Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26049 |
| ensemblid | ENSG00000198780.13 |
| hgncid | 29138 |
| symbol | FAM169A |
| name | family with sequence similarity 169 member A |
| refseq_nuc | NM_001376049.1 |
| refseq_prot | NP_001362978.1 |
| ensembl_nuc | ENST00000687041.1 |
| ensembl_prot | ENSP00000508577.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 74777574 |
| end | 74866387 |
| strand | - |
| ver | v1.2 |
| region | chr5:74777574-74866387 |
| region5000 | chr5:74772574-74871387 |
| regionname0 | FAM169A_chr5_74777574_74866387 |
| regionname5000 | FAM169A_chr5_74772574_74871387 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 670 | 307 | 88 | 64 | 101 | 14 | 38 | 65 | FAM169A_chr5_74772574_74871387 | FAM169A | MAFPV others(665): Show |
chr5 | 74772574 | 74871387 |
| a0002 | 0/0 | 670 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | MAFPV others(665): Show |
chr5 | 74772574 | 74871387 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2010 | 261 | 55 | 55 | 98 | 13 | 38 | FAM169A_chr5_74772574_74871387 | FAM169A | ATGGC others(2005): Show |
chr5 | 74772574 | 74871387 | ||
| a0001c0002 | 0/0 | 2010 | 27 | 24 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | ATGGC others(2005): Show |
chr5 | 74772574 | 74871387 | ||
| a0001c0003 | 0/0 | 2010 | 14 | 9 | 2 | 3 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | ATGGC others(2005): Show |
chr5 | 74772574 | 74871387 | ||
| a0001c0004 | 0/0 | 2010 | 3 | 0 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | ATGGC others(2005): Show |
chr5 | 74772574 | 74871387 | ||
| a0001c0006 | 0/0 | 2010 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | ATGGC others(2005): Show |
chr5 | 74772574 | 74871387 | ||
| a0001c0007 | 0/0 | 2010 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | ATGGC others(2005): Show |
chr5 | 74772574 | 74871387 | ||
| a0002c0005 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | ATGGC others(2005): Show |
chr5 | 74772574 | 74871387 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6125 | 75 | 14 | 19 | 20 | 6 | 16 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0002 | 1/0 | 6125 | 69 | 7 | 11 | 38 | 3 | 9 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0003 | 0/0 | 6124 | 41 | 2 | 9 | 24 | 1 | 5 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0004 | 0/0 | 6123 | 34 | 14 | 11 | 2 | 2 | 5 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6118): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0005 | 0/0 | 6124 | 2 | 2 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0006 | 0/0 | 6124 | 11 | 11 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0008 | 0/0 | 6124 | 7 | 0 | 0 | 7 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0010 | 0/0 | 6119 | 3 | 0 | 2 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6114): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0012 | 0/0 | 6125 | 2 | 0 | 0 | 0 | 0 | 2 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0013 | 0/0 | 6123 | 2 | 2 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6118): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0014 | 0/1 | 6119 | 1 | 0 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6114): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0017 | 0/0 | 6125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0019 | 0/0 | 6125 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0020 | 0/0 | 6125 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0021 | 0/0 | 6125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0022 | 0/0 | 6125 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0023 | 0/0 | 6125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0024 | 0/0 | 6125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0025 | 0/0 | 6124 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0026 | 0/0 | 6124 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0027 | 0/0 | 6124 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0028 | 0/0 | 6123 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6118): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0030 | 0/0 | 6124 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0031 | 0/0 | 6124 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0001t0032 | 0/0 | 6125 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0001c0002t0005 | 0/0 | 6124 | 5 | 5 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0002t0007 | 0/0 | 6123 | 11 | 11 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6118): Show |
chr5 | 74772574 | 74871387 |
| a0001c0002t0009 | 0/0 | 6124 | 6 | 3 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0002t0011 | 0/0 | 6119 | 2 | 2 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6114): Show |
chr5 | 74772574 | 74871387 |
| a0001c0002t0016 | 0/0 | 6124 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0002t0018 | 0/0 | 6119 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6114): Show |
chr5 | 74772574 | 74871387 |
| a0001c0002t0029 | 0/0 | 6123 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6118): Show |
chr5 | 74772574 | 74871387 |
| a0001c0003t0005 | 0/0 | 6124 | 13 | 8 | 2 | 3 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0003t0015 | 0/0 | 6124 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0004t0003 | 0/0 | 6124 | 3 | 0 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| a0001c0006t0010 | 0/0 | 6119 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6114): Show |
chr5 | 74772574 | 74871387 |
| a0001c0007t0002 | 0/0 | 6125 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6120): Show |
chr5 | 74772574 | 74871387 |
| a0002c0005t0003 | 0/0 | 6124 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | AGTGC others(6119): Show |
chr5 | 74772574 | 74871387 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0008g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0008g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0008g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0010g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0010g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0010g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0012g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0012g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0013g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0013g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0014g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0017g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0019g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0020g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0021g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0022g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0023g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0024g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0025g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0026g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0027g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0028g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0030g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0031g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0032g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0009g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0009g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0011g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0011g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0016g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0018g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0029g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0015g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0004t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0004t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0004t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0006t0010g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0007t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0002c0005t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0266 | EUR | GBR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | GBR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00140 | hp2 | a0001 | c0001 | t0010 | g0038 | EUR | GBR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0107 | EUR | FIN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0032 | EUR | FIN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | FIN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00408 | hp1 | a0001 | c0001 | t0023 | g0204 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00438 | hp1 | a0001 | c0003 | t0005 | g0228 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00642 | hp2 | a0001 | c0001 | t0022 | g0181 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0052 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00735 | hp2 | a0001 | c0003 | t0005 | g0227 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0044 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00741 | hp2 | a0001 | c0002 | t0009 | g0247 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01106 | hp2 | a0001 | c0002 | t0009 | g0248 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01109 | hp1 | a0001 | c0004 | t0003 | g0268 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01167 | hp1 | a0001 | c0002 | t0009 | g0243 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01175 | hp2 | a0001 | c0004 | t0003 | g0294 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01243 | hp1 | a0001 | c0001 | t0028 | g0022 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01346 | hp2 | a0001 | c0004 | t0003 | g0267 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01361 | hp1 | a0001 | c0001 | t0010 | g0042 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01361 | hp2 | a0001 | c0007 | t0002 | g0124 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01433 | hp2 | a0001 | c0001 | t0027 | g0272 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | IBS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0036 | EUR | IBS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01516 | hp1 | a0001 | c0006 | t0010 | g0039 | EUR | IBS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0018 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01891 | hp2 | a0001 | c0001 | t0020 | g0079 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0296 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02071 | hp1 | a0001 | c0001 | t0008 | g0284 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02129 | hp1 | a0001 | c0001 | t0025 | g0095 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02135 | hp2 | a0001 | c0001 | t0008 | g0259 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02145 | hp2 | a0001 | c0002 | t0007 | g0069 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | CDX | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | CDX | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02258 | hp1 | a0001 | c0002 | t0009 | g0242 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02293 | hp2 | a0001 | c0003 | t0005 | g0222 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0273 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02451 | hp1 | a0001 | c0003 | t0005 | g0249 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02451 | hp2 | a0001 | c0002 | t0007 | g0070 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02630 | hp1 | a0001 | c0002 | t0007 | g0071 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02647 | hp2 | a0001 | c0002 | t0005 | g0020 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02717 | hp1 | a0001 | c0003 | t0005 | g0251 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02723 | hp1 | a0001 | c0002 | t0007 | g0063 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0027 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0019 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02818 | hp1 | a0001 | c0003 | t0015 | g0241 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02886 | hp1 | a0001 | c0002 | t0007 | g0068 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02895 | hp1 | a0001 | c0002 | t0009 | g0246 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02896 | hp1 | a0001 | c0001 | t0013 | g0306 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02896 | hp2 | a0001 | c0003 | t0005 | g0240 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02897 | hp1 | a0001 | c0001 | t0013 | g0307 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02965 | hp1 | a0001 | c0002 | t0009 | g0244 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02976 | hp1 | a0001 | c0001 | t0019 | g0139 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0298 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03041 | hp2 | a0001 | c0002 | t0011 | g0233 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03098 | hp1 | a0001 | c0003 | t0005 | g0250 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03098 | hp2 | a0001 | c0002 | t0011 | g0232 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03130 | hp2 | a0001 | c0002 | t0005 | g0016 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03139 | hp2 | a0001 | c0002 | t0007 | g0072 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03195 | hp2 | a0001 | c0002 | t0007 | g0064 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0017 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0061 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03516 | hp1 | a0001 | c0002 | t0007 | g0067 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03540 | hp2 | a0001 | c0002 | t0029 | g0245 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03579 | hp2 | a0001 | c0002 | t0007 | g0062 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03654 | hp2 | a0001 | c0001 | t0032 | g0086 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03710 | hp2 | a0001 | c0001 | t0012 | g0229 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04184 | hp2 | a0001 | c0001 | t0012 | g0230 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0287 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18522 | hp2 | a0001 | c0003 | t0005 | g0223 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18906 | hp2 | a0001 | c0002 | t0016 | g0212 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18945 | hp1 | a0001 | c0001 | t0026 | g0303 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18948 | hp2 | a0002 | c0005 | t0003 | g0277 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18952 | hp1 | a0001 | c0001 | t0008 | g0257 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18953 | hp1 | a0001 | c0001 | t0017 | g0120 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18964 | hp1 | a0001 | c0001 | t0031 | g0254 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18964 | hp2 | a0001 | c0001 | t0021 | g0162 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0293 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18981 | hp1 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18982 | hp1 | a0001 | c0003 | t0005 | g0226 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0288 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19001 | hp2 | a0001 | c0003 | t0005 | g0221 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19005 | hp2 | a0001 | c0001 | t0008 | g0258 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19030 | hp2 | a0001 | c0001 | t0030 | g0004 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19043 | hp1 | a0001 | c0003 | t0005 | g0224 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19090 | hp2 | a0001 | c0001 | t0024 | g0207 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19240 | hp2 | a0001 | c0002 | t0007 | g0065 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20129 | hp2 | a0001 | c0003 | t0005 | g0225 | AFR | ASW | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0194 | EUR | TSI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | GIH | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | GIH | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02486 | hp1 | a0001 | c0003 | t0005 | g0103 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02559 | hp2 | a0001 | c0002 | t0007 | g0066 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0301 | AFR | USA | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | USA | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA21309 | hp1 | a0001 | c0002 | t0018 | g0231 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0014 | g0031 | REF | REF | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0160 | REF | REF | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74805254 | C | G | 1 | a0002 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.701G>C | p.Gly234Ala | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 7/13 | 927/6125 | 701/2013 | 234/670 | chr5 | 74805254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74781649 | C | T | 2 | a0001c0002 a0001c0003 |
41 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
synonymous_variant | LOW | c.1824G>A | p.Lys608Lys | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2050/6125 | 1824/2013 | 608/670 | chr5 | 74781649 | |||
| chr5:74801609 | G | A | 1 | a0001c0006 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.933C>T | p.Ala311Ala | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 9/13 | 1159/6125 | 933/2013 | 311/670 | chr5 | 74801609 | |||
| chr5:74813861 | G | A | 1 | a0001c0007 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.649C>T | p.Leu217Leu | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/13 | 875/6125 | 649/2013 | 217/670 | chr5 | 74813861 | |||
| chr5:74813868 | C | A | 1 | a0001c0004 | 3 | HG01109.hp1 HG01175.hp2 HG01346.hp2 |
synonymous_variant | LOW | c.642G>T | p.Arg214Arg | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/13 | 868/6125 | 642/2013 | 214/670 | chr5 | 74813868 | |||
| chr5:74814015 | G | A | 1 | a0001c0003 | 14 | HG00438.hp1 HG00735.hp2 HG02293.hp2 others(11): Show |
synonymous_variant | LOW | c.495C>T | p.Ser165Ser | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/13 | 721/6125 | 495/2013 | 165/670 | chr5 | 74814015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74777590 | AT | A | 5 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0013 others(2): Show |
41 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3869delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 3869 | chr5 | 74777590 | ||||||
| chr5:74777717 | G | A | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(20): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*3743C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 3743 | chr5 | 74777717 | ||||||
| chr5:74777759 | G | C | 2 | a0001c0001t0006 a0001c0001t0030 |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3701C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 3701 | chr5 | 74777759 | ||||||
| chr5:74778223 | C | T | 1 | a0001c0001t0022 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3237G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 3237 | chr5 | 74778223 | ||||||
| chr5:74778387 | A | G | 1 | a0001c0001t0021 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3073T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 3073 | chr5 | 74778387 | ||||||
| chr5:74778597 | TA | T | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(20): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*2862delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2862 | chr5 | 74778597 | ||||||
| chr5:74778625 | T | C | 1 | a0001c0001t0023 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2835A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2835 | chr5 | 74778625 | ||||||
| chr5:74778627 | T | C | 1 | a0001c0001t0020 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2833A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2833 | chr5 | 74778627 | ||||||
| chr5:74779087 | G | A | 1 | a0001c0001t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2373C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2373 | chr5 | 74779087 | ||||||
| chr5:74779088 | A | G | 1 | a0001c0001t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2372T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2372 | chr5 | 74779088 | ||||||
| chr5:74779401 | G | A | 2 | a0001c0001t0024 a0001c0002t0029 |
2 | HG03540.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2059C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2059 | chr5 | 74779401 | ||||||
| chr5:74779442 | C | G | 1 | a0001c0001t0030 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2018 | chr5 | 74779442 | ||||||
| chr5:74779528 | ACAGAG | A | 2 | a0001c0002t0011 a0001c0002t0018 |
3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1927_*1931delCTCT others(1): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1927 | chr5 | 74779528 | ||||||
| chr5:74779529 | C | T | 1 | a0001c0001t0001 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1931G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1931 | chr5 | 74779529 | ||||||
| chr5:74779533 | G | A | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(22): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1927C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1927 | chr5 | 74779533 | ||||||
| chr5:74779604 | C | G | 6 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0019 others(3): Show |
81 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1856G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1856 | chr5 | 74779604 | ||||||
| chr5:74779621 | CT | C | 4 | a0001c0001t0025 a0001c0002t0007 a0001c0002t0016 others(1): Show |
14 | HG02129.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1838delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1838 | chr5 | 74779621 | ||||||
| chr5:74780080 | T | G | 1 | a0001c0001t0026 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1380A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1380 | chr5 | 74780080 | ||||||
| chr5:74780232 | A | G | 1 | a0001c0002t0018 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1228T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1228 | chr5 | 74780232 | ||||||
| chr5:74780385 | T | C | 12 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(9): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1075A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1075 | chr5 | 74780385 | ||||||
| chr5:74780406 | C | G | 1 | a0001c0001t0017 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1054G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1054 | chr5 | 74780406 | ||||||
| chr5:74780454 | G | C | 1 | a0001c0001t0027 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1006C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1006 | chr5 | 74780454 | ||||||
| chr5:74780472 | G | A | 1 | a0001c0001t0028 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*988C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 988 | chr5 | 74780472 | ||||||
| chr5:74780520 | G | A | 1 | a0001c0001t0012 | 2 | HG03710.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*940C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 940 | chr5 | 74780520 | ||||||
| chr5:74780531 | C | T | 2 | a0001c0002t0016 a0001c0003t0015 |
2 | HG02818.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*929G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 929 | chr5 | 74780531 | ||||||
| chr5:74780555 | G | C | 2 | a0001c0002t0009 a0001c0002t0029 |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*905C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 905 | chr5 | 74780555 | ||||||
