6 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0074g0348 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+1090_709+1091d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36244939 | |||||||
| chr9:36245179 | G | A | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.709+852C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245179 | |||||||
| chr9:36245205 | A | G | 6 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0014g0083 others(3): Show |
6 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+826T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245205 | |||||||
| chr9:36245219 | G | A | 3 | a0001c0001t0017g0034 a0001c0001t0017g0063 a0001c0001t0017g0064 |
3 | HG01978.hp1 HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.709+812C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245219 | |||||||
| chr9:36245229 | A | C | 4 | a0001c0001t0001g0106 a0001c0001t0001g0260 a0001c0001t0001g0277 others(1): Show |
4 | HG00438.hp2 HG00621.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.709+802T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245229 | |||||||
| chr9:36245404 | G | T | 5 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(2): Show |
5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.709+627C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245404 | |||||||
| chr9:36245460 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.709+571C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245460 | |||||||
| chr9:36245574 | T | A | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+457A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245574 | |||||||
| chr9:36245762 | A | G | 39 | a0001c0001t0001g0119 a0001c0001t0002g0092 a0001c0001t0002g0093 others(36): Show |
39 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.709+269T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245762 | |||||||
| chr9:36245887 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.709+144T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 3/11 | chr9 | 36245887 | |||||||
| chr9:36246560 | C | T | 7 | a0001c0001t0036g0137 a0001c0001t0036g0138 a0001c0001t0040g0342 others(4): Show |
7 | HG02280.hp1 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-78G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246560 | |||||||
| chr9:36246597 | T | C | 139 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(136): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.258-115A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246597 | |||||||
| chr9:36246660 | C | CT | 15 | a0001c0001t0001g0246 a0001c0001t0001g0255 a0001c0001t0001g0256 others(12): Show |
15 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.258-179dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246660 | |||||||
| chr9:36246660 | CT | C | 41 | a0001c0001t0001g0312 a0001c0001t0002g0078 a0001c0001t0002g0079 others(38): Show |
41 | HG00280.hp2 HG01074.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.258-179delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246660 | |||||||
| chr9:36246660 | CTT | C | 6 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0045g0341 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-180_258-179del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246660 | |||||||
| chr9:36246660 | CTTT | C | 6 | a0001c0001t0035g0350 a0001c0001t0036g0137 a0001c0001t0036g0138 others(3): Show |
6 | HG01255.hp1 HG02257.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-181_258-179del others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246660 | |||||||
| chr9:36246681 | T | G | 216 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(213): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.258-199A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246681 | |||||||
| chr9:36246681 | T | TG | 8 | a0001c0001t0002g0112 a0001c0001t0006g0223 a0001c0001t0006g0224 others(5): Show |
8 | HG01081.hp1 HG01167.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-200_258-199ins others(1): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246681 | |||||||
| chr9:36246693 | A | T | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.258-211T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246693 | |||||||
| chr9:36246869 | A | T | 13 | a0001c0001t0001g0251 a0001c0001t0001g0285 a0001c0001t0001g0302 others(10): Show |
13 | HG00558.hp2 HG00609.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.258-387T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246869 | |||||||
| chr9:36246947 | G | A | 1 | a0001c0001t0073g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.258-465C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246947 | |||||||
| chr9:36246965 | G | A | 224 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(221): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.258-483C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246965 | |||||||
| chr9:36246972 | G | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-490C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36246972 | |||||||
| chr9:36247051 | T | C | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-569A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247051 | |||||||
| chr9:36247122 | T | A | 1 | a0001c0001t0008g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-640A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247122 | |||||||
| chr9:36247201 | C | T | 2 | a0001c0001t0036g0137 a0001c0001t0036g0138 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.258-719G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247201 | |||||||
| chr9:36247276 | C | A | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-794G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247276 | |||||||
| chr9:36247298 | G | A | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-816C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247298 | |||||||
| chr9:36247453 | T | C | 8 | a0001c0001t0036g0137 a0001c0001t0036g0138 a0001c0001t0040g0342 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-971A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247453 | |||||||
| chr9:36247701 | T | A | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-1219A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247701 | |||||||
| chr9:36247733 | A | T | 2 | a0001c0002t0016g0024 a0001c0002t0060g0025 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.258-1251T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247733 | |||||||
| chr9:36247750 | G | A | 1 | a0001c0001t0073g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.258-1268C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247750 | |||||||
| chr9:36247792 | G | C | 231 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(228): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.258-1310C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247792 | |||||||
| chr9:36247829 | C | G | 163 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0001g0157 others(160): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.258-1347G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247829 | |||||||
| chr9:36247983 | G | A | 9 | a0001c0001t0001g0276 a0001c0001t0036g0137 a0001c0001t0036g0138 others(6): Show |
9 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.257+1209C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36247983 | |||||||
| chr9:36248022 | G | A | 4 | a0001c0001t0007g0173 a0001c0001t0007g0175 a0001c0001t0008g0174 others(1): Show |
4 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+1170C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248022 | |||||||
| chr9:36248026 | C | CA | 20 | a0001c0001t0001g0240 a0001c0001t0001g0245 a0001c0001t0001g0268 others(17): Show |
20 | HG00408.hp1 HG01192.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.257+1165dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248026 | |||||||
| chr9:36248026 | CA | C | 36 | a0001c0001t0001g0050 a0001c0001t0001g0158 a0001c0001t0001g0297 others(33): Show |
36 | HG00280.hp1 HG01074.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.257+1165delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248026 | |||||||
| chr9:36248026 | CAA | C | 190 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0001g0157 others(187): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.257+1164_257+1165d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248026 | |||||||
| chr9:36248053 | G | A | 1 | a0001c0001t0031g0091 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.257+1139C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248053 | |||||||
| chr9:36248112 | G | A | 231 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(228): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.257+1080C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248112 | |||||||
| chr9:36248295 | T | C | 139 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(136): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.257+897A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248295 | |||||||
| chr9:36248310 | A | T | 3 | a0001c0002t0016g0024 a0001c0002t0032g0062 a0001c0002t0060g0025 |
3 | HG02647.hp2 HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.257+882T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248310 | |||||||
| chr9:36248316 | T | G | 1 | a0001c0001t0015g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.257+876A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248316 | |||||||
| chr9:36248318 | C | CT | 57 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(54): Show |
59 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.257+873dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248318 | |||||||
| chr9:36248337 | G | A | 1 | a0001c0001t0096g0273 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.257+855C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248337 | |||||||
| chr9:36248443 | T | A | 139 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(136): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.257+749A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248443 | |||||||
| chr9:36248464 | G | A | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+728C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248464 | |||||||
| chr9:36248481 | A | AT | 96 | a0001c0001t0001g0050 a0001c0001t0001g0157 a0001c0001t0001g0158 others(93): Show |
98 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.257+710dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248481 | |||||||
| chr9:36248481 | AT | A | 13 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(10): Show |
13 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+710delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248481 | |||||||
| chr9:36248495 | TG | T | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.257+696delC | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248495 | |||||||
| chr9:36248620 | G | A | 2 | a0001c0001t0007g0160 a0001c0001t0009g0037 |
2 | HG01943.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.257+572C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248620 | |||||||
| chr9:36248694 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+498A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248694 | |||||||
| chr9:36248695 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+497C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248695 | |||||||
| chr9:36248697 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+495G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248697 | |||||||
| chr9:36248699 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+493C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248699 | |||||||
| chr9:36248700 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+492A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248700 | |||||||
| chr9:36248701 | A | G | 3 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0082g0343 |
3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.257+491T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248701 | |||||||
| chr9:36248703 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+489A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248703 | |||||||
| chr9:36248704 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+488C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248704 | |||||||
| chr9:36248705 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+487A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248705 | |||||||
| chr9:36248708 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+484G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248708 | |||||||
| chr9:36248709 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+483A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248709 | |||||||
| chr9:36248710 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+482G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248710 | |||||||
| chr9:36248711 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+481A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248711 | |||||||
| chr9:36248712 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+480G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248712 | |||||||
| chr9:36248713 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+479A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248713 | |||||||
| chr9:36248715 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+477G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248715 | |||||||
| chr9:36248716 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+476A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248716 | |||||||
| chr9:36248717 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+475A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248717 | |||||||
| chr9:36248718 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+474A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248718 | |||||||
| chr9:36248720 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+472G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248720 | |||||||
| chr9:36248721 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+471G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248721 | |||||||
| chr9:36248722 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+470A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248722 | |||||||
| chr9:36248724 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+468C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248724 | |||||||
| chr9:36248725 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+467G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248725 | |||||||
| chr9:36248727 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+465C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248727 | |||||||
| chr9:36248729 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+463A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248729 | |||||||
