Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55159 |
| ensemblid | ENSG00000168411.14 |
| hgncid | 25539 |
| symbol | RFWD3 |
| name | ring finger and WD repeat domain 3 |
| refseq_nuc | NM_018124.4 |
| refseq_prot | NP_060594.3 |
| ensembl_nuc | ENST00000361070.9 |
| ensembl_prot | ENSP00000354361.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 74621399 |
| end | 74666877 |
| strand | - |
| ver | v1.2 |
| region | chr16:74621399-74666877 |
| region5000 | chr16:74616399-74671877 |
| regionname0 | RFWD3_chr16_74621399_74666877 |
| regionname5000 | RFWD3_chr16_74616399_74671877 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 774 | 154 | 27 | 30 | 70 | 3 | 24 | 56 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0002 | 0/0 | 774 | 149 | 40 | 21 | 71 | 10 | 7 | 58 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0003 | 1/1 | 774 | 92 | 17 | 21 | 43 | 3 | 6 | 34 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0004 | 0/0 | 774 | 5 | 0 | 3 | 0 | 0 | 2 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0005 | 0/0 | 774 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0006 | 0/0 | 774 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0007 | 0/0 | 774 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0008 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0009 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0010 | 0/0 | 774 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0011 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0012 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0013 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| a0014 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | MAHEA others(769): Show |
chr16 | 74616399 | 74671877 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2322 | 105 | 20 | 11 | 59 | 0 | 15 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0001c0004 | 0/0 | 2322 | 38 | 6 | 15 | 10 | 2 | 5 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0001c0005 | 0/0 | 2322 | 8 | 0 | 3 | 0 | 1 | 4 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0001c0008 | 0/0 | 2322 | 2 | 1 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0001c0011 | 0/0 | 2322 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0002c0001 | 0/0 | 2322 | 149 | 40 | 21 | 71 | 10 | 7 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0003c0003 | 1/1 | 2322 | 92 | 17 | 21 | 43 | 3 | 6 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0004c0006 | 0/0 | 2322 | 5 | 0 | 3 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0005c0007 | 0/0 | 2322 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0006c0009 | 0/0 | 2322 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0007c0018 | 0/0 | 2322 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0008c0016 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0009c0013 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0010c0017 | 0/0 | 2322 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0011c0015 | 0/0 | 2322 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0012c0010 | 0/0 | 2322 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0013c0012 | 0/0 | 2322 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 | ||
| a0014c0014 | 0/0 | 2322 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | ATGGC others(2317): Show |
chr16 | 74616399 | 74671877 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 4972 | 4 | 0 | 0 | 4 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0002 | 0/0 | 4996 | 59 | 0 | 7 | 41 | 0 | 11 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0006 | 0/0 | 4973 | 11 | 6 | 0 | 4 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4968): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0008 | 0/0 | 5020 | 4 | 0 | 1 | 3 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(5015): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0011 | 0/0 | 4948 | 4 | 4 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0013 | 0/0 | 4996 | 3 | 2 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0014 | 0/0 | 4972 | 3 | 3 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0015 | 0/0 | 5044 | 2 | 0 | 1 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(5039): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0016 | 0/0 | 4996 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0026 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(5015): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0029 | 0/0 | 4996 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0030 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0031 | 0/0 | 4995 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4990): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0032 | 0/0 | 4995 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4990): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0033 | 0/0 | 4996 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0034 | 0/0 | 4996 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0035 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0042 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0044 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0047 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0053 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0001c0002t0054 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0001c0004t0004 | 0/0 | 4947 | 24 | 3 | 15 | 0 | 2 | 4 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4942): Show |
chr16 | 74616399 | 74671877 |
| a0001c0004t0009 | 0/0 | 4995 | 5 | 0 | 0 | 5 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4990): Show |
chr16 | 74616399 | 74671877 |
| a0001c0004t0017 | 0/0 | 4995 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4990): Show |
chr16 | 74616399 | 74671877 |
| a0001c0004t0021 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4942): Show |
chr16 | 74616399 | 74671877 |
| a0001c0004t0023 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4942): Show |
chr16 | 74616399 | 74671877 |
| a0001c0004t0025 | 0/0 | 5043 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(5038): Show |
chr16 | 74616399 | 74671877 |
| a0001c0004t0028 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(5014): Show |
chr16 | 74616399 | 74671877 |
| a0001c0004t0049 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4942): Show |
chr16 | 74616399 | 74671877 |