| chr5:74780948 | T | C | 1 | a0001c0001t0030 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 512 | chr5 | 74780948 | ||||||
| chr5:74780951 | C | T | 1 | a0001c0001t0031 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*509G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 509 | chr5 | 74780951 | ||||||
| chr5:74781107 | T | C | 2 | a0001c0001t0008 a0001c0001t0031 |
8 | HG02071.hp1 HG02135.hp2 NA18952.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*353A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 353 | chr5 | 74781107 | ||||||
| chr5:74781330 | TAGTA | T | 2 | a0001c0001t0010 a0001c0006t0010 |
4 | HG00140.hp2 HG00738.hp2 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*126_*129delTACT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 126 | chr5 | 74781330 | ||||||
| chr5:74781355 | T | C | 1 | a0001c0001t0032 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 105 | chr5 | 74781355 | ||||||
| chr5:74866334 | T | C | 1 | a0001c0001t0013 | 2 | HG02896.hp1 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-173A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/13 | 24658 | chr5 | 74866334 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74782129 | C | A | 2 | a0001c0003t0005g0249 a0001c0003t0005g0250 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1465-121G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 12/12 | chr5 | 74782129 | |||||||
| chr5:74782294 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1465-286T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 12/12 | chr5 | 74782294 | |||||||
| chr5:74782380 | C | T | 6 | a0001c0001t0003g0262 a0001c0001t0003g0273 a0001c0001t0003g0278 others(3): Show |
6 | HG01257.hp2 HG01258.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-372G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 12/12 | chr5 | 74782380 | |||||||
| chr5:74782394 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1465-386C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 12/12 | chr5 | 74782394 | |||||||
| chr5:74783155 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1261-21C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783155 | |||||||
| chr5:74783196 | G | A | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1261-62C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783196 | |||||||
| chr5:74783310 | A | G | 1 | a0001c0001t0002g0196 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1261-176T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783310 | |||||||
| chr5:74783469 | G | T | 148 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(145): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1261-335C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783469 | |||||||
| chr5:74783556 | G | C | 2 | a0001c0001t0002g0113 a0001c0001t0002g0199 |
2 | NA18963.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1261-422C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783556 | |||||||
| chr5:74783667 | A | T | 1 | a0001c0001t0004g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1261-533T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783667 | |||||||
| chr5:74783793 | T | C | 1 | a0001c0001t0030g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1261-659A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783793 | |||||||
| chr5:74783858 | A | T | 1 | a0001c0001t0017g0120 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1261-724T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783858 | |||||||
| chr5:74783904 | G | A | 7 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-770C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783904 | |||||||
| chr5:74783923 | A | T | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1261-789T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783923 | |||||||
| chr5:74784171 | G | A | 6 | a0001c0003t0005g0103 a0001c0003t0005g0224 a0001c0003t0005g0225 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1037C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784171 | |||||||
| chr5:74784210 | A | G | 1 | a0001c0001t0003g0295 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1261-1076T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784210 | |||||||
| chr5:74784510 | C | CA | 9 | a0001c0001t0001g0100 a0001c0001t0001g0182 a0001c0001t0001g0211 others(6): Show |
9 | HG02976.hp1 HG04115.hp2 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-1377dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAA | 9 | a0001c0001t0004g0050 a0001c0002t0007g0063 a0001c0002t0007g0064 others(6): Show |
9 | HG00642.hp1 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-1379_1261-137 others(7): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAA | 56 | a0001c0001t0003g0252 a0001c0001t0003g0255 a0001c0001t0003g0256 others(53): Show |
56 | HG00408.hp2 HG00558.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1261-1380_1261-137 others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAA | 34 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(31): Show |
35 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1261-1381_1261-137 others(9): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAA | 7 | a0001c0001t0003g0264 a0001c0001t0004g0028 a0001c0001t0004g0029 others(4): Show |
7 | HG00140.hp2 HG01069.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-1382_1261-137 others(10): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA | 6 | a0001c0002t0009g0242 a0001c0002t0009g0244 a0001c0002t0009g0246 others(3): Show |
6 | HG00741.hp2 HG01106.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1383_1261-137 others(11): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0005g0061 a0001c0002t0005g0017 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1261-1386_1261-137 others(14): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0005g0060 a0001c0002t0005g0016 a0001c0002t0005g0018 others(3): Show |
6 | HG00735.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1387_1261-137 others(15): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(5): Show |
1 | a0001c0003t0005g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1261-1388_1261-137 others(16): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0006g0010 a0001c0003t0005g0228 |
2 | HG00438.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-1389_1261-137 others(17): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0006g0007 a0001c0001t0006g0012 a0001c0001t0006g0013 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-1390_1261-137 others(18): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(8): Show |
6 | a0001c0001t0006g0005 a0001c0001t0006g0008 a0001c0001t0006g0011 others(3): Show |
6 | HG02293.hp2 HG02723.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1391_1261-137 others(19): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0006g0009 a0001c0003t0005g0221 a0001c0003t0005g0240 |
3 | HG02896.hp2 HG03486.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1261-1392_1261-137 others(20): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0030g0004 a0001c0003t0005g0224 |
2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1261-1393_1261-137 others(21): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(11): Show |
1 | a0001c0003t0005g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1261-1394_1261-137 others(22): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(12): Show |
1 | a0001c0003t0005g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1261-1395_1261-137 others(23): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(13): Show |
1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1261-1377_1261-137 others(24): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(26): Show |
1 | a0001c0003t0005g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1261-1377_1261-137 others(37): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784510 | C | CAAAAAAA others(41): Show |
1 | a0001c0003t0005g0249 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1261-1377_1261-137 others(52): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | |||||||
| chr5:74784607 | T | TA | 16 | a0001c0001t0001g0101 a0001c0001t0002g0119 a0001c0001t0002g0153 others(13): Show |
16 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1261-1474dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784607 | |||||||
| chr5:74784607 | TA | T | 143 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(140): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1261-1474delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784607 | |||||||
| chr5:74784607 | TAA | T | 54 | a0001c0001t0001g0175 a0001c0001t0002g0209 a0001c0001t0004g0003 others(51): Show |
54 | HG00280.hp2 HG00438.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1261-1475_1261-147 others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784607 | |||||||
| chr5:74784607 | TAAA | T | 65 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(62): Show |
66 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1261-1476_1261-147 others(7): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784607 | |||||||
| chr5:74784780 | G | A | 9 | a0001c0001t0002g0153 a0001c0001t0002g0191 a0001c0001t0002g0193 others(6): Show |
9 | HG02451.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-1646C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784780 | |||||||
| chr5:74784792 | G | A | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1261-1658C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784792 | |||||||
| chr5:74784844 | G | A | 1 | a0001c0002t0011g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1261-1710C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784844 | |||||||
| chr5:74784918 | C | CA | 19 | a0001c0001t0002g0180 a0001c0001t0002g0188 a0001c0001t0003g0002 others(16): Show |
19 | HG01243.hp1 HG01433.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1261-1785dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784918 | |||||||
| chr5:74784918 | C | CAA | 7 | a0001c0002t0007g0071 a0001c0002t0009g0242 a0001c0002t0009g0243 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-1786_1261-178 others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784918 | |||||||
| chr5:74784918 | CAA | C | 12 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1261-1786_1261-178 others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784918 | |||||||
| chr5:74784938 | T | A | 1 | a0001c0001t0001g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1261-1804A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784938 | |||||||
| chr5:74784998 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1261-1864T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784998 | |||||||
| chr5:74785027 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1893T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785027 | |||||||
| chr5:74785137 | G | A | 6 | a0001c0001t0002g0122 a0001c0001t0002g0170 a0001c0001t0002g0171 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1261-2003C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785137 | |||||||
| chr5:74785231 | T | G | 1 | a0001c0001t0006g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1261-2097A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785231 | |||||||
| chr5:74785305 | C | T | 107 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1261-2171G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785305 | |||||||
| chr5:74785490 | C | T | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1261-2356G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785490 | |||||||
| chr5:74785491 | G | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0037 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1261-2357C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785491 | |||||||
| chr5:74785535 | G | A | 1 | a0001c0003t0005g0221 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1261-2401C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785535 | |||||||
| chr5:74785737 | G | T | 10 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0034 others(7): Show |
10 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1261-2603C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785737 | |||||||
| chr5:74785815 | C | T | 7 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0054 others(4): Show |
7 | HG00733.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1261-2681G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785815 | |||||||
| chr5:74785914 | T | C | 2 | a0001c0003t0005g0249 a0001c0003t0005g0250 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1261-2780A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785914 | |||||||
| chr5:74786118 | T | C | 44 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 others(41): Show |
44 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1261-2984A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786118 | |||||||
| chr5:74786537 | G | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0093 a0001c0001t0001g0097 others(1): Show |
4 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-3403C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786537 | |||||||
| chr5:74786617 | CTAAGTTC others(18): Show |
C | 1 | a0001c0001t0008g0259 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1261-3508_1261-348 others(29): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786617 | |||||||
| chr5:74786686 | C | G | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1261-3552G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786686 | |||||||
| chr5:74786695 | G | A | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1261-3561C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786695 | |||||||
| chr5:74786752 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1261-3618C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786752 | |||||||
| chr5:74786969 | G | A | 7 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-3835C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786969 | |||||||
| chr5:74786979 | G | A | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1261-3845C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786979 | |||||||
| chr5:74787109 | T | C | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1261-3975A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787109 | |||||||
| chr5:74787157 | G | A | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1261-4023C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787157 | |||||||
| chr5:74787240 | G | A | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1261-4106C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787240 | |||||||
| chr5:74787286 | A | G | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1261-4152T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787286 | |||||||
| chr5:74787496 | C | T | 5 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-4362G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787496 | |||||||
| chr5:74787621 | C | T | 1 | a0001c0003t0005g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1261-4487G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787621 | |||||||
| chr5:74787883 | T | TA | 51 | a0001c0001t0002g0114 a0001c0001t0005g0060 a0001c0001t0005g0061 others(48): Show |
51 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1261-4750dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787883 | |||||||
| chr5:74787892 | G | A | 150 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1261-4758C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787892 | |||||||
| chr5:74788232 | G | A | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1261-5098C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788232 | |||||||
| chr5:74788242 | G | A | 2 | a0001c0001t0006g0007 a0001c0001t0006g0013 |
2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1261-5108C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788242 | |||||||
| chr5:74788425 | G | A | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1261-5291C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788425 | |||||||
| chr5:74788474 | G | A | 12 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1261-5340C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788474 | |||||||
| chr5:74788477 | G | A | 2 | a0001c0001t0003g0252 a0001c0001t0003g0263 |
2 | HG02056.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1261-5343C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788477 | |||||||
| chr5:74788504 | G | A | 1 | a0001c0002t0011g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1261-5370C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788504 | |||||||
| chr5:74788524 | G | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0286 |
2 | NA18953.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1261-5390C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788524 | |||||||
| chr5:74788562 | G | A | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1261-5428C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788562 | |||||||
| chr5:74788620 | G | A | 2 | a0001c0001t0013g0306 a0001c0001t0013g0307 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1261-5486C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788620 | |||||||
| chr5:74789054 | C | T | 2 | a0001c0002t0011g0232 a0001c0002t0011g0233 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1261-5920G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789054 | |||||||
| chr5:74789085 | A | G | 136 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(133): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1261-5951T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789085 | |||||||
| chr5:74789141 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0184 |
2 | HG00735.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1261-6007T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789141 | |||||||
| chr5:74789164 | C | T | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1261-6030G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789164 | |||||||
| chr5:74789209 | T | C | 5 | a0001c0001t0003g0269 a0001c0001t0003g0270 a0001c0001t0003g0281 others(2): Show |
5 | HG00558.hp2 HG02015.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-6075A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789209 | |||||||
| chr5:74789320 | T | C | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1261-6186A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789320 | |||||||
| chr5:74789321 | A | G | 2 | a0001c0001t0004g0021 a0001c0001t0004g0041 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1261-6187T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789321 | |||||||
| chr5:74789332 | G | A | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1261-6198C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789332 | |||||||
| chr5:74789382 | AG | A | 5 | a0001c0001t0001g0074 a0001c0001t0001g0136 a0001c0001t0001g0143 others(2): Show |
5 | NA18945.hp2 NA18975.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-6249delC | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789382 | |||||||
| chr5:74789390 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1261-6256C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789390 | |||||||
| chr5:74789404 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0234 |
2 | HG00323.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1261-6270G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789404 | |||||||
| chr5:74789620 | G | A | 2 | a0001c0002t0011g0232 a0001c0002t0011g0233 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1260+6410C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789620 | |||||||
| chr5:74789758 | G | C | 2 | a0001c0001t0004g0021 a0001c0001t0004g0041 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1260+6272C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789758 | |||||||
| chr5:74789888 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1260+6142G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789888 | |||||||
| chr5:74789898 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1260+6132C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789898 | |||||||
| chr5:74790116 | T | C | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+5914A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790116 | |||||||
| chr5:74790307 | G | C | 1 | a0001c0003t0005g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1260+5723C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790307 | |||||||
| chr5:74790364 | G | T | 291 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(288): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1260+5666C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790364 | |||||||
| chr5:74790545 | C | A | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1260+5485G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790545 | |||||||
| chr5:74790674 | C | G | 1 | a0001c0001t0005g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1260+5356G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790674 | |||||||
| chr5:74790763 | G | A | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1260+5267C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790763 | |||||||
| chr5:74790997 | G | A | 3 | a0001c0002t0011g0232 a0001c0002t0011g0233 a0001c0002t0018g0231 |
3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1260+5033C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790997 | |||||||
| chr5:74791035 | T | C | 6 | a0001c0001t0002g0114 a0001c0003t0005g0221 a0001c0003t0005g0222 others(3): Show |
6 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+4995A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791035 | |||||||
| chr5:74791057 | C | T | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1260+4973G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791057 | |||||||
| chr5:74791077 | G | A | 30 | a0001c0001t0002g0114 a0001c0002t0005g0016 a0001c0002t0005g0017 others(27): Show |
30 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+4953C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791077 | |||||||
| chr5:74791121 | C | T | 3 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0029 |
3 | HG03239.hp2 HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1260+4909G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791121 | |||||||
| chr5:74791206 | C | T | 5 | a0001c0001t0002g0114 a0001c0003t0005g0221 a0001c0003t0005g0222 others(2): Show |
5 | HG00438.hp1 HG00673.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+4824G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791206 | |||||||
| chr5:74791441 | G | A | 1 | a0001c0004t0003g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1260+4589C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791441 | |||||||
| chr5:74791540 | G | A | 30 | a0001c0001t0002g0114 a0001c0002t0005g0016 a0001c0002t0005g0017 others(27): Show |
30 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+4490C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791540 | |||||||
| chr5:74791779 | G | GA | 7 | a0001c0001t0002g0114 a0001c0001t0002g0192 a0001c0003t0005g0221 others(4): Show |
7 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+4250dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791779 | |||||||