| chr9:36248730 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+462A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248730 | |||||||
| chr9:36248737 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+455A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248737 | |||||||
| chr9:36248738 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+454A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248738 | |||||||
| chr9:36248743 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+449A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248743 | |||||||
| chr9:36248744 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+448G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248744 | |||||||
| chr9:36248745 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+447A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248745 | |||||||
| chr9:36248746 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+446A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248746 | |||||||
| chr9:36248747 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+445C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248747 | |||||||
| chr9:36248748 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+444A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248748 | |||||||
| chr9:36248749 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+443A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248749 | |||||||
| chr9:36248750 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+442G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248750 | |||||||
| chr9:36248751 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+441G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248751 | |||||||
| chr9:36248753 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+439A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248753 | |||||||
| chr9:36248755 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+437A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248755 | |||||||
| chr9:36248756 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+436G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248756 | |||||||
| chr9:36248757 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+435A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248757 | |||||||
| chr9:36248759 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+433G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248759 | |||||||
| chr9:36248760 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+432A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248760 | |||||||
| chr9:36248762 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+430G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248762 | |||||||
| chr9:36248763 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+429A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248763 | |||||||
| chr9:36248765 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+427A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248765 | |||||||
| chr9:36248767 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+425A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248767 | |||||||
| chr9:36248770 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+422C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248770 | |||||||
| chr9:36248771 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+421G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248771 | |||||||
| chr9:36248772 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+420A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248772 | |||||||
| chr9:36248773 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+419C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248773 | |||||||
| chr9:36248774 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+418A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248774 | |||||||
| chr9:36248775 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+416_257+417ins others(10): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248775 | |||||||
| chr9:36248775 | T | TGGCCTAT others(372): Show |
1 | a0001c0001t0007g0153 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.257+416_257+417ins others(379): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248775 | |||||||
| chr9:36248776 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+416C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248776 | |||||||
| chr9:36248777 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+415C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248777 | |||||||
| chr9:36248778 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+414G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248778 | |||||||
| chr9:36248779 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+413G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248779 | |||||||
| chr9:36248780 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+412A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248780 | |||||||
| chr9:36248782 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+410A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248782 | |||||||
| chr9:36248786 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+406G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248786 | |||||||
| chr9:36248787 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+405G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248787 | |||||||
| chr9:36248789 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+403C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248789 | |||||||
| chr9:36248790 | T | G | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+402A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248790 | |||||||
| chr9:36248791 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.257+401A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248791 | |||||||
| chr9:36248823 | T | A | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+369A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248823 | |||||||
| chr9:36248828 | A | G | 139 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(136): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.257+364T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248828 | |||||||
| chr9:36248956 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0165 |
2 | NA18947.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.257+236A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248956 | |||||||
| chr9:36248978 | T | C | 4 | a0001c0002t0024g0027 a0001c0002t0025g0026 a0001c0002t0025g0029 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+214A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 2/11 | chr9 | 36248978 | |||||||
| chr9:36249538 | T | C | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-141A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249538 | |||||||
| chr9:36249568 | T | C | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-171A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249568 | |||||||
| chr9:36249614 | T | C | 14 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(11): Show |
14 | HG01074.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.52-217A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249614 | |||||||
| chr9:36249626 | C | T | 1 | a0001c0001t0005g0191 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52-229G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249626 | |||||||
| chr9:36249644 | C | T | 5 | a0001c0001t0005g0202 a0001c0001t0005g0204 a0001c0001t0005g0207 others(2): Show |
5 | HG00438.hp1 HG01981.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-247G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249644 | |||||||
| chr9:36249645 | G | A | 16 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(13): Show |
16 | HG01074.hp2 HG01257.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-248C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249645 | |||||||
| chr9:36249735 | T | A | 1 | a0001c0001t0003g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.52-338A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249735 | |||||||
| chr9:36249745 | G | A | 16 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(13): Show |
16 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-348C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249745 | |||||||
| chr9:36249756 | T | A | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-359A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249756 | |||||||
| chr9:36249756 | T | C | 235 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(232): Show |
237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.52-359A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249756 | |||||||
| chr9:36249764 | G | A | 1 | a0001c0001t0073g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.52-367C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249764 | |||||||
| chr9:36249797 | T | C | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-400A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249797 | |||||||
| chr9:36249860 | G | A | 6 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-463C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249860 | |||||||
| chr9:36249980 | G | C | 4 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0319 others(1): Show |
4 | HG02109.hp1 HG02717.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-583C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249980 | |||||||
| chr9:36249984 | G | A | 4 | a0001c0002t0024g0027 a0001c0002t0025g0026 a0001c0002t0025g0029 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-587C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36249984 | |||||||
| chr9:36250021 | T | C | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-624A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250021 | |||||||
| chr9:36250121 | A | T | 224 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(221): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.52-724T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250121 | |||||||
| chr9:36250158 | G | C | 2 | a0001c0001t0036g0137 a0001c0001t0036g0138 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.52-761C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250158 | |||||||
| chr9:36250212 | G | T | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-815C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250212 | |||||||
| chr9:36250219 | A | G | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-822T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250219 | |||||||
| chr9:36250353 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-956G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250353 | |||||||
| chr9:36250380 | G | C | 145 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(142): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.52-983C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250380 | |||||||
| chr9:36250593 | A | G | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-1196T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250593 | |||||||
| chr9:36250668 | T | C | 231 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(228): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.52-1271A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250668 | |||||||
| chr9:36250801 | C | T | 8 | a0001c0002t0016g0024 a0001c0002t0024g0027 a0001c0002t0025g0026 others(5): Show |
8 | HG01884.hp2 HG01891.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-1404G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36250801 | |||||||
| chr9:36251040 | CTT | C | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-1645_52-1644del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251040 | |||||||
| chr9:36251288 | C | T | 5 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(2): Show |
5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-1891G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251288 | |||||||
| chr9:36251304 | G | A | 231 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(228): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.52-1907C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251304 | |||||||
| chr9:36251323 | C | T | 8 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.52-1926G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251323 | |||||||
| chr9:36251486 | C | T | 4 | a0001c0002t0024g0027 a0001c0002t0025g0026 a0001c0002t0025g0029 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-2089G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251486 | |||||||
| chr9:36251529 | C | T | 244 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(241): Show |
246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.52-2132G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251529 | |||||||
| chr9:36251672 | T | C | 5 | a0001c0002t0024g0027 a0001c0002t0025g0026 a0001c0002t0025g0029 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-2275A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251672 | |||||||
| chr9:36251682 | G | C | 9 | a0001c0001t0046g0011 a0001c0001t0046g0015 a0001c0001t0047g0016 others(6): Show |
9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-2285C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251682 | |||||||
| chr9:36251842 | T | C | 2 | a0001c0001t0022g0217 a0001c0001t0041g0213 |
2 | HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.52-2445A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251842 | |||||||
| chr9:36251986 | C | CT | 211 | a0001c0001t0001g0050 a0001c0001t0001g0119 a0001c0001t0001g0157 others(208): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.52-2590dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251986 | |||||||
| chr9:36251986 | C | CTT | 10 | a0001c0001t0001g0081 a0001c0001t0005g0109 a0001c0001t0005g0216 others(7): Show |
10 | HG01257.hp2 HG01515.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.52-2591_52-2590dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251986 | |||||||
| chr9:36251986 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0088g0353 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.52-2600_52-2590dup others(11): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251986 | |||||||
| chr9:36251986 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0087g0354 a0001c0001t0089g0352 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.52-2601_52-2590dup others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251986 | |||||||
| chr9:36251986 | CT | C | 11 | a0001c0001t0001g0280 a0001c0001t0004g0279 a0001c0001t0034g0290 others(8): Show |
11 | HG01256.hp2 HG02280.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-2590delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36251986 | |||||||
