Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91750 |
| ensemblid | ENSG00000205659.12 |
| hgncid | 19856 |
| symbol | LIN52 |
| name | lin-52 DREAM MuvB core complex component |
| refseq_nuc | NM_001024674.3 |
| refseq_prot | NP_001019845.2 |
| ensembl_nuc | ENST00000555028.7 |
| ensembl_prot | ENSP00000451812.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 74084956 |
| end | 74201493 |
| strand | + |
| ver | v1.2 |
| region | chr14:74084956-74201493 |
| region5000 | chr14:74079956-74206493 |
| regionname0 | LIN52_chr14_74084956_74201493 |
| regionname5000 | LIN52_chr14_74079956_74206493 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 112 | 352 | 82 | 68 | 146 | 12 | 42 | 110 | LIN52_chr14_74079956_74206493 | LIN52 | MASPT others(107): Show |
chr14 | 74079956 | 74206493 |
| a0002 | 0/0 | 112 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | MASPT others(107): Show |
chr14 | 74079956 | 74206493 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 336 | 341 | 71 | 68 | 146 | 12 | 42 | LIN52_chr14_74079956_74206493 | LIN52 | ATGGC others(331): Show |
chr14 | 74079956 | 74206493 | ||
| a0001c0002 | 0/0 | 336 | 11 | 11 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ATGGC others(331): Show |
chr14 | 74079956 | 74206493 | ||
| a0002c0003 | 0/0 | 336 | 2 | 2 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ATGGC others(331): Show |
chr14 | 74079956 | 74206493 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3173 | 72 | 24 | 22 | 15 | 5 | 6 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3168): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0002 | 0/0 | 2875 | 53 | 9 | 7 | 31 | 2 | 4 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2870): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0003 | 0/1 | 2873 | 43 | 1 | 5 | 32 | 1 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2868): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0004 | 0/0 | 2874 | 33 | 10 | 5 | 17 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2869): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0005 | 0/0 | 3177 | 21 | 0 | 4 | 11 | 0 | 6 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3172): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0006 | 0/0 | 2876 | 19 | 3 | 1 | 12 | 0 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2871): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0007 | 0/0 | 2875 | 15 | 0 | 0 | 9 | 0 | 6 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2870): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0008 | 0/0 | 3179 | 15 | 0 | 12 | 1 | 1 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3174): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0010 | 0/0 | 2876 | 7 | 0 | 1 | 2 | 1 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2871): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0011 | 0/0 | 2872 | 6 | 6 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2867): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0012 | 0/0 | 2875 | 5 | 3 | 2 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2870): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0013 | 0/0 | 2875 | 4 | 0 | 1 | 0 | 0 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2870): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0014 | 0/0 | 2873 | 4 | 4 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2868): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0015 | 0/0 | 2875 | 4 | 2 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2870): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0016 | 0/0 | 2872 | 4 | 0 | 0 | 4 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2867): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0017 | 0/0 | 3173 | 3 | 0 | 2 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3168): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0018 | 0/0 | 3175 | 2 | 1 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3170): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0019 | 0/0 | 2874 | 2 | 0 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2869): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0020 | 0/0 | 2862 | 2 | 0 | 2 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2857): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0021 | 0/0 | 2875 | 2 | 2 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2870): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0022 | 0/0 | 2873 | 2 | 0 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2868): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0023 | 0/0 | 3171 | 2 | 0 | 1 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3166): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0024 | 0/0 | 3173 | 2 | 0 | 0 | 0 | 0 | 2 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3168): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0025 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2869): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0026 | 0/0 | 2875 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2870): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0027 | 0/0 | 2872 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2867): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0028 | 0/0 | 2876 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2871): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0029 | 0/0 | 2872 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2867): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0030 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2872): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0031 | 1/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2869): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0033 | 0/0 | 2873 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2868): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0034 | 0/0 | 2877 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2872): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0035 | 0/0 | 2860 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2855): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0036 | 0/0 | 2875 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2870): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0037 | 0/0 | 2876 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2871): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0038 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2869): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0039 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2869): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0040 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2869): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0041 | 0/0 | 3178 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3173): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0042 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3172): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0043 | 0/0 | 3173 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3168): Show |
chr14 | 74079956 | 74206493 |
| a0001c0001t0045 | 0/0 | 2875 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2870): Show |
chr14 | 74079956 | 74206493 |
| a0001c0002t0009 | 0/0 | 2872 | 10 | 10 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2867): Show |
chr14 | 74079956 | 74206493 |
| a0001c0002t0032 | 0/0 | 2873 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(2868): Show |
chr14 | 74079956 | 74206493 |
| a0002c0003t0018 | 0/0 | 3175 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3170): Show |
chr14 | 74079956 | 74206493 |
| a0002c0003t0044 | 0/0 | 3175 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | ACGTG others(3170): Show |
chr14 | 74079956 | 74206493 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0008g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0010g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0010g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0010g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0011g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0011g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0011g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0012g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0012g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0012g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0012g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0012g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0013g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0013g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0013g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0013g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0014g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0014g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0014g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0014g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0015g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0015g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0015g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0015g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0016g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0016g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0016g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0016g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0017g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0017g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0017g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0018g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0018g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0019g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0019g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0020g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0020g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0021g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0021g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0022g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0022g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0023g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0023g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0024g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0024g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0025g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0026g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0027g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0028g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0029g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0030g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0031g0336 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0033g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0034g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0035g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0036g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0037g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0038g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0039g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0040g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0041g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0042g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0043g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0001t0045g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0002t0009g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0002t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0002t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0002t0009g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0002t0009g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0002t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0002t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0002t0009g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0002t0009g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0001c0002t0032g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0002c0003t0018g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| a0002c0003t0044g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | GBR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00099 | hp2 | a0001 | c0001 | t0010 | g0113 | EUR | GBR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00280 | hp1 | a0001 | c0001 | t0017 | g0321 | EUR | FIN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | FIN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0333 | EUR | FIN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0069 | EUR | FIN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00423 | hp1 | a0001 | c0001 | t0035 | g0180 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00438 | hp1 | a0001 | c0001 | t0010 | g0104 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0099 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00558 | hp1 | a0001 | c0001 | t0043 | g0249 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0176 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0212 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00738 | hp1 | a0001 | c0001 | t0010 | g0112 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0334 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01074 | hp2 | a0001 | c0001 | t0034 | g0119 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0111 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0313 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0332 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0348 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01167 | hp1 | a0001 | c0001 | t0020 | g0155 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01167 | hp2 | a0001 | c0001 | t0042 | g0302 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0309 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01169 | hp1 | a0001 | c0001 | t0020 | g0132 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0329 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0086 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0083 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01255 | hp1 | a0001 | c0001 | t0023 | g0337 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0331 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0310 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0326 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01346 | hp2 | a0001 | c0001 | t0041 | g0298 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01433 | hp2 | a0001 | c0001 | t0017 | g0322 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01515 | hp2 | a0001 | c0001 | t0023 | g0343 | EUR | IBS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | IBS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0223 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0063 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01928 | hp2 | a0001 | c0001 | t0017 | g0314 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01934 | hp1 | a0001 | c0001 | t0008 | g0307 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0311 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0325 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0312 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02040 | hp1 | a0001 | c0001 | t0008 | g0308 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0209 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0156 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0297 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0305 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0105 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0174 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02145 | hp2 | a0001 | c0001 | t0037 | g0091 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0327 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | CDX | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02155 | hp2 | a0001 | c0001 | t0007 | g0109 | EAS | CDX | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CDX | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0319 | EAS | CDX | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02258 | hp2 | a0001 | c0002 | t0009 | g0280 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02280 | hp2 | a0001 | c0002 | t0009 | g0278 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02451 | hp2 | a0001 | c0002 | t0009 | g0002 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02572 | hp1 | a0001 | c0001 | t0014 | g0203 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0315 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02602 | hp2 | a0001 | c0001 | t0028 | g0101 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02622 | hp1 | a0001 | c0002 | t0009 | g0283 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02622 | hp2 | a0001 | c0002 | t0009 | g0282 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0204 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0122 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02717 | hp1 | a0001 | c0002 | t0009 | g0284 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0221 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02723 | hp1 | a0001 | c0001 | t0025 | g0087 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0304 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0247 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0299 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02809 | hp1 | a0002 | c0003 | t0018 | g0201 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02809 | hp2 | a0001 | c0001 | t0014 | g0200 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0102 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02895 | hp1 | a0001 | c0001 | t0021 | g0084 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0081 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02922 | hp2 | a0001 | c0002 | t0009 | g0279 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02965 | hp1 | a0001 | c0002 | t0032 | g0285 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02965 | hp2 | a0001 | c0001 | t0018 | g0085 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0344 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02970 | hp2 | a0001 | c0002 | t0009 | g0193 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02976 | hp1 | a0001 | c0001 | t0045 | g0188 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03017 | hp1 | a0001 | c0001 | t0027 | g0124 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03041 | hp1 | a0001 | c0001 | t0014 | g0199 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0198 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0224 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0349 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03209 | hp2 | a0001 | c0002 | t0009 | g0002 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03453 | hp1 | a0001 | c0002 | t0009 | g0281 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0351 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03486 | hp1 | a0001 | c0001 | t0036 | g0082 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0303 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03491 | hp2 | a0001 | c0001 | t0026 | g0186 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03492 | hp1 | a0001 | c0001 | t0024 | g0229 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0306 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03540 | hp1 | a0001 | c0001 | t0021 | g0079 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03579 | hp1 | a0002 | c0003 | t0044 | g0187 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0225 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0114 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03669 | hp2 | a0001 | c0001 | t0024 | g0230 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0162 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03688 | hp2 | a0001 | c0001 | t0013 | g0094 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0115 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03831 | hp2 | a0001 | c0001 | t0013 | g0125 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03834 | hp1 | a0001 | c0001 | t0010 | g0126 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0183 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0168 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03927 | hp2 | a0001 | c0001 | t0008 | g0296 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0330 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03942 | hp2 | a0001 | c0001 | t0013 | g0120 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG04115 | hp2 | a0001 | c0001 | t0010 | g0096 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG04184 | hp1 | a0001 | c0001 | t0029 | g0202 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0341 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG04199 | hp2 | a0001 | c0001 | t0010 | g0106 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0004 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0107 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CHB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18612 | hp2 | a0001 | c0001 | t0016 | g0089 | EAS | CHB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0350 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18906 | hp2 | a0001 | c0001 | t0038 | g0080 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0320 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18946 | hp1 | a0001 | c0001 | t0019 | g0141 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18959 | hp2 | a0001 | c0001 | t0015 | g0039 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18967 | hp2 | a0001 | c0001 | t0033 | g0182 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18984 | hp2 | a0001 | c0001 | t0016 | g0048 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18988 | hp2 | a0001 | c0001 | t0016 | g0010 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18991 | hp1 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18991 | hp2 | a0001 | c0001 | t0022 | g0075 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18999 | hp1 | a0001 | c0001 | t0007 | g0121 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19009 | hp1 | a0001 | c0001 | t0022 | g0056 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19009 | hp2 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0275 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0318 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19030 | hp1 | a0001 | c0001 | t0040 | g0184 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0345 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19043 | hp1 | a0001 | c0001 | t0015 | g0090 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19055 | hp1 | a0001 | c0001 | t0016 | g0051 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19055 | hp2 | a0001 | c0001 | t0019 | g0149 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19057 | hp2 | a0001 | c0001 | t0030 | g0262 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0116 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19067 | hp1 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19075 | hp1 | a0001 | c0001 | t0015 | g0041 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19077 | hp1 | a0001 | c0001 | t0018 | g0271 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19077 | hp2 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19079 | hp1 | a0001 | c0001 | t0007 | g0098 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19082 | hp1 | a0001 | c0001 | t0039 | g0031 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0295 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA19240 | hp2 | a0001 | c0001 | t0015 | g0185 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ASW | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | ASW | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | TSI | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0324 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0078 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0222 | AFR | USA | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | USA | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0061 | REF | REF | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0031 | g0336 | REF | REF | LIN52_chr14_74079956_74206493 | LIN52 | chr14 | 74079956 | 74206493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74198970 | A | G | 1 | a0002 | 2 | HG02809.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.332A>G | p.Lys111Arg | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 351/2874 | 332/339 | 111/112 | chr14 | 74198970 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74198929 | G | A | 1 | a0001c0002 | 11 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
synonymous_variant | LOW | c.291G>A | p.Glu97Glu | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 310/2874 | 291/339 | 97/112 | chr14 | 74198929 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74199022 | C | T | 1 | a0001c0001t0024 | 2 | HG03492.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*45C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 45 | chr14 | 74199022 | ||||||
| chr14:74199028 | C | T | 1 | a0001c0001t0045 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 51 | chr14 | 74199028 | ||||||
| chr14:74199173 | A | T | 1 | a0002c0003t0044 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 196 | chr14 | 74199173 | ||||||
| chr14:74199504 | G | A | 1 | a0001c0001t0025 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*527G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 527 | chr14 | 74199504 | ||||||
| chr14:74199522 | T | C | 6 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0013 others(3): Show |
29 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*545T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 545 | chr14 | 74199522 | ||||||
| chr14:74199862 | G | A | 3 | a0001c0001t0011 a0001c0001t0014 a0001c0001t0029 |
11 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*885G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 885 | chr14 | 74199862 | ||||||
| chr14:74199938 | A | G | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(22): Show |
220 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*961A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 961 | chr14 | 74199938 | ||||||
| chr14:74200076 | A | G | 1 | a0001c0001t0029 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1099A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1099 | chr14 | 74200076 | ||||||
| chr14:74200097 | A | G | 2 | a0001c0001t0013 a0001c0001t0028 |
5 | HG01081.hp1 HG02602.hp2 HG03688.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1120A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1120 | chr14 | 74200097 | ||||||
| chr14:74200121 | A | G | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(22): Show |
220 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1144A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1144 | chr14 | 74200121 | ||||||
| chr14:74200229 | T | TATGGTGA others(302): Show |
11 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(8): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1263_*1264insTCGT others(305): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1264 | INFO_REALIGN_3_PRIME | chr14 | 74200229 | |||||
| chr14:74200229 | T | TATGGTGA others(302): Show |
1 | a0001c0001t0024 | 2 | HG03492.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1263_*1264insTCGT others(305): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1264 | INFO_REALIGN_3_PRIME | chr14 | 74200229 | |||||
| chr14:74200251 | T | TA | 12 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(9): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1278dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1279 | INFO_REALIGN_3_PRIME | chr14 | 74200251 | |||||
| chr14:74200274 | A | G | 12 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(9): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1297A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1297 | chr14 | 74200274 | ||||||
| chr14:74200320 | C | T | 1 | a0001c0001t0040 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1343C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1343 | chr14 | 74200320 | ||||||
| chr14:74200414 | G | GA | 4 | a0001c0001t0012 a0001c0001t0021 a0001c0001t0030 others(1): Show |
9 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1466dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1467 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | |||||
| chr14:74200414 | GA | G | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(9): Show |
129 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1466delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1466 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | |||||
| chr14:74200414 | GAA | G | 6 | a0001c0001t0011 a0001c0001t0016 a0001c0001t0019 others(3): Show |
24 | HG01891.hp1 HG02258.hp2 HG02280.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1465_*1466delAA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1465 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | |||||
| chr14:74200414 | GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0041 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1457_*1466delAAAA others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1457 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | |||||
| chr14:74200414 | GAAAAAAA others(4): Show |
G | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0017 others(1): Show |
40 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1456_*1466delAAAA others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1456 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | |||||
| chr14:74200414 | GAAAAAAA others(6): Show |
G | 7 | a0001c0001t0001 a0001c0001t0018 a0001c0001t0023 others(4): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1454_*1466delAAAA others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1454 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | |||||
| chr14:74200414 | GAAAAAAA others(7): Show |
G | 2 | a0001c0001t0020 a0001c0001t0035 |
3 | HG00423.hp1 HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1453_*1466delAAAA others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1453 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | |||||
| chr14:74200494 | T | C | 1 | a0001c0001t0026 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1517T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1517 | chr14 | 74200494 | ||||||
| chr14:74200640 | C | T | 2 | a0001c0001t0022 a0001c0001t0039 |
3 | NA18991.hp2 NA19009.hp1 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1663C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1663 | chr14 | 74200640 | ||||||
| chr14:74200778 | C | T | 1 | a0001c0001t0042 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1801C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1801 | chr14 | 74200778 | ||||||
| chr14:74200817 | G | T | 2 | a0001c0001t0036 a0001c0001t0038 |
2 | HG03486.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1840G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1840 | chr14 | 74200817 | ||||||
| chr14:74200820 | T | C | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0011 others(12): Show |
114 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1843T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1843 | chr14 | 74200820 | ||||||
| chr14:74200820 | T | TGC | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(13): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1852_*1853dupGC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1854 | INFO_REALIGN_3_PRIME | chr14 | 74200820 | |||||
| chr14:74200820 | T | TGTGC | 7 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0034 others(4): Show |
28 | HG01074.hp2 HG01123.hp2 HG01167.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1844_*1845insTGCG | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1845 | INFO_REALIGN_3_PRIME | chr14 | 74200820 | |||||
| chr14:74200820 | T | TGTGTGC | 1 | a0001c0001t0008 | 15 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1844_*1845insTGTG others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1845 | INFO_REALIGN_3_PRIME | chr14 | 74200820 | |||||
| chr14:74200880 | T | A | 3 | a0001c0001t0021 a0001c0001t0036 a0001c0001t0038 |
4 | HG02895.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1903T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1903 | chr14 | 74200880 | ||||||
| chr14:74201138 | A | G | 5 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0017 others(2): Show |
41 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2161A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 2161 | chr14 | 74201138 | ||||||
| chr14:74201490 | G | A | 1 | a0001c0001t0043 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2513G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 2513 | chr14 | 74201490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74085018 | G | T | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+25G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085018 | |||||||
| chr14:74085082 | T | C | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.19+89T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085082 | |||||||
| chr14:74085267 | G | C | 206 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(203): Show |
208 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.19+274G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085267 | |||||||
| chr14:74085273 | C | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+280C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085273 | |||||||
| chr14:74085345 | T | C | 338 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(335): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.19+352T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085345 | |||||||
| chr14:74085444 | C | G | 1 | a0001c0001t0016g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.19+451C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085444 | |||||||
| chr14:74085502 | A | G | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+509A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085502 | |||||||
| chr14:74085705 | CAATT | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+715_19+718delTT others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74085705 | ||||||
| chr14:74085710 | A | C | 1 | a0001c0001t0002g0197 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.19+717A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085710 | |||||||
| chr14:74085739 | C | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+746C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085739 | |||||||
| chr14:74085807 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19+814C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085807 | |||||||
| chr14:74085840 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.19+847T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085840 | |||||||
| chr14:74085886 | A | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+893A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085886 | |||||||
| chr14:74085967 | G | T | 3 | a0001c0001t0008g0332 a0001c0001t0008g0333 a0001c0001t0008g0334 |
3 | HG00323.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.19+974G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085967 | |||||||
| chr14:74086011 | AT | A | 9 | a0001c0001t0001g0335 a0001c0001t0002g0092 a0001c0001t0004g0206 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1029delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74086011 | ||||||
| chr14:74086041 | T | C | 1 | a0001c0001t0003g0005 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.19+1048T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086041 | |||||||
| chr14:74086092 | C | A | 1 | a0001c0001t0002g0093 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.19+1099C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086092 | |||||||
| chr14:74086186 | G | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.19+1193G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086186 | |||||||
| chr14:74086344 | G | A | 72 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(69): Show |
72 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.19+1351G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086344 | |||||||
| chr14:74086549 | G | C | 2 | a0001c0001t0004g0077 a0001c0001t0012g0078 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.19+1556G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086549 | |||||||
| chr14:74086656 | G | A | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.19+1663G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086656 | |||||||
| chr14:74086669 | GA | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+1685delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74086669 | ||||||
| chr14:74086898 | T | C | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.19+1905T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086898 | |||||||
| chr14:74086948 | G | GA | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+1964dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74086948 | ||||||
| chr14:74086999 | A | G | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0006g0194 |
3 | HG01496.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.19+2006A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086999 | |||||||
| chr14:74087011 | A | C | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+2018A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087011 | |||||||
| chr14:74087109 | G | A | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+2116G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087109 | |||||||
| chr14:74087140 | G | A | 106 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(103): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.19+2147G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087140 | |||||||
| chr14:74087371 | A | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+2378A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087371 | |||||||
| chr14:74087384 | C | T | 1 | a0001c0001t0012g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.19+2391C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087384 | |||||||
| chr14:74087413 | C | CA | 13 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(10): Show |
13 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.19+2443dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74087413 | ||||||
| chr14:74087413 | CA | C | 115 | a0001c0001t0001g0097 a0001c0001t0001g0152 a0001c0001t0001g0161 others(112): Show |
117 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.19+2443delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74087413 | ||||||
| chr14:74087413 | CAA | C | 39 | a0001c0001t0001g0110 a0001c0001t0001g0191 a0001c0001t0002g0117 others(36): Show |
39 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.19+2442_19+2443del others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74087413 | ||||||
| chr14:74087413 | CAAAAAAA others(1): Show |
C | 72 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(69): Show |
72 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.19+2436_19+2443del others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74087413 | ||||||
| chr14:74087413 | CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(6): Show |
9 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2434_19+2443del others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74087413 | ||||||
| chr14:74087469 | G | C | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.19+2476G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087469 | |||||||
| chr14:74087762 | C | T | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.19+2769C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087762 | |||||||
| chr14:74087974 | A | C | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+2981A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087974 | |||||||
| chr14:74088022 | C | T | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+3029C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088022 | |||||||
| chr14:74088024 | C | T | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.19+3031C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088024 | |||||||
| chr14:74088029 | C | T | 3 | a0001c0001t0005g0299 a0001c0001t0005g0330 a0001c0001t0041g0298 |
3 | HG01346.hp2 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.19+3036C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088029 | |||||||
| chr14:74088070 | G | A | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.19+3077G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088070 | |||||||
| chr14:74088167 | T | A | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.20-3065T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088167 | |||||||