| chr5:74791885 | T | C | 23 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0003g0260 others(20): Show |
23 | HG01257.hp2 HG01258.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1260+4145A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791885 | |||||||
| chr5:74792516 | T | G | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+3514A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792516 | |||||||
| chr5:74792517 | C | A | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+3513G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792517 | |||||||
| chr5:74792520 | T | G | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+3510A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792520 | |||||||
| chr5:74792524 | TCCTTGCT others(1): Show |
T | 138 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(135): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1260+3498_1260+350 others(12): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792524 | |||||||
| chr5:74792532 | C | T | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+3498G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792532 | |||||||
| chr5:74792534 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1260+3496G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792534 | |||||||
| chr5:74792660 | CCTGA | C | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+3366_1260+336 others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792660 | |||||||
| chr5:74792920 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1260+3110T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792920 | |||||||
| chr5:74792949 | A | G | 2 | a0001c0002t0011g0232 a0001c0002t0011g0233 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1260+3081T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792949 | |||||||
| chr5:74793123 | G | A | 6 | a0001c0003t0005g0103 a0001c0003t0005g0224 a0001c0003t0005g0225 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1260+2907C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793123 | |||||||
| chr5:74793323 | C | CA | 21 | a0001c0001t0001g0112 a0001c0001t0001g0215 a0001c0001t0002g0119 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1260+2706dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793323 | |||||||
| chr5:74793323 | CA | C | 11 | a0001c0001t0001g0137 a0001c0001t0001g0141 a0001c0001t0003g0286 others(8): Show |
11 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1260+2706delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793323 | |||||||
| chr5:74793519 | G | A | 2 | a0001c0003t0005g0249 a0001c0003t0005g0250 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1260+2511C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793519 | |||||||
| chr5:74793620 | A | G | 150 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1260+2410T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793620 | |||||||
| chr5:74793779 | G | A | 2 | a0001c0002t0011g0232 a0001c0002t0011g0233 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1260+2251C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793779 | |||||||
| chr5:74793858 | C | G | 1 | a0001c0003t0005g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1260+2172G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793858 | |||||||
| chr5:74793902 | C | T | 6 | a0001c0001t0001g0075 a0001c0001t0001g0082 a0001c0001t0001g0096 others(3): Show |
6 | HG01074.hp1 HG01346.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+2128G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793902 | |||||||
| chr5:74793952 | G | A | 3 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0008 |
3 | HG02559.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1260+2078C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793952 | |||||||
| chr5:74794002 | C | CA | 19 | a0001c0001t0001g0179 a0001c0001t0002g0165 a0001c0001t0002g0167 others(16): Show |
19 | HG02071.hp2 HG02145.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.1260+2027dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794002 | |||||||
| chr5:74794167 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1260+1863C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794167 | |||||||
| chr5:74794237 | T | A | 136 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(133): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1260+1793A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794237 | |||||||
| chr5:74794337 | T | A | 1 | a0001c0002t0009g0243 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1260+1693A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794337 | |||||||
| chr5:74794377 | G | C | 1 | a0001c0003t0005g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1260+1653C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794377 | |||||||
| chr5:74794393 | C | CA | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+1636dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794393 | |||||||
| chr5:74794511 | G | T | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1260+1519C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794511 | |||||||
| chr5:74794546 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1260+1484C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794546 | |||||||
| chr5:74794595 | G | A | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1260+1435C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794595 | |||||||
| chr5:74794631 | T | C | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1260+1399A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794631 | |||||||
| chr5:74794768 | A | G | 136 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(133): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1260+1262T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794768 | |||||||
| chr5:74794778 | C | CA | 30 | a0001c0001t0001g0101 a0001c0001t0001g0121 a0001c0001t0001g0143 others(27): Show |
30 | HG00642.hp1 HG01978.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+1251dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794778 | |||||||
| chr5:74794812 | C | G | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+1218G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794812 | |||||||
| chr5:74795029 | G | A | 1 | a0001c0001t0004g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1260+1001C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795029 | |||||||
| chr5:74795060 | C | G | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1260+970G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795060 | |||||||
| chr5:74795127 | G | A | 1 | a0001c0002t0009g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1260+903C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795127 | |||||||
| chr5:74795224 | C | T | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1260+806G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795224 | |||||||
| chr5:74795226 | C | G | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1260+804G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795226 | |||||||
| chr5:74795379 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1260+651C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795379 | |||||||
| chr5:74795399 | A | G | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+631T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795399 | |||||||
| chr5:74795432 | T | C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1260+598A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795432 | |||||||
| chr5:74795525 | AT | A | 29 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(26): Show |
29 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1260+504delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795525 | |||||||
| chr5:74795649 | C | A | 149 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(146): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1260+381G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795649 | |||||||
| chr5:74795709 | A | T | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(37): Show |
40 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1260+321T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795709 | |||||||
| chr5:74795784 | C | T | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1260+246G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795784 | |||||||
| chr5:74795792 | T | C | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1260+238A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795792 | |||||||
| chr5:74795946 | G | A | 2 | a0001c0003t0005g0240 a0001c0003t0015g0241 |
2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1260+84C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795946 | |||||||
| chr5:74796420 | TTC | T | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1104-236_1104-235d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796420 | |||||||
| chr5:74796422 | C | T | 162 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(159): Show |
162 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1104-236G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796422 | |||||||
| chr5:74796466 | C | T | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1104-280G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796466 | |||||||
| chr5:74796475 | G | A | 5 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1104-289C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796475 | |||||||
| chr5:74796632 | G | A | 1 | a0001c0003t0005g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1104-446C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796632 | |||||||
| chr5:74796747 | A | G | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1104-561T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796747 | |||||||
| chr5:74796975 | G | T | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1104-789C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796975 | |||||||
| chr5:74797184 | T | C | 5 | a0001c0001t0004g0040 a0001c0001t0004g0045 a0001c0001t0004g0046 others(2): Show |
5 | HG01081.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1104-998A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797184 | |||||||
| chr5:74797208 | CCT | C | 5 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0034 others(2): Show |
5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1104-1024_1104-102 others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797208 | |||||||
| chr5:74797229 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0234 |
2 | HG00323.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1104-1043A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797229 | |||||||
| chr5:74797344 | T | C | 5 | a0001c0001t0001g0126 a0001c0001t0001g0137 a0001c0001t0001g0146 others(2): Show |
5 | HG01884.hp1 HG02698.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1104-1158A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797344 | |||||||
| chr5:74797388 | G | A | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1104-1202C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797388 | |||||||
| chr5:74797434 | C | T | 15 | a0001c0001t0001g0126 a0001c0001t0001g0130 a0001c0001t0001g0132 others(12): Show |
15 | HG00323.hp2 HG00733.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1104-1248G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797434 | |||||||
| chr5:74797520 | A | C | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1104-1334T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797520 | |||||||
| chr5:74797522 | C | T | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1104-1336G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797522 | |||||||
| chr5:74797750 | A | T | 1 | a0001c0001t0002g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1104-1564T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797750 | |||||||
| chr5:74797808 | C | G | 12 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1104-1622G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797808 | |||||||
| chr5:74797945 | A | T | 24 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(21): Show |
24 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1104-1759T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797945 | |||||||
| chr5:74797960 | A | T | 137 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1104-1774T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797960 | |||||||
| chr5:74798320 | C | T | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1104-2134G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74798320 | |||||||
| chr5:74799035 | T | C | 5 | a0001c0001t0002g0114 a0001c0003t0005g0221 a0001c0003t0005g0222 others(2): Show |
5 | HG00438.hp1 HG00673.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1103+1845A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799035 | |||||||
| chr5:74799594 | G | A | 150 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1103+1286C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799594 | |||||||
| chr5:74799626 | C | T | 22 | a0001c0001t0002g0098 a0001c0001t0002g0113 a0001c0001t0002g0153 others(19): Show |
22 | HG00673.hp1 HG00741.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1103+1254G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799626 | |||||||
| chr5:74799707 | T | C | 6 | a0001c0001t0002g0114 a0001c0003t0005g0221 a0001c0003t0005g0222 others(3): Show |
6 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1103+1173A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799707 | |||||||
| chr5:74799717 | T | C | 24 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0121 others(21): Show |
24 | HG00323.hp2 HG00733.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1103+1163A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799717 | |||||||
| chr5:74799754 | T | A | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1103+1126A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799754 | |||||||
| chr5:74799800 | A | G | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1103+1080T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799800 | |||||||
| chr5:74799814 | C | T | 23 | a0001c0001t0002g0098 a0001c0001t0002g0113 a0001c0001t0002g0153 others(20): Show |
23 | HG00673.hp1 HG00741.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1103+1066G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799814 | |||||||
| chr5:74799821 | C | T | 1 | a0001c0001t0030g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1103+1059G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799821 | |||||||
| chr5:74799880 | CAT | C | 5 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1103+998_1103+999d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799880 | |||||||
| chr5:74799893 | G | T | 7 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0054 others(4): Show |
7 | HG00733.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1103+987C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799893 | |||||||
| chr5:74800009 | T | C | 1 | a0001c0002t0007g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1103+871A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800009 | |||||||
| chr5:74800183 | A | G | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1103+697T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800183 | |||||||
| chr5:74800264 | GT | G | 148 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(145): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1103+615delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800264 | |||||||
| chr5:74800411 | A | T | 1 | a0001c0001t0004g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1103+469T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800411 | |||||||
| chr5:74800458 | T | C | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1103+422A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800458 | |||||||
| chr5:74800463 | C | T | 2 | a0001c0001t0002g0201 a0001c0001t0002g0219 |
2 | NA18956.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1103+417G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800463 | |||||||
| chr5:74800553 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1103+327A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800553 | |||||||
| chr5:74800575 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1103+305A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800575 | |||||||
| chr5:74800584 | C | T | 137 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1103+296G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800584 | |||||||
| chr5:74800608 | T | G | 20 | a0001c0001t0002g0114 a0001c0002t0005g0016 a0001c0002t0005g0017 others(17): Show |
20 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1103+272A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800608 | |||||||
| chr5:74800619 | T | C | 1 | a0001c0001t0002g0153 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1103+261A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800619 | |||||||
| chr5:74800719 | AAAAAGTA others(4): Show |
A | 1 | a0001c0001t0003g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1103+150_1103+160d others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800719 | |||||||
| chr5:74801316 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.952+274G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 9/12 | chr5 | 74801316 | |||||||
| chr5:74801467 | G | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0091 |
3 | HG01081.hp1 HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.952+123C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 9/12 | chr5 | 74801467 | |||||||
| chr5:74801556 | A | C | 49 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0129 others(46): Show |
49 | HG00438.hp1 HG00639.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.952+34T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 9/12 | chr5 | 74801556 | |||||||
| chr5:74801650 | A | C | 1 | a0001c0001t0002g0114 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.913-21T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74801650 | |||||||
| chr5:74801721 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.913-92T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74801721 | |||||||
| chr5:74801727 | T | C | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.913-98A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74801727 | |||||||
| chr5:74802014 | AGTG | A | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.913-388_913-386del others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74802014 | |||||||
| chr5:74802357 | C | T | 1 | a0001c0001t0020g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.913-728G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74802357 | |||||||
| chr5:74802396 | A | G | 1 | a0001c0003t0005g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.913-767T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74802396 | |||||||
| chr5:74802407 | C | A | 1 | a0001c0001t0004g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.913-778G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74802407 | |||||||
| chr5:74802696 | A | G | 12 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.913-1067T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74802696 | |||||||
| chr5:74803225 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.912+1268C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803225 | |||||||
| chr5:74803366 | A | G | 1 | a0001c0001t0028g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.912+1127T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803366 | |||||||
| chr5:74803381 | G | A | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.912+1112C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803381 | |||||||
| chr5:74803476 | G | A | 1 | a0001c0001t0004g0025 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.912+1017C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803476 | |||||||
| chr5:74803564 | A | C | 29 | a0001c0001t0002g0114 a0001c0001t0012g0229 a0001c0001t0012g0230 others(26): Show |
29 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.912+929T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803564 | |||||||
| chr5:74803733 | G | A | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.912+760C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803733 | |||||||
| chr5:74803809 | C | T | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.912+684G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803809 | |||||||
| chr5:74803932 | T | C | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.912+561A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803932 | |||||||
| chr5:74803988 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.912+505C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803988 | |||||||
| chr5:74804018 | T | C | 3 | a0001c0002t0011g0232 a0001c0002t0011g0233 a0001c0002t0018g0231 |
3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.912+475A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74804018 | |||||||
| chr5:74804044 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.912+449A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74804044 | |||||||
| chr5:74804165 | C | T | 1 | a0001c0006t0010g0039 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.912+328G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74804165 | |||||||
| chr5:74804254 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.912+239C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74804254 | |||||||
| chr5:74804771 | C | T | 1 | a0001c0003t0005g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.800-166G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 7/12 | chr5 | 74804771 | |||||||
| chr5:74804816 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.800-211A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 7/12 | chr5 | 74804816 | |||||||
| chr5:74805325 | C | G | 2 | a0001c0001t0004g0050 a0001c0001t0004g0051 |
2 | HG00642.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.671-41G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805325 | |||||||
| chr5:74805442 | ATAAATAA others(6): Show |
A | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.671-171_671-159del others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805442 | |||||||
| chr5:74805522 | C | G | 5 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-238G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805522 | |||||||
| chr5:74805524 | C | CT | 32 | a0001c0001t0001g0074 a0001c0001t0001g0111 a0001c0001t0001g0133 others(29): Show |
32 | HG00621.hp1 HG00621.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.671-241dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805524 | C | CTT | 16 | a0001c0001t0001g0136 a0001c0002t0007g0063 a0001c0002t0007g0064 others(13): Show |
16 | HG01167.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.671-242_671-241dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805524 | C | CTTTTTT | 45 | a0001c0001t0003g0001 a0001c0001t0003g0252 a0001c0001t0003g0253 others(42): Show |
46 | HG00099.hp1 HG00558.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.671-246_671-241dup others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805524 | C | CTTTTTTT | 21 | a0001c0001t0002g0114 a0001c0001t0003g0002 a0001c0001t0003g0271 others(18): Show |
21 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.671-247_671-241dup others(7): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805524 | C | CTTTTTTT others(9): Show |