| chr9:36252064 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.52-2667G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252064 | |||||||
| chr9:36252134 | T | C | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-2737A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252134 | |||||||
| chr9:36252278 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-2881G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252278 | |||||||
| chr9:36252316 | T | C | 2 | a0001c0001t0045g0341 a0001c0001t0045g0345 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.52-2919A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252316 | |||||||
| chr9:36252348 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.52-2951C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252348 | |||||||
| chr9:36252445 | TTTGTATT others(23): Show |
T | 1 | a0001c0001t0001g0306 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.52-3078_52-3049del others(30): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252445 | |||||||
| chr9:36252449 | T | C | 2 | a0001c0001t0049g0072 a0001c0001t0051g0073 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.52-3052A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252449 | |||||||
| chr9:36252476 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.52-3079A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252476 | |||||||
| chr9:36252712 | A | C | 244 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(241): Show |
246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.52-3315T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252712 | |||||||
| chr9:36252751 | T | G | 1 | a0001c0002t0060g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.52-3354A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252751 | |||||||
| chr9:36252828 | G | GCAAA | 231 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(228): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.52-3432_52-3431ins others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252828 | |||||||
| chr9:36252870 | G | T | 1 | a0001c0002t0032g0062 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.52-3473C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252870 | |||||||
| chr9:36252925 | G | A | 1 | a0001c0001t0005g0216 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.52-3528C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36252925 | |||||||
| chr9:36253043 | TCCC | T | 7 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-3649_52-3647del others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253043 | |||||||
| chr9:36253111 | A | G | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-3714T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253111 | |||||||
| chr9:36253208 | T | TACATACA others(1): Show |
6 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-3819_52-3812dup others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253208 | |||||||
| chr9:36253227 | C | T | 2 | a0001c0001t0047g0017 a0001c0001t0096g0273 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.52-3830G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253227 | |||||||
| chr9:36253293 | TA | T | 6 | a0001c0001t0002g0092 a0001c0001t0009g0056 a0001c0001t0016g0114 others(3): Show |
6 | HG01257.hp2 HG03491.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-3897delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253293 | |||||||
| chr9:36253294 | A | T | 223 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(220): Show |
225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.52-3897T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253294 | |||||||
| chr9:36253326 | A | G | 43 | a0001c0001t0005g0109 a0001c0001t0005g0186 a0001c0001t0005g0191 others(40): Show |
43 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.52-3929T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253326 | |||||||
| chr9:36253426 | C | T | 4 | a0001c0001t0014g0236 a0001c0001t0024g0235 a0001c0001t0044g0233 others(1): Show |
4 | HG02965.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-4029G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253426 | |||||||
| chr9:36253466 | C | T | 147 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(144): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.52-4069G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253466 | |||||||
| chr9:36253547 | G | A | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-4150C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253547 | |||||||
| chr9:36253570 | G | A | 1 | a0001c0001t0011g0181 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.52-4173C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253570 | |||||||
| chr9:36253574 | A | T | 2 | a0001c0002t0016g0024 a0001c0002t0060g0025 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.52-4177T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253574 | |||||||
| chr9:36253809 | G | A | 45 | a0001c0001t0001g0119 a0001c0001t0002g0092 a0001c0001t0002g0093 others(42): Show |
45 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.52-4412C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253809 | |||||||
| chr9:36253813 | G | A | 6 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-4416C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253813 | |||||||
| chr9:36253829 | C | T | 226 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(223): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.52-4432G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253829 | |||||||
| chr9:36253842 | A | G | 1 | a0001c0001t0009g0038 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.52-4445T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253842 | |||||||
| chr9:36253994 | A | G | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-4597T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36253994 | |||||||
| chr9:36254205 | A | AAAAT | 164 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0001g0157 others(161): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.52-4812_52-4809dup others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254205 | |||||||
| chr9:36254205 | A | AAAATAAA others(1): Show |
52 | a0001c0001t0001g0050 a0001c0001t0002g0125 a0001c0001t0003g0010 others(49): Show |
54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.52-4816_52-4809dup others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254205 | |||||||
| chr9:36254205 | A | AAAATAAA others(5): Show |
11 | a0001c0001t0003g0020 a0001c0001t0003g0033 a0001c0001t0047g0017 others(8): Show |
11 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-4820_52-4809dup others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254205 | |||||||
| chr9:36254353 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.52-4956G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254353 | |||||||
| chr9:36254411 | G | A | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.52-5014C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254411 | |||||||
| chr9:36254473 | A | G | 16 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(13): Show |
16 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-5076T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254473 | |||||||
| chr9:36254513 | C | T | 239 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(236): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.52-5116G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254513 | |||||||
| chr9:36254544 | A | T | 147 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(144): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.52-5147T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254544 | |||||||
| chr9:36254723 | G | A | 1 | a0001c0001t0008g0145 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.52-5326C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254723 | |||||||
| chr9:36254901 | G | A | 1 | a0001c0001t0020g0166 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.52-5504C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254901 | |||||||
| chr9:36254980 | T | C | 244 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(241): Show |
246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.52-5583A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36254980 | |||||||
| chr9:36255038 | G | T | 3 | a0001c0001t0026g0090 a0001c0001t0031g0088 a0001c0001t0031g0091 |
3 | HG01257.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.52-5641C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255038 | |||||||
| chr9:36255230 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-5833G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255230 | |||||||
| chr9:36255270 | C | T | 1 | a0001c0001t0005g0009 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52-5873G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255270 | |||||||
| chr9:36255341 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.52-5944C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255341 | |||||||
| chr9:36255386 | T | A | 1 | a0001c0001t0004g0278 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.52-5989A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255386 | |||||||
| chr9:36255434 | T | G | 8 | a0001c0001t0011g0351 a0001c0001t0035g0350 a0001c0001t0037g0347 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-6037A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255434 | |||||||
| chr9:36255575 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.52-6178G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255575 | |||||||
| chr9:36255672 | T | C | 1 | a0001c0001t0013g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.52-6275A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255672 | |||||||
| chr9:36255971 | C | G | 4 | a0001c0001t0011g0351 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-6574G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36255971 | |||||||
| chr9:36256027 | C | A | 165 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0001g0157 others(162): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.52-6630G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256027 | |||||||
| chr9:36256142 | G | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG03491.hp1 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.52-6745C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256142 | |||||||
| chr9:36256146 | C | T | 1 | a0001c0001t0005g0009 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52-6749G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256146 | |||||||
| chr9:36256169 | C | T | 2 | a0001c0001t0004g0265 a0001c0001t0004g0266 |
2 | HG02071.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.52-6772G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256169 | |||||||
| chr9:36256170 | G | T | 2 | a0001c0001t0006g0182 a0001c0001t0006g0183 |
2 | HG02080.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.52-6773C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256170 | |||||||
| chr9:36256172 | C | T | 52 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(49): Show |
54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.52-6775G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256172 | |||||||
| chr9:36256239 | C | CT | 23 | a0001c0001t0001g0106 a0001c0001t0001g0249 a0001c0001t0001g0250 others(20): Show |
23 | HG00438.hp2 HG00621.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.52-6843dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | |||||||
| chr9:36256239 | C | CTT | 10 | a0001c0001t0001g0228 a0001c0001t0004g0278 a0001c0001t0019g0318 others(7): Show |
10 | HG02148.hp2 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-6844_52-6843dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | |||||||
| chr9:36256239 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0049g0072 a0001c0001t0051g0073 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.52-6863_52-6843dup others(21): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | |||||||
| chr9:36256239 | CT | C | 30 | a0001c0001t0001g0159 a0001c0001t0001g0257 a0001c0001t0001g0268 others(27): Show |
30 | HG00741.hp2 HG01175.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.52-6843delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | |||||||
| chr9:36256239 | CTT | C | 114 | a0001c0001t0001g0119 a0001c0001t0001g0158 a0001c0001t0001g0162 others(111): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.52-6844_52-6843del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | |||||||
| chr9:36256239 | CTTT | C | 26 | a0001c0001t0001g0081 a0001c0001t0001g0157 a0001c0001t0002g0075 others(23): Show |
26 | HG00280.hp2 HG01069.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.52-6845_52-6843del others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | |||||||
| chr9:36256239 | CTTTTTTT others(1): Show |
C | 46 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0023 others(43): Show |
48 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.52-6850_52-6843del others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256239 | |||||||
| chr9:36256258 | TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0015g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.52-6873_52-6862del others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256258 | |||||||
| chr9:36256264 | TTTGAGA | T | 6 | a0001c0001t0011g0351 a0001c0001t0037g0347 a0001c0001t0037g0349 others(3): Show |
6 | HG01255.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-6873_52-6868del others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256264 | |||||||
| chr9:36256271 | C | G | 9 | a0001c0001t0011g0351 a0001c0001t0015g0039 a0001c0001t0035g0350 others(6): Show |
9 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-6874G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256271 | |||||||
| chr9:36256283 | C | T | 4 | a0001c0001t0011g0351 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-6886G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256283 | |||||||
| chr9:36256314 | G | A | 225 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(222): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52-6917C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256314 | |||||||
| chr9:36256337 | T | C | 244 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(241): Show |
246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.52-6940A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256337 | |||||||
| chr9:36256338 | G | A | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-6941C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256338 | |||||||
| chr9:36256393 | T | C | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-6996A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256393 | |||||||
| chr9:36256484 | A | T | 1 | a0001c0001t0004g0278 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.52-7087T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256484 | |||||||