| chr14:74088204 | C | T | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.20-3028C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088204 | |||||||
| chr14:74088256 | A | G | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.20-2976A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088256 | |||||||
| chr14:74088333 | C | A | 1 | a0001c0001t0007g0099 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.20-2899C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088333 | |||||||
| chr14:74088474 | C | T | 5 | a0001c0001t0004g0206 a0001c0001t0004g0207 a0001c0001t0004g0208 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-2758C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088474 | |||||||
| chr14:74088565 | C | T | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-2667C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088565 | |||||||
| chr14:74088566 | G | A | 61 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(58): Show |
62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.20-2666G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088566 | |||||||
| chr14:74088706 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.20-2526C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088706 | |||||||
| chr14:74088721 | T | G | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-2511T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088721 | |||||||
| chr14:74088753 | C | T | 1 | a0001c0001t0003g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.20-2479C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088753 | |||||||
| chr14:74088911 | T | G | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-2321T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088911 | |||||||
| chr14:74088912 | G | T | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-2320G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088912 | |||||||
| chr14:74089022 | C | T | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.20-2210C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089022 | |||||||
| chr14:74089066 | C | T | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.20-2166C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089066 | |||||||
| chr14:74089087 | GT | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.20-2144delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089087 | |||||||
| chr14:74089370 | A | AT | 123 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0191 others(120): Show |
126 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.20-1846dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74089370 | ||||||
| chr14:74089370 | A | ATT | 37 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0092 others(34): Show |
37 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.20-1847_20-1846dup others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74089370 | ||||||
| chr14:74089560 | T | G | 206 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(203): Show |
208 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.20-1672T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089560 | |||||||
| chr14:74089796 | TA | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-1432delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74089796 | ||||||
| chr14:74089868 | T | C | 1 | a0001c0001t0007g0103 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.20-1364T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089868 | |||||||
| chr14:74089897 | C | A | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-1335C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089897 | |||||||
| chr14:74089952 | C | T | 1 | a0001c0001t0012g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.20-1280C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089952 | |||||||
| chr14:74090018 | C | CT | 148 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(145): Show |
151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.20-1196dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74090018 | ||||||
| chr14:74090018 | C | CTT | 9 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0005g0297 others(6): Show |
9 | HG02071.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1197_20-1196dup others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74090018 | ||||||
| chr14:74090018 | C | CTTT | 9 | a0001c0001t0001g0191 a0001c0001t0002g0092 a0001c0001t0011g0204 others(6): Show |
9 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1198_20-1196dup others(3): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74090018 | ||||||
| chr14:74090181 | A | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-1051A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090181 | |||||||
| chr14:74090219 | A | G | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.20-1013A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090219 | |||||||
| chr14:74090246 | G | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-986G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090246 | |||||||
| chr14:74090317 | C | T | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-915C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090317 | |||||||
| chr14:74090399 | A | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-833A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090399 | |||||||
| chr14:74090428 | C | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-804C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090428 | |||||||
| chr14:74090494 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.20-738C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090494 | |||||||
| chr14:74090563 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.20-669C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090563 | |||||||
| chr14:74090689 | CTTTTTAA others(5): Show |
C | 1 | a0001c0001t0002g0073 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.20-531_20-520delAT others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74090689 | ||||||
| chr14:74090769 | G | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.20-463G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090769 | |||||||
| chr14:74090815 | A | G | 1 | a0001c0001t0003g0072 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.20-417A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090815 | |||||||
| chr14:74090866 | A | G | 5 | a0001c0001t0004g0206 a0001c0001t0004g0207 a0001c0001t0004g0208 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-366A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090866 | |||||||
| chr14:74090889 | G | T | 1 | a0001c0001t0010g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.20-343G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090889 | |||||||
| chr14:74090905 | C | T | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-327C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090905 | |||||||
| chr14:74091144 | T | C | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.20-88T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74091144 | |||||||
| chr14:74091196 | C | A | 5 | a0001c0001t0011g0221 a0001c0001t0011g0222 a0001c0001t0011g0223 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-36C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74091196 | |||||||
| chr14:74091758 | G | A | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+452G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091758 | |||||||
| chr14:74091761 | G | A | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.94+455G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091761 | |||||||
| chr14:74091764 | ACT | A | 87 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(84): Show |
87 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.94+461_94+462delCT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74091764 | ||||||
| chr14:74091767 | C | G | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.94+461C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091767 | |||||||
| chr14:74091768 | T | C | 4 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0136 others(1): Show |
4 | NA18940.hp2 NA18947.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+462T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091768 | |||||||
| chr14:74091769 | G | C | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.94+463G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091769 | |||||||
| chr14:74091772 | T | A | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.94+466T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091772 | |||||||
| chr14:74091773 | C | A | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.94+467C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091773 | |||||||
| chr14:74091773 | C | CA | 13 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0003g0008 others(10): Show |
13 | HG00597.hp1 HG00735.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+491dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74091773 | ||||||
| chr14:74091773 | CA | C | 134 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0191 others(131): Show |
136 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.94+491delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74091773 | ||||||
| chr14:74091773 | CAA | C | 41 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0093 others(38): Show |
41 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.94+490_94+491delAA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74091773 | ||||||
| chr14:74091966 | A | T | 206 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(203): Show |
208 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.94+660A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091966 | |||||||
| chr14:74092101 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.94+795G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092101 | |||||||
| chr14:74092189 | C | A | 2 | a0001c0001t0003g0013 a0001c0001t0004g0014 |
2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.94+883C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092189 | |||||||
| chr14:74092189 | C | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+883C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092189 | |||||||
| chr14:74092195 | C | T | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.94+889C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092195 | |||||||
| chr14:74092235 | G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.94+929G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092235 | |||||||
| chr14:74092281 | T | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+975T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092281 | |||||||
| chr14:74092299 | G | A | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.94+993G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092299 | |||||||
| chr14:74092299 | GTA | G | 220 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(217): Show |
222 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.94+1007_94+1008del others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74092299 | ||||||
| chr14:74092301 | A | G | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.94+995A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092301 | |||||||
| chr14:74092312 | TATG | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+1007_94+1009del others(3): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092312 | |||||||
| chr14:74092316 | T | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+1010T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092316 | |||||||
| chr14:74092328 | G | A | 12 | a0001c0001t0002g0128 a0001c0001t0002g0140 a0001c0001t0002g0142 others(9): Show |
12 | HG00408.hp1 HG02083.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+1022G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092328 | |||||||
| chr14:74092335 | C | T | 1 | a0001c0001t0014g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.94+1029C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092335 | |||||||
| chr14:74092362 | A | G | 1 | a0001c0001t0003g0012 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.94+1056A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092362 | |||||||
| chr14:74092484 | T | G | 2 | a0001c0001t0024g0229 a0001c0001t0024g0230 |
2 | HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.94+1178T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092484 | |||||||
| chr14:74092586 | G | A | 1 | a0001c0001t0045g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94+1280G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092586 | |||||||
| chr14:74092586 | G | T | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.94+1280G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092586 | |||||||
| chr14:74092645 | G | T | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.94+1339G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092645 | |||||||
| chr14:74092862 | A | G | 1 | a0002c0003t0018g0201 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94+1556A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092862 | |||||||
| chr14:74092868 | G | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.94+1562G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092868 | |||||||
| chr14:74092885 | C | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+1579C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092885 | |||||||
| chr14:74092981 | T | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+1675T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092981 | |||||||
| chr14:74093217 | A | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+1911A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093217 | |||||||
| chr14:74093321 | C | CT | 29 | a0001c0001t0001g0220 a0001c0001t0001g0265 a0001c0001t0001g0266 others(26): Show |
29 | HG00280.hp2 HG00735.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.94+2035dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74093321 | ||||||
| chr14:74093321 | CT | C | 19 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0335 others(16): Show |
19 | HG01069.hp1 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+2035delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74093321 | ||||||
| chr14:74093504 | A | G | 347 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(344): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.94+2198A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093504 | |||||||
| chr14:74093553 | A | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+2247A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093553 | |||||||
| chr14:74093623 | G | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.94+2317G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093623 | |||||||
| chr14:74093633 | A | G | 1 | a0001c0001t0027g0124 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-2315A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093633 | |||||||
| chr14:74093634 | T | C | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.95-2314T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093634 | |||||||
| chr14:74093822 | CT | C | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-2125delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093822 | |||||||
| chr14:74094003 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.95-1945C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094003 | |||||||
| chr14:74094039 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.95-1909T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094039 | |||||||
| chr14:74094125 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.95-1823C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094125 | |||||||
| chr14:74094182 | A | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG00642.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.95-1766A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094182 | |||||||
| chr14:74094258 | G | GT | 116 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(113): Show |
118 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.95-1675dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74094258 | ||||||
| chr14:74094263 | T | G | 87 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(84): Show |
87 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.95-1685T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094263 | |||||||
| chr14:74094337 | G | A | 263 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(260): Show |
266 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.95-1611G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094337 | |||||||
| chr14:74094441 | G | C | 1 | a0001c0001t0001g0338 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.95-1507G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094441 | |||||||
| chr14:74094466 | C | G | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.95-1482C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094466 | |||||||
| chr14:74094575 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.95-1373C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094575 | |||||||
| chr14:74094733 | C | CT | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.95-1203dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74094733 | ||||||
| chr14:74094776 | G | T | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-1172G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094776 | |||||||
| chr14:74094880 | G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.95-1068G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094880 | |||||||
| chr14:74094935 | C | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-1013C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094935 | |||||||
| chr14:74094985 | T | C | 7 | a0001c0001t0001g0205 a0001c0001t0001g0231 a0001c0001t0001g0234 others(4): Show |
7 | HG01081.hp2 HG01884.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-963T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094985 | |||||||
| chr14:74094986 | A | G | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-962A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094986 | |||||||
| chr14:74095058 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.95-890C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095058 | |||||||
| chr14:74095149 | G | GT | 23 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(20): Show |
23 | HG01099.hp1 HG01175.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.95-779dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74095149 | ||||||
| chr14:74095149 | G | GTT | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.95-780_95-779dupTT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74095149 | ||||||
| chr14:74095149 | G | GTTTTT | 98 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(95): Show |
100 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.95-783_95-779dupTT others(3): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74095149 | ||||||
| chr14:74095149 | G | GTTTTTT | 18 | a0001c0001t0002g0127 a0001c0001t0002g0138 a0001c0001t0002g0175 others(15): Show |
18 | HG00423.hp1 HG00642.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.95-784_95-779dupTT others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74095149 | ||||||
| chr14:74095186 | C | T | 2 | a0001c0002t0009g0283 a0001c0002t0009g0284 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.95-762C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095186 | |||||||
| chr14:74095324 | G | A | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.95-624G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095324 | |||||||
| chr14:74095678 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.95-270A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095678 | |||||||
| chr14:74095736 | C | G | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-212C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095736 | |||||||
| chr14:74095777 | T | C | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.95-171T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095777 | |||||||
| chr14:74095808 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.95-140C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095808 | |||||||
| chr14:74095838 | CTT | C | 18 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0272 others(15): Show |
18 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.95-109_95-108delTT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095838 | |||||||
| chr14:74096217 | C | T | 1 | a0001c0001t0003g0012 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.132+232C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096217 | |||||||
| chr14:74096259 | C | G | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.132+274C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096259 | |||||||
| chr14:74096342 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.132+357G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096342 | |||||||
| chr14:74096351 | C | T | 10 | a0001c0001t0002g0092 a0001c0001t0011g0204 a0001c0001t0014g0198 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+366C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096351 | |||||||
| chr14:74096467 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.132+482A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096467 | |||||||
| chr14:74096561 | T | G | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.132+576T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096561 | |||||||
| chr14:74096586 | G | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.132+601G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096586 | |||||||
| chr14:74096664 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.132+679C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096664 | |||||||
| chr14:74096874 | T | A | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.132+889T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096874 | |||||||
| chr14:74097079 | T | G | 247 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.133-715T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097079 | |||||||
| chr14:74097115 | G | A | 106 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(103): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.133-679G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097115 | |||||||
| chr14:74097327 | A | T | 1 | a0001c0001t0003g0069 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.133-467A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097327 | |||||||
| chr14:74097425 | C | CT | 81 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(78): Show |
81 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.133-351dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 74097425 | ||||||
| chr14:74097425 | CT | C | 59 | a0001c0001t0001g0239 a0001c0001t0001g0335 a0001c0001t0002g0092 others(56): Show |
61 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.133-351delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 74097425 | ||||||
| chr14:74097425 | CTT | C | 12 | a0001c0001t0004g0206 a0001c0001t0005g0301 a0001c0001t0011g0204 others(9): Show |
12 | HG01167.hp2 HG02572.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-352_133-351del others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 74097425 | ||||||
| chr14:74097425 | CTTT | C | 104 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(101): Show |
105 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.133-353_133-351del others(3): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 74097425 | ||||||
| chr14:74097461 | T | C | 61 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(58): Show |
62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.133-333T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097461 | |||||||
| chr14:74097504 | A | G | 9 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0272 others(6): Show |
9 | HG01192.hp1 HG02027.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.133-290A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097504 | |||||||
| chr14:74097582 | G | A | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.133-212G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097582 | |||||||
| chr14:74097655 | C | T | 11 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(8): Show |
11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.133-139C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097655 | |||||||
| chr14:74097688 | C | T | 1 | a0001c0001t0003g0012 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.133-106C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097688 | |||||||
| chr14:74097765 | G | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.133-29G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097765 | |||||||
| chr14:74097867 | G | A | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
splice_region_variant&intron_variant | LOW | c.199+7G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74097867 | |||||||
| chr14:74097902 | T | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.199+42T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74097902 | |||||||
| chr14:74097906 | C | A | 61 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(58): Show |
62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.199+46C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74097906 | |||||||
| chr14:74098315 | T | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.199+455T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098315 | |||||||
| chr14:74098463 | G | A | 1 | a0001c0001t0003g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.199+603G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098463 | |||||||
| chr14:74098550 | G | GT | 118 | a0001c0001t0001g0110 a0001c0001t0001g0152 a0001c0001t0001g0161 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.199+704dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74098550 | ||||||
| chr14:74098550 | G | GTT | 6 | a0001c0001t0001g0097 a0001c0001t0002g0131 a0001c0001t0002g0179 others(3): Show |
6 | HG01175.hp2 HG01981.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+703_199+704dup others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74098550 | ||||||
| chr14:74098550 | G | T | 1 | a0001c0001t0007g0099 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.199+690G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098550 | |||||||
| chr14:74098672 | C | T | 2 | a0001c0001t0007g0098 a0002c0003t0018g0201 |
2 | HG02809.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.199+812C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098672 | |||||||
| chr14:74098799 | C | T | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+939C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098799 | |||||||
| chr14:74098845 | G | A | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.199+985G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098845 | |||||||
| chr14:74098884 | A | G | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+1024A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098884 | |||||||
| chr14:74098896 | C | G | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+1036C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098896 | |||||||
| chr14:74099125 | A | G | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+1265A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099125 | |||||||
| chr14:74099234 | A | T | 73 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(70): Show |
73 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.199+1374A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099234 | |||||||
| chr14:74099280 | A | T | 1 | a0001c0001t0007g0099 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.199+1420A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099280 | |||||||
| chr14:74099288 | AC | A | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+1429delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099288 | |||||||
| chr14:74099294 | T | G | 1 | a0001c0001t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.199+1434T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099294 | |||||||
| chr14:74099586 | T | G | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.200-1569T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099586 | |||||||
| chr14:74099586 | T | TTGTGTG | 9 | a0001c0001t0002g0192 a0001c0001t0011g0204 a0001c0001t0014g0198 others(6): Show |
9 | HG01109.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.200-1551_200-1546d others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74099586 | ||||||
| chr14:74099586 | T | TTGTGTGT others(1): Show |
93 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.200-1553_200-1546d others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74099586 | ||||||
| chr14:74099586 | T | TTGTGTGT others(3): Show |
13 | a0001c0001t0002g0001 a0001c0001t0002g0093 a0001c0001t0002g0170 others(10): Show |
15 | HG02451.hp2 HG02698.hp1 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.200-1555_200-1546d others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74099586 | ||||||
| chr14:74099586 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0002g0173 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.200-1557_200-1546d others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74099586 | ||||||
| chr14:74099586 | TTG | T | 14 | a0001c0001t0001g0214 a0001c0001t0001g0240 a0001c0001t0004g0077 others(11): Show |
14 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.200-1547_200-1546d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74099586 | ||||||
| chr14:74099691 | G | A | 29 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0007g0004 others(26): Show |
29 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.200-1464G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099691 | |||||||
| chr14:74099719 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.200-1436G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099719 | |||||||
| chr14:74099994 | T | C | 1 | a0001c0001t0011g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.200-1161T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099994 | |||||||
| chr14:74100241 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.200-914G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100241 | |||||||
| chr14:74100574 | C | A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0016g0010 |
3 | NA18975.hp2 NA18988.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.200-581C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100574 | |||||||
| chr14:74100624 | T | C | 247 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.200-531T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100624 | |||||||
| chr14:74100664 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.200-491C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100664 | |||||||
| chr14:74100712 | G | C | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.200-443G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100712 | |||||||
| chr14:74100785 | C | T | 263 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(260): Show |
266 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.200-370C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100785 | |||||||
| chr14:74101033 | T | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.200-122T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74101033 | |||||||
| chr14:74101148 | G | A | 6 | a0001c0001t0012g0081 a0001c0001t0012g0083 a0001c0001t0021g0079 others(3): Show |
6 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.200-7G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74101148 | |||||||
| chr14:74101249 | C | T | 61 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(58): Show |
62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+11C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101249 | |||||||
| chr14:74101386 | A | G | 3 | a0001c0001t0003g0015 a0001c0001t0004g0066 a0001c0001t0004g0067 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.283+148A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101386 | |||||||
| chr14:74101460 | C | CT | 15 | a0001c0001t0001g0292 a0001c0001t0003g0064 a0001c0001t0003g0065 others(12): Show |
15 | HG00673.hp2 HG01109.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+238dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74101460 | ||||||
| chr14:74101460 | CT | C | 115 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.283+238delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74101460 | ||||||
| chr14:74101520 | G | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+282G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101520 | |||||||
| chr14:74101602 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG00280.hp2 HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.283+364G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101602 | |||||||
| chr14:74101607 | C | T | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+369C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101607 | |||||||
| chr14:74101650 | C | T | 1 | a0001c0001t0008g0331 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.283+412C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101650 | |||||||
| chr14:74101661 | C | T | 3 | a0001c0001t0005g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 |
3 | HG01123.hp2 HG01261.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.283+423C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101661 | |||||||
| chr14:74101672 | G | T | 1 | a0001c0001t0002g0177 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.283+434G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101672 | |||||||
| chr14:74101679 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.283+441C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101679 | |||||||
| chr14:74101708 | C | T | 1 | a0001c0002t0032g0285 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.283+470C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101708 | |||||||
| chr14:74101824 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+586G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101824 | |||||||
| chr14:74102045 | G | A | 106 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(103): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+807G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102045 | |||||||
| chr14:74102289 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.283+1051C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102289 | |||||||
| chr14:74102384 | A | G | 1 | a0001c0001t0011g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.283+1146A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102384 | |||||||
| chr14:74102858 | T | C | 2 | a0001c0002t0009g0283 a0001c0002t0009g0284 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.283+1620T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102858 | |||||||
| chr14:74102870 | T | C | 61 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(58): Show |
62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+1632T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102870 | |||||||
| chr14:74102890 | A | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+1652A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102890 | |||||||
| chr14:74102942 | C | T | 10 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(7): Show |
10 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+1704C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102942 | |||||||
| chr14:74102942 | CAT | C | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+1708_283+1709d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74102942 | ||||||
| chr14:74103024 | C | T | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+1786C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103024 | |||||||
| chr14:74103166 | T | C | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+1928T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103166 | |||||||
| chr14:74103178 | A | G | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+1940A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103178 | |||||||
| chr14:74103427 | A | AT | 6 | a0001c0001t0002g0073 a0001c0001t0004g0014 a0001c0001t0004g0021 others(3): Show |
6 | HG00597.hp2 HG01928.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+2211dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103427 | ||||||
| chr14:74103427 | AT | A | 193 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0161 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.283+2211delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103427 | ||||||
| chr14:74103427 | ATT | A | 20 | a0001c0001t0001g0152 a0001c0001t0001g0265 a0001c0001t0001g0273 others(17): Show |
21 | HG01069.hp2 HG01074.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.283+2210_283+2211d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103427 | ||||||
| chr14:74103427 | ATTTTTTT others(6): Show |
A | 24 | a0001c0001t0005g0303 a0001c0001t0005g0304 a0001c0001t0005g0305 others(21): Show |
25 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.283+2199_283+2211d others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103427 | ||||||
| chr14:74103487 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.283+2249C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103487 | |||||||
| chr14:74103506 | T | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+2268T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103506 | |||||||
| chr14:74103558 | G | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+2320G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103558 | |||||||
| chr14:74103564 | C | G | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+2326C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103564 | |||||||
| chr14:74103589 | G | A | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+2351G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103589 | |||||||
| chr14:74103651 | T | C | 196 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(193): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.283+2413T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103651 | |||||||
| chr14:74103684 | C | T | 2 | a0001c0001t0002g0166 a0001c0001t0006g0167 |
2 | NA18956.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.283+2446C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103684 | |||||||
| chr14:74103733 | G | GT | 17 | a0001c0001t0001g0228 a0001c0001t0001g0256 a0001c0001t0001g0257 others(14): Show |
17 | HG01099.hp1 HG01123.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+2531dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | G | GTT | 10 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0258 others(7): Show |
10 | HG01175.hp1 HG01192.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+2530_283+2531d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GT | G | 22 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(19): Show |
22 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+2531delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTT | G | 6 | a0001c0001t0001g0205 a0001c0001t0001g0232 a0001c0001t0001g0234 others(3): Show |
6 | HG01081.hp2 HG01884.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+2530_283+2531d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTTT | G | 6 | a0001c0001t0002g0277 a0001c0001t0003g0013 a0001c0001t0003g0059 others(3): Show |
6 | HG00323.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+2529_283+2531d others(5): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTTTTT | G | 20 | a0001c0001t0002g0276 a0001c0001t0003g0012 a0001c0001t0003g0053 others(17): Show |
20 | HG00438.hp2 HG00597.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.283+2527_283+2531d others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTTTTTT | G | 85 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(82): Show |
86 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.283+2526_283+2531d others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTTTTTTT | G | 19 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0019 others(16): Show |
19 | HG01069.hp1 HG01123.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.283+2525_283+2531d others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTTTTTTT others(1): Show |
G | 6 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(3): Show |
6 | HG01109.hp2 HG02809.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+2524_283+2531d others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTTTTTTT others(3): Show |
G | 16 | a0001c0001t0002g0092 a0001c0001t0002g0127 a0001c0001t0002g0129 others(13): Show |
16 | HG01981.hp2 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.283+2522_283+2531d others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTTTTTTT others(4): Show |