1 | a0001c0003t0005g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.671-256_671-241dup others(16): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805524 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0004g0050 a0001c0002t0005g0016 a0001c0002t0005g0019 |
3 | HG00642.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.671-257_671-241dup others(17): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805524 | C | CTTTTTTT others(11): Show |
3 | a0001c0002t0005g0017 a0001c0002t0005g0018 a0001c0002t0005g0020 |
3 | HG01884.hp2 HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.671-258_671-241dup others(18): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805524 | CTT | C | 30 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(27): Show |
30 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.671-242_671-241del others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805524 | CTTT | C | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.671-243_671-241del others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805524 | CTTTTTTT others(3): Show |
C | 2 | a0001c0002t0011g0232 a0001c0002t0011g0233 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.671-250_671-241del others(10): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805524 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0123 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.671-251_671-241del others(11): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | |||||||
| chr5:74805619 | C | T | 29 | a0001c0001t0002g0114 a0001c0001t0012g0229 a0001c0001t0012g0230 others(26): Show |
29 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.671-335G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805619 | |||||||
| chr5:74805633 | C | T | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.671-349G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805633 | |||||||
| chr5:74805707 | A | G | 1 | a0001c0002t0011g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.671-423T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805707 | |||||||
| chr5:74805752 | A | C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.671-468T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805752 | |||||||
| chr5:74805793 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0184 a0001c0001t0001g0215 |
3 | HG00735.hp1 HG02148.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.671-509A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805793 | |||||||
| chr5:74805976 | C | CA | 15 | a0001c0001t0001g0073 a0001c0001t0001g0111 a0001c0001t0001g0112 others(12): Show |
15 | HG00642.hp1 HG00735.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.671-693dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805976 | |||||||
| chr5:74805976 | C | CAA | 79 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(76): Show |
80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.671-694_671-693dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805976 | |||||||
| chr5:74805976 | C | CAAA | 11 | a0001c0001t0004g0029 a0001c0001t0004g0052 a0001c0001t0004g0053 others(8): Show |
11 | HG00733.hp1 HG01175.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.671-695_671-693dup others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805976 | |||||||
| chr5:74805976 | CA | C | 14 | a0001c0001t0002g0114 a0001c0001t0002g0153 a0001c0001t0002g0161 others(11): Show |
14 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.671-693delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805976 | |||||||
| chr5:74806256 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.671-972C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806256 | |||||||
| chr5:74806440 | A | C | 1 | a0001c0003t0005g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.671-1156T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806440 | |||||||
| chr5:74806493 | C | CA | 152 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(149): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.671-1210dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806493 | |||||||
| chr5:74806591 | T | C | 2 | a0001c0003t0005g0224 a0001c0003t0005g0225 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.671-1307A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806591 | |||||||
| chr5:74806625 | G | A | 1 | a0001c0001t0030g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.671-1341C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806625 | |||||||
| chr5:74806960 | A | AG | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.671-1677dupC | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806960 | |||||||
| chr5:74806984 | A | G | 2 | a0001c0001t0004g0026 a0001c0001t0028g0022 |
2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.671-1700T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806984 | |||||||
| chr5:74807086 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.671-1802G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807086 | |||||||
| chr5:74807263 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.671-1979G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807263 | |||||||
| chr5:74807370 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.671-2086A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807370 | |||||||
| chr5:74807372 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.671-2088C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807372 | |||||||
| chr5:74807453 | A | G | 29 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(26): Show |
29 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.671-2169T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807453 | |||||||
| chr5:74807850 | G | A | 1 | a0001c0001t0031g0254 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.671-2566C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807850 | |||||||
| chr5:74808255 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.671-2971A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808255 | |||||||
| chr5:74808421 | AT | A | 41 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(38): Show |
41 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.671-3138delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808421 | |||||||
| chr5:74808426 | C | G | 41 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(38): Show |
41 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.671-3142G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808426 | |||||||
| chr5:74808544 | T | C | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.671-3260A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808544 | |||||||
| chr5:74808577 | CTG | C | 3 | a0001c0001t0003g0001 a0001c0001t0003g0264 a0001c0001t0003g0266 |
4 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-3295_671-3294d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808577 | |||||||
| chr5:74808664 | A | G | 1 | a0001c0001t0003g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.671-3380T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808664 | |||||||
| chr5:74808686 | T | C | 1 | a0001c0003t0005g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.671-3402A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808686 | |||||||
| chr5:74808709 | A | C | 1 | a0001c0003t0005g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.671-3425T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808709 | |||||||
| chr5:74808742 | G | C | 8 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(5): Show |
8 | HG02559.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-3458C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808742 | |||||||
| chr5:74808757 | C | A | 1 | a0001c0001t0028g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.671-3473G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808757 | |||||||
| chr5:74808984 | T | A | 2 | a0001c0002t0011g0232 a0001c0002t0011g0233 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.671-3700A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808984 | |||||||
| chr5:74809364 | G | A | 1 | a0001c0001t0003g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.671-4080C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809364 | |||||||
| chr5:74809469 | G | A | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.671-4185C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809469 | |||||||
| chr5:74809501 | CAGG | C | 12 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.671-4220_671-4218d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809501 | |||||||
| chr5:74809512 | C | T | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.671-4228G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809512 | |||||||
| chr5:74809513 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG01884.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.671-4229C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809513 | |||||||
| chr5:74809679 | T | C | 1 | a0001c0001t0008g0261 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.670+4161A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809679 | |||||||
| chr5:74809908 | A | G | 1 | a0001c0003t0005g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670+3932T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809908 | |||||||
| chr5:74810233 | C | A | 1 | a0001c0001t0002g0161 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.670+3607G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810233 | |||||||
| chr5:74810414 | C | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG01884.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.670+3426G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810414 | |||||||
| chr5:74810415 | A | G | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.670+3425T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810415 | |||||||
| chr5:74810441 | GTGTACGG others(4): Show |
G | 1 | a0001c0003t0005g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.670+3388_670+3398d others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810441 | |||||||
| chr5:74810675 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.670+3165C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810675 | |||||||
| chr5:74810751 | C | CA | 9 | a0001c0001t0001g0239 a0001c0001t0002g0104 a0001c0001t0002g0106 others(6): Show |
9 | HG00738.hp1 HG01515.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.670+3088dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810751 | |||||||
| chr5:74810751 | CA | C | 86 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0090 others(83): Show |
86 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.670+3088delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810751 | |||||||
| chr5:74810751 | CAA | C | 148 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0076 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.670+3087_670+3088d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810751 | |||||||
| chr5:74810751 | CAAA | C | 17 | a0001c0001t0004g0030 a0001c0002t0007g0062 a0001c0002t0007g0063 others(14): Show |
17 | HG00438.hp1 HG00735.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.670+3086_670+3088d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810751 | |||||||
| chr5:74810819 | C | CT | 17 | a0001c0001t0001g0082 a0001c0001t0001g0096 a0001c0001t0001g0100 others(14): Show |
17 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.670+3020dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810819 | |||||||
| chr5:74810819 | CT | C | 15 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0002g0115 others(12): Show |
15 | HG00323.hp1 HG00741.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+3020delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810819 | |||||||
| chr5:74810819 | CTT | C | 20 | a0001c0001t0006g0010 a0001c0001t0006g0014 a0001c0002t0007g0062 others(17): Show |
20 | HG01167.hp1 HG02145.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.670+3019_670+3020d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810819 | |||||||
| chr5:74810819 | CTTT | C | 19 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(16): Show |
19 | HG00438.hp1 HG00735.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.670+3018_670+3020d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810819 | |||||||
| chr5:74810819 | CTTTTTTT | C | 93 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(90): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.670+3014_670+3020d others(9): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810819 | |||||||
| chr5:74810974 | A | AT | 95 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0100 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.670+2865dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810974 | |||||||
| chr5:74810974 | A | ATT | 25 | a0001c0001t0003g0252 a0001c0001t0003g0255 a0001c0001t0003g0273 others(22): Show |
25 | HG00642.hp1 HG01109.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.670+2864_670+2865d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810974 | |||||||
| chr5:74810974 | AT | A | 36 | a0001c0001t0001g0238 a0001c0001t0005g0060 a0001c0001t0006g0006 others(33): Show |
36 | HG00438.hp1 HG00735.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.670+2865delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810974 | |||||||
| chr5:74811166 | T | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0219 |
2 | NA18956.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.670+2674A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811166 | |||||||
| chr5:74811505 | C | G | 41 | a0001c0001t0030g0004 a0001c0002t0005g0016 a0001c0002t0005g0017 others(38): Show |
41 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.670+2335G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811505 | |||||||
| chr5:74811694 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.670+2146T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811694 | |||||||
| chr5:74811789 | G | A | 119 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(116): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.670+2051C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811789 | |||||||
| chr5:74811832 | T | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0020g0079 |
3 | HG01891.hp2 HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.670+2008A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811832 | |||||||
| chr5:74811912 | C | G | 1 | a0001c0003t0005g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670+1928G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811912 | |||||||
| chr5:74812021 | T | C | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.670+1819A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812021 | |||||||
| chr5:74812185 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0020g0079 |
3 | HG01891.hp2 HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.670+1655C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812185 | |||||||
| chr5:74812255 | C | T | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+1585G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812255 | |||||||
| chr5:74812466 | G | A | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.670+1374C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812466 | |||||||
| chr5:74812565 | C | A | 13 | a0001c0001t0005g0060 a0001c0001t0005g0061 a0001c0001t0006g0005 others(10): Show |
13 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.670+1275G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812565 | |||||||
| chr5:74812653 | C | A | 1 | a0001c0001t0017g0120 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.670+1187G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812653 | |||||||
| chr5:74812819 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.670+1021C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812819 | |||||||
| chr5:74812958 | C | T | 1 | a0001c0002t0011g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.670+882G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812958 | |||||||
| chr5:74813247 | A | T | 6 | a0001c0001t0002g0122 a0001c0001t0002g0170 a0001c0001t0002g0171 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+593T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813247 | |||||||
| chr5:74813249 | A | T | 6 | a0001c0001t0002g0122 a0001c0001t0002g0170 a0001c0001t0002g0171 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+591T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813249 | |||||||
| chr5:74813289 | A | C | 4 | a0001c0001t0002g0122 a0001c0001t0002g0170 a0001c0001t0002g0172 others(1): Show |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+551T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813289 | |||||||
| chr5:74813507 | G | A | 19 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(16): Show |
19 | HG00438.hp1 HG00735.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.670+333C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813507 | |||||||
| chr5:74813677 | G | A | 8 | a0001c0001t0002g0094 a0001c0001t0002g0108 a0001c0001t0002g0152 others(5): Show |
8 | HG00438.hp2 HG02015.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+163C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813677 | |||||||
| chr5:74813691 | A | G | 1 | a0001c0001t0002g0180 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.670+149T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813691 | |||||||
| chr5:74813701 | A | T | 1 | a0001c0002t0007g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.670+139T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813701 | |||||||
| chr5:74813807 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.670+33G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813807 | |||||||
| chr5:74814076 | T | C | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-57A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74814076 | |||||||
| chr5:74814584 | T | C | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.491-565A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74814584 | |||||||
| chr5:74814616 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.491-597A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74814616 | |||||||
| chr5:74815026 | C | A | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-1007G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815026 | |||||||
| chr5:74815161 | AATATACT others(5): Show |
A | 7 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.491-1154_491-1143d others(14): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815161 | |||||||
| chr5:74815196 | CT | C | 151 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(148): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.491-1178delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815196 | |||||||
| chr5:74815228 | T | G | 32 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(29): Show |
32 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.491-1209A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815228 | |||||||
| chr5:74815247 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.491-1228A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815247 | |||||||
| chr5:74815249 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.491-1230C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815249 | |||||||
| chr5:74815338 | C | T | 1 | a0001c0001t0003g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.491-1319G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815338 | |||||||
| chr5:74815339 | G | A | 3 | a0001c0001t0005g0060 a0001c0001t0005g0061 a0001c0003t0005g0228 |
3 | HG00438.hp1 HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-1320C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815339 | |||||||
| chr5:74815380 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.491-1361C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815380 | |||||||
| chr5:74815425 | A | G | 1 | a0001c0001t0004g0025 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.491-1406T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815425 | |||||||
| chr5:74815510 | T | C | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.491-1491A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815510 | |||||||
| chr5:74815576 | C | T | 21 | a0001c0001t0012g0229 a0001c0001t0012g0230 a0001c0002t0005g0016 others(18): Show |
21 | HG00438.hp1 HG00735.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.491-1557G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815576 | |||||||
| chr5:74815878 | T | C | 1 | a0001c0001t0006g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.491-1859A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815878 | |||||||
| chr5:74815912 | C | G | 151 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(148): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.491-1893G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815912 | |||||||
| chr5:74816147 | T | C | 7 | a0001c0001t0012g0229 a0001c0001t0012g0230 a0001c0003t0005g0221 others(4): Show |
7 | HG00438.hp1 HG00735.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.491-2128A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816147 | |||||||
| chr5:74816159 | C | T | 1 | a0001c0003t0005g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.491-2140G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816159 | |||||||
| chr5:74816165 | A | G | 1 | a0001c0001t0006g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.491-2146T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816165 | |||||||
| chr5:74816271 | T | A | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.491-2252A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816271 | |||||||
| chr5:74816409 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.491-2390A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816409 | |||||||
| chr5:74816445 | A | T | 1 | a0001c0001t0004g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.491-2426T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816445 | |||||||
| chr5:74816465 | C | T | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.491-2446G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816465 | |||||||
| chr5:74817010 | G | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.491-2991C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74817010 | |||||||
| chr5:74817395 | C | T | 119 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(116): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.491-3376G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74817395 | |||||||
| chr5:74817797 | C | T | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.491-3778G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74817797 | |||||||
| chr5:74817869 | T | C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.491-3850A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74817869 | |||||||
| chr5:74818570 | G | GC | 39 | a0001c0001t0001g0073 a0001c0001t0001g0088 a0001c0001t0001g0096 others(36): Show |
39 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.491-4552dupG | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818570 | |||||||
| chr5:74818572 | C | G | 2 | a0001c0001t0004g0057 a0001c0001t0004g0058 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.491-4553G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818572 | |||||||