| chr9:36256488 | G | T | 4 | a0001c0001t0020g0149 a0001c0001t0042g0144 a0001c0001t0042g0178 others(1): Show |
4 | HG00741.hp1 HG01255.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-7091C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256488 | |||||||
| chr9:36256702 | A | G | 1 | a0001c0001t0038g0110 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.52-7305T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256702 | |||||||
| chr9:36256814 | T | C | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-7417A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256814 | |||||||
| chr9:36256916 | T | A | 1 | a0001c0001t0005g0206 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.52-7519A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256916 | |||||||
| chr9:36256954 | C | G | 9 | a0001c0001t0046g0011 a0001c0001t0046g0015 a0001c0001t0047g0016 others(6): Show |
9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-7557G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256954 | |||||||
| chr9:36256965 | G | A | 4 | a0001c0001t0011g0351 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-7568C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256965 | |||||||
| chr9:36256966 | G | A | 4 | a0001c0001t0011g0351 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-7569C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256966 | |||||||
| chr9:36256998 | G | A | 225 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(222): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52-7601C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36256998 | |||||||
| chr9:36257065 | A | G | 10 | a0001c0001t0003g0035 a0001c0001t0003g0043 a0001c0001t0003g0044 others(7): Show |
10 | HG00544.hp1 HG02015.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.52-7668T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257065 | |||||||
| chr9:36257092 | T | C | 1 | a0001c0001t0073g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.52-7695A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257092 | |||||||
| chr9:36257154 | A | G | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-7757T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257154 | |||||||
| chr9:36257246 | G | T | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-7849C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257246 | |||||||
| chr9:36257379 | G | C | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.52-7982C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257379 | |||||||
| chr9:36257380 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.52-7983C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257380 | |||||||
| chr9:36257477 | G | T | 1 | a0001c0002t0052g0340 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.52-8080C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257477 | |||||||
| chr9:36257492 | C | T | 225 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(222): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52-8095G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257492 | |||||||
| chr9:36257541 | C | T | 4 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-8144G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257541 | |||||||
| chr9:36257758 | G | T | 9 | a0001c0001t0005g0191 a0001c0001t0005g0202 a0001c0001t0005g0204 others(6): Show |
9 | HG00438.hp1 HG01981.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-8361C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257758 | |||||||
| chr9:36257767 | C | A | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-8370G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257767 | |||||||
| chr9:36257800 | C | T | 146 | a0001c0001t0001g0119 a0001c0001t0001g0157 a0001c0001t0001g0158 others(143): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.52-8403G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257800 | |||||||
| chr9:36257802 | C | A | 6 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-8405G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CA | 67 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0226 others(64): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.52-8406dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAA | 58 | a0001c0001t0001g0228 a0001c0001t0001g0230 a0001c0001t0001g0244 others(55): Show |
58 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.52-8407_52-8406dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAA | 49 | a0001c0001t0001g0050 a0001c0001t0001g0243 a0001c0001t0001g0300 others(46): Show |
50 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.52-8408_52-8406dup others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAAA | 13 | a0001c0001t0001g0253 a0001c0001t0001g0311 a0001c0001t0001g0313 others(10): Show |
13 | HG00438.hp1 HG01074.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-8409_52-8406dup others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0045g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.52-8415_52-8406dup others(10): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0026g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.52-8416_52-8406dup others(11): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0073g0082 a0001c0001t0076g0231 a0001c0002t0060g0025 |
3 | HG02615.hp1 HG03225.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.52-8417_52-8406dup others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0014g0083 a0001c0001t0014g0084 |
2 | HG01074.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.52-8418_52-8406dup others(13): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0016g0098 a0001c0001t0047g0016 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.52-8419_52-8406dup others(14): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0046g0015 |
3 | HG02622.hp1 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.52-8420_52-8406dup others(15): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0093g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52-8422_52-8406dup others(17): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0014g0087 a0001c0001t0084g0179 |
2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.52-8424_52-8406dup others(19): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0091g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.52-8426_52-8406dup others(21): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | CA | C | 7 | a0001c0001t0001g0159 a0001c0001t0001g0255 a0001c0001t0001g0269 others(4): Show |
7 | HG00738.hp1 HG01257.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-8406delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | CAAAAAAA | C | 12 | a0001c0001t0001g0119 a0001c0001t0002g0103 a0001c0001t0002g0126 others(9): Show |
12 | HG01106.hp1 HG01109.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.52-8412_52-8406del others(7): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | CAAAAAAA others(1): Show |
C | 20 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(17): Show |
20 | HG00621.hp2 HG02723.hp2 HG02896.hp1 others(17): Show |
intron_variant | MODIFIER | c.52-8413_52-8406del others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0035g0350 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.52-8416_52-8406del others(11): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0037g0347 a0001c0001t0037g0349 a0001c0001t0053g0346 others(1): Show |
4 | HG01255.hp1 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-8417_52-8406del others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257802 | CAAAAAAA others(11): Show |
C | 3 | a0001c0001t0011g0208 a0001c0001t0011g0209 a0001c0001t0081g0219 |
3 | HG01069.hp1 HG01071.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.52-8423_52-8406del others(18): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257802 | |||||||
| chr9:36257918 | G | T | 5 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(2): Show |
5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-8521C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257918 | |||||||
| chr9:36257995 | G | T | 225 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(222): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52-8598C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36257995 | |||||||
| chr9:36258174 | C | T | 2 | a0001c0001t0036g0137 a0001c0001t0036g0138 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.52-8777G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258174 | |||||||
| chr9:36258270 | G | T | 1 | a0001c0001t0011g0351 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.52-8873C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258270 | |||||||
| chr9:36258273 | G | T | 1 | a0001c0001t0009g0037 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.52-8876C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258273 | |||||||
| chr9:36258297 | C | G | 1 | a0001c0001t0038g0110 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.52-8900G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258297 | |||||||
| chr9:36258550 | C | T | 48 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.52-9153G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258550 | |||||||
| chr9:36258577 | C | G | 2 | a0001c0001t0004g0261 a0001c0001t0004g0275 |
2 | HG00735.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.52-9180G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258577 | |||||||
| chr9:36258633 | T | A | 1 | a0001c0001t0047g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.52-9236A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258633 | |||||||
| chr9:36258780 | G | T | 50 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(47): Show |
52 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.52-9383C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258780 | |||||||
| chr9:36258798 | T | C | 8 | a0001c0001t0011g0351 a0001c0001t0035g0350 a0001c0001t0037g0347 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-9401A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258798 | |||||||
| chr9:36258849 | C | T | 3 | a0001c0001t0087g0354 a0001c0001t0088g0353 a0001c0001t0089g0352 |
3 | HG02572.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.52-9452G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258849 | |||||||
| chr9:36258889 | G | A | 1 | a0001c0001t0009g0049 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.52-9492C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258889 | |||||||
| chr9:36258898 | A | G | 1 | a0001c0002t0052g0340 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.52-9501T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36258898 | |||||||
| chr9:36259040 | G | A | 6 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0299 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-9643C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259040 | |||||||
| chr9:36259057 | G | A | 6 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-9660C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259057 | |||||||
| chr9:36259116 | C | A | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-9719G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259116 | |||||||
| chr9:36259200 | C | A | 1 | a0001c0001t0002g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.52-9803G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259200 | |||||||
| chr9:36259290 | C | A | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-9893G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259290 | |||||||
| chr9:36259392 | CT | C | 9 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(6): Show |
9 | HG01255.hp1 HG02257.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-9996delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259392 | |||||||
| chr9:36259392 | CTT | C | 229 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(226): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.52-9997_52-9996del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259392 | |||||||
| chr9:36259392 | CTTT | C | 6 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-9998_52-9996del others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259392 | |||||||
| chr9:36259585 | C | T | 4 | a0001c0001t0011g0351 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-10188G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259585 | |||||||
| chr9:36259699 | C | T | 1 | a0001c0001t0005g0206 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.52-10302G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259699 | |||||||
| chr9:36259723 | C | T | 40 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.52-10326G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259723 | |||||||
| chr9:36259799 | T | C | 225 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(222): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52-10402A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259799 | |||||||
| chr9:36259984 | C | T | 238 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(235): Show |
240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.52-10587G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259984 | |||||||
| chr9:36259997 | G | A | 3 | a0001c0001t0003g0035 a0001c0001t0071g0022 a0001c0001t0075g0021 |
3 | HG02015.hp1 HG02056.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.52-10600C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36259997 | |||||||
| chr9:36260132 | C | T | 2 | a0001c0001t0045g0341 a0001c0001t0045g0345 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.52-10735G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260132 | |||||||
| chr9:36260281 | T | TA | 48 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(45): Show |
50 | HG00408.hp2 HG01109.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.52-10885dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260281 | |||||||
| chr9:36260281 | T | TAA | 9 | a0001c0001t0067g0053 a0001c0002t0016g0024 a0001c0002t0024g0027 others(6): Show |
9 | HG00544.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-10886_52-10885d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260281 | |||||||
| chr9:36260281 | TA | T | 14 | a0001c0001t0001g0158 a0001c0001t0001g0237 a0001c0001t0001g0244 others(11): Show |
14 | HG01069.hp2 HG01167.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.52-10885delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260281 | |||||||
| chr9:36260290 | A | C | 1 | a0001c0001t0001g0337 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.52-10893T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260290 | |||||||
| chr9:36260294 | A | G | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-10897T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260294 | |||||||
| chr9:36260315 | T | A | 8 | a0001c0001t0011g0351 a0001c0001t0035g0350 a0001c0001t0037g0347 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-10918A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260315 | |||||||