G | 62 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0191 others(59): Show |
63 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.283+2521_283+2531d others(13): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTTTTTTT others(5): Show |
G | 35 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(32): Show |
36 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.283+2520_283+2531d others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTTTTTTT others(6): Show |
G | 3 | a0001c0001t0001g0213 a0001c0001t0007g0105 a0001c0001t0007g0121 |
3 | HG02027.hp2 HG02132.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.283+2519_283+2531d others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103733 | GTTTTTTT others(7): Show |
G | 8 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0241 others(5): Show |
8 | NA18947.hp2 NA18962.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+2518_283+2531d others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | ||||||
| chr14:74103748 | T | G | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+2510T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103748 | |||||||
| chr14:74103896 | C | CT | 13 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(10): Show |
13 | HG01109.hp2 HG01169.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.283+2672dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103896 | ||||||
| chr14:74104017 | G | T | 3 | a0001c0001t0011g0222 a0001c0001t0011g0223 a0001c0001t0011g0224 |
3 | HG01891.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.283+2779G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104017 | |||||||
| chr14:74104173 | A | G | 1 | a0001c0001t0004g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.283+2935A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104173 | |||||||
| chr14:74104220 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.283+2982A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104220 | |||||||
| chr14:74104247 | C | A | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+3009C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104247 | |||||||
| chr14:74104319 | A | G | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.283+3081A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104319 | |||||||
| chr14:74104355 | C | G | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+3117C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104355 | |||||||
| chr14:74104576 | A | G | 1 | a0001c0001t0004g0020 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.283+3338A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104576 | |||||||
| chr14:74104588 | T | G | 2 | a0001c0001t0006g0156 a0001c0001t0033g0182 |
2 | HG02071.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.283+3350T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104588 | |||||||
| chr14:74104591 | A | AT | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+3365dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74104591 | ||||||
| chr14:74104670 | A | T | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+3432A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104670 | |||||||
| chr14:74104699 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.283+3461G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104699 | |||||||
| chr14:74104813 | C | T | 347 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(344): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.283+3575C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104813 | |||||||
| chr14:74104823 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.283+3585G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104823 | |||||||
| chr14:74105085 | TATTA | T | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+3848_283+3851d others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105085 | |||||||
| chr14:74105104 | G | C | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.283+3866G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105104 | |||||||
| chr14:74105161 | A | G | 2 | a0001c0001t0003g0013 a0001c0001t0004g0014 |
2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.283+3923A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105161 | |||||||
| chr14:74105171 | G | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+3933G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105171 | |||||||
| chr14:74105395 | C | A | 247 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.283+4157C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105395 | |||||||
| chr14:74105578 | AT | A | 204 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(201): Show |
206 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.283+4353delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74105578 | ||||||
| chr14:74105578 | ATT | A | 43 | a0001c0001t0003g0007 a0001c0001t0003g0323 a0001c0001t0005g0295 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.283+4352_283+4353d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74105578 | ||||||
| chr14:74105657 | A | G | 263 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(260): Show |
266 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.283+4419A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105657 | |||||||
| chr14:74105719 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+4481G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105719 | |||||||
| chr14:74105801 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.283+4563T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105801 | |||||||
| chr14:74105984 | A | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+4746A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105984 | |||||||
| chr14:74106080 | T | C | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+4842T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106080 | |||||||
| chr14:74106312 | C | G | 1 | a0001c0001t0005g0315 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.283+5074C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106312 | |||||||
| chr14:74106356 | A | G | 1 | a0001c0001t0003g0017 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.283+5118A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106356 | |||||||
| chr14:74106725 | A | C | 1 | a0001c0001t0003g0052 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.283+5487A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106725 | |||||||
| chr14:74106887 | G | A | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+5649G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106887 | |||||||
| chr14:74106981 | G | A | 2 | a0001c0001t0002g0192 a0001c0001t0015g0185 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.283+5743G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106981 | |||||||
| chr14:74107019 | A | G | 247 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.283+5781A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107019 | |||||||
| chr14:74107076 | T | C | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+5838T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107076 | |||||||
| chr14:74107267 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.283+6029A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107267 | |||||||
| chr14:74107442 | C | G | 1 | a0001c0001t0006g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.283+6204C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107442 | |||||||
| chr14:74107452 | G | A | 1 | a0001c0001t0002g0276 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+6214G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107452 | |||||||
| chr14:74107460 | G | A | 105 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(102): Show |
106 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.283+6222G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107460 | |||||||
| chr14:74107460 | G | C | 1 | a0001c0001t0002g0148 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.283+6222G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107460 | |||||||
| chr14:74107534 | T | A | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+6296T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107534 | |||||||
| chr14:74107538 | G | A | 1 | a0001c0001t0017g0322 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.283+6300G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107538 | |||||||
| chr14:74107583 | G | A | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+6345G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107583 | |||||||
| chr14:74107682 | T | C | 3 | a0001c0001t0003g0023 a0001c0001t0003g0053 a0001c0001t0003g0054 |
3 | HG00423.hp2 HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.283+6444T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107682 | |||||||
| chr14:74107702 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+6464A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107702 | |||||||
| chr14:74107712 | G | A | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+6474G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107712 | |||||||
| chr14:74107858 | G | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+6620G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107858 | |||||||
| chr14:74108062 | C | A | 5 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0251 others(2): Show |
5 | HG00639.hp1 HG01261.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+6824C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108062 | |||||||
| chr14:74108202 | GCTTT | G | 4 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0263 others(1): Show |
4 | HG00099.hp1 HG00642.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+6973_283+6976d others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74108202 | ||||||
| chr14:74108262 | A | G | 1 | a0001c0001t0005g0315 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.283+7024A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108262 | |||||||
| chr14:74108349 | A | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+7111A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108349 | |||||||
| chr14:74108368 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+7130C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108368 | |||||||
| chr14:74108554 | T | C | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+7316T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108554 | |||||||
| chr14:74108610 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.283+7372A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108610 | |||||||
| chr14:74108672 | T | C | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+7434T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108672 | |||||||
| chr14:74109004 | G | A | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+7766G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109004 | |||||||
| chr14:74109017 | A | G | 1 | a0001c0001t0006g0169 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.283+7779A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109017 | |||||||
| chr14:74109070 | T | C | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+7832T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109070 | |||||||
| chr14:74109345 | A | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+8107A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109345 | |||||||
| chr14:74109414 | C | T | 1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+8176C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109414 | |||||||
| chr14:74109488 | C | T | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+8250C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109488 | |||||||
| chr14:74109694 | T | C | 1 | a0001c0001t0036g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.283+8456T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109694 | |||||||
| chr14:74109720 | T | C | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+8482T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109720 | |||||||
| chr14:74110041 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.283+8803A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110041 | |||||||
| chr14:74110110 | T | C | 82 | a0001c0001t0001g0205 a0001c0001t0001g0231 a0001c0001t0001g0234 others(79): Show |
82 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.283+8872T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110110 | |||||||
| chr14:74110299 | A | T | 1 | a0001c0001t0017g0314 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.283+9061A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110299 | |||||||
| chr14:74110363 | A | C | 1 | a0001c0001t0002g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283+9125A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110363 | |||||||
| chr14:74110610 | C | T | 3 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0034g0119 |
3 | HG01074.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.283+9372C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110610 | |||||||
| chr14:74110884 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.283+9646T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110884 | |||||||
| chr14:74110897 | T | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+9659T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110897 | |||||||
| chr14:74110898 | G | A | 10 | a0001c0001t0002g0092 a0001c0001t0011g0204 a0001c0001t0014g0198 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+9660G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110898 | |||||||
| chr14:74110920 | C | T | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+9682C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110920 | |||||||
| chr14:74110923 | G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+9685G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110923 | |||||||
| chr14:74110938 | C | A | 1 | a0001c0001t0002g0276 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+9700C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110938 | |||||||
| chr14:74110994 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+9756C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110994 | |||||||
| chr14:74111058 | A | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+9820A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111058 | |||||||
| chr14:74111131 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+9893C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111131 | |||||||
| chr14:74111408 | C | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+10170C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111408 | |||||||
| chr14:74111414 | G | A | 3 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.283+10176G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111414 | |||||||
| chr14:74111414 | G | C | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+10176G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111414 | |||||||
| chr14:74111444 | A | G | 4 | a0001c0001t0013g0094 a0001c0001t0013g0120 a0001c0001t0013g0125 others(1): Show |
4 | HG02602.hp2 HG03688.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+10206A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111444 | |||||||
| chr14:74111455 | AT | A | 117 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(114): Show |
119 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.283+10232delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111455 | ||||||
| chr14:74111455 | ATT | A | 130 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(127): Show |
131 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.283+10231_283+1023 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111455 | ||||||
| chr14:74111508 | C | T | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.283+10270C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111508 | |||||||
| chr14:74111535 | C | T | 1 | a0001c0001t0016g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.283+10297C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111535 | |||||||
| chr14:74111594 | G | A | 1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+10356G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111594 | |||||||
| chr14:74111606 | G | GTATT | 31 | a0001c0001t0001g0218 a0001c0001t0001g0227 a0001c0001t0001g0241 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.283+10410_283+1041 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | ||||||
| chr14:74111606 | G | GTATTTAT others(1): Show |
50 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0002g0276 others(47): Show |
50 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.283+10406_283+1041 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | ||||||
| chr14:74111606 | G | GTATTTAT others(5): Show |
4 | a0001c0001t0003g0015 a0001c0001t0003g0074 a0001c0001t0004g0066 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+10402_283+1041 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | ||||||
| chr14:74111606 | GTATT | G | 54 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(51): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.283+10410_283+1041 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | ||||||
| chr14:74111606 | GTATTTAT others(1): Show |
G | 92 | a0001c0001t0001g0161 a0001c0001t0002g0093 a0001c0001t0002g0127 others(89): Show |
93 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.283+10406_283+1041 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | ||||||
| chr14:74111606 | GTATTTAT others(5): Show |
G | 12 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(9): Show |
12 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+10402_283+1041 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | ||||||
| chr14:74111664 | A | G | 3 | a0001c0001t0003g0015 a0001c0001t0004g0066 a0001c0001t0004g0067 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.283+10426A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111664 | |||||||
| chr14:74111707 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+10469C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111707 | |||||||
| chr14:74111796 | T | C | 3 | a0001c0001t0002g0001 a0001c0001t0002g0170 a0001c0001t0006g0178 |
4 | NA18963.hp2 NA18971.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+10558T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111796 | |||||||
| chr14:74111867 | TTTTTTTT others(1): Show |
T | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+10645_283+1065 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111867 | ||||||
| chr14:74111914 | C | T | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+10676C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111914 | |||||||
| chr14:74111938 | T | C | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+10700T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111938 | |||||||
| chr14:74111941 | C | T | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+10703C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111941 | |||||||
| chr14:74111957 | C | T | 3 | a0001c0001t0003g0023 a0001c0001t0003g0053 a0001c0001t0003g0054 |
3 | HG00423.hp2 HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.283+10719C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111957 | |||||||
| chr14:74111974 | T | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+10736T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111974 | |||||||
| chr14:74112127 | A | T | 1 | a0001c0001t0007g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.283+10889A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112127 | |||||||
| chr14:74112266 | A | G | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+11028A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112266 | |||||||
| chr14:74112290 | T | A | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+11052T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112290 | |||||||
| chr14:74112333 | G | A | 1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+11095G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112333 | |||||||
| chr14:74112376 | C | T | 8 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(5): Show |
9 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+11138C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112376 | |||||||
| chr14:74112621 | G | A | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+11383G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112621 | |||||||
| chr14:74112635 | C | G | 1 | a0001c0001t0003g0038 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.283+11397C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112635 | |||||||
| chr14:74112766 | T | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+11528T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112766 | |||||||
| chr14:74112919 | A | G | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+11681A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112919 | |||||||
| chr14:74113025 | A | AGAG | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+11788_283+1179 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74113025 | ||||||
| chr14:74113264 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283+12026C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74113264 | |||||||
| chr14:74113403 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.283+12165A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74113403 | |||||||
| chr14:74113457 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0015g0090 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+12219G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74113457 | |||||||
| chr14:74113694 | T | A | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+12456T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74113694 | |||||||
| chr14:74113868 | G | A | 72 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(69): Show |
72 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.283+12630G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74113868 | |||||||
| chr14:74113970 | C | CT | 40 | a0001c0001t0001g0213 a0001c0001t0001g0237 a0001c0001t0001g0255 others(37): Show |
40 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.283+12742dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74113970 | ||||||
| chr14:74114174 | T | TTG | 8 | a0001c0001t0012g0086 a0001c0001t0025g0087 a0001c0002t0009g0278 others(5): Show |
8 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+12936_283+1293 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114174 | |||||||
| chr14:74114174 | T | TTGTGTG | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+12936_283+1293 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114174 | |||||||
| chr14:74114174 | TAG | T | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+12937_283+1293 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114174 | |||||||
| chr14:74114175 | A | AGT | 34 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0341 others(31): Show |
34 | HG00423.hp1 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+12974_283+1297 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114175 | A | AGTGT | 35 | a0001c0001t0001g0205 a0001c0001t0001g0231 a0001c0001t0001g0236 others(32): Show |
36 | HG00438.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.283+12972_283+1297 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114175 | A | AGTGTGT | 31 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0213 others(28): Show |
31 | HG00741.hp2 HG01175.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.283+12970_283+1297 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114175 | A | AGTGTGTG others(1): Show |
16 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0007 others(13): Show |
16 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.283+12968_283+1297 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114175 | A | AGTGTGTG others(3): Show |
41 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(38): Show |
41 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.283+12966_283+1297 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114175 | A | AGTGTGTG others(5): Show |
9 | a0001c0001t0003g0012 a0001c0001t0003g0033 a0001c0001t0003g0034 others(6): Show |
9 | HG00408.hp2 HG00673.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+12964_283+1297 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114175 | A | AGTGTGTG others(7): Show |
2 | a0001c0001t0003g0068 a0001c0001t0003g0088 |
2 | HG03017.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.283+12962_283+1297 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114175 | A | AGTGTGTG others(9): Show |
2 | a0001c0001t0001g0152 a0001c0001t0016g0051 |
2 | HG01069.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.283+12960_283+1297 others(20): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114175 | A | T | 13 | a0001c0001t0011g0204 a0001c0001t0012g0086 a0001c0001t0014g0203 others(10): Show |
13 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.283+12937A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114175 | |||||||
| chr14:74114175 | AGT | A | 49 | a0001c0001t0001g0233 a0001c0001t0001g0255 a0001c0001t0001g0339 others(46): Show |
50 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.283+12974_283+1297 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114175 | AGTGT | A | 42 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.283+12972_283+1297 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114175 | AGTGTGT | A | 6 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0001g0291 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+12970_283+1297 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | ||||||
| chr14:74114492 | G | A | 1 | a0001c0001t0042g0302 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.283+13254G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114492 | |||||||
| chr14:74114510 | C | A | 1 | a0001c0001t0019g0141 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.283+13272C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114510 | |||||||
| chr14:74114511 | G | A | 2 | a0001c0001t0003g0053 a0001c0001t0006g0156 |
2 | HG02071.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.283+13273G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114511 | |||||||
| chr14:74114534 | AC | A | 5 | a0001c0001t0011g0221 a0001c0001t0011g0222 a0001c0001t0011g0223 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+13298delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114534 | ||||||
| chr14:74114593 | T | TAAC | 6 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+13373_283+1337 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114593 | ||||||
| chr14:74114603 | A | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+13365A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114603 | |||||||
| chr14:74114818 | G | A | 268 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(265): Show |
271 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.283+13580G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114818 | |||||||
| chr14:74115010 | A | C | 1 | a0001c0001t0014g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.283+13772A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115010 | |||||||
| chr14:74115146 | A | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+13908A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115146 | |||||||
| chr14:74115451 | A | T | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+14213A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115451 | |||||||
| chr14:74115459 | G | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+14221G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115459 | |||||||
| chr14:74115476 | CTG | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+14242_283+1424 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74115476 | ||||||
| chr14:74115666 | A | G | 7 | a0001c0001t0005g0295 a0001c0001t0005g0300 a0001c0001t0005g0301 others(4): Show |
7 | NA18967.hp1 NA19003.hp1 NA19010.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+14428A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115666 | |||||||
| chr14:74115693 | A | G | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+14455A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115693 | |||||||
| chr14:74115803 | C | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+14565C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115803 | |||||||
| chr14:74115826 | C | T | 1 | a0001c0001t0004g0026 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.283+14588C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115826 | |||||||
| chr14:74116004 | G | A | 263 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(260): Show |
266 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.283+14766G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116004 | |||||||
| chr14:74116018 | A | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0272 a0001c0001t0018g0271 |
3 | HG02027.hp2 NA18944.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.283+14780A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116018 | |||||||
| chr14:74116092 | T | C | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+14854T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116092 | |||||||
| chr14:74116192 | A | G | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+14954A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116192 | |||||||
| chr14:74116302 | CAAAAAAT | C | 26 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0007g0004 others(23): Show |
26 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.283+15078_283+1508 others(11): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74116302 | ||||||
| chr14:74116309 | TAAAAAA | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+15072_283+1507 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116309 | |||||||
| chr14:74116435 | G | C | 2 | a0001c0001t0011g0223 a0001c0001t0011g0224 |
2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.283+15197G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116435 | |||||||
| chr14:74116774 | A | G | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+15536A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116774 | |||||||
| chr14:74116790 | G | A | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+15552G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116790 | |||||||
| chr14:74116830 | G | GT | 7 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(4): Show |
7 | HG02559.hp1 HG02738.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+15607dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74116830 | ||||||
| chr14:74116835 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.283+15597T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116835 | |||||||
| chr14:74116846 | C | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+15608C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116846 | |||||||
| chr14:74117128 | T | C | 1 | a0001c0001t0006g0167 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.283+15890T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117128 | |||||||
| chr14:74117469 | A | AT | 13 | a0001c0001t0002g0177 a0001c0001t0008g0296 a0001c0001t0013g0120 others(10): Show |
14 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+16234dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74117469 | ||||||
| chr14:74117473 | C | T | 347 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(344): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.283+16235C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117473 | |||||||
| chr14:74117491 | GC | G | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+16254delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117491 | |||||||
| chr14:74117789 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.283+16551A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117789 | |||||||
| chr14:74117855 | A | C | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+16617A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117855 | |||||||
| chr14:74117868 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283+16630A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117868 | |||||||
| chr14:74117927 | CA | C | 61 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(58): Show |
62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+16697delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74117927 | ||||||
| chr14:74118055 | C | G | 247 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.283+16817C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118055 | |||||||
| chr14:74118120 | G | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+16882G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118120 | |||||||
| chr14:74118225 | C | T | 1 | a0001c0001t0007g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.283+16987C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118225 | |||||||
| chr14:74118234 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+16996C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118234 | |||||||
| chr14:74118399 | G | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+17161G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118399 | |||||||
| chr14:74118614 | A | G | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283+17376A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118614 | |||||||
| chr14:74118874 | C | T | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+17636C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118874 | |||||||
| chr14:74118949 | A | ACTT | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+17712_283+1771 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74118949 | ||||||
| chr14:74119160 | C | CT | 81 | a0001c0001t0001g0226 a0001c0001t0001g0239 a0001c0001t0001g0342 others(78): Show |
81 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.283+17941dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119160 | ||||||
| chr14:74119160 | CT | C | 167 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(164): Show |
170 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.283+17941delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119160 | ||||||
| chr14:74119164 | T | C | 7 | a0001c0001t0001g0205 a0001c0001t0001g0231 a0001c0001t0001g0234 others(4): Show |
7 | HG01081.hp2 HG01884.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+17926T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119164 | |||||||
| chr14:74119247 | C | T | 1 | a0001c0001t0004g0044 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.283+18009C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119247 | |||||||
| chr14:74119286 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+18048C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119286 | |||||||
| chr14:74119307 | GC | G | 40 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(37): Show |
41 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.283+18076delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119307 | ||||||
| chr14:74119314 | C | G | 1 | a0001c0001t0025g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.283+18076C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119314 | |||||||
| chr14:74119329 | A | AT | 5 | a0001c0001t0011g0221 a0001c0001t0011g0222 a0001c0001t0011g0223 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+18099dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119329 | ||||||
| chr14:74119355 | A | G | 1 | a0001c0001t0005g0320 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.283+18117A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119355 | |||||||
| chr14:74119374 | T | C | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+18136T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119374 | |||||||
| chr14:74119407 | G | T | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+18169G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119407 | |||||||
| chr14:74119573 | A | G | 14 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(11): Show |
14 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+18335A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119573 | |||||||
| chr14:74119665 | G | A | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+18427G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119665 | |||||||
| chr14:74119836 | C | CT | 20 | a0001c0001t0001g0239 a0001c0001t0001g0335 a0001c0001t0002g0092 others(17): Show |
20 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.283+18615dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119836 | ||||||
| chr14:74119836 | CT | C | 6 | a0001c0001t0001g0242 a0001c0001t0002g0175 a0001c0001t0003g0046 others(3): Show |
6 | HG01167.hp1 HG01168.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+18615delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119836 | ||||||
| chr14:74119969 | G | A | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+18731G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119969 | |||||||
| chr14:74119984 | C | A | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+18746C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119984 | |||||||
| chr14:74119984 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+18746C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119984 | |||||||
| chr14:74120307 | G | C | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+19069G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120307 | |||||||
| chr14:74120354 | C | T | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+19116C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120354 | |||||||
| chr14:74120376 | C | T | 268 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(265): Show |
271 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.283+19138C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120376 | |||||||
| chr14:74120472 | AGGCCAGG others(1): Show |
A | 11 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(8): Show |
11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+19236_283+1924 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74120472 | ||||||
| chr14:74120481 | G | T | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+19243G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120481 | |||||||
| chr14:74120612 | G | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+19374G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120612 | |||||||
| chr14:74120687 | G | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+19449G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120687 | |||||||
| chr14:74120703 | C | T | 22 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0022 others(19): Show |
22 | HG00438.hp2 HG00544.hp2 NA18940.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+19465C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120703 | |||||||
| chr14:74120754 | C | CA | 80 | a0001c0001t0001g0248 a0001c0001t0002g0027 a0001c0001t0002g0073 others(77): Show |
80 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.283+19534dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74120754 | ||||||
| chr14:74120781 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG02559.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.283+19543G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120781 | |||||||
| chr14:74120795 | G | A | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.283+19557G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120795 | |||||||
| chr14:74120913 | G | GA | 14 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(11): Show |
14 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+19685dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74120913 | ||||||
| chr14:74121403 | A | G | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+20165A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121403 | |||||||
| chr14:74121445 | T | C | 10 | a0001c0001t0002g0092 a0001c0001t0011g0204 a0001c0001t0014g0198 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+20207T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121445 | |||||||
| chr14:74121470 | C | T | 247 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.283+20232C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121470 | |||||||
| chr14:74121530 | G | A | 5 | a0001c0001t0005g0303 a0001c0001t0005g0304 a0001c0001t0005g0305 others(2): Show |
5 | HG02129.hp2 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+20292G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121530 | |||||||
| chr14:74121575 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.283+20337G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121575 | |||||||
| chr14:74121653 | T | G | 247 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.283+20415T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121653 | |||||||
| chr14:74121725 | CT | C | 237 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(234): Show |