| chr5:74818577 | C | G | 2 | a0001c0001t0003g0275 a0001c0001t0003g0286 |
2 | NA18953.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.491-4558G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818577 | |||||||
| chr5:74818704 | A | G | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-4685T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818704 | |||||||
| chr5:74818736 | C | T | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-4717G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818736 | |||||||
| chr5:74818737 | G | A | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-4718C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818737 | |||||||
| chr5:74818753 | G | A | 1 | a0001c0001t0019g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.491-4734C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818753 | |||||||
| chr5:74818770 | G | GCT | 15 | a0001c0001t0001g0073 a0001c0001t0001g0087 a0001c0001t0001g0121 others(12): Show |
15 | HG00673.hp1 HG01192.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.491-4753_491-4752d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | |||||||
| chr5:74818770 | GCT | G | 10 | a0001c0001t0001g0237 a0001c0001t0004g0051 a0001c0001t0006g0009 others(7): Show |
10 | HG01884.hp2 HG02647.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-4753_491-4752d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | |||||||
| chr5:74818770 | GCTCT | G | 14 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(11): Show |
14 | HG01167.hp1 HG02258.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.491-4755_491-4752d others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | |||||||
| chr5:74818770 | GCTCTCT | G | 3 | a0001c0001t0001g0096 a0001c0001t0003g0300 a0001c0001t0004g0052 |
3 | HG00733.hp1 HG02027.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.491-4757_491-4752d others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | |||||||
| chr5:74818770 | GCTCTCTC others(1): Show |
G | 59 | a0001c0001t0002g0161 a0001c0001t0002g0166 a0001c0001t0002g0167 others(56): Show |
59 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.491-4759_491-4752d others(10): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | |||||||
| chr5:74818770 | GCTCTCTC others(3): Show |
G | 3 | a0001c0002t0007g0066 a0001c0002t0007g0070 a0001c0002t0007g0071 |
3 | HG02451.hp2 HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.491-4761_491-4752d others(12): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | |||||||
| chr5:74818789 | CTCTCTCT others(9): Show |
C | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-4786_491-4771d others(18): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818789 | |||||||
| chr5:74818795 | CTCTCTCT others(3): Show |
C | 8 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(5): Show |
8 | HG02145.hp2 HG02723.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-4786_491-4777d others(12): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818795 | |||||||
| chr5:74818797 | C | A | 1 | a0001c0001t0004g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.491-4778G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818797 | |||||||
| chr5:74818797 | C | CTA | 4 | a0001c0001t0004g0034 a0001c0001t0004g0036 a0001c0001t0004g0047 others(1): Show |
4 | HG01069.hp2 HG01515.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-4779_491-4778i others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818797 | |||||||
| chr5:74818797 | CTCTCTCT others(1): Show |
C | 12 | a0001c0001t0002g0094 a0001c0001t0002g0108 a0001c0001t0002g0152 others(9): Show |
13 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.491-4786_491-4779d others(10): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818797 | |||||||
| chr5:74818797 | CTCTCTCT others(5): Show |
C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.491-4790_491-4779d others(14): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818797 | |||||||
| chr5:74818799 | C | A | 9 | a0001c0001t0001g0081 a0001c0001t0004g0030 a0001c0001t0004g0034 others(6): Show |
9 | HG01069.hp2 HG01081.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.491-4780G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818799 | |||||||
| chr5:74818799 | C | CTA | 10 | a0001c0001t0004g0021 a0001c0001t0004g0024 a0001c0001t0004g0035 others(7): Show |
10 | HG00140.hp2 HG01071.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.491-4781_491-4780i others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818799 | |||||||
| chr5:74818799 | C | CTATA | 3 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0040 |
3 | HG00280.hp2 HG01255.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.491-4781_491-4780i others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818799 | |||||||
| chr5:74818799 | CTCTCTA | C | 3 | a0001c0002t0009g0247 a0001c0002t0009g0248 a0001c0002t0018g0231 |
3 | HG00741.hp2 HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.491-4786_491-4781d others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818799 | |||||||
| chr5:74818801 | C | A | 24 | a0001c0001t0001g0081 a0001c0001t0004g0003 a0001c0001t0004g0021 others(21): Show |
24 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.491-4782G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818801 | |||||||
| chr5:74818801 | C | CTA | 4 | a0001c0001t0004g0026 a0001c0001t0004g0029 a0001c0001t0010g0044 others(1): Show |
4 | HG00738.hp2 HG01243.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-4783_491-4782i others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818801 | |||||||
| chr5:74818801 | CTCTA | C | 3 | a0001c0003t0005g0222 a0001c0003t0005g0227 a0001c0003t0005g0228 |
3 | HG00438.hp1 HG00735.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.491-4786_491-4783d others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818801 | |||||||
| chr5:74818803 | C | A | 59 | a0001c0001t0001g0075 a0001c0001t0001g0081 a0001c0001t0001g0082 others(56): Show |
59 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.491-4784G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818803 | |||||||
| chr5:74818803 | C | CTA | 8 | a0001c0001t0001g0102 a0001c0001t0001g0302 a0001c0001t0002g0114 others(5): Show |
8 | HG00673.hp2 HG01074.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-4786_491-4785d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818803 | |||||||
| chr5:74818803 | C | CTATATA | 4 | a0001c0001t0004g0023 a0001c0001t0004g0037 a0001c0001t0005g0060 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-4790_491-4785d others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818803 | |||||||
| chr5:74818803 | CTA | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0002t0005g0017 |
3 | HG02083.hp2 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.491-4786_491-4785d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818803 | |||||||
| chr5:74818803 | CTATA | C | 3 | a0001c0002t0011g0232 a0001c0003t0005g0221 a0001c0003t0005g0226 |
3 | HG03098.hp2 NA18982.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.491-4788_491-4785d others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818803 | |||||||
| chr5:74818805 | A | C | 82 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0080 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.491-4786T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818805 | |||||||
| chr5:74818807 | A | C | 56 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0080 others(53): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.491-4788T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818807 | |||||||
| chr5:74818809 | A | C | 14 | a0001c0001t0001g0084 a0001c0001t0001g0135 a0001c0001t0001g0305 others(11): Show |
14 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.491-4790T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818809 | |||||||
| chr5:74818811 | A | C | 3 | a0001c0001t0002g0163 a0001c0001t0002g0196 a0001c0001t0002g0202 |
3 | HG00741.hp1 HG01978.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.491-4792T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818811 | |||||||
| chr5:74818841 | C | A | 149 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(146): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.491-4822G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818841 | |||||||
| chr5:74818947 | C | T | 13 | a0001c0001t0005g0060 a0001c0001t0005g0061 a0001c0001t0006g0005 others(10): Show |
13 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-4928G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818947 | |||||||
| chr5:74819024 | G | A | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.491-5005C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819024 | |||||||
| chr5:74819162 | C | T | 109 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.491-5143G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819162 | |||||||
| chr5:74819257 | C | A | 1 | a0001c0001t0003g0298 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.491-5238G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819257 | |||||||
| chr5:74819362 | C | G | 1 | a0001c0001t0002g0194 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.491-5343G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819362 | |||||||
| chr5:74819501 | A | C | 1 | a0001c0001t0010g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.491-5482T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819501 | |||||||
| chr5:74819513 | G | A | 178 | a0001c0001t0002g0098 a0001c0001t0002g0113 a0001c0001t0002g0122 others(175): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.491-5494C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819513 | |||||||
| chr5:74819665 | A | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.491-5646T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819665 | |||||||
| chr5:74819804 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.491-5785T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819804 | |||||||
| chr5:74819911 | G | T | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-5892C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819911 | |||||||
| chr5:74819924 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.491-5905A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819924 | |||||||
| chr5:74819993 | C | CT | 68 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0100 others(65): Show |
68 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.491-5975dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819993 | |||||||
| chr5:74819993 | C | CTT | 15 | a0001c0001t0003g0001 a0001c0001t0003g0264 a0001c0001t0003g0266 others(12): Show |
16 | HG00099.hp1 HG00408.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.491-5976_491-5975d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819993 | |||||||
| chr5:74819993 | C | CTTT | 38 | a0001c0001t0004g0003 a0001c0001t0004g0023 a0001c0001t0004g0024 others(35): Show |
38 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.491-5977_491-5975d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819993 | |||||||
| chr5:74819993 | CTTTT | C | 6 | a0001c0003t0005g0103 a0001c0003t0005g0224 a0001c0003t0005g0225 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-5978_491-5975d others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819993 | |||||||
| chr5:74820059 | G | A | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-6040C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74820059 | |||||||
| chr5:74820610 | C | T | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-6591G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74820610 | |||||||
| chr5:74820951 | G | C | 8 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(5): Show |
8 | HG02559.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-6932C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74820951 | |||||||
| chr5:74821195 | T | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.491-7176A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821195 | |||||||
| chr5:74821328 | T | C | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-7309A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821328 | |||||||
| chr5:74821671 | A | G | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-7652T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821671 | |||||||
| chr5:74821697 | C | T | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-7678G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821697 | |||||||
| chr5:74821814 | T | G | 1 | a0001c0001t0008g0288 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.491-7795A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821814 | |||||||
| chr5:74821949 | G | A | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.491-7930C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821949 | |||||||
| chr5:74822117 | T | G | 1 | a0001c0004t0003g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.491-8098A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822117 | |||||||
| chr5:74822132 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.491-8113C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822132 | |||||||
| chr5:74822483 | A | G | 1 | a0001c0003t0005g0226 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.491-8464T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822483 | |||||||
| chr5:74822660 | C | T | 1 | a0001c0001t0006g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.491-8641G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822660 | |||||||
| chr5:74822812 | ACTC | A | 5 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-8796_491-8794d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822812 | |||||||
| chr5:74822893 | T | C | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-8874A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822893 | |||||||
| chr5:74822970 | T | C | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-8951A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822970 | |||||||
| chr5:74823006 | G | A | 40 | a0001c0001t0030g0004 a0001c0002t0005g0016 a0001c0002t0005g0017 others(37): Show |
40 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.491-8987C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823006 | |||||||
| chr5:74823121 | C | T | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-9102G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823121 | |||||||
| chr5:74823289 | C | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0142 a0001c0001t0001g0211 |
3 | HG01516.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.491-9270G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823289 | |||||||
| chr5:74823355 | C | T | 2 | a0001c0002t0011g0232 a0001c0002t0011g0233 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.491-9336G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823355 | |||||||
| chr5:74823477 | G | A | 119 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(116): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.491-9458C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823477 | |||||||
| chr5:74823636 | G | A | 1 | a0001c0001t0021g0162 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.491-9617C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823636 | |||||||
| chr5:74823661 | G | A | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.491-9642C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823661 | |||||||
| chr5:74823713 | G | A | 2 | a0001c0001t0008g0257 a0001c0001t0008g0258 |
2 | NA18952.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.491-9694C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823713 | |||||||
| chr5:74823850 | T | G | 1 | a0001c0001t0002g0168 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.491-9831A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823850 | |||||||
| chr5:74823901 | C | G | 13 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0081 others(10): Show |
13 | HG01074.hp1 HG01346.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-9882G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823901 | |||||||
| chr5:74824141 | C | T | 135 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(132): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.491-10122G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824141 | |||||||
| chr5:74824157 | T | C | 1 | a0001c0003t0005g0249 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.491-10138A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824157 | |||||||
| chr5:74824301 | T | C | 1 | a0001c0002t0007g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490+10125A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824301 | |||||||
| chr5:74824334 | G | A | 1 | a0001c0001t0004g0048 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.490+10092C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824334 | |||||||
| chr5:74824402 | C | T | 7 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0025 others(4): Show |
7 | HG02735.hp1 HG03239.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.490+10024G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824402 | |||||||
| chr5:74824677 | GCT | G | 13 | a0001c0001t0005g0060 a0001c0001t0005g0061 a0001c0001t0006g0005 others(10): Show |
13 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.490+9747_490+9748d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824677 | |||||||
| chr5:74824708 | TAC | T | 49 | a0001c0001t0001g0073 a0001c0001t0004g0024 a0001c0001t0004g0025 others(46): Show |
49 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.490+9716_490+9717d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824708 | |||||||
| chr5:74824708 | TACAC | T | 96 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(93): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.490+9714_490+9717d others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824708 | |||||||
| chr5:74824972 | C | T | 1 | a0001c0001t0004g0029 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.490+9454G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824972 | |||||||
| chr5:74825577 | C | T | 44 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 others(41): Show |
44 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.490+8849G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74825577 | |||||||
| chr5:74825773 | C | T | 8 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(5): Show |
8 | HG02145.hp2 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.490+8653G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74825773 | |||||||
| chr5:74825797 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.490+8629A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74825797 | |||||||
| chr5:74825815 | T | C | 5 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+8611A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74825815 | |||||||
| chr5:74825821 | G | A | 44 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 others(41): Show |
44 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.490+8605C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74825821 | |||||||
| chr5:74826250 | A | G | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+8176T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74826250 | |||||||
| chr5:74826503 | G | A | 108 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(105): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.490+7923C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74826503 | |||||||
| chr5:74826574 | T | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.490+7852A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74826574 | |||||||
| chr5:74826602 | C | T | 7 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.490+7824G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74826602 | |||||||
| chr5:74826658 | T | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.490+7768A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74826658 | |||||||
| chr5:74827144 | T | C | 1 | a0001c0001t0003g0256 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.490+7282A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827144 | |||||||
| chr5:74827302 | G | A | 150 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.490+7124C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827302 | |||||||
| chr5:74827669 | C | CT | 11 | a0001c0001t0002g0114 a0001c0001t0002g0155 a0001c0001t0003g0281 others(8): Show |
11 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+6756dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827669 | |||||||
| chr5:74827694 | T | G | 7 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.490+6732A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827694 | |||||||
| chr5:74827706 | A | T | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+6720T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827706 | |||||||
| chr5:74827837 | A | AT | 59 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(56): Show |
60 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.490+6588dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827837 | |||||||
| chr5:74827930 | T | A | 1 | a0001c0001t0002g0206 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.490+6496A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827930 | |||||||
| chr5:74827937 | A | G | 1 | a0001c0001t0003g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+6489T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827937 | |||||||
| chr5:74827979 | T | C | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+6447A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827979 | |||||||
| chr5:74828021 | A | G | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+6405T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828021 | |||||||
| chr5:74828054 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.490+6372A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828054 | |||||||
| chr5:74828092 | T | C | 1 | a0001c0002t0011g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490+6334A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828092 | |||||||
| chr5:74828119 | T | C | 3 | a0001c0001t0004g0034 a0001c0001t0004g0035 a0001c0001t0004g0036 |
3 | HG01069.hp2 HG01071.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.490+6307A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828119 | |||||||
| chr5:74828209 | T | C | 1 | a0001c0001t0003g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+6217A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828209 | |||||||
| chr5:74828307 | C | T | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490+6119G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828307 | |||||||
| chr5:74828456 | T | A | 1 | a0001c0001t0003g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+5970A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828456 | |||||||
| chr5:74828460 | T | A | 1 | a0001c0001t0003g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+5966A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828460 | |||||||
| chr5:74828461 | T | A | 1 | a0001c0001t0003g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+5965A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828461 | |||||||
| chr5:74828501 | C | T | 138 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(135): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.490+5925G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828501 | |||||||