| chr9:36260375 | G | T | 1 | a0001c0001t0001g0311 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.52-10978C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260375 | |||||||
| chr9:36260429 | T | C | 1 | a0001c0001t0001g0314 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.52-11032A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260429 | |||||||
| chr9:36260583 | A | G | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-11186T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260583 | |||||||
| chr9:36260598 | G | A | 2 | a0001c0001t0049g0072 a0001c0001t0051g0073 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.52-11201C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260598 | |||||||
| chr9:36260657 | G | C | 8 | a0001c0001t0011g0351 a0001c0001t0035g0350 a0001c0001t0037g0347 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-11260C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260657 | |||||||
| chr9:36260684 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.52-11287T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260684 | |||||||
| chr9:36260721 | T | C | 1 | a0001c0001t0047g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.52-11324A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260721 | |||||||
| chr9:36260725 | C | T | 52 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(49): Show |
54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.52-11328G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260725 | |||||||
| chr9:36260762 | G | A | 51 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(48): Show |
53 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.52-11365C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260762 | |||||||
| chr9:36260786 | G | A | 9 | a0001c0001t0046g0011 a0001c0001t0046g0015 a0001c0001t0047g0016 others(6): Show |
9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-11389C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260786 | |||||||
| chr9:36260868 | C | CA | 20 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0244 others(17): Show |
20 | HG00621.hp1 HG00735.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.52-11472dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | |||||||
| chr9:36260868 | C | CAA | 15 | a0001c0001t0001g0243 a0001c0001t0001g0249 a0001c0001t0001g0268 others(12): Show |
15 | HG00438.hp2 HG01109.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-11473_52-11472d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | |||||||
| chr9:36260868 | C | CAAA | 11 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0319 others(8): Show |
11 | HG00140.hp1 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-11474_52-11472d others(5): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | |||||||
| chr9:36260868 | C | CAAAA | 9 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0325 others(6): Show |
9 | HG00408.hp1 HG00544.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-11475_52-11472d others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | |||||||
| chr9:36260868 | CA | C | 17 | a0001c0001t0001g0229 a0001c0001t0001g0242 a0001c0001t0001g0246 others(14): Show |
17 | HG00558.hp1 HG00558.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.52-11472delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | |||||||
| chr9:36260868 | CAAAAA | C | 13 | a0001c0001t0005g0206 a0001c0001t0005g0207 a0001c0001t0005g0222 others(10): Show |
13 | HG00438.hp1 HG01167.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.52-11476_52-11472d others(7): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | |||||||
| chr9:36260868 | CAAAAAA | C | 101 | a0001c0001t0001g0050 a0001c0001t0001g0157 a0001c0001t0001g0158 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.52-11477_52-11472d others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | |||||||
| chr9:36260868 | CAAAAAAA | C | 111 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0002g0078 others(108): Show |
113 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.52-11478_52-11472d others(9): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260868 | |||||||
| chr9:36260883 | A | C | 2 | a0001c0001t0045g0341 a0001c0001t0045g0345 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.52-11486T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260883 | |||||||
| chr9:36260886 | A | C | 9 | a0001c0001t0046g0011 a0001c0001t0046g0015 a0001c0001t0047g0016 others(6): Show |
9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-11489T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260886 | |||||||
| chr9:36260887 | A | C | 3 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0082g0343 |
3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52-11490T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260887 | |||||||
| chr9:36260890 | A | C | 2 | a0001c0001t0045g0341 a0001c0001t0045g0345 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.52-11493T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260890 | |||||||
| chr9:36260893 | A | C | 215 | a0001c0001t0001g0050 a0001c0001t0001g0119 a0001c0001t0001g0157 others(212): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.52-11496T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260893 | |||||||
| chr9:36260894 | A | C | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.52-11497T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36260894 | |||||||
| chr9:36261114 | A | G | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.52-11717T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261114 | |||||||
| chr9:36261409 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-12012G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261409 | |||||||
| chr9:36261410 | G | C | 1 | a0001c0001t0001g0337 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.52-12013C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261410 | |||||||
| chr9:36261422 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.52-12025C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261422 | |||||||
| chr9:36261426 | G | A | 1 | a0001c0001t0008g0152 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.52-12029C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261426 | |||||||
| chr9:36261463 | G | A | 1 | a0001c0002t0050g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-12066C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261463 | |||||||
| chr9:36261524 | G | A | 1 | a0001c0001t0001g0327 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.52-12127C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261524 | |||||||
| chr9:36261532 | G | A | 1 | a0001c0001t0084g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.52-12135C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261532 | |||||||
| chr9:36261552 | C | CA | 91 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0251 others(88): Show |
93 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.52-12156dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261552 | |||||||
| chr9:36261552 | CA | C | 11 | a0001c0001t0008g0156 a0001c0001t0011g0351 a0001c0001t0035g0350 others(8): Show |
11 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-12156delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261552 | |||||||
| chr9:36261566 | A | T | 1 | a0001c0001t0078g0284 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.52-12169T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261566 | |||||||
| chr9:36261661 | T | C | 1 | a0001c0001t0010g0274 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.52-12264A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261661 | |||||||
| chr9:36261799 | T | A | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-12402A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261799 | |||||||
| chr9:36261800 | G | A | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.52-12403C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261800 | |||||||
| chr9:36261814 | G | T | 231 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(228): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.52-12417C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261814 | |||||||
| chr9:36261815 | C | T | 232 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(229): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.52-12418G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261815 | |||||||
| chr9:36261816 | G | T | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.52-12419C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261816 | |||||||
| chr9:36261848 | G | A | 60 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(57): Show |
62 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.52-12451C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261848 | |||||||
| chr9:36261922 | CA | C | 217 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0119 others(214): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.52-12526delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261922 | |||||||
| chr9:36261922 | CAA | C | 12 | a0001c0001t0006g0193 a0001c0001t0008g0156 a0001c0001t0039g0146 others(9): Show |
12 | HG01109.hp1 HG01168.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.52-12527_52-12526d others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36261922 | |||||||
| chr9:36262086 | A | C | 2 | a0001c0001t0014g0236 a0001c0001t0090g0234 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.52-12689T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36262086 | |||||||
| chr9:36262123 | C | T | 144 | a0001c0001t0001g0050 a0001c0001t0001g0119 a0001c0001t0002g0092 others(141): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.52-12726G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36262123 | |||||||
| chr9:36262423 | G | A | 1 | a0001c0001t0008g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.52-13026C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36262423 | |||||||
| chr9:36262629 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.52-13232C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36262629 | |||||||
| chr9:36262740 | G | A | 48 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.52-13343C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36262740 | |||||||
| chr9:36263114 | A | G | 4 | a0001c0001t0011g0351 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-13717T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263114 | |||||||
| chr9:36263150 | T | C | 1 | a0001c0001t0004g0329 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.51+13744A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263150 | |||||||
| chr9:36263176 | C | CT | 115 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0001g0254 others(112): Show |
115 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.51+13717dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263176 | |||||||
| chr9:36263429 | G | A | 1 | a0001c0001t0046g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.51+13465C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263429 | |||||||
| chr9:36263434 | G | A | 2 | a0001c0001t0049g0072 a0001c0001t0051g0073 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.51+13460C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263434 | |||||||
| chr9:36263438 | T | G | 48 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+13456A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263438 | |||||||
| chr9:36263445 | A | G | 8 | a0001c0001t0011g0351 a0001c0001t0035g0350 a0001c0001t0037g0347 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+13449T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263445 | |||||||
| chr9:36263447 | G | A | 6 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+13447C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263447 | |||||||
| chr9:36263456 | C | T | 1 | a0001c0001t0011g0192 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.51+13438G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263456 | |||||||
| chr9:36263528 | T | C | 3 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0082g0343 |
3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.51+13366A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263528 | |||||||
| chr9:36263555 | AC | A | 7 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0045g0341 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+13338delG | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263555 | |||||||
| chr9:36263580 | A | G | 17 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(14): Show |
17 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+13314T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263580 | |||||||
| chr9:36263657 | A | G | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+13237T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263657 | |||||||
| chr9:36263658 | G | A | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+13236C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263658 | |||||||
| chr9:36263662 | A | T | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+13232T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263662 | |||||||
| chr9:36263672 | T | C | 1 | a0001c0001t0069g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.51+13222A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263672 | |||||||
| chr9:36263803 | G | A | 53 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(50): Show |
55 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.51+13091C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263803 | |||||||
| chr9:36263903 | G | A | 5 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(2): Show |
5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+12991C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263903 | |||||||
| chr9:36263924 | A | G | 1 | a0001c0001t0046g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.51+12970T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36263924 | |||||||
| chr9:36264108 | A | G | 1 | a0001c0001t0004g0278 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.51+12786T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264108 | |||||||
| chr9:36264115 | TTTTA | T | 4 | a0001c0001t0011g0351 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+12775_51+12778d others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264115 | |||||||
| chr9:36264259 | A | G | 1 | a0001c0001t0031g0091 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.51+12635T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264259 | |||||||
| chr9:36264300 | G | T | 8 | a0001c0001t0011g0351 a0001c0001t0035g0350 a0001c0001t0037g0347 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+12594C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264300 | |||||||
| chr9:36264449 | A | G | 44 | a0001c0001t0005g0109 a0001c0001t0005g0186 a0001c0001t0005g0191 others(41): Show |