240 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.283+20503delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74121725 | ||||||
| chr14:74121725 | CTT | C | 8 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(5): Show |
8 | HG02258.hp1 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+20502_283+2050 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74121725 | ||||||
| chr14:74121747 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.283+20509G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121747 | |||||||
| chr14:74121805 | C | T | 2 | a0001c0002t0009g0283 a0001c0002t0009g0284 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.283+20567C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121805 | |||||||
| chr14:74121816 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+20578C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121816 | |||||||
| chr14:74121851 | A | G | 268 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(265): Show |
271 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.283+20613A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121851 | |||||||
| chr14:74121869 | G | A | 63 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(60): Show |
65 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.283+20631G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121869 | |||||||
| chr14:74121895 | G | A | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+20657G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121895 | |||||||
| chr14:74122003 | CTCATAT | C | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+20768_283+2077 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74122003 | ||||||
| chr14:74122015 | T | TGAG | 206 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(203): Show |
208 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.283+20778_283+2078 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74122015 | ||||||
| chr14:74122115 | C | G | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+20877C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122115 | |||||||
| chr14:74122153 | C | T | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+20915C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122153 | |||||||
| chr14:74122284 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+21046C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122284 | |||||||
| chr14:74122299 | C | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+21061C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122299 | |||||||
| chr14:74122537 | G | C | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0006g0194 |
3 | HG01496.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.283+21299G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122537 | |||||||
| chr14:74122741 | C | G | 106 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(103): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+21503C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122741 | |||||||
| chr14:74122742 | T | C | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+21504T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122742 | |||||||
| chr14:74122877 | A | G | 1 | a0001c0001t0007g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.283+21639A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122877 | |||||||
| chr14:74122884 | CAAACAA | C | 108 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(105): Show |
110 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.283+21663_283+2166 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74122884 | ||||||
| chr14:74122901 | A | AAAAAC | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+21664_283+2166 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74122901 | ||||||
| chr14:74122943 | C | T | 130 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(127): Show |
132 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.283+21705C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122943 | |||||||
| chr14:74122999 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.283+21761G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122999 | |||||||
| chr14:74123100 | T | A | 2 | a0001c0002t0009g0283 a0001c0002t0009g0284 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.283+21862T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123100 | |||||||
| chr14:74123328 | A | C | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+22090A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123328 | |||||||
| chr14:74123374 | C | T | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+22136C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123374 | |||||||
| chr14:74123527 | T | C | 61 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(58): Show |
62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+22289T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123527 | |||||||
| chr14:74123664 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+22426C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123664 | |||||||
| chr14:74123668 | G | A | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+22430G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123668 | |||||||
| chr14:74123672 | T | C | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+22434T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123672 | |||||||
| chr14:74123680 | A | G | 2 | a0001c0001t0004g0206 a0001c0001t0012g0209 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.283+22442A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123680 | |||||||
| chr14:74123782 | G | C | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+22544G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123782 | |||||||
| chr14:74123789 | G | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+22551G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123789 | |||||||
| chr14:74123843 | T | C | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283+22605T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123843 | |||||||
| chr14:74123890 | A | G | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+22652A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123890 | |||||||
| chr14:74123972 | G | T | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+22734G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123972 | |||||||
| chr14:74124065 | A | T | 4 | a0001c0001t0011g0221 a0001c0001t0011g0222 a0001c0001t0011g0223 others(1): Show |
4 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+22827A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124065 | |||||||
| chr14:74124098 | A | G | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+22860A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124098 | |||||||
| chr14:74124119 | G | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+22881G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124119 | |||||||
| chr14:74124292 | C | G | 1 | a0001c0001t0013g0111 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.283+23054C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124292 | |||||||
| chr14:74124517 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.283+23279T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124517 | |||||||
| chr14:74124538 | T | C | 247 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.283+23300T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124538 | |||||||
| chr14:74124637 | C | G | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+23399C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124637 | |||||||
| chr14:74124684 | C | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+23446C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124684 | |||||||
| chr14:74124810 | C | CA | 8 | a0001c0001t0001g0227 a0001c0001t0001g0231 a0001c0001t0001g0346 others(5): Show |
8 | HG00438.hp2 HG01123.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+23595dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | ||||||
| chr14:74124810 | C | CAAAA | 11 | a0001c0001t0002g0146 a0001c0001t0002g0177 a0001c0001t0006g0165 others(8): Show |
11 | HG00673.hp1 HG02145.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+23592_283+2359 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | ||||||
| chr14:74124810 | C | CAAAAA | 53 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0191 others(50): Show |
54 | HG00408.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.283+23591_283+2359 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | ||||||
| chr14:74124810 | C | CAAAAAA | 29 | a0001c0001t0002g0118 a0001c0001t0002g0127 a0001c0001t0002g0131 others(26): Show |
30 | HG00099.hp2 HG00423.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.283+23590_283+2359 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | ||||||
| chr14:74124810 | C | CAAAAAAA | 16 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(13): Show |
16 | HG00438.hp1 HG00544.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.283+23589_283+2359 others(11): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | ||||||
| chr14:74124810 | CA | C | 57 | a0001c0001t0001g0248 a0001c0001t0002g0276 a0001c0001t0002g0277 others(54): Show |
58 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.283+23595delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | ||||||
| chr14:74125321 | A | G | 76 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(73): Show |
76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+24083A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125321 | |||||||
| chr14:74125515 | C | A | 263 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(260): Show |
266 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.283+24277C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125515 | |||||||
| chr14:74125575 | A | G | 106 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(103): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+24337A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125575 | |||||||
| chr14:74125601 | C | G | 1 | a0001c0001t0005g0297 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.283+24363C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125601 | |||||||
| chr14:74125674 | G | A | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+24436G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125674 | |||||||
| chr14:74125729 | T | C | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.283+24491T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125729 | |||||||
| chr14:74125804 | C | T | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+24566C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125804 | |||||||
| chr14:74125861 | G | A | 3 | a0001c0001t0003g0008 a0001c0001t0003g0018 a0001c0001t0004g0009 |
3 | HG00597.hp1 HG02083.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.283+24623G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125861 | |||||||
| chr14:74126036 | T | TA | 166 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(163): Show |
168 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.283+24812dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74126036 | ||||||
| chr14:74126047 | AAAAG | A | 57 | a0001c0001t0001g0152 a0001c0001t0002g0001 a0001c0001t0002g0127 others(54): Show |
58 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.283+24813_283+2481 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74126047 | ||||||
| chr14:74126050 | AGAAAT | A | 4 | a0001c0001t0001g0161 a0001c0001t0002g0093 a0001c0001t0002g0157 others(1): Show |
4 | HG01516.hp1 HG02071.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+24815_283+2481 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74126050 | ||||||
| chr14:74126055 | T | A | 57 | a0001c0001t0001g0152 a0001c0001t0002g0001 a0001c0001t0002g0127 others(54): Show |
58 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.283+24817T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126055 | |||||||
| chr14:74126137 | T | C | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+24899T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126137 | |||||||
| chr14:74126227 | C | G | 12 | a0001c0001t0002g0092 a0001c0001t0011g0204 a0001c0001t0014g0198 others(9): Show |
13 | HG02145.hp2 HG02451.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+24989C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126227 | |||||||
| chr14:74126240 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+25002G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126240 | |||||||
| chr14:74126303 | A | G | 2 | a0001c0001t0003g0054 a0001c0001t0042g0302 |
2 | HG01167.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.283+25065A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126303 | |||||||
| chr14:74126338 | G | C | 7 | a0001c0001t0008g0296 a0001c0001t0008g0308 a0001c0001t0008g0309 others(4): Show |
7 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+25100G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126338 | |||||||
| chr14:74126422 | T | C | 29 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0007g0004 others(26): Show |
29 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.283+25184T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126422 | |||||||
| chr14:74126470 | G | A | 1 | a0001c0001t0007g0098 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.283+25232G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126470 | |||||||
| chr14:74127025 | T | C | 11 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(8): Show |
11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+25787T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127025 | |||||||
| chr14:74127307 | G | A | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+26069G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127307 | |||||||
| chr14:74127556 | C | T | 10 | a0001c0001t0002g0092 a0001c0001t0011g0204 a0001c0001t0014g0198 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+26318C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127556 | |||||||
| chr14:74127627 | A | C | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+26389A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127627 | |||||||
| chr14:74127659 | G | A | 2 | a0001c0001t0003g0013 a0001c0001t0004g0014 |
2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.283+26421G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127659 | |||||||
| chr14:74127690 | G | A | 1 | a0001c0001t0043g0249 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.283+26452G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127690 | |||||||
| chr14:74127743 | A | T | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+26505A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127743 | |||||||
| chr14:74127800 | T | C | 268 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(265): Show |
271 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.283+26562T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127800 | |||||||
| chr14:74127885 | G | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+26647G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127885 | |||||||
| chr14:74127978 | A | C | 1 | a0001c0001t0002g0276 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+26740A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127978 | |||||||
| chr14:74128016 | G | A | 1 | a0001c0001t0004g0207 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.283+26778G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128016 | |||||||
| chr14:74128276 | C | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+27038C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128276 | |||||||
| chr14:74128707 | T | C | 246 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(243): Show |
249 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.283+27469T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128707 | |||||||
| chr14:74128715 | G | A | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+27477G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128715 | |||||||
| chr14:74128817 | G | A | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+27579G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128817 | |||||||
| chr14:74128848 | G | T | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+27610G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128848 | |||||||
| chr14:74128869 | G | C | 3 | a0001c0001t0007g0107 a0001c0001t0010g0096 a0001c0001t0010g0106 |
3 | HG04115.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.283+27631G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128869 | |||||||
| chr14:74129042 | G | T | 3 | a0001c0001t0008g0332 a0001c0001t0008g0333 a0001c0001t0008g0334 |
3 | HG00323.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.283+27804G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129042 | |||||||
| chr14:74129281 | A | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+28043A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129281 | |||||||
| chr14:74129344 | G | T | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+28106G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129344 | |||||||
| chr14:74129412 | G | A | 45 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(42): Show |
45 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.283+28174G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129412 | |||||||
| chr14:74129497 | G | A | 1 | a0001c0001t0011g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283+28259G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129497 | |||||||
| chr14:74129731 | A | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+28493A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129731 | |||||||
| chr14:74130027 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+28789C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130027 | |||||||
| chr14:74130128 | C | G | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.283+28890C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130128 | |||||||
| chr14:74130238 | A | G | 1 | a0001c0001t0007g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.283+29000A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130238 | |||||||
| chr14:74130259 | A | G | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+29021A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130259 | |||||||
| chr14:74130270 | A | ATTTTTTG others(17): Show |
44 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(41): Show |
44 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.283+29039_283+2904 others(28): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130270 | ||||||
| chr14:74130270 | A | ATTTTTTG others(18): Show |
2 | a0001c0001t0003g0074 a0001c0001t0004g0036 |
2 | HG02027.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.283+29039_283+2904 others(29): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130270 | ||||||
| chr14:74130270 | A | ATTTTTTG others(18): Show |
1 | a0001c0001t0004g0028 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.283+29039_283+2904 others(29): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130270 | ||||||
| chr14:74130277 | G | GGTTTTTT others(16): Show |
1 | a0001c0001t0025g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.283+29050_283+2905 others(27): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130277 | ||||||
| chr14:74130277 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0004g0014 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.283+29039_283+2904 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130277 | |||||||
| chr14:74130277 | G | GTTTTTTT others(16): Show |
20 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0013 others(17): Show |
20 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.283+29039_283+2904 others(27): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130277 | |||||||
| chr14:74130277 | G | GTTTTTTT others(18): Show |
4 | a0001c0001t0003g0019 a0001c0001t0004g0044 a0001c0001t0004g0057 others(1): Show |
4 | HG00438.hp2 HG01928.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+29039_283+2904 others(29): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130277 | |||||||
| chr14:74130277 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0004g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283+29039_283+2904 others(28): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130277 | |||||||
| chr14:74130278 | G | GTGTTTTT others(12): Show |
1 | a0001c0001t0024g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.283+29041_283+2904 others(23): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTGTTTTT others(13): Show |
1 | a0001c0001t0024g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.283+29041_283+2904 others(24): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTGTTT others(7): Show |
1 | a0002c0003t0018g0201 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.283+29043_283+2904 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTGTTT others(8): Show |
5 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(2): Show |
6 | HG02451.hp2 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+29043_283+2904 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTGTTT others(11): Show |
1 | a0001c0001t0014g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.283+29043_283+2904 others(22): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTGTTT others(12): Show |
1 | a0001c0001t0011g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283+29043_283+2904 others(23): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTGTTT others(13): Show |
1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+29043_283+2904 others(24): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTGTTT others(22): Show |
1 | a0001c0001t0015g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+29043_283+2904 others(33): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(3): Show |
32 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0300 others(29): Show |
33 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.283+29049_283+2905 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(4): Show |
15 | a0001c0001t0005g0297 a0001c0001t0005g0299 a0001c0001t0005g0301 others(12): Show |
15 | HG01099.hp2 HG01106.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+29048_283+2905 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(5): Show |
4 | a0001c0001t0008g0312 a0001c0001t0011g0221 a0001c0001t0011g0222 others(1): Show |
4 | HG01981.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+29047_283+2905 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(6): Show |
3 | a0001c0001t0011g0223 a0001c0001t0011g0224 a0001c0001t0011g0225 |
3 | HG01891.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.283+29046_283+2905 others(17): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(8): Show |
2 | a0001c0001t0004g0349 a0001c0001t0004g0350 |
2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+29044_283+2905 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(9): Show |
6 | a0001c0001t0001g0287 a0001c0001t0001g0293 a0001c0001t0001g0294 others(3): Show |
6 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+29043_283+2905 others(20): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(10): Show |
10 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0234 others(7): Show |
10 | HG01074.hp1 HG01099.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+29042_283+2905 others(21): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(11): Show |
24 | a0001c0001t0001g0205 a0001c0001t0001g0227 a0001c0001t0001g0232 others(21): Show |
24 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.283+29041_283+2905 others(22): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(12): Show |
17 | a0001c0001t0001g0216 a0001c0001t0001g0219 a0001c0001t0001g0228 others(14): Show |
17 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+29058_283+2905 others(23): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(13): Show |
14 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0218 others(11): Show |
14 | HG01175.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.283+29058_283+2905 others(24): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(14): Show |
5 | a0001c0001t0001g0231 a0001c0001t0001g0254 a0001c0001t0001g0257 others(2): Show |
5 | HG01358.hp2 HG03486.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+29058_283+2905 others(25): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(15): Show |
1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283+29058_283+2905 others(26): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(21): Show |
1 | a0001c0001t0004g0344 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.283+29058_283+2905 others(32): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(22): Show |
1 | a0001c0001t0037g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.283+29058_283+2905 others(33): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | GTTTTTTT others(27): Show |
1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283+29058_283+2905 others(38): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | ||||||
| chr14:74130278 | G | T | 51 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(48): Show |
51 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.283+29040G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130278 | |||||||
| chr14:74130279 | T | TTTTTTTT others(15): Show |
1 | a0001c0001t0012g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.283+29050_283+2905 others(26): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130279 | ||||||
| chr14:74130280 | T | TTG | 103 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(100): Show |
104 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.283+29043_283+2904 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130280 | ||||||
| chr14:74130436 | C | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+29198C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130436 | |||||||
| chr14:74130467 | A | T | 1 | a0001c0001t0002g0173 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.283+29229A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130467 | |||||||
| chr14:74130524 | C | T | 89 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(86): Show |
89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+29286C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130524 | |||||||
| chr14:74130538 | A | C | 10 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0241 others(7): Show |
10 | HG01358.hp2 NA18947.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+29300A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130538 | |||||||
| chr14:74130588 | A | AT | 74 | a0001c0001t0001g0191 a0001c0001t0001g0205 a0001c0001t0001g0213 others(71): Show |
74 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.283+29374dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130588 | ||||||
| chr14:74130588 | A | ATT | 93 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(90): Show |
95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.283+29373_283+2937 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130588 | ||||||
| chr14:74130588 | A | ATTT | 31 | a0001c0001t0001g0110 a0001c0001t0002g0137 a0001c0001t0002g0170 others(28): Show |
31 | HG00099.hp2 HG00423.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.283+29372_283+2937 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130588 | ||||||
| chr14:74130588 | AT | A | 17 | a0001c0001t0001g0242 a0001c0001t0001g0273 a0001c0001t0003g0058 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+29374delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130588 | ||||||
| chr14:74130785 | C | G | 1 | a0001c0001t0004g0009 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.283+29547C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130785 | |||||||
| chr14:74130948 | AT | A | 14 | a0001c0001t0001g0216 a0001c0001t0001g0220 a0001c0001t0001g0232 others(11): Show |
14 | HG00280.hp2 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+29715delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130948 | ||||||
| chr14:74130954 | A | ATTAT | 33 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(30): Show |
33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.283+29734_283+2973 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130954 | ||||||
| chr14:74130954 | A | ATTATTTA others(5): Show |
1 | a0001c0001t0013g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283+29726_283+2973 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130954 | ||||||
| chr14:74131008 | C | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+29770C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131008 | |||||||
| chr14:74131124 | T | C | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+29886T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131124 | |||||||
| chr14:74131131 | G | A | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+29893G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131131 | |||||||
| chr14:74131146 | G | A | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+29908G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131146 | |||||||
| chr14:74131160 | C | A | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+29922C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131160 | |||||||
| chr14:74131188 | G | GTATACTT others(10): Show |
114 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(111): Show |
116 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.283+29954_283+2995 others(21): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131188 | ||||||
| chr14:74131190 | A | ATACTTTG others(10): Show |
4 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(1): Show |
4 | HG02258.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+29954_283+2995 others(21): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131190 | ||||||
| chr14:74131264 | G | A | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+30026G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131264 | |||||||
| chr14:74131319 | C | CT | 8 | a0001c0001t0001g0228 a0001c0001t0003g0072 a0001c0001t0004g0029 others(5): Show |
8 | HG02055.hp2 HG02135.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+30097dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131319 | ||||||
| chr14:74131319 | C | CTT | 41 | a0001c0001t0001g0335 a0001c0001t0003g0323 a0001c0001t0005g0295 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+30096_283+3009 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131319 | ||||||
| chr14:74131319 | CT | C | 10 | a0001c0001t0002g0073 a0001c0001t0011g0204 a0001c0001t0011g0221 others(7): Show |
10 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+30097delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131319 | ||||||
| chr14:74131429 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+30191C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131429 | |||||||
| chr14:74131486 | CTT | C | 7 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0011g0221 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+30252_283+3025 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131486 | ||||||
| chr14:74131612 | G | A | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.283+30374G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131612 | |||||||
| chr14:74131614 | C | T | 1 | a0001c0001t0007g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.283+30376C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131614 | |||||||
| chr14:74131659 | A | C | 1 | a0001c0001t0002g0181 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.283+30421A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131659 | |||||||
| chr14:74131698 | T | G | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.283+30460T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131698 | |||||||
| chr14:74131771 | G | A | 5 | a0001c0001t0011g0221 a0001c0001t0011g0222 a0001c0001t0011g0223 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+30533G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131771 | |||||||
| chr14:74131915 | T | C | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.283+30677T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131915 | |||||||
| chr14:74131964 | A | G | 3 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.283+30726A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131964 | |||||||
| chr14:74132077 | T | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+30839T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132077 | |||||||
| chr14:74132461 | G | A | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+31223G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132461 | |||||||
| chr14:74132572 | A | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+31334A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132572 | |||||||
| chr14:74132648 | A | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+31410A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132648 | |||||||
| chr14:74132710 | T | C | 1 | a0001c0001t0016g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.283+31472T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132710 | |||||||
| chr14:74132728 | C | T | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+31490C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132728 | |||||||
| chr14:74132798 | C | T | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+31560C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132798 | |||||||
| chr14:74132862 | T | A | 1 | a0001c0001t0007g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.283+31624T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132862 | |||||||
| chr14:74133014 | T | TA | 9 | a0001c0001t0001g0259 a0001c0001t0002g0276 a0001c0001t0002g0277 others(6): Show |
9 | HG01433.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+31787dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74133014 | ||||||
| chr14:74133031 | C | G | 1 | a0001c0002t0009g0282 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.283+31793C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74133031 | |||||||
| chr14:74133689 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.283+32451A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74133689 | |||||||
| chr14:74133834 | C | A | 1 | a0001c0001t0006g0183 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.283+32596C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74133834 | |||||||
| chr14:74134093 | A | C | 5 | a0001c0001t0004g0206 a0001c0001t0004g0207 a0001c0001t0004g0208 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+32855A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134093 | |||||||
| chr14:74134128 | G | A | 2 | a0001c0001t0003g0025 a0001c0001t0003g0071 |
2 | NA18954.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.283+32890G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134128 | |||||||
| chr14:74134146 | C | G | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.283+32908C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134146 | |||||||
| chr14:74134315 | G | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+33077G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134315 | |||||||
| chr14:74134640 | AT | A | 61 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(58): Show |
62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+33406delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74134640 | ||||||
| chr14:74134688 | T | C | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+33450T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134688 | |||||||
| chr14:74134693 | T | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+33455T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134693 | |||||||
| chr14:74134795 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+33557G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134795 | |||||||
| chr14:74134858 | A | G | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+33620A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134858 | |||||||
| chr14:74135027 | A | G | 7 | a0001c0001t0008g0296 a0001c0001t0008g0308 a0001c0001t0008g0309 others(4): Show |
7 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+33789A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135027 | |||||||
| chr14:74135055 | T | TTTG | 3 | a0001c0001t0002g0164 a0001c0001t0006g0156 a0001c0001t0033g0182 |
3 | HG02071.hp1 NA18967.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.283+33831_283+3383 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74135055 | ||||||
| chr14:74135055 | TTTG | T | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+33831_283+3383 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74135055 | ||||||
| chr14:74135140 | C | G | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.283+33902C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135140 | |||||||
| chr14:74135185 | C | T | 108 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(105): Show |
110 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.283+33947C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135185 | |||||||
| chr14:74135276 | G | T | 3 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0034g0119 |
3 | HG01074.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.283+34038G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135276 | |||||||
| chr14:74135286 | A | G | 1 | a0001c0001t0011g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.283+34048A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135286 | |||||||
| chr14:74135303 | T | A | 2 | a0001c0001t0003g0024 a0001c0001t0003g0033 |
2 | NA19057.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.283+34065T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135303 | |||||||
| chr14:74135547 | A | AT | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+34318dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74135547 | ||||||
| chr14:74135547 | AT | A | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+34318delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74135547 | ||||||
| chr14:74135556 | T | A | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+34318T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135556 | |||||||
| chr14:74135657 | A | T | 61 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(58): Show |
62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+34419A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135657 | |||||||
| chr14:74135664 | T | G | 1 | a0001c0001t0010g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.283+34426T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135664 | |||||||
| chr14:74135690 | T | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+34452T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135690 | |||||||
| chr14:74135727 | T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34489T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135727 | |||||||
| chr14:74135768 | T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34530T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135768 | |||||||
| chr14:74135819 | GT | G | 242 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(239): Show |
245 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.283+34593delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74135819 | ||||||
| chr14:74135895 | T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34657T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135895 | |||||||
| chr14:74136156 | C | T | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.283+34918C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136156 | |||||||
| chr14:74136190 | T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34952T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136190 | |||||||
| chr14:74136191 | T | C | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34953T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136191 | |||||||
| chr14:74136193 | T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34955T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136193 | |||||||
| chr14:74136194 | T | G | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34956T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136194 | |||||||
| chr14:74136195 | T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34957T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136195 | |||||||
| chr14:74136198 | T | G | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34960T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136198 | |||||||
| chr14:74136199 | T | C | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34961T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136199 | |||||||
| chr14:74136200 | C | G | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34962C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136200 | |||||||
| chr14:74136201 | A | T | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34963A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136201 | |||||||