| a0001c0004t0050 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4942): Show |
chr16 | 74616399 | 74671877 |
| a0001c0004t0051 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(5011): Show |
chr16 | 74616399 | 74671877 |
| a0001c0005t0007 | 0/0 | 4948 | 8 | 0 | 3 | 0 | 1 | 4 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0001c0008t0027 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(5015): Show |
chr16 | 74616399 | 74671877 |
| a0001c0008t0046 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0001c0011t0002 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0001 | 0/0 | 4972 | 104 | 25 | 13 | 52 | 8 | 6 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0002 | 0/0 | 4996 | 26 | 3 | 5 | 16 | 1 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0008 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(5015): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0010 | 0/0 | 4972 | 5 | 5 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0012 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0018 | 0/0 | 4972 | 2 | 1 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0024 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0037 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0038 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0039 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0040 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4968): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0041 | 0/0 | 4971 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4966): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0043 | 0/0 | 4972 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0048 | 0/0 | 4948 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0002c0001t0052 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0003c0003t0003 | 1/0 | 4948 | 70 | 10 | 16 | 38 | 2 | 3 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0003c0003t0005 | 0/1 | 4948 | 19 | 7 | 2 | 5 | 1 | 3 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0003c0003t0012 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0003c0003t0020 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0003c0003t0022 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0004c0006t0001 | 0/0 | 4972 | 4 | 0 | 3 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0004c0006t0019 | 0/0 | 4972 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0005c0007t0002 | 0/0 | 4996 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0006c0009t0008 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(5015): Show |
chr16 | 74616399 | 74671877 |
| a0007c0018t0005 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0008c0016t0036 | 0/0 | 4996 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0009c0013t0045 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| a0010c0017t0012 | 0/0 | 4948 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4943): Show |
chr16 | 74616399 | 74671877 |
| a0011c0015t0002 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0012c0010t0002 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4991): Show |
chr16 | 74616399 | 74671877 |
| a0013c0012t0009 | 0/0 | 4995 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4990): Show |
chr16 | 74616399 | 74671877 |
| a0014c0014t0001 | 0/0 | 4972 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | GGCAG others(4967): Show |
chr16 | 74616399 | 74671877 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0004 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0008g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0008g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0008g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0013g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0014g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0014g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0014g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0015g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0015g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0016g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0016g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0026g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0029g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0030g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0031g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0032g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0033g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0034g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0035g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0042g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0044g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0047g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0053g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0054g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0009g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0009g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0009g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0009g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0009g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0017g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0021g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0023g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0025g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0028g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0049g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0050g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0051g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0008t0027g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0008t0046g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0011t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0012 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0010g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0010g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0010g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0012g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0018g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0018g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0024g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0037g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0038g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0039g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0040g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0041g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0043g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0048g0374 