44 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.51+12445T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264449 | |||||||
| chr9:36264545 | C | A | 7 | a0001c0001t0006g0212 a0001c0001t0011g0208 a0001c0001t0011g0209 others(4): Show |
7 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+12349G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264545 | |||||||
| chr9:36264651 | A | T | 1 | a0001c0001t0026g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.51+12243T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264651 | |||||||
| chr9:36264652 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51+12242C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264652 | |||||||
| chr9:36264677 | G | C | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG01496.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.51+12217C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264677 | |||||||
| chr9:36264815 | T | C | 1 | a0001c0001t0001g0330 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.51+12079A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264815 | |||||||
| chr9:36264879 | G | A | 52 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(49): Show |
54 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.51+12015C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264879 | |||||||
| chr9:36264933 | T | C | 1 | a0001c0001t0026g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.51+11961A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264933 | |||||||
| chr9:36264955 | T | C | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+11939A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36264955 | |||||||
| chr9:36265008 | G | T | 7 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0045g0341 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+11886C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265008 | |||||||
| chr9:36265031 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.51+11863C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265031 | |||||||
| chr9:36265032 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.51+11862G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265032 | |||||||
| chr9:36265100 | A | G | 5 | a0001c0001t0014g0232 a0001c0001t0014g0236 a0001c0001t0024g0235 others(2): Show |
5 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+11794T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265100 | |||||||
| chr9:36265127 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | NA18944.hp2 NA18957.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.51+11767G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265127 | |||||||
| chr9:36265162 | G | A | 225 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(222): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.51+11732C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265162 | |||||||
| chr9:36265356 | A | G | 1 | a0001c0001t0032g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.51+11538T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265356 | |||||||
| chr9:36265469 | C | T | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+11425G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265469 | |||||||
| chr9:36265737 | T | C | 245 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(242): Show |
247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.51+11157A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265737 | |||||||
| chr9:36265774 | C | T | 4 | a0001c0001t0011g0351 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+11120G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265774 | |||||||
| chr9:36265801 | C | A | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+11093G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265801 | |||||||
| chr9:36265828 | G | A | 8 | a0001c0001t0011g0351 a0001c0001t0035g0350 a0001c0001t0037g0347 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+11066C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265828 | |||||||
| chr9:36265957 | TCTCA | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0276 others(3): Show |
6 | HG02056.hp2 NA18946.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+10933_51+10936d others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265957 | |||||||
| chr9:36265990 | C | T | 1 | a0001c0001t0065g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.51+10904G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36265990 | |||||||
| chr9:36266015 | G | C | 4 | a0001c0001t0014g0236 a0001c0001t0024g0235 a0001c0001t0044g0233 others(1): Show |
4 | HG02965.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+10879C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266015 | |||||||
| chr9:36266049 | T | A | 2 | a0001c0001t0020g0171 a0001c0001t0021g0154 |
2 | HG00738.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.51+10845A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266049 | |||||||
| chr9:36266087 | G | A | 48 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+10807C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266087 | |||||||
| chr9:36266151 | G | A | 3 | a0001c0001t0007g0169 a0001c0001t0007g0170 a0001c0001t0007g0180 |
3 | NA18944.hp1 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.51+10743C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266151 | |||||||
| chr9:36266200 | C | G | 53 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(50): Show |
55 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.51+10694G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266200 | |||||||
| chr9:36266270 | C | T | 7 | a0001c0002t0016g0024 a0001c0002t0024g0027 a0001c0002t0025g0026 others(4): Show |
7 | HG01884.hp2 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+10624G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266270 | |||||||
| chr9:36266287 | G | A | 2 | a0001c0001t0020g0171 a0001c0001t0021g0154 |
2 | HG00738.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.51+10607C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266287 | |||||||
| chr9:36266439 | G | A | 1 | a0001c0001t0003g0051 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.51+10455C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266439 | |||||||
| chr9:36266585 | T | A | 40 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.51+10309A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266585 | |||||||
| chr9:36266591 | C | T | 1 | a0001c0001t0013g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51+10303G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266591 | |||||||
| chr9:36266826 | G | A | 1 | a0001c0001t0041g0213 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.51+10068C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266826 | |||||||
| chr9:36266886 | A | G | 245 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(242): Show |
247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.51+10008T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266886 | |||||||
| chr9:36266891 | T | C | 4 | a0001c0001t0011g0351 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+10003A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266891 | |||||||
| chr9:36266898 | C | CA | 7 | a0001c0001t0020g0149 a0001c0001t0042g0144 a0001c0001t0042g0178 others(4): Show |
7 | HG00741.hp1 HG01123.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+9995dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266898 | |||||||
| chr9:36266915 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51+9979T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266915 | |||||||
| chr9:36266937 | C | T | 2 | a0001c0001t0071g0022 a0001c0001t0075g0021 |
2 | HG02056.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.51+9957G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36266937 | |||||||
| chr9:36267020 | C | T | 53 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(50): Show |
55 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.51+9874G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267020 | |||||||
| chr9:36267264 | A | G | 100 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0002g0092 others(97): Show |
100 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.51+9630T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267264 | |||||||
| chr9:36267350 | A | G | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+9544T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267350 | |||||||
| chr9:36267416 | G | A | 1 | a0001c0001t0010g0282 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.51+9478C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267416 | |||||||
| chr9:36267552 | C | T | 1 | a0001c0001t0014g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.51+9342G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267552 | |||||||
| chr9:36267692 | TCAAA | T | 8 | a0001c0001t0003g0035 a0001c0001t0017g0034 a0001c0001t0017g0063 others(5): Show |
8 | HG01255.hp1 HG01978.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+9198_51+9201del others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267692 | |||||||
| chr9:36267692 | TCAAACAA others(5): Show |
T | 7 | a0001c0002t0016g0024 a0001c0002t0024g0027 a0001c0002t0025g0026 others(4): Show |
7 | HG01884.hp2 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+9190_51+9201del others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267692 | |||||||
| chr9:36267748 | A | T | 21 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(18): Show |
21 | HG01074.hp2 HG01255.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.51+9146T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267748 | |||||||
| chr9:36267828 | G | A | 2 | a0001c0001t0018g0060 a0001c0001t0018g0061 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.51+9066C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36267828 | |||||||
| chr9:36268008 | G | T | 3 | a0001c0002t0016g0024 a0001c0002t0032g0062 a0001c0002t0060g0025 |
3 | HG02647.hp2 HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.51+8886C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268008 | |||||||
| chr9:36268044 | C | G | 245 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(242): Show |
247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.51+8850G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268044 | |||||||
| chr9:36268077 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.51+8817G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268077 | |||||||
| chr9:36268220 | C | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+8674G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268220 | |||||||
| chr9:36268254 | A | T | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+8640T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268254 | |||||||
| chr9:36268280 | C | T | 98 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0002g0092 others(95): Show |
98 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.51+8614G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268280 | |||||||
| chr9:36268387 | T | C | 245 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(242): Show |
247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.51+8507A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268387 | |||||||
| chr9:36268410 | A | T | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+8484T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268410 | |||||||
| chr9:36268438 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.51+8456C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268438 | |||||||
| chr9:36268852 | G | T | 5 | a0001c0001t0002g0075 a0001c0001t0002g0078 a0001c0001t0002g0079 others(2): Show |
5 | NA18967.hp2 NA18973.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+8042C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268852 | |||||||
| chr9:36268950 | C | T | 1 | a0001c0001t0003g0054 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.51+7944G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36268950 | |||||||
| chr9:36269045 | G | T | 3 | a0001c0001t0010g0267 a0001c0001t0010g0281 a0001c0001t0010g0282 |
3 | HG00609.hp1 NA18954.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.51+7849C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269045 | |||||||
| chr9:36269101 | G | A | 1 | a0001c0001t0059g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.51+7793C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269101 | |||||||
| chr9:36269129 | C | CA | 58 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(55): Show |
58 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.51+7764dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269129 | |||||||
| chr9:36269158 | A | G | 2 | a0001c0001t0049g0072 a0001c0001t0051g0073 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.51+7736T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269158 | |||||||
| chr9:36269271 | C | T | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+7623G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269271 | |||||||
| chr9:36269320 | G | A | 2 | a0001c0001t0049g0072 a0001c0001t0051g0073 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.51+7574C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269320 | |||||||
| chr9:36269415 | T | C | 4 | a0001c0001t0007g0173 a0001c0001t0007g0175 a0001c0001t0008g0174 others(1): Show |
4 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+7479A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269415 | |||||||
| chr9:36269664 | C | CT | 19 | a0001c0001t0001g0081 a0001c0001t0001g0226 a0001c0001t0001g0228 others(16): Show |
19 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.51+7229dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269664 | |||||||
| chr9:36269664 | C | CTT | 107 | a0001c0001t0001g0050 a0001c0001t0001g0157 a0001c0001t0001g0158 others(104): Show |
109 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.51+7228_51+7229dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269664 | |||||||
| chr9:36269664 | C | CTTT | 19 | a0001c0001t0003g0033 a0001c0001t0008g0152 a0001c0001t0013g0067 others(16): Show |
19 | HG01109.hp1 HG01243.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.51+7227_51+7229dup others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269664 | |||||||
| chr9:36269664 | C | CTTTT | 87 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0002g0092 others(84): Show |
87 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.51+7226_51+7229dup others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269664 | |||||||
| chr9:36269684 | C | T | 6 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+7210G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269684 | |||||||
| chr9:36269700 | C | A | 46 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(43): Show |