| chr14:74136204 | G | T | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34966G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136204 | |||||||
| chr14:74136279 | T | C | 3 | a0001c0001t0011g0222 a0001c0001t0011g0223 a0001c0001t0011g0224 |
3 | HG01891.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.283+35041T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136279 | |||||||
| chr14:74136564 | T | C | 4 | a0001c0001t0013g0094 a0001c0001t0013g0120 a0001c0001t0013g0125 others(1): Show |
4 | HG02602.hp2 HG03688.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+35326T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136564 | |||||||
| chr14:74136685 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+35447C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136685 | |||||||
| chr14:74136700 | A | C | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+35462A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136700 | |||||||
| chr14:74136764 | T | A | 2 | a0001c0002t0009g0283 a0001c0002t0009g0284 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.283+35526T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136764 | |||||||
| chr14:74136797 | A | T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+35559A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136797 | |||||||
| chr14:74137010 | A | G | 1 | a0001c0001t0003g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.283+35772A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137010 | |||||||
| chr14:74137110 | G | A | 344 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(341): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.283+35872G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137110 | |||||||
| chr14:74137137 | G | A | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+35899G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137137 | |||||||
| chr14:74137155 | AAT | A | 108 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(105): Show |
109 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.283+35934_283+3593 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137155 | ||||||
| chr14:74137169 | TA | T | 4 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0008g0327 others(1): Show |
4 | HG01346.hp2 HG01884.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+35932delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137169 | |||||||
| chr14:74137169 | TATA | T | 5 | a0001c0001t0007g0105 a0001c0001t0011g0204 a0001c0001t0014g0203 others(2): Show |
5 | HG02132.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+35932_283+3593 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137169 | |||||||
| chr14:74137170 | A | T | 2 | a0001c0001t0003g0038 a0001c0001t0013g0094 |
2 | HG03688.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.283+35932A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137170 | |||||||
| chr14:74137171 | TA | T | 47 | a0001c0001t0001g0347 a0001c0001t0002g0092 a0001c0001t0003g0018 others(44): Show |
49 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.283+35934delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137171 | |||||||
| chr14:74137172 | A | T | 173 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0215 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.283+35934A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137172 | |||||||
| chr14:74137246 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.283+36008G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137246 | |||||||
| chr14:74137247 | C | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0010g0112 others(1): Show |
4 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+36009C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137247 | |||||||
| chr14:74137307 | ATAT | A | 106 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(103): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+36073_283+3607 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137307 | ||||||
| chr14:74137364 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283+36126C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137364 | |||||||
| chr14:74137445 | C | T | 4 | a0001c0001t0002g0166 a0001c0001t0006g0167 a0001c0001t0020g0132 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+36207C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137445 | |||||||
| chr14:74137485 | T | G | 347 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(344): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.283+36247T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137485 | |||||||
| chr14:74137495 | T | G | 3 | a0001c0001t0007g0107 a0001c0001t0010g0096 a0001c0001t0010g0106 |
3 | HG04115.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.283+36257T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137495 | |||||||
| chr14:74137496 | C | CTTTTTTT | 4 | a0001c0001t0004g0077 a0001c0001t0004g0349 a0001c0001t0004g0351 others(1): Show |
4 | HG02897.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+36259_283+3626 others(11): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137496 | ||||||
| chr14:74137496 | C | CTTTTTTT others(1): Show |
7 | a0001c0001t0004g0350 a0001c0001t0012g0078 a0001c0001t0012g0083 others(4): Show |
7 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+36259_283+3626 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137496 | ||||||
| chr14:74137498 | C | CT | 9 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0228 others(6): Show |
9 | HG00099.hp1 HG00642.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+36278dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137498 | C | CTCT | 8 | a0001c0001t0002g0142 a0001c0001t0002g0190 a0001c0001t0002g0197 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+36261_283+3626 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137498 | C | CTCTT | 62 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0191 others(59): Show |
63 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.283+36261_283+3626 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137498 | C | CTCTTT | 35 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(32): Show |
35 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.283+36261_283+3626 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137498 | C | CTTTTTTT others(4): Show |
6 | a0001c0001t0003g0012 a0001c0001t0003g0060 a0001c0001t0012g0086 others(3): Show |
6 | HG01243.hp1 HG01256.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+36268_283+3627 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137498 | C | CTTTTTTT others(5): Show |
66 | a0001c0001t0002g0027 a0001c0001t0003g0005 a0001c0001t0003g0007 others(63): Show |
66 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.283+36267_283+3627 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137498 | C | CTTTTTTT others(6): Show |
10 | a0001c0001t0002g0073 a0001c0001t0003g0017 a0001c0001t0003g0032 others(7): Show |
10 | HG02135.hp1 HG03471.hp1 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+36266_283+3627 others(17): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137498 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0002g0092 a0001c0001t0004g0070 a0001c0001t0039g0031 |
3 | HG03831.hp1 HG06807.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.283+36265_283+3627 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137498 | C | CTTTTTTT others(8): Show |
4 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0012g0209 others(1): Show |
4 | HG02055.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+36264_283+3627 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137498 | C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0210 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+36263_283+3627 others(20): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137498 | C | T | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+36260C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137498 | |||||||
| chr14:74137498 | CT | C | 50 | a0001c0001t0001g0205 a0001c0001t0001g0231 a0001c0001t0001g0234 others(47): Show |
51 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.283+36278delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | ||||||
| chr14:74137548 | G | C | 2 | a0001c0001t0013g0094 a0001c0001t0013g0125 |
2 | HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.283+36310G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137548 | |||||||
| chr14:74137585 | C | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+36347C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137585 | |||||||
| chr14:74137747 | C | G | 3 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0034g0119 |
3 | HG01074.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.283+36509C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137747 | |||||||
| chr14:74137788 | G | A | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+36550G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137788 | |||||||
| chr14:74137790 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283+36552G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137790 | |||||||
| chr14:74137871 | A | T | 3 | a0001c0001t0005g0297 a0001c0001t0005g0319 a0001c0001t0005g0320 |
3 | HG02071.hp2 HG02165.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.283+36633A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137871 | |||||||
| chr14:74137951 | T | G | 1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283+36713T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137951 | |||||||
| chr14:74138182 | C | T | 1 | a0001c0001t0011g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283+36944C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138182 | |||||||
| chr14:74138445 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.283+37207G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138445 | |||||||
| chr14:74138465 | T | A | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+37227T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138465 | |||||||
| chr14:74138520 | A | C | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+37282A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138520 | |||||||
| chr14:74138522 | G | A | 9 | a0001c0001t0001g0213 a0001c0001t0001g0272 a0001c0001t0002g0260 others(6): Show |
9 | HG02027.hp2 HG02155.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+37284G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138522 | |||||||
| chr14:74138587 | T | C | 1 | a0001c0001t0010g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.283+37349T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138587 | |||||||
| chr14:74138627 | C | A | 4 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0004g0344 others(1): Show |
4 | HG01123.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+37389C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138627 | |||||||
| chr14:74138641 | T | C | 8 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(5): Show |
9 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+37403T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138641 | |||||||
| chr14:74138769 | C | CA | 233 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(230): Show |
235 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.283+37547dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74138769 | ||||||
| chr14:74138769 | C | CAA | 10 | a0001c0001t0004g0036 a0001c0001t0004g0070 a0001c0001t0004g0348 others(7): Show |
10 | HG01109.hp2 HG02027.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+37546_283+3754 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74138769 | ||||||
| chr14:74138824 | T | C | 1 | a0001c0001t0003g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.283+37586T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138824 | |||||||
| chr14:74138935 | AT | A | 100 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0213 others(97): Show |
101 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.283+37712delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74138935 | ||||||
| chr14:74138935 | ATT | A | 168 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0191 others(165): Show |
170 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.283+37711_283+3771 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74138935 | ||||||
| chr14:74139020 | TA | T | 61 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0002g0001 others(58): Show |
62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+37785delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74139020 | ||||||
| chr14:74139217 | G | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0010g0112 others(1): Show |
4 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+37979G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74139217 | |||||||
| chr14:74139669 | T | C | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+38431T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74139669 | |||||||
| chr14:74139702 | G | T | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.283+38464G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74139702 | |||||||
| chr14:74139715 | G | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+38477G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74139715 | |||||||
| chr14:74139739 | T | A | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+38501T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74139739 | |||||||
| chr14:74140044 | TTTA | T | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+38810_283+3881 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74140044 | ||||||
| chr14:74140079 | C | CTT | 206 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(203): Show |
208 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.283+38842_283+3884 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74140079 | ||||||
| chr14:74140289 | C | A | 1 | a0001c0001t0012g0081 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.283+39051C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140289 | |||||||
| chr14:74140305 | G | A | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+39067G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140305 | |||||||
| chr14:74140582 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+39344C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140582 | |||||||
| chr14:74140621 | G | C | 118 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(115): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+39383G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140621 | |||||||
| chr14:74140625 | C | T | 4 | a0001c0001t0003g0034 a0001c0001t0004g0026 a0001c0002t0009g0002 others(1): Show |
5 | HG02451.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+39387C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140625 | |||||||
| chr14:74140711 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.283+39473A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140711 | |||||||
| chr14:74140927 | C | T | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+39689C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140927 | |||||||
| chr14:74141572 | A | T | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+40334A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74141572 | |||||||
| chr14:74142140 | T | C | 1 | a0001c0001t0037g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.283+40902T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142140 | |||||||
| chr14:74142317 | T | A | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+41079T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142317 | |||||||
| chr14:74142630 | G | A | 2 | a0001c0001t0004g0077 a0001c0001t0012g0078 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.283+41392G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142630 | |||||||
| chr14:74142643 | A | G | 1 | a0001c0001t0006g0135 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.283+41405A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142643 | |||||||
| chr14:74142716 | T | C | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.283+41478T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142716 | |||||||
| chr14:74142757 | A | T | 2 | a0001c0001t0011g0204 a0001c0001t0014g0203 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.283+41519A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142757 | |||||||
| chr14:74142796 | T | C | 1 | a0001c0001t0007g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.283+41558T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142796 | |||||||
| chr14:74142898 | C | G | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+41660C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142898 | |||||||
| chr14:74142991 | A | G | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+41753A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142991 | |||||||
| chr14:74143063 | G | A | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+41825G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143063 | |||||||
| chr14:74143172 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.283+41934C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143172 | |||||||
| chr14:74143287 | T | C | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.283+42049T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143287 | |||||||
| chr14:74143362 | G | A | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+42124G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143362 | |||||||
| chr14:74143395 | C | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+42157C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143395 | |||||||
| chr14:74143524 | A | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+42286A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143524 | |||||||
| chr14:74143564 | T | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+42326T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143564 | |||||||
| chr14:74143610 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+42372A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143610 | |||||||
| chr14:74143611 | G | GT | 230 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(227): Show |
231 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.283+42382dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74143611 | ||||||
| chr14:74143622 | A | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+42384A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143622 | |||||||
| chr14:74143772 | T | G | 5 | a0001c0001t0004g0206 a0001c0001t0004g0207 a0001c0001t0004g0208 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+42534T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143772 | |||||||
| chr14:74143899 | C | T | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+42661C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143899 | |||||||
| chr14:74143988 | A | AT | 7 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0011g0221 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+42761dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74143988 | ||||||
| chr14:74144127 | AT | A | 234 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(231): Show |
235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.283+42904delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74144127 | ||||||
| chr14:74144162 | T | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+42924T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144162 | |||||||
| chr14:74144194 | G | A | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+42956G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144194 | |||||||
| chr14:74144279 | A | AT | 8 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(5): Show |
8 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+43054dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74144279 | ||||||
| chr14:74144279 | AT | A | 11 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(8): Show |
11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+43054delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74144279 | ||||||
| chr14:74144346 | C | T | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+43108C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144346 | |||||||
| chr14:74144386 | C | G | 6 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+43148C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144386 | |||||||
| chr14:74144471 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+43233A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144471 | |||||||
| chr14:74144487 | G | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+43249G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144487 | |||||||
| chr14:74144568 | A | G | 190 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(187): Show |
190 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.283+43330A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144568 | |||||||
| chr14:74144617 | A | AAATTAGA others(1): Show |
288 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.283+43380_283+4338 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74144617 | ||||||
| chr14:74144700 | A | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+43462A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144700 | |||||||
| chr14:74144754 | G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+43516G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144754 | |||||||
| chr14:74144784 | G | A | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+43546G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144784 | |||||||
| chr14:74144985 | G | C | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+43747G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144985 | |||||||
| chr14:74145051 | C | T | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+43813C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145051 | |||||||
| chr14:74145313 | T | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+44075T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145313 | |||||||
| chr14:74145383 | T | A | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+44145T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145383 | |||||||
| chr14:74145397 | T | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+44159T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145397 | |||||||
| chr14:74145452 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+44214A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145452 | |||||||
| chr14:74145480 | T | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+44242T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145480 | |||||||
| chr14:74145615 | C | G | 2 | a0001c0001t0006g0156 a0001c0002t0009g0281 |
2 | HG02071.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.283+44377C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145615 | |||||||
| chr14:74145695 | G | C | 3 | a0001c0001t0002g0128 a0001c0001t0002g0147 a0001c0001t0019g0149 |
3 | NA18954.hp2 NA19055.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.283+44457G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145695 | |||||||
| chr14:74145791 | C | T | 3 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.283+44553C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145791 | |||||||
| chr14:74145807 | C | A | 1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283+44569C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145807 | |||||||
| chr14:74145966 | T | C | 4 | a0001c0001t0021g0079 a0001c0001t0021g0084 a0001c0001t0036g0082 others(1): Show |
4 | HG02895.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+44728T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145966 | |||||||
| chr14:74146009 | T | C | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+44771T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146009 | |||||||
| chr14:74146025 | T | C | 4 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+44787T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146025 | |||||||
| chr14:74146192 | G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+44954G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146192 | |||||||
| chr14:74146257 | A | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+45019A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146257 | |||||||
| chr14:74146260 | C | T | 1 | a0001c0001t0003g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.283+45022C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146260 | |||||||
| chr14:74146271 | A | C | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+45033A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146271 | |||||||
| chr14:74146308 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+45070A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146308 | |||||||
| chr14:74146348 | A | G | 1 | a0001c0001t0005g0297 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.283+45110A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146348 | |||||||
| chr14:74146401 | C | T | 10 | a0001c0001t0002g0092 a0001c0001t0011g0204 a0001c0001t0014g0198 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+45163C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146401 | |||||||
| chr14:74146581 | A | G | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+45343A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146581 | |||||||
| chr14:74146663 | C | T | 2 | a0001c0001t0002g0192 a0001c0001t0015g0185 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.283+45425C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146663 | |||||||
| chr14:74146692 | G | A | 4 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0004g0344 others(1): Show |
4 | HG01123.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+45454G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146692 | |||||||
| chr14:74147022 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.283+45784G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147022 | |||||||
| chr14:74147025 | G | A | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+45787G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147025 | |||||||
| chr14:74147126 | C | T | 1 | a0001c0001t0010g0113 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.283+45888C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147126 | |||||||
| chr14:74147189 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+45951C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147189 | |||||||
| chr14:74147190 | G | A | 7 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0011g0221 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+45952G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147190 | |||||||
| chr14:74147197 | G | A | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+45959G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147197 | |||||||
| chr14:74147260 | A | G | 1 | a0001c0001t0005g0325 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.283+46022A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147260 | |||||||
| chr14:74147387 | G | A | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+46149G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147387 | |||||||
| chr14:74147470 | G | A | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+46232G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147470 | |||||||
| chr14:74147796 | A | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+46558A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147796 | |||||||
| chr14:74147857 | T | G | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+46619T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147857 | |||||||
| chr14:74147863 | T | C | 81 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.283+46625T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147863 | |||||||
| chr14:74147925 | G | C | 1 | a0001c0001t0007g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.283+46687G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147925 | |||||||
| chr14:74148001 | G | T | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.283+46763G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148001 | |||||||
| chr14:74148002 | C | T | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.283+46764C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148002 | |||||||
| chr14:74148040 | A | G | 288 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.283+46802A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148040 | |||||||
| chr14:74148134 | A | G | 10 | a0001c0001t0002g0129 a0001c0001t0002g0133 a0001c0001t0002g0134 others(7): Show |
10 | NA18940.hp2 NA18944.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+46896A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148134 | |||||||
| chr14:74148195 | C | G | 1 | a0001c0001t0015g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+46957C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148195 | |||||||
| chr14:74148213 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0253 |
2 | NA19072.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.283+46975C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148213 | |||||||
| chr14:74148234 | T | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+46996T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148234 | |||||||
| chr14:74148290 | A | G | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+47052A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148290 | |||||||
| chr14:74148316 | T | C | 1 | a0001c0001t0007g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.283+47078T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148316 | |||||||
| chr14:74148327 | A | C | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.283+47089A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148327 | |||||||
| chr14:74148392 | G | A | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+47154G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148392 | |||||||
| chr14:74148558 | A | G | 4 | a0001c0001t0002g0131 a0001c0001t0002g0138 a0001c0001t0002g0160 others(1): Show |
4 | HG00642.hp1 HG00735.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+47320A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148558 | |||||||
| chr14:74148627 | T | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+47389T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148627 | |||||||
| chr14:74148675 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.283+47437C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148675 | |||||||
| chr14:74148741 | G | GA | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+47513dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74148741 | ||||||
| chr14:74148801 | G | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.283+47563G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148801 | |||||||
| chr14:74148915 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+47677G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148915 | |||||||
| chr14:74149111 | A | G | 243 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(240): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.283+47873A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149111 | |||||||
| chr14:74149206 | A | T | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.283+47968A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149206 | |||||||
| chr14:74149373 | T | G | 2 | a0001c0001t0021g0079 a0001c0001t0021g0084 |
2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.283+48135T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149373 | |||||||
| chr14:74149596 | T | A | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+48358T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149596 | |||||||
| chr14:74149647 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.283+48409A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149647 | |||||||
| chr14:74149706 | T | C | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+48468T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149706 | |||||||
| chr14:74149718 | A | G | 1 | a0001c0001t0003g0055 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.283+48480A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149718 | |||||||
| chr14:74149790 | T | C | 241 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(238): Show |
242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.283+48552T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149790 | |||||||
| chr14:74150071 | T | C | 1 | a0001c0001t0004g0014 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.283+48833T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150071 | |||||||
| chr14:74150405 | C | A | 5 | a0001c0001t0004g0206 a0001c0001t0004g0207 a0001c0001t0004g0208 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-48517C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150405 | |||||||
| chr14:74150474 | A | T | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.284-48448A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150474 | |||||||
| chr14:74150519 | T | C | 6 | a0001c0001t0002g0092 a0001c0001t0014g0198 a0001c0001t0014g0199 others(3): Show |
6 | HG02145.hp2 HG02809.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-48403T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150519 | |||||||
| chr14:74150634 | T | A | 1 | a0001c0001t0003g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.284-48288T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150634 | |||||||
| chr14:74150646 | T | C | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-48276T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150646 | |||||||
| chr14:74150735 | A | T | 45 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(42): Show |
45 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-48187A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150735 | |||||||
| chr14:74150804 | G | T | 4 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0004g0344 others(1): Show |
4 | HG01123.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-48118G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150804 | |||||||
| chr14:74150927 | G | C | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-47995G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150927 | |||||||
| chr14:74150965 | C | T | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-47957C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150965 | |||||||
| chr14:74150974 | T | A | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-47948T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150974 | |||||||
| chr14:74151264 | A | T | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-47658A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74151264 | |||||||
| chr14:74151504 | TTAAAA | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-47417_284-4741 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74151504 | |||||||
| chr14:74151647 | T | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-47275T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74151647 | |||||||
| chr14:74151982 | C | T | 1 | a0001c0001t0007g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.284-46940C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74151982 | |||||||
| chr14:74151994 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.284-46928C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74151994 | |||||||
| chr14:74152097 | T | C | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-46825T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152097 | |||||||
| chr14:74152124 | A | G | 1 | a0001c0001t0010g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.284-46798A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152124 | |||||||
| chr14:74152129 | G | A | 2 | a0001c0001t0011g0204 a0001c0001t0014g0203 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.284-46793G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152129 | |||||||
| chr14:74152262 | C | CA | 82 | a0001c0001t0001g0335 a0001c0001t0002g0177 a0001c0001t0002g0276 others(79): Show |
83 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.284-46645dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152262 | ||||||
| chr14:74152262 | C | CAA | 72 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(69): Show |
72 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.284-46646_284-4664 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152262 | ||||||
| chr14:74152331 | TACTG | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-46590_284-4658 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152331 | |||||||
| chr14:74152447 | A | G | 1 | a0001c0001t0003g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.284-46475A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152447 | |||||||
| chr14:74152488 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-46434C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152488 | |||||||
| chr14:74152506 | G | A | 5 | a0001c0001t0004g0206 a0001c0001t0004g0207 a0001c0001t0004g0208 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-46416G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152506 | |||||||
| chr14:74152519 | C | T | 2 | a0001c0001t0003g0065 a0001c0001t0004g0029 |
2 | HG00673.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.284-46403C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152519 | |||||||
| chr14:74152839 | A | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-46083A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152839 | |||||||
| chr14:74152901 | A | G | 5 | a0001c0001t0011g0221 a0001c0001t0011g0222 a0001c0001t0011g0223 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-46021A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152901 | |||||||
| chr14:74152959 | C | CA | 34 | a0001c0001t0001g0097 a0001c0001t0001g0161 a0001c0001t0001g0191 others(31): Show |
34 | HG00673.hp2 HG00735.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.284-45940dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152959 | ||||||
| chr14:74152959 | C | CAA | 11 | a0001c0001t0001g0205 a0001c0001t0001g0231 a0001c0001t0001g0234 others(8): Show |
11 | HG01081.hp2 HG01109.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-45941_284-4594 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152959 | ||||||
| chr14:74152959 | CA | C | 12 | a0001c0001t0001g0263 a0001c0001t0001g0287 a0001c0001t0001g0288 others(9): Show |
13 | HG00099.hp1 HG00323.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.284-45940delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152959 | ||||||
| chr14:74152959 | CAA | C | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-45941_284-4594 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152959 | ||||||
| chr14:74152961 | A | C | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-45961A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152961 | |||||||
| chr14:74153164 | G | T | 2 | a0001c0001t0017g0321 a0001c0001t0017g0322 |
2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.284-45758G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153164 | |||||||
| chr14:74153401 | T | C | 1 | a0001c0001t0015g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-45521T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153401 | |||||||
| chr14:74153408 | CT | C | 13 | a0001c0001t0003g0017 a0001c0001t0003g0023 a0001c0001t0003g0053 others(10): Show |
13 | HG00423.hp2 HG02165.hp1 NA18975.hp2 others(10): Show |
intron_variant | MODIFIER | c.284-45513delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153408 | |||||||
| chr14:74153548 | A | AT | 21 | a0001c0001t0001g0286 a0001c0001t0001g0335 a0001c0001t0002g0197 others(18): Show |
21 | HG01074.hp1 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-45360dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74153548 | ||||||
| chr14:74153548 | AT | A | 11 | a0001c0001t0002g0092 a0001c0001t0003g0016 a0001c0001t0005g0299 others(8): Show |
11 | HG00280.hp1 HG01167.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-45360delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74153548 | ||||||
| chr14:74153629 | A | T | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-45293A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153629 | |||||||
| chr14:74153764 | G | A | 1 | a0001c0001t0017g0322 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.284-45158G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153764 | |||||||
| chr14:74153791 | G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-45131G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153791 | |||||||
| chr14:74153873 | A | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-45049A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153873 | |||||||