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0052g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0002 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0012g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0020g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0022g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0004c0006t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0004c0006t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0004c0006t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0004c0006t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0004c0006t0019g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0005c0007t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0005c0007t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0006c0009t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0006c0009t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0007c0018t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0008c0016t0036g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0009c0013t0045g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0010c0017t0012g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0011c0015t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0012c0010t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0013c0012t0009g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0014c0014t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0004 | g0010 | EUR | GBR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00099 | hp2 | a0001 | c0004 | t0004 | g0127 | EUR | GBR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00140 | hp1 | a0001 | c0005 | t0007 | g0047 | EUR | GBR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00140 | hp2 | a0002 | c0001 | t0001 | g0331 | EUR | GBR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00280 | hp1 | a0003 | c0003 | t0005 | g0043 | EUR | FIN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00280 | hp2 | a0003 | c0003 | t0003 | g0077 | EUR | FIN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0271 | EUR | FIN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00323 | hp2 | a0002 | c0001 | t0002 | g0162 | EUR | FIN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00408 | hp1 | a0003 | c0003 | t0003 | g0097 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00408 | hp2 | a0001 | c0002 | t0053 | g0381 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0303 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0323 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00544 | hp1 | a0003 | c0003 | t0003 | g0099 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00544 | hp2 | a0002 | c0001 | t0002 | g0012 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0308 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00558 | hp2 | a0001 | c0004 | t0017 | g0016 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0305 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00597 | hp2 | a0003 | c0003 | t0003 | g0048 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0312 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00609 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0296 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00621 | hp2 | a0003 | c0003 | t0003 | g0074 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00639 | hp1 | a0002 | c0001 | t0002 | g0157 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00639 | hp2 | a0001 | c0004 | t0004 | g0129 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00642 | hp2 | a0003 | c0003 | t0003 | g0028 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00673 | hp1 | a0001 | c0002 | t0006 | g0359 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00673 | hp2 | a0001 | c0002 | t0015 | g0138 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0328 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00733 | hp2 | a0001 | c0004 | t0004 | g0001 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00735 | hp1 | a0003 | c0003 | t0003 | g0050 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00735 | hp2 | a0002 | c0001 | t0002 | g0158 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00738 | hp1 | a0001 | c0002 | t0013 | g0164 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00738 | hp2 | a0003 | c0003 | t0005 | g0045 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00741 | hp1 | a0003 | c0003 | t0020 | g0066 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00741 | hp2 | a0001 | c0004 | t0004 | g0125 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01069 | hp1 | a0002 | c0001 | t0002 | g0014 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01069 | hp2 | a0002 | c0001 | t0001 | g0332 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01070 | hp1 | a0002 | c0001 | t0001 | g0304 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01070 | hp2 | a0001 | c0004 | t0004 | g0123 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01071 | hp1 | a0002 | c0001 | t0002 | g0014 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0307 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0285 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01074 | hp2 | a0002 | c0001 | t0002 | g0159 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0275 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01081 | hp2 | a0003 | c0003 | t0022 | g0039 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0177 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0260 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01106 | hp2 | a0003 | c0003 | t0003 | g0108 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01109 | hp1 | a0002 | c0001 | t0018 | g0378 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01109 | hp2 | a0002 | c0001 | t0012 | g0059 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0290 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0189 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0289 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01169 | hp2 | a0003 | c0003 | t0012 | g0058 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01192 | hp1 | a0003 | c0003 | t0003 | g0055 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01192 | hp2 | a0001 | c0005 | t0007 | g0112 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0322 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01243 | hp2 | a0003 | c0003 | t0003 | g0094 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01255 | hp1 | a0001 | c0004 | t0004 | g0117 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01255 | hp2 | a0003 | c0003 | t0003 | g0079 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01256 | hp1 | a0003 | c0003 | t0003 | g0062 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01256 | hp2 | a0001 | c0002 | t0008 | g0147 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01257 | hp1 | a0003 | c0003 | t0003 | g0002 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01257 | hp2 | a0001 | c0005 | t0007 | g0111 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01261 | hp1 | a0001 | c0002 | t0015 | g0139 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0176 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01358 | hp1 | a0001 | c0004 | t0004 | g0134 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0264 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01361 | hp1 | a0003 | c0003 | t0003 | g0027 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01361 | hp2 | a0003 | c0003 | t0005 | g0042 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01433 | hp1 | a0001 | c0005 | t0007 | g0092 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01433 | hp2 | a0004 | c0006 | t0001 | g0272 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0273 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01496 | hp2 | a0001 | c0004 | t0004 | g0135 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0259 | EUR | IBS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01515 | hp2 | a0002 | c0001 | t0048 | g0374 | EUR | IBS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0263 | EUR | IBS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01516 | hp2 | a0002 | c0001 | t0001 | g0242 | EUR | IBS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01884 | hp1 | a0002 | c0001 | t0001 | g0018 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01884 | hp2 | a0001 | c0002 | t0011 | g0025 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01928 | hp1 | a0003 | c0003 | t0003 | g0054 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01928 | hp2 | a0001 | c0004 | t0004 | g0122 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01943 | hp1 | a0003 | c0003 | t0003 | g0053 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0203 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01952 | hp1 | a0001 | c0004 | t0004 | g0001 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01952 | hp2 | a0001 | c0002 | t0031 | g0204 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01975 | hp1 | a0001 | c0004 | t0004 | g0001 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01975 | hp2 | a0003 | c0003 | t0003 | g0081 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0178 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01978 | hp2 | a0001 | c0004 | t0004 | g0121 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0252 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01981 | hp2 | a0004 | c0006 | t0001 | g0258 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01993 | hp1 | a0001 | c0008 | t0027 | g0140 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01993 | hp2 | a0003 | c0003 | t0003 | g0008 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02004 | hp1 | a0003 | c0003 | t0003 | g0113 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02004 | hp2 | a0001 | c0004 | t0004 | g0001 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02027 | hp1 | a0001 | c0004 | t0025 | g0137 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02027 | hp2 | a0002 | c0001 | t0008 | g0143 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02040 | hp1 | a0003 | c0003 | t0003 | g0070 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0244 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0317 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02080 | hp2 | a0001 | c0004 | t0009 | g0174 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02083 | hp1 | a0003 | c0003 | t0003 | g0105 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02083 | hp2 | a0002 | c0001 | t0002 | g0155 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02132 | hp1 | a0003 | c0003 | t0003 | g0071 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02135 | hp1 | a0003 | c0003 | t0003 | g0061 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02135 | hp2 | a0001 | c0002 | t0032 | g0199 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02145 | hp1 | a0002 | c0001 | t0010 | g0321 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02145 | hp2 | a0002 | c0001 | t0001 | g0347 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02155 | hp1 | a0001 | c0002 | t0026 | g0146 | EAS | CDX | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02155 | hp2 | a0001 | c0002 | t0008 | g0145 | EAS | CDX | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02165 | hp2 | a0001 | c0002 | t0030 | g0190 | EAS | CDX | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02257 | hp1 | a0001 | c0002 | t0033 | g0171 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02257 | hp2 | a0003 | c0003 | t0005 | g0033 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02258 | hp1 | a0003 | c0003 | t0003 | g0078 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02258 | hp2 | a0001 | c0002 | t0044 | g0373 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02273 | hp1 | a0003 | c0003 | t0003 | g0115 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02273 | hp2 | a0001 | c0004 | t0004 | g0001 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02280 | hp1 | a0003 | c0003 | t0003 | g0002 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0018 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02293 | hp1 | a0004 | c0006 | t0001 | g0257 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02293 | hp2 | a0003 | c0003 | t0003 | g0080 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02300 | hp1 | a0007 | c0018 | t0005 | g0040 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02300 | hp2 | a0001 | c0004 | t0004 | g0126 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02451 | hp1 | a0003 | c0003 | t0005 | g0037 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02451 | hp2 | a0001 | c0002 | t0006 | g0364 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02523 | hp1 | a0002 | c0001 | t0008 | g0141 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02572 | hp1 | a0001 | c0002 | t0006 | g0361 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0287 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02602 | hp1 | a0003 | c0003 | t0005 | g0041 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02602 | hp2 | a0003 | c0003 | t0003 | g0052 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02615 | hp1 | a0002 | c0001 | t0018 | g0379 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0362 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02622 | hp1 | a0001 | c0004 | t0049 | g0376 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02622 | hp2 | a0002 | c0001 | t0001 | g0277 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02630 | hp1 | a0002 | c0001 | t0001 | g0345 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02630 | hp2 | a0001 | c0002 | t0006 | g0355 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02647 | hp1 | a0003 | c0003 | t0005 | g0032 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0313 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02683 | hp1 | a0003 | c0003 | t0005 | g0044 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02683 | hp2 | a0001 | c0004 | t0004 | g0010 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02698 | hp2 | a0004 | c0006 | t0001 | g0274 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02723 | hp1 | a0001 | c0002 | t0042 | g0339 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02723 | hp2 | a0002 | c0001 | t0001 | g0265 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02735 | hp1 | a0003 | c0003 | t0003 | g0002 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02738 | hp1 | a0003 | c0003 | t0003 | g0084 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02738 | hp2 | a0001 | c0002 | t0016 | g0215 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02809 | hp1 | a0008 | c0016 | t0036 | g0154 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02809 | hp2 | a0002 | c0001 | t0038 | g0284 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02818 | hp1 | a0003 | c0003 | t0003 | g0090 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0022 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02886 | hp1 | a0001 | c0002 | t0014 | g0254 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02886 | hp2 | a0003 | c0003 | t0003 | g0107 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02895 | hp1 | a0003 | c0003 | t0005 | g0034 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02895 | hp2 | a0002 | c0001 | t0002 | g0163 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02896 | hp1 | a0001 | c0004 | t0004 | g0131 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02896 | hp2 | a0003 | c0003 | t0005 | g0035 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02897 | hp1 | a0002 | c0001 | t0002 | g0160 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02897 | hp2 | a0001 | c0004 | t0004 | g0132 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02922 | hp1 | a0002 | c0001 | t0010 | g0340 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02922 | hp2 | a0001 | c0004 | t0023 | g0130 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02970 | hp1 | a0002 | c0001 | t0001 | g0288 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02970 | hp2 | a0001 | c0002 | t0014 | g0354 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02976 | hp1 | a0003 | c0003 | t0005 | g0036 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0266 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03017 | hp1 | a0001 | c0005 | t0007 | g0009 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03017 | hp2 | a0001 | c0002 | t0016 | g0214 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03041 | hp1 | a0002 | c0001 | t0002 | g0012 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0356 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0075 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03098 | hp2 | a0002 | c0001 | t0010 | g0250 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03139 | hp1 | a0002 | c0001 | t0001 | g0281 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03139 | hp2 | a0002 | c0001 | t0001 | g0269 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03195 | hp1 | a0002 | c0001 | t0039 | g0249 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03195 | hp2 | a0002 | c0001 | t0010 | g0267 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03225 | hp1 | a0009 | c0013 | t0045 | g0319 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03225 | hp2 | a0001 | c0002 | t0011 | g0029 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03453 | hp1 | a0001 | c0002 | t0047 | g0349 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03453 | hp2 | a0003 | c0003 | t0003 | g0098 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03486 | hp1 | a0002 | c0001 | t0001 | g0282 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03486 | hp2 | a0001 | c0002 | t0013 | g0152 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0015 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03490 | hp2 | a0001 | c0005 | t0007 | g0110 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0217 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03492 | hp2 | a0001 | c0005 | t0007 | g0009 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0352 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03516 | hp2 | a0001 | c0002 | t0013 | g0153 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03540 | hp1 | a0002 | c0001 | t0024 | g0136 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03540 | hp2 | a0001 | c0004 | t0050 | g0375 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0344 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0350 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03654 | hp1 | a0002 | c0001 | t0002 | g0161 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03654 | hp2 | a0001 | c0004 | t0021 | g0124 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0333 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0169 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03704 | hp1 | a0001 | c0004 | t0004 | g0119 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03704 | hp2 | a0005 | c0007 | t0002 | g0168 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03710 | hp1 | a0005 | c0007 | t0002 | g0167 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03710 | hp2 | a0002 | c0001 | t0001 | g0314 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0295 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0222 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0324 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0208 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03942 | hp2 | a0004 | c0006 | t0019 | g0021 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04115 | hp1 | a0003 | c0003 | t0005 | g0046 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0180 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04184 | hp1 | a0002 | c0001 | t0001 | g0268 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04199 | hp1 | a0001 | c0004 | t0004 | g0120 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0210 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04204 | hp1 | a0010 | c0017 | t0012 | g0060 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04204 | hp2 | a0001 | c0004 | t0004 | g0118 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0280 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04228 | hp2 | a0001 | c0002 | t0006 | g0360 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18522 | hp1 | a0002 | c0001 | t0001 | g0336 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18522 | hp2 | a0001 | c0002 | t0006 | g0365 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | CHB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0315 | EAS | CHB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18906 | hp1 | a0002 | c0001 | t0037 | g0283 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18906 | hp2 | a0002 | c0001 | t0001 | g0270 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18939 | hp1 | a0003 | c0003 | t0003 | g0102 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0318 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18941 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18942 | hp1 | a0003 | c0003 | t0003 | g0064 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0342 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18944 | hp1 | a0003 | c0003 | t0005 | g0083 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18945 | hp1 | a0001 | c0004 | t0009 | g0185 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0368 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18946 | hp2 | a0006 | c0009 | t0008 | g0148 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0367 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18948 | hp1 | a0003 | c0003 | t0003 | g0100 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18948 | hp2 | a0001 | c0002 | t0035 | g0228 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18949 | hp2 | a0003 | c0003 | t0003 | g0093 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18950 | hp1 | a0001 | c0004 | t0028 | g0144 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0343 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0298 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18954 | hp1 | a0001 | c0002 | t0006 | g0363 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0302 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18959 | hp2 | a0002 | c0001 | t0001 | g0299 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18960 | hp1 | a0011 | c0015 | t0002 | g0235 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0316 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18962 | hp1 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0256 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18963 | hp2 | a0002 | c0001 | t0001 | g0243 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0253 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18964 | hp2 | a0002 | c0001 | t0002 | g0221 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0293 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18966 | hp1 | a0003 | c0003 | t0003 | g0076 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0366 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0371 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0326 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18968 | hp1 | a0002 | c0001 | t0041 | g0309 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18969 | hp2 | a0003 | c0003 | t0003 | g0067 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0338 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18971 | hp2 | a0012 | c0010 | t0002 | g0191 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18972 | hp1 | a0002 | c0001 | t0001 | g0240 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18972 | hp2 | a0003 | c0003 | t0003 | g0104 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18973 | hp2 | a0002 | c0001 | t0001 | g0330 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18975 | hp1 | a0003 | c0003 | t0003 | g0073 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0325 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18977 | hp1 | a0003 | c0003 | t0003 | g0088 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18977 | hp2 | a0003 | c0003 | t0005 | g0007 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18978 | hp1 | a0001 | c0004 | t0009 | g0184 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18978 | hp2 | a0002 | c0001 | t0001 | g0248 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18981 | hp2 | a0003 | c0003 | t0003 | g0114 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18982 | hp2 | a0001 | c0004 | t0051 | g0377 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18984 | hp1 | a0001 | c0004 | t0009 | g0183 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18984 | hp2 | a0002 | c0001 | t0001 | g0297 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18985 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18985 | hp2 | a0001 | c0002 | t0008 | g0142 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18989 | hp1 | a0002 | c0001 | t0001 | g0291 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18990 | hp1 | a0002 | c0001 | t0001 | g0306 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0341 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18993 