46 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.51+7194G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269700 | |||||||
| chr9:36269724 | T | C | 4 | a0001c0002t0024g0027 a0001c0002t0025g0026 a0001c0002t0025g0029 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+7170A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269724 | |||||||
| chr9:36269937 | C | T | 8 | a0001c0001t0011g0351 a0001c0001t0035g0350 a0001c0001t0037g0347 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+6957G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269937 | |||||||
| chr9:36269950 | C | A | 2 | a0001c0001t0045g0341 a0001c0001t0045g0345 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.51+6944G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269950 | |||||||
| chr9:36269958 | G | A | 4 | a0001c0001t0011g0351 a0001c0001t0087g0354 a0001c0001t0088g0353 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+6936C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269958 | |||||||
| chr9:36269961 | C | T | 4 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+6933G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36269961 | |||||||
| chr9:36270081 | C | G | 4 | a0001c0001t0020g0149 a0001c0001t0042g0144 a0001c0001t0042g0178 others(1): Show |
4 | HG00741.hp1 HG01255.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+6813G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270081 | |||||||
| chr9:36270172 | A | G | 60 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(57): Show |
62 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.51+6722T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270172 | |||||||
| chr9:36270183 | G | A | 1 | a0001c0001t0031g0091 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.51+6711C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270183 | |||||||
| chr9:36270372 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.51+6522A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270372 | |||||||
| chr9:36270456 | G | A | 1 | a0001c0001t0067g0053 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.51+6438C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270456 | |||||||
| chr9:36270468 | C | T | 48 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+6426G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270468 | |||||||
| chr9:36270516 | C | CT | 6 | a0001c0001t0001g0268 a0001c0001t0001g0283 a0001c0001t0001g0315 others(3): Show |
6 | HG00621.hp1 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+6377dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270516 | |||||||
| chr9:36270516 | CT | C | 64 | a0001c0001t0001g0050 a0001c0001t0001g0244 a0001c0001t0001g0245 others(61): Show |
65 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.51+6377delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270516 | |||||||
| chr9:36270541 | G | A | 165 | a0001c0001t0001g0081 a0001c0001t0001g0106 a0001c0001t0001g0119 others(162): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.51+6353C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270541 | |||||||
| chr9:36270566 | G | A | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | NA18943.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.51+6328C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270566 | |||||||
| chr9:36270566 | G | C | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+6328C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270566 | |||||||
| chr9:36270567 | T | G | 245 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(242): Show |
247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.51+6327A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270567 | |||||||
| chr9:36270579 | A | G | 240 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(237): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.51+6315T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270579 | |||||||
| chr9:36270603 | C | T | 9 | a0001c0001t0046g0011 a0001c0001t0046g0015 a0001c0001t0047g0016 others(6): Show |
9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.51+6291G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270603 | |||||||
| chr9:36270604 | G | A | 1 | a0001c0001t0007g0177 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.51+6290C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270604 | |||||||
| chr9:36270619 | A | G | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+6275T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270619 | |||||||
| chr9:36270630 | A | G | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+6264T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270630 | |||||||
| chr9:36270672 | C | T | 8 | a0001c0001t0011g0351 a0001c0001t0035g0350 a0001c0001t0037g0347 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+6222G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270672 | |||||||
| chr9:36270675 | G | A | 5 | a0001c0001t0033g0131 a0001c0001t0033g0132 a0001c0001t0040g0342 others(2): Show |
5 | HG03195.hp1 HG06807.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+6219C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270675 | |||||||
| chr9:36270679 | G | A | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+6215C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270679 | |||||||
| chr9:36270708 | G | A | 6 | a0001c0001t0013g0067 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+6186C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270708 | |||||||
| chr9:36270883 | C | T | 165 | a0001c0001t0001g0081 a0001c0001t0001g0106 a0001c0001t0001g0119 others(162): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.51+6011G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270883 | |||||||
| chr9:36270991 | T | A | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+5903A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36270991 | |||||||
| chr9:36271036 | A | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+5858T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271036 | |||||||
| chr9:36271130 | G | A | 2 | a0001c0001t0049g0072 a0001c0001t0051g0073 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.51+5764C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271130 | |||||||
| chr9:36271405 | G | A | 8 | a0001c0001t0011g0351 a0001c0001t0035g0350 a0001c0001t0037g0347 others(5): Show |
8 | HG01255.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+5489C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271405 | |||||||
| chr9:36271481 | C | T | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+5413G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271481 | |||||||
| chr9:36271482 | T | C | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+5412A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271482 | |||||||
| chr9:36271483 | C | T | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+5411G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271483 | |||||||
| chr9:36271505 | C | T | 2 | a0001c0001t0045g0341 a0001c0001t0045g0345 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.51+5389G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271505 | |||||||
| chr9:36271997 | A | G | 1 | a0001c0001t0011g0351 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.51+4897T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36271997 | |||||||
| chr9:36272067 | C | G | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4827G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272067 | |||||||
| chr9:36272100 | A | T | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4794T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272100 | |||||||
| chr9:36272103 | C | G | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4791G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272103 | |||||||
| chr9:36272126 | A | T | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4768T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272126 | |||||||
| chr9:36272129 | A | T | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4765T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272129 | |||||||
| chr9:36272130 | C | G | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4764G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272130 | |||||||
| chr9:36272131 | A | C | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4763T>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272131 | |||||||
| chr9:36272138 | G | A | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4756C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272138 | |||||||
| chr9:36272140 | A | G | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4754T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272140 | |||||||
| chr9:36272147 | C | A | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4747G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272147 | |||||||
| chr9:36272202 | A | G | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4692T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272202 | |||||||
| chr9:36272203 | T | G | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4691A>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272203 | |||||||
| chr9:36272233 | G | C | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4661C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272233 | |||||||
| chr9:36272234 | C | A | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4660G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272234 | |||||||
| chr9:36272235 | A | T | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4659T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272235 | |||||||
| chr9:36272252 | A | T | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4642T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272252 | |||||||
| chr9:36272253 | G | A | 1 | a0001c0001t0004g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.51+4641C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272253 | |||||||
| chr9:36272264 | C | A | 2 | a0001c0001t0045g0341 a0001c0001t0045g0345 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.51+4630G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272264 | |||||||
| chr9:36272479 | G | A | 1 | a0001c0001t0028g0133 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.51+4415C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272479 | |||||||
| chr9:36272492 | G | A | 17 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(14): Show |
17 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+4402C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272492 | |||||||
| chr9:36272620 | C | CA | 24 | a0001c0001t0001g0227 a0001c0001t0001g0240 a0001c0001t0001g0241 others(21): Show |
24 | HG00438.hp2 HG00621.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.51+4273dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | |||||||
| chr9:36272620 | C | CAA | 7 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
7 | HG03491.hp1 HG03492.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+4272_51+4273dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | |||||||
| chr9:36272620 | CA | C | 20 | a0001c0001t0001g0280 a0001c0001t0001g0321 a0001c0001t0004g0248 others(17): Show |
20 | HG00609.hp2 HG01891.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.51+4273delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | |||||||
| chr9:36272620 | CAA | C | 13 | a0001c0001t0002g0075 a0001c0001t0002g0079 a0001c0001t0003g0054 others(10): Show |
13 | HG01346.hp2 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.51+4272_51+4273del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | |||||||
| chr9:36272620 | CAAA | C | 127 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0157 others(124): Show |
129 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.51+4271_51+4273del others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | |||||||
| chr9:36272620 | CAAAA | C | 95 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0002g0092 others(92): Show |
95 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.51+4270_51+4273del others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272620 | |||||||
| chr9:36272685 | G | A | 1 | a0001c0001t0031g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.51+4209C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272685 | |||||||
| chr9:36272801 | T | A | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | NA19064.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.51+4093A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272801 | |||||||
| chr9:36272914 | AT | A | 4 | a0001c0001t0006g0183 a0001c0001t0006g0188 a0001c0001t0073g0082 others(1): Show |
4 | HG03225.hp1 NA18946.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+3979delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272914 | |||||||
| chr9:36272915 | T | A | 5 | a0001c0001t0005g0186 a0001c0001t0006g0182 a0001c0001t0006g0184 others(2): Show |
5 | HG02080.hp1 NA18953.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+3979A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272915 | |||||||
| chr9:36272916 | AC | A | 135 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0001g0157 others(132): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.51+3977delG | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272916 | |||||||
| chr9:36272917 | C | A | 28 | a0001c0001t0001g0106 a0001c0001t0002g0092 a0001c0001t0002g0096 others(25): Show |
28 | HG00735.hp1 HG01168.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.51+3977G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272917 | |||||||
| chr9:36272917 | C | CA | 27 | a0001c0001t0001g0227 a0001c0001t0001g0253 a0001c0001t0001g0254 others(24): Show |
27 | HG00408.hp1 HG00438.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.51+3976dupT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272917 | |||||||
| chr9:36272917 | CA | C | 48 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0023 others(45): Show |
50 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.51+3976delT | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272917 | |||||||
| chr9:36272924 | A | T | 1 | a0001c0001t0080g0148 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.51+3970T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272924 | |||||||
| chr9:36272925 | A | T | 1 | a0001c0001t0008g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.51+3969T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272925 | |||||||
| chr9:36272926 | A | T | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | NA19002.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.51+3968T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272926 | |||||||
| chr9:36272964 | A | G | 1 | a0001c0001t0022g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.51+3930T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272964 | |||||||
| chr9:36272971 | G | A | 3 | a0001c0001t0003g0058 a0001c0001t0003g0059 a0001c0001t0063g0031 |