| chr14:74153961 | A | G | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG02559.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.284-44961A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153961 | |||||||
| chr14:74154008 | C | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-44914C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154008 | |||||||
| chr14:74154041 | G | A | 1 | a0001c0001t0006g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.284-44881G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154041 | |||||||
| chr14:74154173 | G | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-44749G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154173 | |||||||
| chr14:74154174 | T | C | 1 | a0001c0001t0006g0165 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.284-44748T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154174 | |||||||
| chr14:74154176 | A | G | 5 | a0001c0001t0011g0221 a0001c0001t0011g0222 a0001c0001t0011g0223 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-44746A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154176 | |||||||
| chr14:74154249 | A | AAT | 7 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0011g0221 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-44672_284-4467 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74154249 | ||||||
| chr14:74154583 | T | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-44339T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154583 | |||||||
| chr14:74154711 | G | A | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-44211G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154711 | |||||||
| chr14:74154736 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.284-44186T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154736 | |||||||
| chr14:74154753 | A | C | 2 | a0001c0001t0002g0192 a0001c0001t0015g0185 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.284-44169A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154753 | |||||||
| chr14:74154845 | T | C | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-44077T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154845 | |||||||
| chr14:74154882 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.284-44040T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154882 | |||||||
| chr14:74155131 | G | A | 6 | a0001c0001t0002g0128 a0001c0001t0002g0144 a0001c0001t0002g0145 others(3): Show |
6 | NA18946.hp1 NA18954.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-43791G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155131 | |||||||
| chr14:74155354 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.284-43568C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155354 | |||||||
| chr14:74155412 | C | T | 1 | a0001c0001t0003g0042 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.284-43510C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155412 | |||||||
| chr14:74155575 | T | C | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-43347T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155575 | |||||||
| chr14:74155588 | T | C | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-43334T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155588 | |||||||
| chr14:74155631 | C | G | 243 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(240): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.284-43291C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155631 | |||||||
| chr14:74155790 | G | A | 3 | a0001c0001t0011g0222 a0001c0001t0011g0223 a0001c0001t0011g0224 |
3 | HG01891.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.284-43132G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155790 | |||||||
| chr14:74155950 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-42972C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155950 | |||||||
| chr14:74156415 | G | C | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-42507G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156415 | |||||||
| chr14:74156493 | T | G | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.284-42429T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156493 | |||||||
| chr14:74156494 | G | T | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.284-42428G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156494 | |||||||
| chr14:74156496 | T | C | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.284-42426T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156496 | |||||||
| chr14:74156550 | A | G | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-42372A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156550 | |||||||
| chr14:74156717 | A | T | 1 | a0001c0001t0007g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.284-42205A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156717 | |||||||
| chr14:74156854 | A | T | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-42068A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156854 | |||||||
| chr14:74156988 | A | G | 81 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-41934A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156988 | |||||||
| chr14:74157002 | T | G | 1 | a0001c0001t0007g0103 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.284-41920T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157002 | |||||||
| chr14:74157035 | C | CTT | 181 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0215 others(178): Show |
181 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.284-41874_284-4187 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157035 | ||||||
| chr14:74157035 | C | CTTT | 44 | a0001c0001t0001g0213 a0001c0001t0001g0264 a0001c0001t0003g0323 others(41): Show |
45 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-41875_284-4187 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157035 | ||||||
| chr14:74157102 | G | A | 1 | a0001c0001t0007g0108 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.284-41820G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157102 | |||||||
| chr14:74157222 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-41700A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157222 | |||||||
| chr14:74157455 | A | ATT | 9 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0256 others(6): Show |
9 | HG00558.hp1 HG01192.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-41466_284-4146 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157455 | ||||||
| chr14:74157457 | A | AT | 13 | a0001c0001t0001g0205 a0001c0001t0001g0231 a0001c0001t0001g0234 others(10): Show |
13 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.284-41464dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157457 | ||||||
| chr14:74157457 | A | ATT | 49 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0217 others(46): Show |
49 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.284-41464_284-4146 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157457 | ||||||
| chr14:74157457 | A | T | 12 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0256 others(9): Show |
12 | HG00558.hp1 HG01192.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-41465A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157457 | |||||||
| chr14:74157458 | TA | T | 3 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.284-41463delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157458 | |||||||
| chr14:74157459 | A | AT | 9 | a0001c0001t0004g0210 a0001c0001t0004g0348 a0001c0001t0004g0349 others(6): Show |
9 | HG01109.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-41457dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157459 | ||||||
| chr14:74157459 | A | ATAT | 22 | a0001c0001t0002g0276 a0001c0001t0003g0323 a0001c0001t0005g0297 others(19): Show |
23 | HG00280.hp1 HG00639.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.284-41462_284-4146 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157459 | ||||||
| chr14:74157459 | A | ATT | 17 | a0001c0001t0001g0215 a0001c0001t0001g0220 a0001c0001t0001g0250 others(14): Show |
17 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-41458_284-4145 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157459 | ||||||
| chr14:74157459 | A | ATTT | 10 | a0001c0001t0002g0277 a0001c0001t0005g0300 a0001c0001t0005g0301 others(7): Show |
10 | HG01123.hp2 HG01978.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-41459_284-4145 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157459 | ||||||
| chr14:74157459 | A | T | 128 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0205 others(125): Show |
128 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.284-41463A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157459 | |||||||
| chr14:74157460 | T | TA | 83 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(80): Show |
83 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.284-41462_284-4146 others(5): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157460 | |||||||
| chr14:74157460 | T | TATA | 9 | a0001c0001t0005g0303 a0001c0001t0005g0304 a0001c0001t0005g0305 others(6): Show |
9 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-41462_284-4146 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157460 | |||||||
| chr14:74157461 | T | A | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.284-41461T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157461 | |||||||
| chr14:74157493 | G | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-41429G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157493 | |||||||
| chr14:74157660 | G | A | 1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.284-41262G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157660 | |||||||
| chr14:74157705 | G | A | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-41217G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157705 | |||||||
| chr14:74157894 | T | C | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-41028T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157894 | |||||||
| chr14:74157952 | A | G | 2 | a0001c0001t0001g0338 a0001c0001t0001g0340 |
2 | HG01106.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.284-40970A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157952 | |||||||
| chr14:74157955 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.284-40967C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157955 | |||||||
| chr14:74158117 | A | AT | 12 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(9): Show |
12 | HG00323.hp1 HG02071.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-40804dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158117 | ||||||
| chr14:74158118 | TA | T | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-40803delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158118 | |||||||
| chr14:74158119 | A | AT | 28 | a0001c0001t0005g0299 a0001c0001t0005g0303 a0001c0001t0005g0304 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.284-40802dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158119 | ||||||
| chr14:74158119 | A | ATT | 25 | a0001c0001t0001g0205 a0001c0001t0001g0215 a0001c0001t0001g0231 others(22): Show |
25 | HG01074.hp1 HG01081.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.284-40802_284-4080 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158119 | ||||||
| chr14:74158119 | A | ATTT | 16 | a0001c0001t0001g0213 a0001c0001t0001g0272 a0001c0001t0001g0338 others(13): Show |
16 | HG01106.hp1 HG01243.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-40802_284-4080 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158119 | ||||||
| chr14:74158119 | A | T | 18 | a0001c0001t0001g0341 a0001c0001t0002g0195 a0001c0001t0002g0196 others(15): Show |
18 | HG00323.hp1 HG01496.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-40803A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158119 | |||||||
| chr14:74158121 | A | ATT | 64 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.284-40800_284-4079 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158121 | ||||||
| chr14:74158121 | A | T | 130 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(127): Show |
131 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.284-40801A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158121 | |||||||
| chr14:74158123 | A | ATTTT | 71 | a0001c0001t0001g0214 a0001c0001t0002g0027 a0001c0001t0002g0073 others(68): Show |
71 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.284-40798_284-4079 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158123 | ||||||
| chr14:74158123 | A | T | 205 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(202): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.284-40799A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158123 | |||||||
| chr14:74158124 | TA | T | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-40797delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158124 | |||||||
| chr14:74158125 | A | T | 290 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0161 others(287): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.284-40797A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158125 | |||||||
| chr14:74158127 | T | A | 1 | a0001c0001t0035g0180 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.284-40795T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158127 | |||||||
| chr14:74158184 | G | A | 1 | a0001c0001t0005g0310 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.284-40738G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158184 | |||||||
| chr14:74158254 | C | T | 3 | a0001c0001t0003g0008 a0001c0001t0003g0018 a0001c0001t0004g0009 |
3 | HG00597.hp1 HG02083.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.284-40668C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158254 | |||||||
| chr14:74158260 | C | T | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-40662C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158260 | |||||||
| chr14:74158273 | C | T | 3 | a0001c0001t0022g0056 a0001c0001t0022g0075 a0001c0001t0039g0031 |
3 | NA18991.hp2 NA19009.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.284-40649C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158273 | |||||||
| chr14:74158306 | T | G | 81 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-40616T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158306 | |||||||
| chr14:74158402 | C | T | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.284-40520C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158402 | |||||||
| chr14:74158429 | C | T | 2 | a0001c0001t0003g0018 a0001c0001t0004g0009 |
2 | HG00597.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.284-40493C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158429 | |||||||
| chr14:74158481 | TG | T | 81 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-40440delG | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158481 | |||||||
| chr14:74158486 | A | G | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.284-40436A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158486 | |||||||
| chr14:74158531 | T | C | 1 | a0001c0001t0007g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.284-40391T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158531 | |||||||
| chr14:74158571 | C | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-40351C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158571 | |||||||
| chr14:74158776 | C | T | 81 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-40146C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158776 | |||||||
| chr14:74158777 | C | T | 1 | a0001c0001t0005g0299 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.284-40145C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158777 | |||||||
| chr14:74158782 | G | A | 1 | a0001c0001t0012g0081 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.284-40140G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158782 | |||||||
| chr14:74158873 | C | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-40049C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158873 | |||||||
| chr14:74158991 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-39931C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158991 | |||||||
| chr14:74159040 | G | C | 1 | a0001c0001t0015g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-39882G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159040 | |||||||
| chr14:74159070 | T | C | 7 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0011g0221 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-39852T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159070 | |||||||
| chr14:74159168 | T | TATTA | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-39753_284-3975 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74159168 | ||||||
| chr14:74159348 | T | C | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-39574T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159348 | |||||||
| chr14:74159428 | C | T | 1 | a0001c0001t0002g0166 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.284-39494C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159428 | |||||||
| chr14:74159503 | C | T | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-39419C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159503 | |||||||
| chr14:74159566 | TG | T | 3 | a0001c0001t0001g0110 a0001c0001t0010g0113 a0001c0001t0010g0126 |
3 | HG00099.hp2 HG00741.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.284-39355delG | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159566 | |||||||
| chr14:74159567 | G | T | 2 | a0001c0001t0001g0097 a0001c0001t0010g0112 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.284-39355G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159567 | |||||||
| chr14:74159567 | GT | G | 270 | a0001c0001t0001g0191 a0001c0001t0001g0205 a0001c0001t0001g0213 others(267): Show |
271 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.284-39335delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74159567 | ||||||
| chr14:74159567 | GTT | G | 9 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(6): Show |
10 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-39336_284-3933 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74159567 | ||||||
| chr14:74159574 | T | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284-39348T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159574 | |||||||
| chr14:74159575 | T | G | 229 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(226): Show |
230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.284-39347T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159575 | |||||||
| chr14:74159576 | T | G | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.284-39346T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159576 | |||||||
| chr14:74159588 | G | A | 6 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-39334G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159588 | |||||||
| chr14:74159791 | C | T | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-39131C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159791 | |||||||
| chr14:74159841 | T | G | 243 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(240): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.284-39081T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159841 | |||||||
| chr14:74159862 | G | A | 1 | a0001c0001t0005g0320 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.284-39060G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159862 | |||||||
| chr14:74159904 | C | A | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-39018C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159904 | |||||||
| chr14:74160055 | A | G | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-38867A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160055 | |||||||
| chr14:74160070 | C | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-38852C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160070 | |||||||
| chr14:74160118 | G | A | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-38804G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160118 | |||||||
| chr14:74160191 | A | G | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-38731A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160191 | |||||||
| chr14:74160261 | G | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-38661G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160261 | |||||||
| chr14:74160337 | T | G | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-38585T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160337 | |||||||
| chr14:74160439 | C | T | 76 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(73): Show |
76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.284-38483C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160439 | |||||||
| chr14:74160632 | C | T | 42 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(39): Show |
43 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.284-38290C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160632 | |||||||
| chr14:74160732 | T | C | 2 | a0001c0001t0002g0192 a0001c0001t0015g0185 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.284-38190T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160732 | |||||||
| chr14:74160918 | A | G | 1 | a0001c0001t0008g0311 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.284-38004A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160918 | |||||||
| chr14:74160931 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-37991C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160931 | |||||||
| chr14:74160981 | C | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-37941C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160981 | |||||||
| chr14:74160987 | T | C | 1 | a0001c0001t0011g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.284-37935T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160987 | |||||||
| chr14:74161010 | A | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-37912A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161010 | |||||||
| chr14:74161295 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-37627C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161295 | |||||||
| chr14:74161477 | G | A | 1 | a0001c0001t0034g0119 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.284-37445G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161477 | |||||||
| chr14:74161486 | C | T | 1 | a0001c0001t0008g0312 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.284-37436C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161486 | |||||||
| chr14:74161495 | G | A | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-37427G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161495 | |||||||
| chr14:74161700 | G | C | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-37222G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161700 | |||||||
| chr14:74161936 | G | C | 73 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(70): Show |
73 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.284-36986G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161936 | |||||||
| chr14:74162104 | T | G | 1 | a0001c0001t0002g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.284-36818T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162104 | |||||||
| chr14:74162282 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-36640C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162282 | |||||||
| chr14:74162292 | A | G | 4 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0062 others(1): Show |
4 | HG00323.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-36630A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162292 | |||||||
| chr14:74162443 | C | T | 29 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0007g0004 others(26): Show |
29 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.284-36479C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162443 | |||||||
| chr14:74162462 | A | G | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-36460A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162462 | |||||||
| chr14:74162475 | C | CA | 53 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0233 others(50): Show |
53 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.284-36427dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74162475 | ||||||
| chr14:74162475 | C | CAA | 77 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(74): Show |
77 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.284-36428_284-3642 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74162475 | ||||||
| chr14:74162475 | CA | C | 50 | a0001c0001t0001g0152 a0001c0001t0002g0196 a0001c0001t0003g0015 others(47): Show |
51 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.284-36427delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74162475 | ||||||
| chr14:74162477 | A | C | 3 | a0001c0002t0009g0282 a0001c0002t0009g0283 a0001c0002t0009g0284 |
3 | HG02622.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.284-36445A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162477 | |||||||
| chr14:74162478 | A | C | 5 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-36444A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162478 | |||||||
| chr14:74162479 | A | C | 3 | a0001c0002t0009g0282 a0001c0002t0009g0283 a0001c0002t0009g0284 |
3 | HG02622.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.284-36443A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162479 | |||||||
| chr14:74162480 | A | C | 5 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-36442A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162480 | |||||||
| chr14:74162513 | C | T | 1 | a0001c0001t0025g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.284-36409C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162513 | |||||||
| chr14:74162528 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.284-36394T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162528 | |||||||
| chr14:74162563 | GA | G | 6 | a0001c0001t0001g0240 a0001c0001t0002g0260 a0001c0001t0002g0261 others(3): Show |
6 | HG02040.hp2 HG02155.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-36350delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74162563 | ||||||
| chr14:74162630 | G | C | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-36292G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162630 | |||||||
| chr14:74162780 | C | T | 243 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(240): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.284-36142C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162780 | |||||||
| chr14:74162957 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-35965C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162957 | |||||||
| chr14:74162965 | T | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-35957T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162965 | |||||||
| chr14:74162998 | TTAAG | T | 5 | a0001c0001t0011g0221 a0001c0001t0011g0222 a0001c0001t0011g0223 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-35919_284-3591 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74162998 | ||||||
| chr14:74163151 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.284-35771A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163151 | |||||||
| chr14:74163331 | C | A | 1 | a0001c0001t0007g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.284-35591C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163331 | |||||||
| chr14:74163362 | G | A | 1 | a0001c0001t0041g0298 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.284-35560G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163362 | |||||||
| chr14:74163362 | G | T | 6 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0001g0291 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-35560G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163362 | |||||||
| chr14:74163467 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.284-35455A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163467 | |||||||
| chr14:74163472 | C | G | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0006g0194 |
3 | HG01496.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.284-35450C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163472 | |||||||
| chr14:74163496 | G | A | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-35426G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163496 | |||||||
| chr14:74163635 | T | A | 16 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(13): Show |
16 | HG00438.hp1 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-35287T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163635 | |||||||
| chr14:74163801 | G | A | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-35121G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163801 | |||||||
| chr14:74163814 | G | A | 2 | a0001c0001t0001g0338 a0001c0001t0001g0340 |
2 | HG01106.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.284-35108G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163814 | |||||||
| chr14:74163881 | A | C | 45 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-35041A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163881 | |||||||
| chr14:74163892 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-35030C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163892 | |||||||
| chr14:74163984 | A | AT | 82 | a0001c0001t0001g0097 a0001c0001t0001g0205 a0001c0001t0001g0213 others(79): Show |
82 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.284-34923dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74163984 | ||||||
| chr14:74164138 | T | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-34784T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164138 | |||||||
| chr14:74164253 | T | C | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-34669T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164253 | |||||||
| chr14:74164287 | G | GT | 234 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(231): Show |
235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.284-34626dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74164287 | ||||||
| chr14:74164297 | G | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-34625G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164297 | |||||||
| chr14:74164384 | A | G | 6 | a0001c0001t0002g0128 a0001c0001t0002g0144 a0001c0001t0002g0145 others(3): Show |
6 | NA18946.hp1 NA18954.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-34538A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164384 | |||||||
| chr14:74164407 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.284-34515C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164407 | |||||||
| chr14:74164420 | G | A | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-34502G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164420 | |||||||
| chr14:74164434 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-34488A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164434 | |||||||
| chr14:74164477 | G | A | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-34445G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164477 | |||||||
| chr14:74164613 | C | T | 5 | a0001c0001t0004g0206 a0001c0001t0004g0207 a0001c0001t0004g0208 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-34309C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164613 | |||||||
| chr14:74164664 | C | G | 74 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(71): Show |
74 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.284-34258C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164664 | |||||||
| chr14:74164700 | T | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-34222T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164700 | |||||||
| chr14:74164786 | A | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-34136A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164786 | |||||||
| chr14:74164919 | A | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-34003A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164919 | |||||||
| chr14:74164987 | A | G | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-33935A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164987 | |||||||
| chr14:74165054 | A | C | 122 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(119): Show |
123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.284-33868A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165054 | |||||||
| chr14:74165082 | A | C | 1 | a0001c0001t0003g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.284-33840A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165082 | |||||||
| chr14:74165107 | G | A | 4 | a0001c0001t0021g0079 a0001c0001t0021g0084 a0001c0001t0036g0082 others(1): Show |
4 | HG02895.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-33815G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165107 | |||||||
| chr14:74165117 | T | C | 9 | a0001c0001t0005g0303 a0001c0001t0005g0304 a0001c0001t0005g0305 others(6): Show |
9 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-33805T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165117 | |||||||
| chr14:74165217 | G | A | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-33705G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165217 | |||||||
| chr14:74165237 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.284-33685T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165237 | |||||||
| chr14:74165267 | AG | A | 9 | a0001c0001t0001g0205 a0001c0001t0001g0231 a0001c0001t0001g0234 others(6): Show |
10 | HG01081.hp2 HG01884.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-33650delG | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165267 | ||||||
| chr14:74165327 | C | T | 1 | a0001c0001t0006g0165 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.284-33595C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165327 | |||||||
| chr14:74165444 | G | T | 38 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(35): Show |
39 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.284-33478G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165444 | |||||||
| chr14:74165513 | C | CTT | 9 | a0001c0001t0003g0008 a0001c0001t0004g0077 a0001c0001t0012g0078 others(6): Show |
9 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-33395_284-3339 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTCTT others(6): Show |
8 | a0001c0001t0001g0191 a0001c0001t0002g0190 a0001c0001t0002g0192 others(5): Show |
8 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-33405_284-3340 others(17): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTCTT others(7): Show |
3 | a0001c0001t0001g0097 a0001c0001t0002g0189 a0001c0001t0010g0113 |
3 | HG00099.hp2 HG01175.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.284-33405_284-3340 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTCTT others(8): Show |
2 | a0001c0001t0001g0110 a0001c0001t0010g0112 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.284-33405_284-3340 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0004g0009 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.284-33402_284-3340 others(17): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0005g0310 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.284-33403_284-3339 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTTTT others(4): Show |
38 | a0001c0001t0002g0073 a0001c0001t0003g0069 a0001c0001t0003g0323 others(35): Show |
39 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.284-33404_284-3339 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTTTT others(5): Show |
95 | a0001c0001t0001g0335 a0001c0001t0002g0027 a0001c0001t0002g0092 others(92): Show |
96 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.284-33405_284-3339 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTTTT others(6): Show |
28 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0003g0015 others(25): Show |
28 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.284-33406_284-3339 others(17): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTTTT others(7): Show |
10 | a0001c0001t0003g0033 a0001c0001t0007g0098 a0001c0001t0007g0115 others(7): Show |
10 | HG02647.hp2 HG03017.hp1 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-33407_284-3339 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTTTT others(8): Show |
9 | a0001c0001t0007g0095 a0001c0001t0007g0107 a0001c0001t0010g0096 others(6): Show |
9 | HG01081.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-33408_284-3339 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165513 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0014g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.284-33394_284-3339 others(20): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | ||||||
| chr14:74165526 | T | TTTGAGAC others(4): Show |
1 | a0001c0001t0043g0249 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.284-33394_284-3338 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165526 | ||||||
| chr14:74165589 | A | G | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-33333A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165589 | |||||||
| chr14:74165853 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-33069A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165853 | |||||||
| chr14:74165894 | A | AT | 15 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0002g0092 others(12): Show |
16 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-33014dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165894 | ||||||
| chr14:74165894 | AT | A | 16 | a0001c0001t0001g0191 a0001c0001t0001g0236 a0001c0001t0001g0268 others(13): Show |
16 | HG00323.hp2 HG01081.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-33014delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165894 | ||||||
| chr14:74165984 | C | T | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-32938C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165984 | |||||||
| chr14:74166235 | A | G | 1 | a0001c0001t0035g0180 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.284-32687A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166235 | |||||||
| chr14:74166252 | C | T | 1 | a0001c0001t0016g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.284-32670C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166252 | |||||||
| chr14:74166457 | C | T | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-32465C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166457 | |||||||
| chr14:74166502 | C | T | 2 | a0001c0001t0003g0034 a0001c0001t0004g0026 |
2 | NA18956.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.284-32420C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166502 | |||||||
| chr14:74166503 | G | A | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-32419G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166503 | |||||||
| chr14:74166583 | A | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-32339A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166583 | |||||||
| chr14:74166906 | G | A | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-32016G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166906 | |||||||
| chr14:74166907 | C | T | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-32015C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166907 | |||||||
| chr14:74167044 | G | A | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-31878G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167044 | |||||||
| chr14:74167107 | T | C | 1 | a0001c0001t0003g0323 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.284-31815T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167107 | |||||||
| chr14:74167112 | C | CT | 94 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0258 others(91): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.284-31790dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74167112 | ||||||
| chr14:74167112 | C | CTT | 97 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(94): Show |
97 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.284-31791_284-3179 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74167112 | ||||||
| chr14:74167112 | C | CTTTT | 67 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(64): Show |
67 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.284-31793_284-3179 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74167112 | ||||||
| chr14:74167162 | G | C | 241 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(238): Show |
242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.284-31760G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167162 | |||||||
| chr14:74167208 | A | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-31714A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167208 | |||||||
| chr14:74167527 | A | C | 2 | a0001c0001t0017g0321 a0001c0001t0017g0322 |
2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.284-31395A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167527 | |||||||