| chr5:74828715 | C | T | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.490+5711G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828715 | |||||||
| chr5:74828780 | G | A | 1 | a0001c0002t0007g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490+5646C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828780 | |||||||
| chr5:74828964 | C | T | 108 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(105): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.490+5462G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828964 | |||||||
| chr5:74828973 | G | A | 1 | a0001c0001t0017g0120 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.490+5453C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828973 | |||||||
| chr5:74829056 | G | A | 54 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(51): Show |
55 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.490+5370C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829056 | |||||||
| chr5:74829056 | G | T | 1 | a0001c0001t0002g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.490+5370C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829056 | |||||||
| chr5:74829065 | A | G | 16 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(13): Show |
16 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.490+5361T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829065 | |||||||
| chr5:74829437 | A | T | 22 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0083 others(19): Show |
22 | HG00639.hp1 HG01074.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.490+4989T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829437 | |||||||
| chr5:74829463 | C | T | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490+4963G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829463 | |||||||
| chr5:74829475 | A | T | 8 | a0001c0001t0002g0114 a0001c0001t0012g0229 a0001c0001t0012g0230 others(5): Show |
8 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+4951T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829475 | |||||||
| chr5:74829611 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.490+4815A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829611 | |||||||
| chr5:74829615 | G | A | 2 | a0001c0002t0007g0070 a0001c0002t0007g0072 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.490+4811C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829615 | |||||||
| chr5:74829636 | C | A | 1 | a0001c0001t0003g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+4790G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829636 | |||||||
| chr5:74829668 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.490+4758A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829668 | |||||||
| chr5:74829680 | T | C | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.490+4746A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829680 | |||||||
| chr5:74829684 | A | C | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+4742T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829684 | |||||||
| chr5:74829771 | C | T | 1 | a0001c0002t0007g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490+4655G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829771 | |||||||
| chr5:74829825 | T | C | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.490+4601A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829825 | |||||||
| chr5:74830517 | A | G | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+3909T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74830517 | |||||||
| chr5:74830532 | T | C | 1 | a0001c0001t0004g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490+3894A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74830532 | |||||||
| chr5:74830539 | A | C | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+3887T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74830539 | |||||||
| chr5:74830785 | G | A | 1 | a0001c0002t0016g0212 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.490+3641C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74830785 | |||||||
| chr5:74831057 | C | A | 1 | a0001c0001t0004g0024 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.490+3369G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831057 | |||||||
| chr5:74831138 | GA | G | 3 | a0001c0001t0003g0001 a0001c0001t0003g0264 a0001c0001t0003g0266 |
4 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+3287delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831138 | |||||||
| chr5:74831157 | C | T | 109 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.490+3269G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831157 | |||||||
| chr5:74831286 | C | T | 151 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(148): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.490+3140G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831286 | |||||||
| chr5:74831360 | T | G | 1 | a0001c0001t0002g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490+3066A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831360 | |||||||
| chr5:74831879 | T | C | 1 | a0001c0001t0004g0036 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.490+2547A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831879 | |||||||
| chr5:74831985 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0020g0079 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.490+2441G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831985 | |||||||
| chr5:74832377 | A | C | 2 | a0001c0003t0005g0240 a0001c0003t0015g0241 |
2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.490+2049T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74832377 | |||||||
| chr5:74832576 | C | T | 149 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(146): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.490+1850G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74832576 | |||||||
| chr5:74832587 | A | T | 1 | a0001c0001t0027g0272 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.490+1839T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74832587 | |||||||
| chr5:74832672 | T | C | 1 | a0001c0003t0005g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.490+1754A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74832672 | |||||||
| chr5:74832675 | A | G | 5 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0034 others(2): Show |
5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+1751T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74832675 | |||||||
| chr5:74833008 | A | C | 2 | a0001c0001t0004g0050 a0001c0001t0004g0051 |
2 | HG00642.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.490+1418T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833008 | |||||||
| chr5:74833123 | A | G | 1 | a0001c0003t0005g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.490+1303T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833123 | |||||||
| chr5:74833139 | A | G | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.490+1287T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833139 | |||||||
| chr5:74833181 | G | A | 2 | a0001c0001t0003g0270 a0001c0001t0003g0281 |
2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.490+1245C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833181 | |||||||
| chr5:74833285 | AAAC | A | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.490+1138_490+1140d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833285 | |||||||
| chr5:74833292 | A | G | 8 | a0001c0001t0030g0004 a0001c0002t0009g0242 a0001c0002t0009g0243 others(5): Show |
8 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.490+1134T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833292 | |||||||
| chr5:74833679 | A | C | 1 | a0001c0001t0002g0114 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.490+747T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833679 | |||||||
| chr5:74833738 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.490+688A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833738 | |||||||
| chr5:74833935 | T | C | 1 | a0001c0002t0011g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.490+491A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833935 | |||||||
| chr5:74834029 | A | C | 8 | a0001c0001t0001g0078 a0001c0002t0009g0242 a0001c0002t0009g0243 others(5): Show |
8 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.490+397T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74834029 | |||||||
| chr5:74834217 | G | A | 1 | a0001c0003t0005g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.490+209C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74834217 | |||||||
| chr5:74834295 | C | T | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+131G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74834295 | |||||||
| chr5:74834329 | T | A | 1 | a0001c0001t0002g0202 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.490+97A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74834329 | |||||||
| chr5:74834353 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.490+73A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74834353 | |||||||
| chr5:74834779 | C | T | 3 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0217 |
3 | HG02056.hp2 NA18949.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.319-182G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834779 | |||||||
| chr5:74834839 | T | A | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.319-242A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834839 | |||||||
| chr5:74834840 | C | A | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.319-243G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834840 | |||||||
| chr5:74834848 | A | G | 1 | a0001c0002t0009g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.319-251T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834848 | |||||||
| chr5:74834999 | T | TA | 102 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(99): Show |
103 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.319-403dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834999 | |||||||
| chr5:74834999 | T | TAA | 44 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0024 others(41): Show |
44 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.319-404_319-403dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834999 | |||||||
| chr5:74835041 | C | T | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.319-444G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835041 | |||||||
| chr5:74835185 | T | C | 1 | a0001c0001t0004g0043 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.319-588A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835185 | |||||||
| chr5:74835250 | A | G | 6 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
6 | HG01243.hp2 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-653T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835250 | |||||||
| chr5:74835276 | C | T | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.319-679G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835276 | |||||||
| chr5:74835405 | C | T | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.319-808G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835405 | |||||||
| chr5:74835601 | C | CA | 68 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0096 others(65): Show |
68 | HG00140.hp2 HG00673.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.319-1005dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835601 | |||||||
| chr5:74835601 | CA | C | 71 | a0001c0001t0001g0141 a0001c0001t0002g0094 a0001c0001t0002g0154 others(68): Show |
72 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.319-1005delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835601 | |||||||
| chr5:74836326 | GTTT | G | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(37): Show |
40 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.319-1732_319-1730d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836326 | |||||||
| chr5:74836458 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.319-1861C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836458 | |||||||
| chr5:74836514 | A | C | 1 | a0001c0003t0005g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.319-1917T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836514 | |||||||
| chr5:74836662 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.319-2065G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836662 | |||||||
| chr5:74836663 | G | A | 2 | a0001c0001t0006g0007 a0001c0001t0006g0013 |
2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.319-2066C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836663 | |||||||
| chr5:74836872 | C | T | 4 | a0001c0001t0001g0109 a0001c0001t0001g0176 a0001c0001t0001g0178 others(1): Show |
4 | HG01928.hp2 HG01975.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+2093G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836872 | |||||||
| chr5:74836892 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0082 a0001c0001t0001g0134 |
3 | HG01346.hp1 HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.318+2073C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836892 | |||||||
| chr5:74836935 | G | C | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.318+2030C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836935 | |||||||
| chr5:74836943 | CA | C | 171 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0101 others(168): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.318+2021delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836943 | |||||||
| chr5:74837184 | T | C | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.318+1781A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74837184 | |||||||
| chr5:74837461 | G | T | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.318+1504C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74837461 | |||||||
| chr5:74837692 | G | A | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.318+1273C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74837692 | |||||||
| chr5:74837737 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0020g0079 |
3 | HG01891.hp2 HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.318+1228C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74837737 | |||||||
| chr5:74837939 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.318+1026C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74837939 | |||||||
| chr5:74838114 | C | CA | 35 | a0001c0001t0001g0184 a0001c0001t0002g0106 a0001c0001t0002g0108 others(32): Show |
35 | HG00438.hp1 HG00738.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.318+850dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838114 | |||||||
| chr5:74838208 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.318+757A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838208 | |||||||
| chr5:74838418 | A | G | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.318+547T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838418 | |||||||
| chr5:74838434 | A | G | 1 | a0001c0001t0003g0265 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.318+531T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838434 | |||||||
| chr5:74838489 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.318+476G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838489 | |||||||
| chr5:74838515 | A | G | 1 | a0001c0003t0005g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.318+450T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838515 | |||||||
| chr5:74838802 | G | A | 4 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0140 others(1): Show |
4 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+163C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838802 | |||||||
| chr5:74838829 | C | T | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.318+136G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838829 | |||||||
| chr5:74838917 | T | C | 38 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(35): Show |
38 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.318+48A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838917 | |||||||
| chr5:74838951 | G | GAGGATCT others(4): Show |
1 | a0001c0001t0001g0182 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.318+3_318+13dupAAC others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838951 | |||||||
| chr5:74839131 | G | C | 5 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-81C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839131 | |||||||
| chr5:74839386 | T | C | 1 | a0001c0004t0003g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.233-336A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839386 | |||||||
| chr5:74839463 | C | T | 1 | a0001c0003t0005g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.233-413G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839463 | |||||||
| chr5:74839465 | T | C | 2 | a0001c0003t0005g0249 a0001c0003t0005g0250 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.233-415A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839465 | |||||||
| chr5:74839522 | A | ATT | 13 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(10): Show |
13 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.233-474_233-473dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839522 | |||||||
| chr5:74839522 | AT | A | 91 | a0001c0001t0001g0085 a0001c0001t0001g0141 a0001c0001t0002g0110 others(88): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.233-473delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839522 | |||||||
| chr5:74839617 | T | C | 1 | a0001c0004t0003g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.232+457A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839617 | |||||||
| chr5:74839627 | C | T | 3 | a0001c0002t0011g0232 a0001c0002t0011g0233 a0001c0002t0018g0231 |
3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.232+447G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839627 | |||||||
| chr5:74839989 | T | C | 1 | a0001c0001t0008g0259 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.232+85A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839989 | |||||||
| chr5:74840006 | C | A | 6 | a0001c0001t0002g0122 a0001c0001t0002g0170 a0001c0001t0002g0171 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+68G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74840006 | |||||||
| chr5:74840057 | A | C | 1 | a0001c0001t0001g0214 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.232+17T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74840057 | |||||||
| chr5:74840290 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.133-117C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840290 | |||||||
| chr5:74840374 | T | C | 46 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(43): Show |
46 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.133-201A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840374 | |||||||
| chr5:74840396 | T | C | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.133-223A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840396 | |||||||
| chr5:74840526 | TA | T | 15 | a0001c0001t0004g0027 a0001c0001t0005g0060 a0001c0001t0005g0061 others(12): Show |
15 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.133-354delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840526 | |||||||
| chr5:74840567 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.133-394T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840567 | |||||||
| chr5:74840646 | A | G | 4 | a0001c0001t0001g0082 a0001c0001t0001g0131 a0001c0001t0001g0142 others(1): Show |
4 | HG01516.hp2 HG02735.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-473T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840646 | |||||||
| chr5:74840657 | A | G | 1 | a0001c0001t0004g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.133-484T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840657 | |||||||
| chr5:74840791 | T | A | 1 | a0001c0001t0032g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133-618A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840791 | |||||||
| chr5:74840974 | T | C | 2 | a0001c0001t0012g0229 a0001c0001t0012g0230 |
2 | HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.132+571A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840974 | |||||||
| chr5:74841716 | T | C | 24 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0003g0260 others(21): Show |
24 | HG01257.hp2 HG01258.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3-37A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74841716 | |||||||
| chr5:74841809 | G | A | 2 | a0001c0002t0011g0232 a0001c0002t0011g0233 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-3-130C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74841809 | |||||||
| chr5:74841914 | T | C | 5 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-235A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74841914 | |||||||
| chr5:74842010 | A | T | 1 | a0001c0001t0002g0193 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-3-331T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842010 | |||||||
| chr5:74842011 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-3-332G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842011 | |||||||
| chr5:74842041 | G | A | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-362C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842041 | |||||||
| chr5:74842043 | G | T | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-364C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842043 | |||||||
| chr5:74842057 | A | T | 1 | a0001c0001t0003g0287 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-3-378T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842057 | |||||||
| chr5:74842058 | A | C | 1 | a0001c0001t0003g0287 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-3-379T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842058 | |||||||
| chr5:74842125 | AT | A | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-447delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842125 | |||||||
| chr5:74842144 | G | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-3-465C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842144 | |||||||
| chr5:74842193 | AG | A | 152 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(149): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-3-515delC | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842193 | |||||||
| chr5:74842231 | G | A | 1 | a0001c0004t0003g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-3-552C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842231 | |||||||
| chr5:74842420 | C | CA | 28 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0091 others(25): Show |
28 | HG00408.hp1 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.-3-742dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842420 | C | CAA | 20 | a0001c0001t0001g0149 a0001c0001t0001g0182 a0001c0001t0002g0168 others(17): Show |
20 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.-3-743_-3-742dupTT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842420 | C | CAAA | 25 | a0001c0001t0003g0252 a0001c0001t0003g0256 a0001c0001t0003g0262 others(22): Show |