3 | NA18956.hp1 NA19064.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.51+3923C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36272971 | |||||||
| chr9:36273041 | C | T | 1 | a0001c0001t0093g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.51+3853G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273041 | |||||||
| chr9:36273064 | G | A | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+3830C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273064 | |||||||
| chr9:36273110 | T | C | 3 | a0001c0002t0016g0024 a0001c0002t0032g0062 a0001c0002t0060g0025 |
3 | HG02647.hp2 HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.51+3784A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273110 | |||||||
| chr9:36273112 | G | T | 1 | a0001c0001t0002g0136 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.51+3782C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273112 | |||||||
| chr9:36273119 | T | C | 1 | a0001c0001t0084g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.51+3775A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273119 | |||||||
| chr9:36273178 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | NA18944.hp2 NA18957.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.51+3716G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273178 | |||||||
| chr9:36273221 | A | AT | 70 | a0001c0001t0001g0081 a0001c0001t0001g0157 a0001c0001t0001g0158 others(67): Show |
70 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.51+3672dupA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273221 | |||||||
| chr9:36273221 | A | ATT | 15 | a0001c0001t0002g0136 a0001c0001t0007g0141 a0001c0001t0013g0067 others(12): Show |
15 | HG01099.hp1 HG01168.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.51+3671_51+3672dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273221 | |||||||
| chr9:36273221 | A | ATTT | 86 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0002g0092 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.51+3670_51+3672dup others(3): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273221 | |||||||
| chr9:36273221 | A | T | 2 | a0001c0001t0014g0236 a0001c0001t0090g0234 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.51+3673T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273221 | |||||||
| chr9:36273221 | AT | A | 7 | a0001c0001t0003g0030 a0001c0001t0018g0060 a0001c0001t0018g0061 others(4): Show |
7 | HG01515.hp2 HG01517.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+3672delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273221 | |||||||
| chr9:36273577 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.51+3317T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273577 | |||||||
| chr9:36273660 | CT | C | 122 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0157 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.51+3233delA | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273660 | |||||||
| chr9:36273701 | A | G | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+3193T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273701 | |||||||
| chr9:36273702 | G | A | 1 | a0001c0001t0007g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.51+3192C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273702 | |||||||
| chr9:36273763 | C | G | 3 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0082g0343 |
3 | HG03195.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.51+3131G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273763 | |||||||
| chr9:36273820 | G | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.51+3074C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273820 | |||||||
| chr9:36273831 | G | A | 225 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(222): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.51+3063C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273831 | |||||||
| chr9:36273841 | C | T | 1 | a0001c0001t0029g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.51+3053G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273841 | |||||||
| chr9:36273917 | G | A | 53 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(50): Show |
55 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.51+2977C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273917 | |||||||
| chr9:36273925 | G | A | 1 | a0001c0001t0038g0099 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.51+2969C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36273925 | |||||||
| chr9:36274068 | C | CTG | 6 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(3): Show |
6 | HG02280.hp1 HG02683.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+2824_51+2825dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | C | CTGTGTG | 4 | a0001c0001t0002g0075 a0001c0001t0024g0235 a0001c0001t0035g0350 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2820_51+2825dup others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | C | CTGTGTGT others(1): Show |
3 | a0001c0001t0037g0349 a0001c0001t0074g0348 a0001c0001t0090g0234 |
3 | HG01255.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.51+2818_51+2825dup others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | C | CTGTGTGT others(3): Show |
2 | a0001c0001t0014g0232 a0001c0001t0044g0233 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.51+2816_51+2825dup others(10): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0037g0347 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.51+2814_51+2825dup others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | CTG | C | 7 | a0001c0001t0001g0081 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG02735.hp2 HG03195.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2824_51+2825del others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | CTGTG | C | 24 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(21): Show |
24 | HG00609.hp2 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.51+2822_51+2825del others(4): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | CTGTGTG | C | 20 | a0001c0001t0001g0260 a0001c0001t0001g0268 a0001c0001t0001g0269 others(17): Show |
20 | HG00609.hp1 HG00735.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.51+2820_51+2825del others(6): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | CTGTGTGT others(1): Show |
C | 45 | a0001c0001t0001g0277 a0001c0001t0001g0280 a0001c0001t0001g0283 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.51+2818_51+2825del others(8): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | CTGTGTGT others(3): Show |
C | 26 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(23): Show |
26 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.51+2816_51+2825del others(10): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | CTGTGTGT others(5): Show |
C | 19 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0334 others(16): Show |
19 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.51+2814_51+2825del others(12): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | CTGTGTGT others(7): Show |
C | 100 | a0001c0001t0001g0050 a0001c0001t0001g0106 a0001c0001t0001g0119 others(97): Show |
102 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.51+2812_51+2825del others(14): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | CTGTGTGT others(9): Show |
C | 83 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(80): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.51+2810_51+2825del others(16): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | CTGTGTGT others(11): Show |
C | 5 | a0001c0001t0006g0223 a0001c0001t0006g0224 a0001c0001t0007g0180 others(2): Show |
5 | HG01081.hp1 HG01243.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2808_51+2825del others(18): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274068 | CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0045g0345 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.51+2806_51+2825del others(20): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274068 | |||||||
| chr9:36274115 | T | A | 7 | a0001c0001t0001g0338 a0001c0001t0012g0003 a0001c0001t0012g0004 others(4): Show |
7 | HG02056.hp2 HG02451.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2779A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274115 | |||||||
| chr9:36274363 | T | C | 48 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+2531A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274363 | |||||||
| chr9:36274465 | A | G | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2429T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274465 | |||||||
| chr9:36274846 | C | CCG | 226 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(223): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.51+2046_51+2047dup others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274846 | |||||||
| chr9:36274868 | A | G | 90 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0002g0092 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.51+2026T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274868 | |||||||
| chr9:36274876 | T | C | 1 | a0001c0001t0013g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51+2018A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274876 | |||||||
| chr9:36274879 | T | C | 1 | a0001c0001t0013g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51+2015A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274879 | |||||||
| chr9:36274885 | G | T | 1 | a0001c0001t0011g0181 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.51+2009C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274885 | |||||||
| chr9:36274959 | C | T | 1 | a0001c0001t0076g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.51+1935G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274959 | |||||||
| chr9:36274970 | G | A | 1 | a0001c0001t0004g0339 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.51+1924C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274970 | |||||||
| chr9:36274974 | T | C | 1 | a0001c0001t0053g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+1920A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36274974 | |||||||
| chr9:36275046 | A | T | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+1848T>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275046 | |||||||
| chr9:36275065 | T | C | 17 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(14): Show |
17 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+1829A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275065 | |||||||
| chr9:36275204 | C | T | 1 | a0001c0001t0003g0020 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.51+1690G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275204 | |||||||
| chr9:36275403 | G | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG03491.hp1 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.51+1491C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275403 | |||||||
| chr9:36275448 | G | C | 17 | a0001c0001t0001g0081 a0001c0001t0002g0075 a0001c0001t0002g0078 others(14): Show |
17 | HG01074.hp2 HG01257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+1446C>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275448 | |||||||
| chr9:36275564 | G | T | 4 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
4 | NA18945.hp2 NA18957.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+1330C>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275564 | |||||||
| chr9:36275702 | C | G | 9 | a0001c0001t0046g0011 a0001c0001t0046g0015 a0001c0001t0047g0016 others(6): Show |
9 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.51+1192G>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275702 | |||||||
| chr9:36275724 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.51+1170T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275724 | |||||||
| chr9:36275851 | T | C | 7 | a0001c0001t0040g0342 a0001c0001t0040g0344 a0001c0001t0045g0341 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+1043A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275851 | |||||||
| chr9:36275894 | A | G | 1 | a0001c0001t0007g0139 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.51+1000T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275894 | |||||||
| chr9:36275895 | G | A | 1 | a0001c0001t0006g0065 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.51+999C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275895 | |||||||
| chr9:36275910 | C | A | 1 | a0001c0001t0032g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.51+984G>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275910 | |||||||
| chr9:36275920 | C | T | 1 | a0001c0001t0003g0010 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.51+974G>A | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275920 | |||||||
| chr9:36275930 | T | C | 92 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0002g0092 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.51+964A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36275930 | |||||||
| chr9:36276027 | G | A | 48 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+867C>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276027 | |||||||
| chr9:36276059 | A | G | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+835T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276059 | |||||||
| chr9:36276175 | AACAC | A | 44 | a0001c0001t0002g0218 a0001c0001t0005g0186 a0001c0001t0005g0191 others(41): Show |
44 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.51+715_51+718delGT others(2): Show |
GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276175 | |||||||
| chr9:36276186 | A | G | 60 | a0001c0001t0001g0050 a0001c0001t0003g0010 a0001c0001t0003g0020 others(57): Show |
62 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.51+708T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276186 | |||||||
| chr9:36276282 | A | G | 4 | a0001c0001t0035g0350 a0001c0001t0037g0347 a0001c0001t0037g0349 others(1): Show |
4 | HG01255.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+612T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276282 | |||||||
| chr9:36276546 | T | A | 233 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+348A>T | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276546 | |||||||
| chr9:36276600 | A | G | 1 | a0001c0001t0005g0009 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.51+294T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276600 | |||||||
| chr9:36276831 | T | C | 1 | a0001c0001t0028g0225 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.51+63A>G | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276831 | |||||||
| chr9:36276860 | A | G | 225 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0106 others(222): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.51+34T>C | GNE | ENSG00000159921.20 | transcript | ENST00000396594.8 | protein_coding | 1/11 | chr9 | 36276860 |