| chr14:74167950 | G | A | 1 | a0001c0001t0003g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.284-30972G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167950 | |||||||
| chr14:74167966 | A | AT | 222 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(219): Show |
223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.284-30952dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74167966 | ||||||
| chr14:74167978 | GGTTT | G | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-30939_284-3093 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74167978 | ||||||
| chr14:74168049 | G | A | 240 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(237): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.284-30873G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168049 | |||||||
| chr14:74168104 | A | G | 1 | a0001c0001t0001g0340 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.284-30818A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168104 | |||||||
| chr14:74168397 | G | A | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-30525G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168397 | |||||||
| chr14:74168464 | C | T | 1 | a0001c0001t0004g0009 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.284-30458C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168464 | |||||||
| chr14:74168467 | G | C | 5 | a0001c0001t0004g0206 a0001c0001t0004g0207 a0001c0001t0004g0208 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-30455G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168467 | |||||||
| chr14:74168476 | G | C | 2 | a0001c0001t0004g0206 a0001c0001t0012g0209 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.284-30446G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168476 | |||||||
| chr14:74168669 | G | GA | 9 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(6): Show |
9 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-30243dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74168669 | ||||||
| chr14:74168708 | T | A | 1 | a0001c0001t0028g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.284-30214T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168708 | |||||||
| chr14:74168741 | C | A | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-30181C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168741 | |||||||
| chr14:74168840 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.284-30082G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168840 | |||||||
| chr14:74168873 | C | T | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-30049C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168873 | |||||||
| chr14:74168916 | G | A | 2 | a0001c0001t0002g0137 a0001c0001t0002g0150 |
2 | HG01358.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.284-30006G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168916 | |||||||
| chr14:74168926 | G | A | 1 | a0001c0001t0001g0347 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.284-29996G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168926 | |||||||
| chr14:74168932 | C | T | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-29990C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168932 | |||||||
| chr14:74168948 | G | A | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.284-29974G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168948 | |||||||
| chr14:74169046 | T | G | 45 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(42): Show |
45 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-29876T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169046 | |||||||
| chr14:74169180 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.284-29742T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169180 | |||||||
| chr14:74169329 | C | T | 1 | a0001c0001t0003g0323 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.284-29593C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169329 | |||||||
| chr14:74169387 | G | T | 1 | a0001c0001t0003g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.284-29535G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169387 | |||||||
| chr14:74169696 | A | AC | 9 | a0001c0001t0001g0215 a0001c0001t0001g0238 a0001c0001t0003g0065 others(6): Show |
9 | HG00673.hp2 HG01978.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-29221dupC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74169696 | ||||||
| chr14:74169701 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.284-29221C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169701 | |||||||
| chr14:74169705 | T | A | 1 | a0001c0001t0002g0151 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.284-29217T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169705 | |||||||
| chr14:74169827 | A | T | 1 | a0001c0001t0002g0151 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.284-29095A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169827 | |||||||
| chr14:74169879 | T | G | 10 | a0001c0001t0002g0092 a0001c0001t0011g0204 a0001c0001t0014g0198 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-29043T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169879 | |||||||
| chr14:74169934 | G | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-28988G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169934 | |||||||
| chr14:74169983 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-28939A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169983 | |||||||
| chr14:74170075 | G | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-28847G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170075 | |||||||
| chr14:74170129 | G | C | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.284-28793G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170129 | |||||||
| chr14:74170170 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-28752A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170170 | |||||||
| chr14:74170215 | C | G | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-28707C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170215 | |||||||
| chr14:74170475 | G | A | 288 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.284-28447G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170475 | |||||||
| chr14:74170506 | CA | C | 148 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(145): Show |
149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.284-28405delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74170506 | ||||||
| chr14:74170741 | G | A | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-28181G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170741 | |||||||
| chr14:74170881 | A | T | 1 | a0001c0001t0013g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.284-28041A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170881 | |||||||
| chr14:74170881 | AT | A | 141 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.284-28036delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74170881 | ||||||
| chr14:74170882 | T | A | 99 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0002g0092 others(96): Show |
99 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.284-28040T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170882 | |||||||
| chr14:74170932 | A | G | 1 | a0001c0001t0002g0276 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.284-27990A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170932 | |||||||
| chr14:74170995 | A | G | 3 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.284-27927A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170995 | |||||||
| chr14:74171018 | C | CAA | 90 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0002g0276 others(87): Show |
91 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.284-27888_284-2788 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171018 | ||||||
| chr14:74171138 | CTT | C | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-27782_284-2778 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171138 | ||||||
| chr14:74171363 | T | TA | 21 | a0001c0001t0001g0215 a0001c0001t0001g0335 a0001c0001t0001g0341 others(18): Show |
21 | HG00642.hp1 HG01109.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-27544dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171363 | ||||||
| chr14:74171464 | G | A | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-27458G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74171464 | |||||||
| chr14:74171697 | ATAT | A | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-27220_284-2721 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171697 | ||||||
| chr14:74171705 | TTA | T | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-27215_284-2721 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171705 | ||||||
| chr14:74171736 | C | CT | 53 | a0001c0001t0001g0191 a0001c0001t0002g0117 a0001c0001t0002g0118 others(50): Show |
53 | HG00438.hp1 HG00544.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.284-27166dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171736 | ||||||
| chr14:74171736 | C | CTT | 94 | a0001c0001t0001g0335 a0001c0001t0002g0027 a0001c0001t0002g0073 others(91): Show |
95 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.284-27167_284-2716 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171736 | ||||||
| chr14:74171736 | C | CTTT | 56 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0003g0323 others(53): Show |
57 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.284-27168_284-2716 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171736 | ||||||
| chr14:74171736 | C | CTTTT | 6 | a0001c0001t0005g0299 a0001c0001t0005g0319 a0001c0001t0008g0296 others(3): Show |
6 | HG01243.hp1 HG02165.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-27169_284-2716 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171736 | ||||||
| chr14:74171736 | CTTTTTTT | C | 81 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-27172_284-2716 others(11): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171736 | ||||||
| chr14:74171765 | G | A | 1 | a0001c0001t0013g0111 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.284-27157G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74171765 | |||||||
| chr14:74171789 | A | G | 1 | a0001c0001t0004g0349 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.284-27133A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74171789 | |||||||
| chr14:74171802 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.284-27120G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74171802 | |||||||
| chr14:74171846 | C | G | 1 | a0001c0001t0004g0029 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.284-27076C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74171846 | |||||||
| chr14:74172095 | G | T | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-26827G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172095 | |||||||
| chr14:74172096 | T | C | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-26826T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172096 | |||||||
| chr14:74172197 | T | C | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-26725T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172197 | |||||||
| chr14:74172422 | T | C | 1 | a0001c0001t0025g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.284-26500T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172422 | |||||||
| chr14:74172615 | T | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG00280.hp2 HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.284-26307T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172615 | |||||||
| chr14:74172769 | C | G | 7 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0011g0221 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-26153C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172769 | |||||||
| chr14:74172902 | T | C | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.284-26020T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172902 | |||||||
| chr14:74172909 | C | G | 9 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0272 others(6): Show |
9 | HG01192.hp1 HG02027.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-26013C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172909 | |||||||
| chr14:74173052 | G | C | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-25870G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173052 | |||||||
| chr14:74173265 | G | T | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-25657G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173265 | |||||||
| chr14:74173327 | A | C | 1 | a0001c0001t0041g0298 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.284-25595A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173327 | |||||||
| chr14:74173434 | G | A | 83 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(80): Show |
83 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.284-25488G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173434 | |||||||
| chr14:74173477 | G | A | 4 | a0001c0001t0002g0131 a0001c0001t0002g0138 a0001c0001t0002g0160 others(1): Show |
4 | HG00642.hp1 HG00735.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-25445G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173477 | |||||||
| chr14:74173659 | A | T | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284-25263A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173659 | |||||||
| chr14:74173809 | T | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-25113T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173809 | |||||||
| chr14:74173889 | C | A | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-25033C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173889 | |||||||
| chr14:74173900 | G | T | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-25022G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173900 | |||||||
| chr14:74173998 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-24924C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173998 | |||||||
| chr14:74174269 | A | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-24653A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174269 | |||||||
| chr14:74174283 | C | T | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-24639C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174283 | |||||||
| chr14:74174357 | T | G | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-24565T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174357 | |||||||
| chr14:74174504 | T | C | 1 | a0001c0001t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.284-24418T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174504 | |||||||
| chr14:74174508 | G | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-24414G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174508 | |||||||
| chr14:74174535 | T | C | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-24387T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174535 | |||||||
| chr14:74174550 | G | A | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-24372G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174550 | |||||||
| chr14:74174650 | G | A | 1 | a0001c0001t0005g0304 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.284-24272G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174650 | |||||||
| chr14:74174770 | A | T | 2 | a0001c0001t0012g0086 a0001c0001t0025g0087 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-24152A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174770 | |||||||
| chr14:74174789 | G | GA | 137 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0002g0092 others(134): Show |
138 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.284-24123dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74174789 | ||||||
| chr14:74174789 | G | GAA | 103 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(100): Show |
103 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.284-24124_284-2412 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74174789 | ||||||
| chr14:74174871 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-24051A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174871 | |||||||
| chr14:74175020 | A | AAATAAT | 4 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0004g0344 others(1): Show |
4 | HG01123.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-23883_284-2387 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | ||||||
| chr14:74175020 | A | AAATAATA others(5): Show |
14 | a0001c0001t0001g0232 a0001c0001t0002g0277 a0001c0001t0011g0222 others(11): Show |
14 | HG01891.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-23889_284-2387 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | ||||||
| chr14:74175020 | A | AAATAATA others(8): Show |
16 | a0001c0001t0002g0276 a0001c0001t0003g0024 a0001c0001t0003g0033 others(13): Show |
16 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-23892_284-2387 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | ||||||
| chr14:74175020 | A | AAATAATA others(11): Show |
141 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(138): Show |
141 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.284-23895_284-2387 others(22): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | ||||||
| chr14:74175020 | A | AAATAATA others(14): Show |
49 | a0001c0001t0001g0226 a0001c0001t0001g0258 a0001c0001t0001g0287 others(46): Show |
50 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.284-23898_284-2387 others(25): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | ||||||
| chr14:74175020 | A | AAATAATA others(17): Show |
14 | a0001c0001t0001g0235 a0001c0001t0001g0342 a0001c0001t0003g0025 others(11): Show |
14 | HG00558.hp1 HG01943.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-23901_284-2387 others(28): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | ||||||
| chr14:74175020 | A | AAATAATA others(23): Show |
1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.284-23878_284-2387 others(34): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | ||||||
| chr14:74175020 | AAAT | A | 47 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(44): Show |
48 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.284-23880_284-2387 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | ||||||
| chr14:74175040 | A | G | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284-23882A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175040 | |||||||
| chr14:74175072 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.284-23850A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175072 | |||||||
| chr14:74175083 | T | C | 1 | a0001c0001t0007g0103 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.284-23839T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175083 | |||||||
| chr14:74175220 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.284-23702A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175220 | |||||||
| chr14:74175242 | C | CTGTA | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-23679_284-2367 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175242 | ||||||
| chr14:74175529 | C | CA | 5 | a0001c0001t0001g0240 a0001c0001t0008g0312 a0001c0001t0034g0119 others(2): Show |
6 | HG01074.hp2 HG01981.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-23381dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175529 | ||||||
| chr14:74175529 | CA | C | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-23381delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175529 | ||||||
| chr14:74175566 | G | A | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-23356G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175566 | |||||||
| chr14:74175577 | G | A | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-23345G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175577 | |||||||
| chr14:74175586 | A | G | 81 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-23336A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175586 | |||||||
| chr14:74175711 | T | C | 1 | a0001c0001t0016g0048 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.284-23211T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175711 | |||||||
| chr14:74175711 | T | TAC | 34 | a0001c0001t0002g0128 a0001c0001t0002g0140 a0001c0001t0002g0144 others(31): Show |
34 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.284-23172_284-2317 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175711 | T | TACAC | 39 | a0001c0001t0001g0152 a0001c0001t0002g0001 a0001c0001t0002g0131 others(36): Show |
41 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.284-23174_284-2317 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175711 | T | TACACAC | 35 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0002g0137 others(32): Show |
35 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.284-23176_284-2317 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175711 | T | TACACACA others(1): Show |
16 | a0001c0001t0003g0007 a0001c0001t0003g0024 a0001c0001t0003g0025 others(13): Show |
16 | HG00438.hp2 HG02027.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-23178_284-2317 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175711 | T | TACACACA others(3): Show |
9 | a0001c0001t0001g0097 a0001c0001t0003g0038 a0001c0001t0004g0037 others(6): Show |
9 | HG00099.hp2 HG00738.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-23180_284-2317 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175711 | T | TACACACA others(5): Show |
3 | a0001c0001t0004g0349 a0001c0001t0004g0350 a0001c0001t0004g0351 |
3 | HG03195.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.284-23182_284-2317 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175711 | T | TACACACA others(7): Show |
1 | a0001c0001t0004g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.284-23184_284-2317 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175711 | TAC | T | 12 | a0001c0001t0001g0228 a0001c0001t0001g0240 a0001c0001t0001g0255 others(9): Show |
12 | HG01106.hp1 HG02040.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-23172_284-2317 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175711 | TACAC | T | 56 | a0001c0001t0001g0205 a0001c0001t0001g0215 a0001c0001t0001g0216 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.284-23174_284-2317 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175711 | TACACAC | T | 10 | a0001c0001t0001g0227 a0001c0001t0001g0339 a0001c0001t0002g0276 others(7): Show |
10 | HG01516.hp2 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-23176_284-2317 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175711 | TACACACA others(3): Show |
T | 2 | a0001c0001t0023g0337 a0001c0001t0023g0343 |
2 | HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.284-23180_284-2317 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | ||||||
| chr14:74175732 | ACACACAC others(13): Show |
A | 10 | a0001c0002t0009g0002 a0001c0002t0009g0193 a0001c0002t0009g0278 others(7): Show |
11 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-23188_284-2316 others(24): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175732 | ||||||
| chr14:74175746 | ACACACC | A | 7 | a0001c0001t0001g0335 a0001c0001t0004g0077 a0001c0001t0004g0206 others(4): Show |
7 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-23174_284-2316 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175746 | ||||||
| chr14:74175748 | A | ACACACAC others(4): Show |
2 | a0001c0001t0007g0099 a0001c0001t0010g0123 |
2 | HG00544.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.284-23171_284-2317 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | ||||||
| chr14:74175748 | A | ACACACAC others(11): Show |
1 | a0001c0001t0006g0100 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.284-23171_284-2317 others(22): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | ||||||
| chr14:74175748 | A | ACACACAC others(9): Show |
1 | a0001c0001t0013g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.284-23171_284-2317 others(20): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | ||||||
| chr14:74175748 | A | ACACACAC others(7): Show |
3 | a0001c0001t0007g0098 a0001c0001t0007g0122 a0001c0001t0027g0124 |
3 | HG02698.hp1 HG03017.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.284-23171_284-2317 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | ||||||
| chr14:74175748 | A | ACACACAC others(5): Show |
8 | a0001c0001t0007g0004 a0001c0001t0007g0095 a0001c0001t0007g0108 others(5): Show |
8 | HG00438.hp1 HG03704.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.284-23171_284-2317 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | ||||||
| chr14:74175748 | A | ACACACAC others(3): Show |
12 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0006g0102 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-23171_284-2317 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | ||||||
| chr14:74175748 | A | C | 1 | a0001c0001t0001g0253 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.284-23174A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175748 | |||||||
| chr14:74175748 | ACACC | A | 11 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0012g0078 others(8): Show |
11 | HG01192.hp1 HG02027.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-23172_284-2316 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | ||||||
| chr14:74175750 | A | C | 33 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(30): Show |
33 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.284-23172A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175750 | |||||||
| chr14:74175750 | ACC | A | 14 | a0001c0001t0001g0272 a0001c0001t0002g0260 a0001c0001t0002g0261 others(11): Show |
14 | HG01243.hp2 HG01257.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.284-23168_284-2316 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175750 | ||||||
| chr14:74175751 | C | CACACACA others(4): Show |
1 | a0001c0001t0001g0110 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.284-23171_284-2317 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175751 | |||||||
| chr14:74175752 | C | A | 112 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(109): Show |
113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.284-23170C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175752 | |||||||
| chr14:74175753 | C | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0074 a0001c0001t0006g0211 |
3 | NA18950.hp1 NA19012.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.284-23169C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175753 | |||||||
| chr14:74175848 | C | T | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284-23074C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175848 | |||||||
| chr14:74176031 | G | A | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-22891G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176031 | |||||||
| chr14:74176089 | A | G | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-22833A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176089 | |||||||
| chr14:74176224 | G | T | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-22698G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176224 | |||||||
| chr14:74176227 | A | G | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-22695A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176227 | |||||||
| chr14:74176297 | A | G | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-22625A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176297 | |||||||
| chr14:74176301 | G | A | 1 | a0001c0001t0004g0009 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.284-22621G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176301 | |||||||
| chr14:74176540 | A | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-22382A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176540 | |||||||
| chr14:74176853 | T | C | 230 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(227): Show |
231 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.284-22069T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176853 | |||||||
| chr14:74176963 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG02559.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.284-21959G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176963 | |||||||
| chr14:74177030 | C | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-21892C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177030 | |||||||
| chr14:74177218 | G | A | 4 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0004g0344 others(1): Show |
4 | HG01123.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-21704G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177218 | |||||||
| chr14:74177249 | C | T | 4 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0062 others(1): Show |
4 | HG00323.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-21673C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177249 | |||||||
| chr14:74177376 | T | C | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-21546T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177376 | |||||||
| chr14:74177418 | A | G | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-21504A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177418 | |||||||
| chr14:74177480 | AAT | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-21440_284-2143 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74177480 | ||||||
| chr14:74177531 | A | G | 1 | a0001c0001t0004g0207 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284-21391A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177531 | |||||||
| chr14:74177743 | G | A | 1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.284-21179G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177743 | |||||||
| chr14:74177808 | C | T | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-21114C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177808 | |||||||
| chr14:74177904 | A | G | 10 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0241 others(7): Show |
10 | HG01358.hp2 NA18947.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-21018A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177904 | |||||||
| chr14:74178119 | G | A | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.284-20803G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178119 | |||||||
| chr14:74178355 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.284-20567A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178355 | |||||||
| chr14:74178460 | A | AT | 53 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0216 others(50): Show |
53 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.284-20447dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74178460 | ||||||
| chr14:74178476 | G | A | 1 | a0001c0001t0042g0302 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.284-20446G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178476 | |||||||
| chr14:74178542 | C | A | 3 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.284-20380C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178542 | |||||||
| chr14:74178568 | G | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-20354G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178568 | |||||||
| chr14:74178572 | G | A | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-20350G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178572 | |||||||
| chr14:74178632 | AT | A | 243 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(240): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.284-20283delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74178632 | ||||||
| chr14:74178878 | C | G | 1 | a0001c0001t0008g0331 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.284-20044C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178878 | |||||||
| chr14:74179223 | T | C | 1 | a0001c0001t0037g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.284-19699T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179223 | |||||||
| chr14:74179374 | T | G | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-19548T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179374 | |||||||
| chr14:74179406 | T | G | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-19516T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179406 | |||||||
| chr14:74179469 | C | T | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-19453C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179469 | |||||||
| chr14:74179503 | T | C | 73 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(70): Show |
73 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.284-19419T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179503 | |||||||
| chr14:74179520 | G | A | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-19402G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179520 | |||||||
| chr14:74179562 | G | A | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-19360G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179562 | |||||||
| chr14:74179655 | CA | C | 135 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(132): Show |
136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.284-19253delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74179655 | ||||||
| chr14:74179655 | CAA | C | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-19254_284-1925 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74179655 | ||||||
| chr14:74179673 | AAAAAAG | A | 76 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(73): Show |
76 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.284-19243_284-1923 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74179673 | ||||||
| chr14:74179674 | AAAAAG | A | 67 | a0001c0001t0001g0205 a0001c0001t0001g0231 a0001c0001t0001g0234 others(64): Show |
68 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.284-19243_284-1923 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74179674 | ||||||
| chr14:74179692 | A | C | 1 | a0001c0001t0001g0339 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-19230A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179692 | |||||||
| chr14:74179696 | C | A | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-19226C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179696 | |||||||
| chr14:74179700 | G | A | 2 | a0001c0001t0003g0034 a0001c0001t0004g0026 |
2 | NA18956.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.284-19222G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179700 | |||||||
| chr14:74179890 | A | G | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-19032A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179890 | |||||||
| chr14:74179896 | T | C | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-19026T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179896 | |||||||
| chr14:74179912 | A | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-19010A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179912 | |||||||
| chr14:74179972 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-18950C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179972 | |||||||
| chr14:74180002 | C | T | 4 | a0001c0001t0002g0166 a0001c0001t0006g0167 a0001c0001t0020g0132 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-18920C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180002 | |||||||
| chr14:74180129 | C | T | 45 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-18793C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180129 | |||||||
| chr14:74180191 | A | G | 73 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(70): Show |
73 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.284-18731A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180191 | |||||||
| chr14:74180219 | A | T | 81 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-18703A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180219 | |||||||
| chr14:74180262 | A | AT | 17 | a0001c0001t0002g0147 a0001c0001t0004g0077 a0001c0001t0004g0206 others(14): Show |
17 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-18639dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74180262 | ||||||
| chr14:74180262 | A | ATT | 79 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(76): Show |
79 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.284-18640_284-1863 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74180262 | ||||||
| chr14:74180262 | A | ATTT | 11 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0226 others(8): Show |
11 | HG00099.hp1 HG00735.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-18641_284-1863 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74180262 | ||||||
| chr14:74180262 | AT | A | 122 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0002g0092 others(119): Show |
123 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.284-18639delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74180262 | ||||||
| chr14:74180271 | T | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-18651T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180271 | |||||||
| chr14:74180359 | G | A | 3 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.284-18563G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180359 | |||||||
| chr14:74180394 | T | C | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-18528T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180394 | |||||||
| chr14:74180422 | T | C | 243 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(240): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.284-18500T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180422 | |||||||
| chr14:74180432 | AT | A | 9 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0272 others(6): Show |
9 | HG01192.hp1 HG02027.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-18479delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74180432 | ||||||
| chr14:74180460 | T | C | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-18462T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180460 | |||||||
| chr14:74180501 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-18421A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180501 | |||||||
| chr14:74180715 | A | G | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-18207A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180715 | |||||||
| chr14:74180879 | C | T | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-18043C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180879 | |||||||
| chr14:74181033 | A | G | 1 | a0001c0001t0012g0083 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.284-17889A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181033 | |||||||
| chr14:74181056 | T | C | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-17866T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181056 | |||||||
| chr14:74181080 | C | T | 1 | a0001c0001t0005g0305 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.284-17842C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181080 | |||||||
| chr14:74181107 | C | CA | 10 | a0001c0001t0002g0129 a0001c0001t0002g0146 a0001c0001t0002g0175 others(7): Show |
10 | HG01168.hp2 HG02027.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-17794dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181107 | ||||||
| chr14:74181107 | CA | C | 25 | a0001c0001t0002g0092 a0001c0001t0003g0060 a0001c0001t0011g0204 others(22): Show |
26 | HG01243.hp1 HG01243.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.284-17794delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181107 | ||||||
| chr14:74181107 | CAA | C | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-17795_284-1779 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181107 | ||||||
| chr14:74181107 | CAAAA | C | 132 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(129): Show |
133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.284-17797_284-1779 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181107 | ||||||
| chr14:74181123 | A | G | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-17799A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181123 | |||||||
| chr14:74181128 | A | G | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-17794A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181128 | |||||||
| chr14:74181201 | A | G | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-17721A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181201 | |||||||
| chr14:74181237 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.284-17685A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181237 | |||||||
| chr14:74181259 | T | C | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-17663T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181259 | |||||||
| chr14:74181435 | C | CA | 43 | a0001c0001t0002g0173 a0001c0001t0002g0192 a0001c0001t0003g0323 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.284-17471dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181435 | ||||||