25 | HG01109.hp1 HG01175.hp2 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.-3-744_-3-742dupTT others(1): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842420 | C | CAAAA | 8 | a0001c0001t0001g0150 a0001c0001t0003g0255 a0001c0001t0003g0260 others(5): Show |
8 | HG00408.hp2 HG00558.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-745_-3-742dupTT others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842420 | CA | C | 61 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
61 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.-3-742delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842420 | CAA | C | 19 | a0001c0001t0001g0082 a0001c0001t0001g0102 a0001c0001t0001g0131 others(16): Show |
19 | HG00733.hp1 HG01074.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.-3-743_-3-742delTT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842420 | CAAA | C | 22 | a0001c0001t0001g0081 a0001c0001t0001g0130 a0001c0001t0001g0175 others(19): Show |
22 | HG00642.hp1 HG00733.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-3-744_-3-742delTT others(1): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842420 | CAAAA | C | 19 | a0001c0001t0004g0003 a0001c0001t0004g0025 a0001c0001t0004g0027 others(16): Show |
19 | HG01109.hp2 HG01243.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.-3-745_-3-742delTT others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842420 | CAAAAA | C | 16 | a0001c0001t0004g0021 a0001c0001t0004g0023 a0001c0001t0004g0024 others(13): Show |
16 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-3-746_-3-742delTT others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842420 | CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0005g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-3-754_-3-742delTT others(11): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842420 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-3-756_-3-742delTT others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | |||||||
| chr5:74842456 | A | G | 1 | a0001c0003t0005g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3-777T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842456 | |||||||
| chr5:74842535 | CT | C | 17 | a0001c0001t0004g0030 a0001c0001t0006g0005 a0001c0001t0006g0006 others(14): Show |
17 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-3-857delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842535 | |||||||
| chr5:74842830 | T | TCAATC | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-3-1152_-3-1151ins others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842830 | |||||||
| chr5:74842891 | G | A | 1 | a0001c0001t0003g0280 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-3-1212C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842891 | |||||||
| chr5:74843014 | C | T | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-1335G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74843014 | |||||||
| chr5:74843111 | G | C | 1 | a0001c0001t0002g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-3-1432C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74843111 | |||||||
| chr5:74843529 | T | C | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-1850A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74843529 | |||||||
| chr5:74843671 | T | C | 1 | a0001c0001t0003g0270 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-3-1992A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74843671 | |||||||
| chr5:74843776 | A | G | 150 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-3-2097T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74843776 | |||||||
| chr5:74844142 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-3-2463C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844142 | |||||||
| chr5:74844336 | C | A | 1 | a0001c0001t0002g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-3-2657G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844336 | |||||||
| chr5:74844384 | C | T | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-3-2705G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844384 | |||||||
| chr5:74844401 | G | A | 8 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(5): Show |
8 | HG02145.hp2 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-2722C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844401 | |||||||
| chr5:74844570 | G | A | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-3-2891C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844570 | |||||||
| chr5:74844631 | A | G | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-3-2952T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844631 | |||||||
| chr5:74844710 | G | A | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-3031C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844710 | |||||||
| chr5:74844758 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-3-3079C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844758 | |||||||
| chr5:74844792 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-3-3113C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844792 | |||||||
| chr5:74845027 | C | T | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-3348G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845027 | |||||||
| chr5:74845130 | T | C | 24 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0003g0260 others(21): Show |
24 | HG01257.hp2 HG01258.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3-3451A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845130 | |||||||
| chr5:74845198 | T | G | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-3-3519A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845198 | |||||||
| chr5:74845257 | G | A | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-3578C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845257 | |||||||
| chr5:74845406 | T | C | 1 | a0001c0003t0005g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-3-3727A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845406 | |||||||
| chr5:74845505 | G | A | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-3-3826C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845505 | |||||||
| chr5:74845738 | T | C | 6 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG00323.hp1 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-4059A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845738 | |||||||
| chr5:74845795 | G | A | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-4116C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845795 | |||||||
| chr5:74846211 | A | C | 2 | a0001c0001t0012g0229 a0001c0001t0012g0230 |
2 | HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-3-4532T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846211 | |||||||
| chr5:74846352 | C | T | 150 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-3-4673G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846352 | |||||||
| chr5:74846380 | A | G | 1 | a0001c0001t0006g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-3-4701T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846380 | |||||||
| chr5:74846476 | T | C | 1 | a0001c0001t0003g0255 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-3-4797A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846476 | |||||||
| chr5:74846811 | T | C | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-3-5132A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846811 | |||||||
| chr5:74846904 | T | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0305 |
2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.-3-5225A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846904 | |||||||
| chr5:74846910 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-3-5231C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846910 | |||||||
| chr5:74847019 | A | C | 1 | a0001c0003t0005g0222 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-3-5340T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847019 | |||||||
| chr5:74847040 | C | T | 76 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(73): Show |
76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-3-5361G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847040 | |||||||
| chr5:74847133 | T | C | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-5454A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847133 | |||||||
| chr5:74847262 | G | C | 63 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(60): Show |
64 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-3-5583C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847262 | |||||||
| chr5:74847380 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-3-5701C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847380 | |||||||
| chr5:74847499 | A | G | 1 | a0001c0001t0004g0024 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-3-5820T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847499 | |||||||
| chr5:74847555 | T | G | 1 | a0001c0001t0010g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-3-5876A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847555 | |||||||
| chr5:74847571 | G | A | 122 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(119): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-3-5892C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847571 | |||||||
| chr5:74847700 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-3-6021A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847700 | |||||||
| chr5:74847733 | T | C | 1 | a0001c0001t0030g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-6054A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847733 | |||||||
| chr5:74847741 | C | T | 1 | a0001c0001t0030g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-6062G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847741 | |||||||
| chr5:74847850 | T | C | 6 | a0001c0001t0002g0122 a0001c0001t0002g0170 a0001c0001t0002g0171 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-6171A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847850 | |||||||
| chr5:74847909 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-3-6230A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847909 | |||||||
| chr5:74847935 | G | A | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-6256C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847935 | |||||||
| chr5:74847939 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-3-6260T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847939 | |||||||
| chr5:74847963 | T | C | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-6284A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847963 | |||||||
| chr5:74848338 | T | C | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-6659A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848338 | |||||||
| chr5:74848378 | A | G | 96 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(93): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-3-6699T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848378 | |||||||
| chr5:74848497 | A | C | 1 | a0001c0001t0022g0181 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-3-6818T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848497 | |||||||
| chr5:74848616 | T | C | 3 | a0001c0002t0011g0232 a0001c0002t0011g0233 a0001c0002t0018g0231 |
3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-3-6937A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848616 | |||||||
| chr5:74848656 | T | C | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-3-6977A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848656 | |||||||
| chr5:74848744 | T | G | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-7065A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848744 | |||||||
| chr5:74848919 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-3-7240G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848919 | |||||||
| chr5:74849066 | G | A | 1 | a0001c0003t0005g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-3-7387C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849066 | |||||||
| chr5:74849132 | A | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0080 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-3-7453T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849132 | |||||||
| chr5:74849330 | T | C | 1 | a0001c0001t0030g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-7651A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849330 | |||||||
| chr5:74849391 | G | C | 3 | a0001c0002t0007g0070 a0001c0002t0007g0071 a0001c0002t0007g0072 |
3 | HG02451.hp2 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-3-7712C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849391 | |||||||
| chr5:74849479 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-3-7800A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849479 | |||||||
| chr5:74849573 | T | G | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-3-7894A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849573 | |||||||
| chr5:74849753 | A | G | 96 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(93): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-3-8074T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849753 | |||||||
| chr5:74849822 | C | T | 1 | a0001c0003t0005g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-3-8143G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849822 | |||||||
| chr5:74850035 | C | G | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-3-8356G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850035 | |||||||
| chr5:74850130 | A | G | 2 | a0001c0002t0007g0070 a0001c0002t0007g0072 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-3-8451T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850130 | |||||||
| chr5:74850181 | A | G | 3 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0217 |
3 | HG02056.hp2 NA18949.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-3-8502T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850181 | |||||||
| chr5:74850208 | T | G | 1 | a0001c0002t0029g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-3-8529A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850208 | |||||||
| chr5:74850253 | G | A | 7 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-8574C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850253 | |||||||
| chr5:74850260 | G | C | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-3-8581C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850260 | |||||||
| chr5:74850327 | A | C | 1 | a0001c0003t0005g0222 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-3-8648T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850327 | |||||||
| chr5:74850424 | T | C | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-8745A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850424 | |||||||
| chr5:74850648 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-3-8969A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850648 | |||||||
| chr5:74850897 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-3-9218G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850897 | |||||||
| chr5:74850980 | G | A | 2 | a0001c0003t0005g0249 a0001c0003t0005g0250 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-3-9301C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850980 | |||||||
| chr5:74851048 | TAAG | T | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-3-9372_-3-9370del others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851048 | |||||||
| chr5:74851237 | T | TCCTC | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-9562_-3-9559dup others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851237 | |||||||
| chr5:74851253 | T | TTCGTAGT others(6): Show |
1 | a0001c0001t0002g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-3-9587_-3-9575dup others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851253 | |||||||
| chr5:74851739 | C | T | 7 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-10060G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851739 | |||||||
| chr5:74851856 | C | G | 2 | a0001c0001t0003g0001 a0001c0001t0003g0264 |
3 | HG01069.hp1 HG01071.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-3-10177G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851856 | |||||||
| chr5:74851860 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-3-10181C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851860 | |||||||
| chr5:74851898 | G | T | 1 | a0001c0001t0003g0256 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-3-10219C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851898 | |||||||
| chr5:74851945 | G | A | 2 | a0001c0002t0011g0232 a0001c0002t0011g0233 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-3-10266C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851945 | |||||||
| chr5:74852014 | G | T | 1 | a0001c0003t0005g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-3-10335C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852014 | |||||||
| chr5:74852176 | C | T | 11 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-10497G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852176 | |||||||
| chr5:74852200 | C | T | 1 | a0001c0001t0030g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-10521G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852200 | |||||||
| chr5:74852381 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-3-10702C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852381 | |||||||
| chr5:74852403 | G | A | 28 | a0001c0001t0012g0229 a0001c0001t0012g0230 a0001c0002t0005g0016 others(25): Show |
28 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-3-10724C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852403 | |||||||
| chr5:74852426 | T | C | 106 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-3-10747A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852426 | |||||||
| chr5:74852477 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-3-10798C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852477 | |||||||
| chr5:74852665 | T | A | 1 | a0001c0003t0005g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-3-10986A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852665 | |||||||
| chr5:74852820 | T | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0176 a0001c0001t0001g0178 others(1): Show |
4 | HG01928.hp2 HG01975.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-11141A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852820 | |||||||
| chr5:74852876 | C | T | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-3-11197G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852876 | |||||||
| chr5:74853485 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0239 |
2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-3-11806G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853485 | |||||||
| chr5:74853547 | G | C | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(58): Show |
62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-11868C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853547 | |||||||
| chr5:74853653 | T | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-3-11974A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853653 | |||||||
| chr5:74853701 | A | AT | 17 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0123 others(14): Show |
17 | HG01106.hp2 HG01109.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.-3-12023dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853701 | |||||||
| chr5:74853701 | A | T | 2 | a0001c0001t0004g0027 a0001c0001t0004g0028 |
2 | HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-3-12022T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853701 | |||||||
| chr5:74853701 | AT | A | 91 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0002g0122 others(88): Show |
92 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-3-12023delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853701 | |||||||
| chr5:74853701 | ATT | A | 14 | a0001c0001t0003g0296 a0001c0001t0004g0057 a0001c0001t0004g0058 others(11): Show |
14 | HG01975.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3-12024_-3-12023d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853701 | |||||||
| chr5:74853733 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-3-12054T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853733 | |||||||
| chr5:74853905 | A | G | 151 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(148): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-3-12226T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853905 | |||||||
| chr5:74854264 | G | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0179 a0001c0001t0002g0180 |
3 | HG02572.hp2 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-4+11901C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854264 | |||||||
| chr5:74854357 | T | C | 151 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(148): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-4+11808A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854357 | |||||||
| chr5:74854358 | G | A | 3 | a0001c0002t0011g0232 a0001c0002t0011g0233 a0001c0002t0018g0231 |
3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-4+11807C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854358 | |||||||
| chr5:74854397 | AAAT | A | 135 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(132): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-4+11765_-4+11767d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854397 | |||||||
| chr5:74854871 | C | A | 149 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(146): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-4+11294G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854871 | |||||||
| chr5:74854875 | G | A | 1 | a0001c0001t0003g0280 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-4+11290C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854875 | |||||||
| chr5:74854885 | C | G | 1 | a0001c0003t0005g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-4+11280G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854885 | |||||||
| chr5:74855115 | G | A | 1 | a0001c0001t0003g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-4+11050C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855115 | |||||||
| chr5:74855126 | T | C | 1 | a0001c0001t0030g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-4+11039A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855126 | |||||||
| chr5:74855215 | C | G | 137 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-4+10950G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855215 | |||||||
| chr5:74855261 | T | A | 1 | a0001c0001t0001g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-4+10904A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855261 | |||||||
| chr5:74855472 | A | C | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+10693T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855472 | |||||||
| chr5:74855511 | G | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4+10654C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855511 | |||||||
| chr5:74855548 | C | A | 1 | a0001c0001t0003g0282 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-4+10617G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855548 | |||||||
| chr5:74855573 | G | C | 1 | a0001c0001t0025g0095 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-4+10592C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855573 | |||||||
| chr5:74855619 | T | C | 1 | a0001c0001t0030g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-4+10546A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855619 | |||||||
| chr5:74855995 | C | T | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-4+10170G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855995 | |||||||
| chr5:74855996 | G | A | 93 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(90): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-4+10169C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855996 | |||||||
| chr5:74856412 | T | C | 22 | a0001c0001t0002g0098 a0001c0001t0002g0113 a0001c0001t0002g0191 others(19): Show |
22 | HG00673.hp1 HG00741.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-4+9753A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74856412 | |||||||
| chr5:74856583 | T | C | 1 | a0001c0003t0005g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-4+9582A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74856583 | |||||||
| chr5:74856589 | A | T | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-4+9576T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74856589 | |||||||
| chr5:74856612 | T | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4+9553A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74856612 | |||||||
| chr5:74856813 | GA | G | 10 | a0001c0001t0002g0122 a0001c0001t0003g0286 a0001c0002t0007g0062 others(7): Show |
10 | HG02145.hp2 HG02559.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4+9351delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74856813 | |||||||
| chr5:74857044 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-4+9121C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857044 | |||||||
| chr5:74857108 | C | CA | 100 | a0001c0001t0001g0078 a0001c0001t0001g0096 a0001c0001t0001g0097 others(97): Show |
101 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-4+9056dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857108 | |||||||
| chr5:74857108 | C | CAA | 13 | a0001c0001t0002g0205 a0001c0001t0002g0206 a0001c0001t0002g0219 others(10): Show |
13 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-4+9055_-4+9056dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857108 | |||||||
| chr5:74857108 | CA | C | 47 | a0001c0001t0001g0074 a0001c0001t0001g0121 a0001c0001t0002g0115 others(44): Show |
47 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.-4+9056delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857108 | |||||||
| chr5:74857187 | T | C | 138 | a0001c0001t0002g0114 a0001c0001t0003g0001 a0001c0001t0003g0002 others(135): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-4+8978A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857187 | |||||||
| chr5:74857368 | C | T | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | NA18948.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-4+8797G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857368 | |||||||
| chr5:74857369 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-4+8796C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857369 | |||||||
| chr5:74857380 | G | A | 2 | a0001c0001t0004g0045 a0001c0001t0004g0046 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-4+8785C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857380 | |||||||
| chr5:74857447 | G | C | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | NA18948.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-4+8718C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857447 | |||||||
| chr5:74857456 | G | A | 1 | a0001c0003t0005g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-4+8709C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857456 | |||||||
| chr5:74857475 | G | A | 2 | a0001c0003t0005g0224 a0001c0003t0005g0225 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-4+8690C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857475 | |||||||
| chr5:74857567 | C | T | 1 | a0001c0001t0017g0120 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-4+8598G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857567 | |||||||
| chr5:74857571 | G | GA | 8 | a0001c0002t0005g0018 a0001c0002t0005g0019 a0001c0002t0005g0020 others(5): Show |
8 | HG01884.hp2 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4+8593_-4+8594ins others(1): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | |||||||
| chr5:74857571 | G | GAA | 10 | a0001c0001t0012g0229 a0001c0002t0007g0062 a0001c0002t0007g0065 others(7): Show |
10 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-4+8593_-4+8594ins others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | |||||||
| chr5:74857571 | G | GAAA | 6 | a0001c0001t0002g0114 a0001c0001t0012g0230 a0001c0002t0007g0072 others(3): Show |
6 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+8593_-4+8594ins others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | |||||||
| chr5:74857571 | G | GAAAAAAA others(3): Show |
1 | a0001c0002t0009g0246 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-4+8593_-4+8594ins others(10): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | |||||||
| chr5:74857571 | G | GAAAAAAA others(5): Show |
2 | a0001c0002t0009g0247 a0001c0002t0009g0248 |
2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-4+8593_-4+8594ins others(12): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | |||||||
| chr5:74857571 | GGAAAAAA | G | 16 | a0001c0001t0003g0002 a0001c0001t0003g0260 a0001c0001t0003g0286 others(13): Show |
16 | HG00408.hp2 HG01175.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4+8587_-4+8593del others(7): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | |||||||
| chr5:74857571 | GGAAAAAA others(1): Show |
G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0252 a0001c0001t0003g0253 others(42): Show |
46 | HG00099.hp1 HG00558.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-4+8586_-4+8593del others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | |||||||
| chr5:74857572 | G | A | 41 | a0001c0001t0002g0114 a0001c0001t0012g0229 a0001c0001t0012g0230 others(38): Show |
41 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-4+8593C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | |||||||
| chr5:74857572 | G | GA | 48 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(45): Show |
48 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-4+8592dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | |||||||
| chr5:74857572 | G | GAA | 23 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0001g0092 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4+8591_-4+8592dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | |||||||
| chr5:74857572 | G | GAAA | 12 | a0001c0001t0001g0083 a0001c0001t0001g0093 a0001c0001t0001g0096 others(9): Show |
12 | HG00639.hp1 HG00639.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4+8590_-4+8592dup others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | |||||||
| chr5:74857572 | GA | G | 16 | a0001c0001t0002g0122 a0001c0001t0002g0170 a0001c0001t0002g0171 others(13): Show |
16 | HG01978.hp2 HG02615.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4+8592delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | |||||||
| chr5:74857572 | GAA | G | 7 | a0001c0001t0005g0060 a0001c0001t0006g0006 a0001c0001t0006g0007 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+8591_-4+8592del others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | |||||||
| chr5:74857572 | GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-4+8582_-4+8592del others(11): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | |||||||
| chr5:74857572 | GAAAAAAA others(6): Show |
G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0142 a0001c0001t0001g0211 |
3 | HG01516.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-4+8580_-4+8592del others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | |||||||
| chr5:74857572 | GAAAAAAA others(7): Show |
G | 2 | a0001c0001t0002g0094 a0001c0001t0004g0048 |
2 | HG01109.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.-4+8579_-4+8592del others(14): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | |||||||
| chr5:74857572 | GAAAAAAA others(8): Show |
G | 33 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(30): Show |
33 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-4+8578_-4+8592del others(15): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | |||||||
| chr5:74857573 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-4+8592T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857573 | |||||||
| chr5:74857585 | A | G | 1 | a0001c0001t0006g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-4+8580T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857585 | |||||||
| chr5:74857666 | TCTGTATA others(19): Show |
T | 12 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+8473_-4+8498del others(26): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857666 | |||||||
| chr5:74857702 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-4+8463A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857702 | |||||||
| chr5:74857794 | G | A | 43 | a0001c0001t0002g0114 a0001c0001t0012g0229 a0001c0001t0012g0230 others(40): Show |
43 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-4+8371C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857794 | |||||||
| chr5:74857833 | C | G | 7 | a0001c0001t0004g0003 a0001c0001t0004g0024 a0001c0001t0004g0025 others(4): Show |
7 | HG02735.hp1 HG03239.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+8332G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857833 | |||||||
| chr5:74857861 | C | T | 5 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
5 | HG03491.hp1 HG03492.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+8304G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857861 | |||||||
| chr5:74857949 | A | G | 1 | a0001c0001t0003g0260 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-4+8216T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857949 | |||||||
| chr5:74858113 | C | A | 60 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(57): Show |
61 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4+8052G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858113 | |||||||
| chr5:74858203 | T | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4+7962A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858203 | |||||||
| chr5:74858301 | T | C | 1 | a0001c0001t0003g0296 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-4+7864A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858301 | |||||||
| chr5:74858574 | G | A | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4+7591C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858574 | |||||||
| chr5:74858837 | T | C | 7 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+7328A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858837 | |||||||
| chr5:74858907 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-4+7258A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858907 | |||||||
| chr5:74858920 | A | C | 60 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(57): Show |
61 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4+7245T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858920 | |||||||
| chr5:74858980 | A | G | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+7185T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858980 | |||||||
| chr5:74859287 | C | CT | 18 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0100 others(15): Show |
19 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-4+6877dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859287 | |||||||
| chr5:74859345 | C | T | 60 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(57): Show |
61 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4+6820G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859345 | |||||||
| chr5:74859450 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-4+6715A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859450 | |||||||
| chr5:74859523 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-4+6642G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859523 | |||||||
| chr5:74859690 | A | G | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-4+6475T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859690 | |||||||
| chr5:74859720 | C | T | 1 | a0001c0001t0030g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-4+6445G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859720 | |||||||
| chr5:74859746 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-4+6419C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859746 | |||||||
| chr5:74859821 | C | T | 148 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(145): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-4+6344G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859821 | |||||||
| chr5:74859946 | G | A | 1 | a0001c0002t0016g0212 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-4+6219C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859946 | |||||||
| chr5:74859993 | G | A | 94 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(91): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-4+6172C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859993 | |||||||
| chr5:74860166 | T | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4+5999A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860166 | |||||||
| chr5:74860231 | A | G | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+5934T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860231 | |||||||
| chr5:74860453 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-4+5712T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860453 | |||||||
| chr5:74860519 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-4+5646G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860519 | |||||||
| chr5:74860726 | T | A | 3 | a0001c0002t0011g0232 a0001c0002t0011g0233 a0001c0002t0018g0231 |
3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-4+5439A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860726 | |||||||
| chr5:74860733 | C | T | 1 | a0001c0001t0003g0297 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-4+5432G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860733 | |||||||
| chr5:74860734 | T | C | 1 | a0001c0001t0003g0297 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-4+5431A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860734 | |||||||
| chr5:74860827 | T | TA | 17 | a0001c0001t0001g0101 a0001c0001t0001g0213 a0001c0001t0001g0214 others(14): Show |
17 | HG01109.hp2 HG01175.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.-4+5337dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860827 | |||||||
| chr5:74860827 | TA | T | 56 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(53): Show |
56 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.-4+5337delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860827 | |||||||
| chr5:74860895 | T | C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-4+5270A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860895 | |||||||
| chr5:74860980 | T | C | 94 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(91): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-4+5185A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860980 | |||||||
| chr5:74861037 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-4+5128A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861037 | |||||||
| chr5:74861056 | G | A | 3 | a0001c0002t0011g0232 a0001c0002t0011g0233 a0001c0002t0018g0231 |
3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-4+5109C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861056 | |||||||
| chr5:74861069 | T | G | 149 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(146): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-4+5096A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861069 | |||||||
| chr5:74861087 | A | G | 1 | a0001c0001t0003g0255 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-4+5078T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861087 | |||||||
| chr5:74861190 | T | C | 1 | a0001c0002t0007g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-4+4975A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861190 | |||||||
| chr5:74861416 | T | A | 2 | a0001c0002t0011g0232 a0001c0002t0011g0233 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-4+4749A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861416 | |||||||
| chr5:74861489 | C | G | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+4676G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861489 | |||||||
| chr5:74861532 | T | C | 1 | a0001c0001t0004g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-4+4633A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861532 | |||||||
| chr5:74861622 | G | A | 2 | a0001c0001t0005g0060 a0001c0001t0005g0061 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-4+4543C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861622 | |||||||
| chr5:74862003 | CTG | C | 7 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0054 others(4): Show |
7 | HG00733.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+4160_-4+4161del others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862003 | |||||||
| chr5:74862127 | C | T | 1 | a0001c0001t0004g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-4+4038G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862127 | |||||||
| chr5:74862411 | G | A | 60 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(57): Show |
61 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4+3754C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862411 | |||||||
| chr5:74862411 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-4+3754C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862411 | |||||||
| chr5:74862415 | T | A | 5 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+3750A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862415 | |||||||
| chr5:74862515 | C | G | 60 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(57): Show |
61 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4+3650G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862515 | |||||||
| chr5:74862541 | G | A | 4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG02809.hp1 HG03041.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+3624C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862541 | |||||||
| chr5:74862764 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-4+3401C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862764 | |||||||
| chr5:74862790 | A | T | 4 | a0001c0001t0002g0104 a0001c0001t0002g0105 a0001c0001t0002g0106 others(1): Show |
4 | HG00280.hp1 HG00738.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+3375T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862790 | |||||||
| chr5:74863023 | T | TAA | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4+3140_-4+3141dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863023 | |||||||
| chr5:74863023 | TA | T | 37 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4+3141delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863023 | |||||||
| chr5:74863043 | A | G | 118 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(115): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-4+3122T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863043 | |||||||
| chr5:74863046 | G | A | 11 | a0001c0002t0007g0062 a0001c0002t0007g0063 a0001c0002t0007g0064 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+3119C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863046 | |||||||
| chr5:74863143 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-4+3022T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863143 | |||||||
| chr5:74863312 | C | T | 119 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(116): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-4+2853G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863312 | |||||||
| chr5:74863332 | T | C | 34 | a0001c0001t0004g0003 a0001c0001t0004g0021 a0001c0001t0004g0023 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4+2833A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863332 | |||||||
| chr5:74863504 | C | T | 1 | a0001c0001t0003g0253 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-4+2661G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863504 | |||||||
| chr5:74863871 | T | G | 7 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+2294A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863871 | |||||||
| chr5:74863960 | T | C | 2 | a0001c0003t0005g0240 a0001c0003t0015g0241 |
2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-4+2205A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863960 | |||||||
| chr5:74864126 | T | C | 71 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0253 others(68): Show |
72 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-4+2039A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864126 | |||||||
| chr5:74864225 | A | G | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-4+1940T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864225 | |||||||
| chr5:74864294 | G | A | 7 | a0001c0002t0009g0242 a0001c0002t0009g0243 a0001c0002t0009g0244 others(4): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+1871C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864294 | |||||||
| chr5:74864497 | G | C | 3 | a0001c0003t0005g0249 a0001c0003t0005g0250 a0001c0003t0005g0251 |
3 | HG02451.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-4+1668C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864497 | |||||||
| chr5:74864532 | T | C | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-4+1633A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864532 | |||||||
| chr5:74864630 | A | G | 100 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(97): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.-4+1535T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864630 | |||||||
| chr5:74864829 | G | A | 54 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0252 others(51): Show |
55 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-4+1336C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864829 | |||||||
| chr5:74864972 | GATC | G | 12 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0007 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+1190_-4+1192del others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864972 | |||||||
| chr5:74865251 | C | T | 1 | a0001c0001t0004g0003 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-4+914G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74865251 | |||||||
| chr5:74865806 | T | TGGGGAGA others(6): Show |
1 | a0001c0001t0001g0302 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-4+346_-4+358dupTC others(11): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74865806 | |||||||
| chr5:74865951 | G | A | 2 | a0001c0001t0003g0304 a0001c0001t0026g0303 |
2 | NA18945.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-4+214C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74865951 | |||||||
| chr5:74865992 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4+173G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74865992 | |||||||
| chr5:74866069 | G | C | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-4+96C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74866069 |