| chr14:74181512 | G | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0253 |
2 | NA19072.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.284-17410G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181512 | |||||||
| chr14:74181548 | C | G | 1 | a0001c0001t0007g0105 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.284-17374C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181548 | |||||||
| chr14:74181650 | TACAG | T | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-17269_284-1726 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181650 | ||||||
| chr14:74182037 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.284-16885G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182037 | |||||||
| chr14:74182157 | CATG | C | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-16764_284-1676 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182157 | |||||||
| chr14:74182403 | A | G | 288 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.284-16519A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182403 | |||||||
| chr14:74182426 | A | G | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-16496A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182426 | |||||||
| chr14:74182447 | A | C | 1 | a0001c0001t0005g0330 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.284-16475A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182447 | |||||||
| chr14:74182454 | G | A | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-16468G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182454 | |||||||
| chr14:74182477 | T | C | 2 | a0001c0001t0003g0034 a0001c0001t0004g0026 |
2 | NA18956.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.284-16445T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182477 | |||||||
| chr14:74182499 | A | AGCCAAGT others(27): Show |
41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-16398_284-1639 others(38): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74182499 | ||||||
| chr14:74182561 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.284-16361A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182561 | |||||||
| chr14:74182577 | C | T | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-16345C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182577 | |||||||
| chr14:74182659 | T | G | 81 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-16263T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182659 | |||||||
| chr14:74182828 | C | T | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.284-16094C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182828 | |||||||
| chr14:74182877 | C | A | 1 | a0001c0001t0001g0339 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-16045C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182877 | |||||||
| chr14:74183102 | TC | T | 148 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(145): Show |
149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.284-15819delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183102 | |||||||
| chr14:74183103 | C | T | 139 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(136): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.284-15819C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183103 | |||||||
| chr14:74183108 | T | C | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-15814T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183108 | |||||||
| chr14:74183157 | A | G | 143 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-15765A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183157 | |||||||
| chr14:74183252 | C | CA | 72 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(69): Show |
72 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.284-15669dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74183252 | ||||||
| chr14:74183254 | C | T | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG01496.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.284-15668C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183254 | |||||||
| chr14:74183282 | G | A | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-15640G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183282 | |||||||
| chr14:74183290 | G | A | 1 | a0001c0001t0008g0307 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.284-15632G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183290 | |||||||
| chr14:74183608 | T | A | 1 | a0001c0001t0002g0181 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.284-15314T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183608 | |||||||
| chr14:74183635 | T | C | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-15287T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183635 | |||||||
| chr14:74183657 | C | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-15265C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183657 | |||||||
| chr14:74183765 | C | G | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-15157C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183765 | |||||||
| chr14:74183795 | C | T | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-15127C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183795 | |||||||
| chr14:74184282 | T | C | 2 | a0001c0001t0003g0065 a0001c0001t0004g0029 |
2 | HG00673.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.284-14640T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184282 | |||||||
| chr14:74184305 | G | A | 7 | a0001c0001t0001g0205 a0001c0001t0001g0231 a0001c0001t0001g0234 others(4): Show |
7 | HG01081.hp2 HG01884.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-14617G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184305 | |||||||
| chr14:74184363 | G | A | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-14559G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184363 | |||||||
| chr14:74184374 | T | C | 4 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-14548T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184374 | |||||||
| chr14:74184411 | A | G | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-14511A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184411 | |||||||
| chr14:74184535 | C | T | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-14387C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184535 | |||||||
| chr14:74184559 | C | G | 1 | a0001c0001t0019g0149 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.284-14363C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184559 | |||||||
| chr14:74184627 | G | A | 243 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(240): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.284-14295G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184627 | |||||||
| chr14:74184738 | C | T | 129 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(126): Show |
130 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.284-14184C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184738 | |||||||
| chr14:74184930 | A | C | 88 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(85): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.284-13992A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184930 | |||||||
| chr14:74185038 | T | C | 3 | a0001c0001t0011g0204 a0001c0001t0014g0203 a0001c0001t0029g0202 |
3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-13884T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185038 | |||||||
| chr14:74185068 | A | T | 1 | a0001c0001t0002g0134 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.284-13854A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185068 | |||||||
| chr14:74185209 | A | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-13713A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185209 | |||||||
| chr14:74185309 | C | CT | 81 | a0001c0001t0001g0205 a0001c0001t0001g0215 a0001c0001t0001g0216 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-13590dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74185309 | ||||||
| chr14:74185309 | C | CTT | 35 | a0001c0001t0001g0214 a0001c0001t0001g0248 a0001c0001t0001g0272 others(32): Show |
35 | HG00735.hp2 HG01074.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.284-13591_284-1359 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74185309 | ||||||
| chr14:74185309 | C | CTTT | 97 | a0001c0001t0001g0213 a0001c0001t0001g0335 a0001c0001t0002g0073 others(94): Show |
98 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.284-13592_284-1359 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74185309 | ||||||
| chr14:74185309 | C | CTTTT | 21 | a0001c0001t0002g0027 a0001c0001t0003g0016 a0001c0001t0003g0019 others(18): Show |
21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.284-13593_284-1359 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74185309 | ||||||
| chr14:74185309 | C | CTTTTT | 9 | a0001c0001t0004g0036 a0001c0001t0005g0318 a0001c0001t0005g0328 others(6): Show |
9 | HG02027.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-13594_284-1359 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74185309 | ||||||
| chr14:74185313 | T | C | 8 | a0001c0001t0002g0130 a0001c0001t0002g0166 a0001c0001t0006g0154 others(5): Show |
8 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-13609T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185313 | |||||||
| chr14:74185372 | T | C | 1 | a0001c0001t0037g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.284-13550T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185372 | |||||||
| chr14:74185504 | G | A | 129 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(126): Show |
130 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.284-13418G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185504 | |||||||
| chr14:74185564 | C | T | 1 | a0001c0001t0014g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.284-13358C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185564 | |||||||
| chr14:74185572 | G | C | 10 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0241 others(7): Show |
10 | HG01358.hp2 NA18947.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-13350G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185572 | |||||||
| chr14:74185602 | C | T | 1 | a0001c0001t0017g0322 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.284-13320C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185602 | |||||||
| chr14:74185750 | T | C | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-13172T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185750 | |||||||
| chr14:74185823 | G | A | 45 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(42): Show |
45 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-13099G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185823 | |||||||
| chr14:74185839 | A | G | 72 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(69): Show |
72 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.284-13083A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185839 | |||||||
| chr14:74185908 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284-13014A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185908 | |||||||
| chr14:74185990 | G | T | 7 | a0001c0001t0008g0296 a0001c0001t0008g0308 a0001c0001t0008g0309 others(4): Show |
7 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-12932G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185990 | |||||||
| chr14:74186010 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.284-12912C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186010 | |||||||
| chr14:74186164 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(1): Show |
4 | HG02258.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-12758A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186164 | |||||||
| chr14:74186206 | C | T | 9 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0272 others(6): Show |
9 | HG01192.hp1 HG02027.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-12716C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186206 | |||||||
| chr14:74186229 | C | T | 288 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0191 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.284-12693C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186229 | |||||||
| chr14:74186295 | AAAAC | A | 5 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0001g0291 others(2): Show |
5 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-12607_284-1260 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74186295 | ||||||
| chr14:74186428 | A | G | 1 | a0001c0001t0004g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.284-12494A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186428 | |||||||
| chr14:74186453 | G | A | 1 | a0001c0001t0025g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.284-12469G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186453 | |||||||
| chr14:74186783 | G | A | 10 | a0001c0001t0002g0092 a0001c0001t0011g0204 a0001c0001t0014g0198 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-12139G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186783 | |||||||
| chr14:74186877 | A | G | 1 | a0001c0001t0013g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.284-12045A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186877 | |||||||
| chr14:74186933 | G | T | 2 | a0001c0001t0017g0321 a0001c0001t0017g0322 |
2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.284-11989G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186933 | |||||||
| chr14:74186948 | A | G | 231 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(228): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-11974A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186948 | |||||||
| chr14:74187037 | A | C | 1 | a0001c0001t0002g0261 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.284-11885A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187037 | |||||||
| chr14:74187238 | G | T | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-11684G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187238 | |||||||
| chr14:74187447 | C | A | 1 | a0001c0001t0002g0153 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.284-11475C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187447 | |||||||
| chr14:74187450 | A | G | 75 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(72): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.284-11472A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187450 | |||||||
| chr14:74187489 | C | T | 241 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(238): Show |
242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.284-11433C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187489 | |||||||
| chr14:74187549 | T | C | 5 | a0001c0001t0001g0152 a0001c0001t0002g0137 a0001c0001t0002g0150 others(2): Show |
5 | HG01069.hp2 HG01346.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-11373T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187549 | |||||||
| chr14:74187803 | T | C | 1 | a0001c0001t0004g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.284-11119T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187803 | |||||||
| chr14:74188027 | A | G | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-10895A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188027 | |||||||
| chr14:74188174 | A | G | 1 | a0001c0002t0009g0282 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.284-10748A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188174 | |||||||
| chr14:74188418 | T | C | 243 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(240): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.284-10504T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188418 | |||||||
| chr14:74188440 | A | AT | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-10475dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74188440 | ||||||
| chr14:74188447 | T | A | 3 | a0001c0001t0013g0094 a0001c0001t0013g0125 a0001c0001t0028g0101 |
3 | HG02602.hp2 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.284-10475T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188447 | |||||||
| chr14:74188519 | A | G | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-10403A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188519 | |||||||
| chr14:74188571 | C | T | 94 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(91): Show |
94 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-10351C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188571 | |||||||
| chr14:74188671 | C | T | 3 | a0001c0001t0014g0198 a0001c0001t0014g0199 a0001c0001t0014g0200 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.284-10251C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188671 | |||||||
| chr14:74188714 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.284-10208G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188714 | |||||||
| chr14:74188761 | A | G | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.284-10161A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188761 | |||||||
| chr14:74188880 | T | G | 3 | a0001c0001t0002g0164 a0001c0001t0006g0156 a0001c0001t0033g0182 |
3 | HG02071.hp1 NA18967.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.284-10042T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188880 | |||||||
| chr14:74188955 | C | T | 102 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-9967C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188955 | |||||||
| chr14:74189025 | G | C | 1 | a0001c0001t0004g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.284-9897G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189025 | |||||||
| chr14:74189175 | C | T | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-9747C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189175 | |||||||
| chr14:74189193 | T | C | 7 | a0001c0001t0011g0204 a0001c0001t0014g0198 a0001c0001t0014g0199 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-9729T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189193 | |||||||
| chr14:74189249 | T | C | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-9673T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189249 | |||||||
| chr14:74189359 | T | A | 1 | a0001c0001t0003g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.284-9563T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189359 | |||||||
| chr14:74189477 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284-9445C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189477 | |||||||
| chr14:74189497 | A | G | 8 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0241 others(5): Show |
8 | NA18947.hp2 NA18962.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-9425A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189497 | |||||||
| chr14:74189626 | A | G | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.284-9296A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189626 | |||||||
| chr14:74189710 | A | G | 2 | a0001c0001t0012g0081 a0001c0001t0012g0083 |
2 | HG01243.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.284-9212A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189710 | |||||||
| chr14:74189938 | G | A | 2 | a0001c0001t0006g0100 a0001c0001t0006g0102 |
2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.284-8984G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189938 | |||||||
| chr14:74189963 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.284-8959A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189963 | |||||||
| chr14:74190230 | T | C | 1 | a0001c0001t0027g0124 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.284-8692T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190230 | |||||||
| chr14:74190345 | G | A | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-8577G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190345 | |||||||
| chr14:74190360 | T | C | 232 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(229): Show |
233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-8562T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190360 | |||||||
| chr14:74190389 | C | CTT | 13 | a0001c0001t0001g0243 a0001c0001t0001g0263 a0001c0001t0001g0274 others(10): Show |
13 | HG00099.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.284-8514_284-8513d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | ||||||
| chr14:74190389 | C | CTTT | 81 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(78): Show |
81 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-8515_284-8513d others(5): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | ||||||
| chr14:74190389 | C | CTTTT | 7 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0292 others(4): Show |
7 | HG01175.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-8516_284-8513d others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | ||||||
| chr14:74190389 | C | CTTTTT | 11 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0011g0221 others(8): Show |
11 | HG01243.hp2 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-8517_284-8513d others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | ||||||
| chr14:74190389 | C | CTTTTTT | 6 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-8518_284-8513d others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | ||||||
| chr14:74190389 | C | CTTTTTTT others(1): Show |
58 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(55): Show |
58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.284-8520_284-8513d others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | ||||||
| chr14:74190389 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0022 others(3): Show |
6 | HG00408.hp2 HG00544.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-8521_284-8513d others(11): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | ||||||
| chr14:74190389 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0003g0076 a0001c0001t0004g0036 a0001c0001t0015g0041 others(1): Show |
4 | HG01943.hp2 HG02027.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-8522_284-8513d others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | ||||||
| chr14:74190389 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.284-8533C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190389 | |||||||
| chr14:74190389 | CTTT | C | 39 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(36): Show |
40 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.284-8515_284-8513d others(5): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | ||||||
| chr14:74190519 | G | C | 1 | a0001c0001t0015g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.284-8403G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190519 | |||||||
| chr14:74190597 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.284-8325G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190597 | |||||||
| chr14:74190828 | T | C | 11 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(8): Show |
11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-8094T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190828 | |||||||
| chr14:74191263 | G | A | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-7659G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191263 | |||||||
| chr14:74191326 | C | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-7596C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191326 | |||||||
| chr14:74191719 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-7203C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191719 | |||||||
| chr14:74191727 | G | A | 7 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0340 others(4): Show |
7 | HG01106.hp1 HG01255.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-7195G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191727 | |||||||
| chr14:74191734 | C | T | 1 | a0001c0001t0005g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.284-7188C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191734 | |||||||
| chr14:74191790 | C | T | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-7132C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191790 | |||||||
| chr14:74191801 | T | C | 1 | a0001c0001t0003g0018 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.284-7121T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191801 | |||||||
| chr14:74191949 | T | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-6973T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191949 | |||||||
| chr14:74192086 | AC | A | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-6834delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74192086 | ||||||
| chr14:74192231 | A | C | 1 | a0001c0001t0013g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.284-6691A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192231 | |||||||
| chr14:74192265 | G | A | 4 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-6657G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192265 | |||||||
| chr14:74192268 | GTTGTTTT others(12): Show |
G | 1 | a0001c0001t0002g0145 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.284-6638_284-6620d others(21): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74192268 | ||||||
| chr14:74192442 | C | G | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-6480C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192442 | |||||||
| chr14:74192497 | G | A | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.284-6425G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192497 | |||||||
| chr14:74192505 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.284-6417C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192505 | |||||||
| chr14:74192608 | G | C | 1 | a0001c0001t0002g0093 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.284-6314G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192608 | |||||||
| chr14:74192677 | A | G | 2 | a0001c0001t0004g0047 a0001c0001t0004g0049 |
2 | NA18942.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.284-6245A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192677 | |||||||
| chr14:74192934 | G | T | 145 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(142): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.284-5988G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192934 | |||||||
| chr14:74192987 | T | G | 145 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(142): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.284-5935T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192987 | |||||||
| chr14:74193038 | G | A | 1 | a0001c0001t0011g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.284-5884G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193038 | |||||||
| chr14:74193087 | A | C | 47 | a0001c0001t0001g0161 a0001c0001t0001g0215 a0001c0001t0001g0216 others(44): Show |
47 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.284-5835A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193087 | |||||||
| chr14:74193240 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.284-5682G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193240 | |||||||
| chr14:74193247 | C | CA | 134 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(131): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.284-5661dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74193247 | ||||||
| chr14:74193247 | C | CAA | 11 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-5662_284-5661d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74193247 | ||||||
| chr14:74193247 | CA | C | 100 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0002g0092 others(97): Show |
101 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.284-5661delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74193247 | ||||||
| chr14:74193286 | T | C | 145 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(142): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.284-5636T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193286 | |||||||
| chr14:74193401 | G | A | 1 | a0001c0001t0007g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.284-5521G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193401 | |||||||
| chr14:74193417 | TA | T | 138 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(135): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.284-5491delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74193417 | ||||||
| chr14:74193422 | A | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-5500A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193422 | |||||||
| chr14:74193515 | A | G | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-5407A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193515 | |||||||
| chr14:74193599 | G | A | 145 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(142): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.284-5323G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193599 | |||||||
| chr14:74193617 | T | G | 41 | a0001c0001t0003g0323 a0001c0001t0005g0295 a0001c0001t0005g0297 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-5305T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193617 | |||||||
| chr14:74193668 | T | C | 1 | a0001c0001t0011g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.284-5254T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193668 | |||||||
| chr14:74193805 | A | G | 145 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(142): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.284-5117A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193805 | |||||||
| chr14:74193964 | T | C | 2 | a0001c0001t0003g0059 a0001c0001t0003g0060 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.284-4958T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193964 | |||||||
| chr14:74194021 | A | C | 244 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(241): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.284-4901A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194021 | |||||||
| chr14:74194095 | T | C | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-4827T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194095 | |||||||
| chr14:74194228 | T | G | 7 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0011g0221 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-4694T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194228 | |||||||
| chr14:74194314 | G | A | 1 | a0001c0001t0004g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.284-4608G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194314 | |||||||
| chr14:74194656 | C | T | 1 | a0001c0001t0005g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.284-4266C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194656 | |||||||
| chr14:74194714 | G | A | 2 | a0001c0002t0009g0002 a0001c0002t0009g0193 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-4208G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194714 | |||||||
| chr14:74194734 | C | T | 2 | a0001c0001t0002g0138 a0001c0001t0006g0176 |
2 | HG00642.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.284-4188C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194734 | |||||||
| chr14:74194791 | G | C | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-4131G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194791 | |||||||
| chr14:74194794 | G | A | 103 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(100): Show |
103 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.284-4128G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194794 | |||||||
| chr14:74194795 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0015g0090 a0001c0001t0037g0091 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-4127C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194795 | |||||||
| chr14:74194796 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.284-4126G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194796 | |||||||
| chr14:74194947 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.284-3975C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194947 | |||||||
| chr14:74194978 | G | A | 3 | a0001c0001t0003g0008 a0001c0001t0003g0018 a0001c0001t0004g0009 |
3 | HG00597.hp1 HG02083.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.284-3944G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194978 | |||||||
| chr14:74195058 | A | C | 46 | a0001c0001t0001g0161 a0001c0001t0001g0215 a0001c0001t0001g0216 others(43): Show |
46 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.284-3864A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195058 | |||||||
| chr14:74195070 | G | A | 6 | a0001c0001t0001g0335 a0001c0001t0004g0206 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-3852G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195070 | |||||||
| chr14:74195468 | A | C | 1 | a0001c0001t0003g0323 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.284-3454A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195468 | |||||||
| chr14:74195477 | G | A | 8 | a0001c0001t0004g0077 a0001c0001t0012g0078 a0001c0001t0012g0081 others(5): Show |
8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-3445G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195477 | |||||||
| chr14:74195556 | A | ACG | 12 | a0001c0001t0004g0077 a0001c0001t0004g0348 a0001c0001t0004g0349 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-3366_284-3365i others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195556 | |||||||
| chr14:74195556 | A | ATG | 239 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0161 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.284-3347_284-3346d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74195556 | ||||||
| chr14:74195556 | A | ATGTG | 9 | a0001c0001t0011g0204 a0001c0001t0011g0223 a0001c0001t0011g0224 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-3349_284-3346d others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74195556 | ||||||
| chr14:74195556 | A | ATGTGTG | 12 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0005g0303 others(9): Show |
12 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-3351_284-3346d others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74195556 | ||||||
| chr14:74195575 | T | TGC | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-3343_284-3342d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74195575 | ||||||
| chr14:74195579 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.284-3343C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195579 | |||||||
| chr14:74195616 | G | A | 1 | a0001c0001t0006g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.284-3306G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195616 | |||||||
| chr14:74195713 | A | T | 1 | a0001c0001t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.284-3209A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195713 | |||||||
| chr14:74195775 | T | G | 244 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0213 others(241): Show |
246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.284-3147T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195775 | |||||||
| chr14:74196671 | CT | C | 9 | a0001c0001t0001g0191 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-2250delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196671 | |||||||
| chr14:74196692 | T | C | 3 | a0001c0001t0003g0032 a0001c0001t0003g0038 a0001c0001t0003g0052 |
3 | NA18960.hp1 NA18961.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.284-2230T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196692 | |||||||
| chr14:74196693 | G | A | 3 | a0001c0001t0003g0032 a0001c0001t0003g0038 a0001c0001t0003g0052 |
3 | NA18960.hp1 NA18961.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.284-2229G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196693 | |||||||
| chr14:74196718 | C | T | 8 | a0001c0002t0009g0278 a0001c0002t0009g0279 a0001c0002t0009g0280 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-2204C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196718 | |||||||
| chr14:74196755 | C | T | 4 | a0001c0001t0004g0348 a0001c0001t0004g0349 a0001c0001t0004g0350 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-2167C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196755 | |||||||
| chr14:74196782 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.284-2140T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196782 | |||||||
| chr14:74196839 | A | C | 1 | a0001c0001t0012g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.284-2083A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196839 | |||||||
| chr14:74196848 | G | A | 5 | a0001c0001t0011g0221 a0001c0001t0011g0222 a0001c0001t0011g0223 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-2074G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196848 | |||||||
| chr14:74196895 | G | A | 34 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0002g0117 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-2027G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196895 | |||||||
| chr14:74197163 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.284-1759T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197163 | |||||||
| chr14:74197266 | A | G | 74 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0003g0005 others(71): Show |
74 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.284-1656A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197266 | |||||||
| chr14:74197291 | G | A | 3 | a0001c0001t0004g0206 a0001c0001t0012g0209 a0001c0001t0045g0188 |
3 | HG02055.hp2 HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.284-1631G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197291 | |||||||
| chr14:74197303 | C | G | 1 | a0001c0001t0003g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.284-1619C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197303 | |||||||
| chr14:74197303 | C | T | 1 | a0001c0001t0005g0324 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.284-1619C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197303 | |||||||
| chr14:74197315 | G | A | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284-1607G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197315 | |||||||
| chr14:74197513 | A | G | 2 | a0001c0001t0011g0204 a0001c0001t0014g0203 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.284-1409A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197513 | |||||||
| chr14:74197794 | A | G | 1 | a0001c0001t0002g0134 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.284-1128A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197794 | |||||||
| chr14:74197795 | C | G | 2 | a0001c0001t0001g0251 a0001c0001t0029g0202 |
2 | HG00639.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.284-1127C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197795 | |||||||
| chr14:74197961 | A | G | 1 | a0001c0001t0023g0343 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.284-961A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197961 | |||||||
| chr14:74197998 | C | T | 24 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0003g0059 others(21): Show |
24 | HG00558.hp1 HG01167.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.284-924C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197998 | |||||||
| chr14:74198007 | T | C | 16 | a0001c0001t0002g0189 a0001c0001t0003g0088 a0001c0001t0015g0090 others(13): Show |
17 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-915T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198007 | |||||||
| chr14:74198117 | A | T | 1 | a0001c0001t0005g0315 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.284-805A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198117 | |||||||
| chr14:74198268 | A | G | 7 | a0001c0001t0001g0205 a0001c0001t0001g0236 a0001c0001t0001g0238 others(4): Show |
7 | HG01081.hp2 HG02145.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-654A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198268 | |||||||
| chr14:74198418 | G | T | 11 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0192 others(8): Show |
11 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-504G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198418 | |||||||
| chr14:74198637 | T | G | 11 | a0001c0001t0002g0136 a0001c0001t0003g0016 a0001c0001t0003g0040 others(8): Show |
11 | HG01928.hp1 HG01943.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-285T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198637 | |||||||
| chr14:74198690 | G | C | 36 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0006g0100 others(33): Show |
36 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.284-232G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198690 | |||||||
| chr14:74198700 | A | G | 1 | a0001c0001t0003g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.284-222A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198700 | |||||||
| chr14:74198840 | G | A | 114 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0152 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.284-82G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198840 |