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18993 | hp2 | a0003 | c0003 | t0003 | g0056 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18995 | hp1 | a0003 | c0003 | t0003 | g0103 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0255 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18998 | hp2 | a0002 | c0001 | t0001 | g0311 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0241 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18999 | hp2 | a0003 | c0003 | t0003 | g0087 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19000 | hp2 | a0003 | c0003 | t0003 | g0106 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19001 | hp1 | a0003 | c0003 | t0003 | g0057 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19001 | hp2 | a0002 | c0001 | t0001 | g0294 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19002 | hp1 | a0001 | c0002 | t0006 | g0358 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0372 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19003 | hp1 | a0013 | c0012 | t0009 | g0219 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19003 | hp2 | a0003 | c0003 | t0003 | g0089 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19004 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19007 | hp1 | a0003 | c0003 | t0003 | g0101 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19007 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19009 | hp1 | a0003 | c0003 | t0005 | g0007 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19009 | hp2 | a0002 | c0001 | t0002 | g0151 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19010 | hp1 | a0003 | c0003 | t0003 | g0085 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0334 | AFR | LWK | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0251 | AFR | LWK | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19055 | hp1 | a0003 | c0003 | t0003 | g0095 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19055 | hp2 | a0014 | c0014 | t0001 | g0327 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19056 | hp1 | a0003 | c0003 | t0003 | g0049 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19056 | hp2 | a0002 | c0001 | t0002 | g0172 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19057 | hp2 | a0003 | c0003 | t0003 | g0109 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19060 | hp1 | a0001 | c0004 | t0009 | g0182 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0246 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19062 | hp1 | a0001 | c0002 | t0054 | g0382 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19063 | hp1 | a0002 | c0001 | t0002 | g0011 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19064 | hp1 | a0003 | c0003 | t0003 | g0024 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19064 | hp2 | a0002 | c0001 | t0002 | g0156 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19065 | hp1 | a0006 | c0009 | t0008 | g0149 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19065 | hp2 | a0003 | c0003 | t0003 | g0072 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0292 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19066 | hp2 | a0003 | c0003 | t0005 | g0006 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19067 | hp1 | a0002 | c0001 | t0002 | g0165 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19067 | hp2 | a0003 | c0003 | t0003 | g0065 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0301 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19074 | hp1 | a0002 | c0001 | t0002 | g0179 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19078 | hp1 | a0003 | c0003 | t0003 | g0068 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19078 | hp2 | a0001 | c0002 | t0008 | g0150 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19079 | hp1 | a0002 | c0001 | t0002 | g0011 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19080 | hp1 | a0002 | c0001 | t0002 | g0013 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0247 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19081 | hp1 | a0002 | c0001 | t0002 | g0013 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19082 | hp1 | a0002 | c0001 | t0001 | g0310 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0337 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19085 | hp1 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19085 | hp2 | a0001 | c0004 | t0017 | g0016 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19086 | hp1 | a0002 | c0001 | t0001 | g0300 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19087 | hp2 | a0001 | c0002 | t0006 | g0357 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19089 | hp1 | a0003 | c0003 | t0003 | g0051 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19090 | hp1 | a0003 | c0003 | t0005 | g0006 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19090 | hp2 | a0001 | c0011 | t0002 | g0213 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19091 | hp1 | a0003 | c0003 | t0003 | g0082 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0370 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19240 | hp1 | a0001 | c0002 | t0011 | g0026 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19240 | hp2 | a0003 | c0003 | t0003 | g0002 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20129 | hp1 | a0003 | c0003 | t0003 | g0023 | AFR | ASW | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20129 | hp2 | a0002 | c0001 | t0001 | g0261 | AFR | ASW | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0279 | EUR | TSI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0335 | EUR | TSI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20805 | hp1 | a0003 | c0003 | t0003 | g0096 | EUR | TSI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0329 | EUR | TSI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20905 | hp1 | a0001 | c0002 | t0034 | g0197 | SAS | GIH | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20905 | hp2 | a0001 | c0005 | t0007 | g0091 | SAS | GIH | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01123 | hp1 | a0001 | c0004 | t0004 | g0128 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01123 | hp2 | a0002 | c0001 | t0043 | g0276 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02109 | hp1 | a0001 | c0002 | t0011 | g0133 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0351 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02486 | hp1 | a0001 | c0002 | t0029 | g0166 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0346 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02559 | hp1 | a0002 | c0001 | t0010 | g0262 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02559 | hp2 | a0002 | c0001 | t0040 | g0286 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03471 | hp1 | a0001 | c0004 | t0004 | g0116 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03471 | hp2 | a0001 | c0002 | t0014 | g0353 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG06807 | hp1 | a0003 | c0003 | t0005 | g0038 | AFR | USA | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0320 | AFR | USA | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20300 | hp1 | a0003 | c0003 | t0003 | g0030 | AFR | USA | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20300 | hp2 | a0002 | c0001 | t0052 | g0380 | AFR | USA | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA21309 | hp1 | a0001 | c0008 | t0046 | g0348 | AFR | LWK | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA21309 | hp2 | a0002 | c0001 | t0001 | g0278 | AFR | LWK | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0005 | g0031 | REF | REF | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0003 | g0063 | REF | REF | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74623954 | T | C | 1 | a0010 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.2299A>G | p.Met767Val | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2393/4948 | 2299/2325 | 767/774 | chr16 | 74623954 | |||
| chr16:74626549 | T | A | 1 | a0013 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.1975A>T | p.Asn659Tyr | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/13 | 2069/4948 | 1975/2325 | 659/774 | chr16 | 74626549 | |||
| chr16:74630845 | T | C | 4 | a0002 a0004 a0008 others(1): Show |
156 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
missense_variant | MODERATE | c.1690A>G | p.Ile564Val | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/13 | 1784/4948 | 1690/2325 | 564/774 | chr16 | 74630845 | |||
| chr16:74632641 | T | G | 1 | a0006 | 2 | NA18946.hp2 NA19065.hp1 |
missense_variant | MODERATE | c.1459A>C | p.Met487Leu | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/13 | 1553/4948 | 1459/2325 | 487/774 | chr16 | 74632641 | |||
| chr16:74636468 | T | G | 1 | a0007 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.1304A>C | p.Lys435Thr | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/13 | 1398/4948 | 1304/2325 | 435/774 | chr16 | 74636468 | |||
| chr16:74637950 | A | G | 1 | a0005 | 2 | HG03704.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.1100T>C | p.Met367Thr | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/13 | 1194/4948 | 1100/2325 | 367/774 | chr16 | 74637950 | |||
| chr16:74637968 | G | A | 1 | a0004 | 5 | HG01433.hp2 HG01981.hp2 HG02293.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.1082C>T | p.Ser361Phe | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/13 | 1176/4948 | 1082/2325 | 361/774 | chr16 | 74637968 | |||
| chr16:74644407 | C | T | 1 | a0012 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.1034G>A | p.Arg345Gln | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/13 | 1128/4948 | 1034/2325 | 345/774 | chr16 | 74644407 | |||
| chr16:74649149 | T | C | 1 | a0009 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.775A>G | p.Lys259Glu | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/13 | 869/4948 | 775/2325 | 259/774 | chr16 | 74649149 | |||
| chr16:74660975 | G | A | 1 | a0014 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.475C>T | p.Arg159Trp | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/13 | 569/4948 | 475/2325 | 159/774 | chr16 | 74660975 | |||
| chr16:74660987 | C | A | 1 | a0011 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.463G>T | p.Val155Leu | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/13 | 557/4948 | 463/2325 | 155/774 | chr16 | 74660987 | |||
| chr16:74661181 | G | T | 10 | a0001 a0002 a0004 others(7): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
missense_variant | MODERATE | c.269C>A | p.Thr90Asn | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/13 | 363/4948 | 269/2325 | 90/774 | chr16 | 74661181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74630800 | A | G | 1 | a0001c0005 | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
synonymous_variant | LOW | c.1735T>C | p.Leu579Leu | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/13 | 1829/4948 | 1735/2325 | 579/774 | chr16 | 74630800 | |||
| chr16:74630912 | A | T | 11 | a0001c0002 a0001c0011 a0002c0001 others(8): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
synonymous_variant | LOW | c.1623T>A | p.Pro541Pro | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/13 | 1717/4948 | 1623/2325 | 541/774 | chr16 | 74630912 | |||
| chr16:74636560 | C | T | 10 | a0001c0002 a0001c0008 a0002c0001 others(7): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
synonymous_variant | LOW | c.1212G>A | p.Thr404Thr | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/13 | 1306/4948 | 1212/2325 | 404/774 | chr16 | 74636560 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74621532 | G | A | 1 | a0001c0004t0050 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2396C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2396 | chr16 | 74621532 | ||||||
| chr16:74621636 | G | A | 3 | a0002c0001t0010 a0002c0001t0037 a0002c0001t0038 |
7 | HG02145.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2292C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2292 | chr16 | 74621636 | ||||||
| chr16:74621663 | G | A | 1 | a0002c0001t0038 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2265C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2265 | chr16 | 74621663 | ||||||
| chr16:74621694 | T | TG | 41 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0006 others(38): Show |
263 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*2233dupC | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2233 | chr16 | 74621694 | ||||||
| chr16:74621699 | G | GT | 2 | a0001c0002t0006 a0002c0001t0040 |
12 | HG00673.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2228dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2228 | chr16 | 74621699 | ||||||
| chr16:74621703 | G | GT | 12 | a0001c0002t0031 a0001c0004t0004 a0001c0004t0009 others(9): Show |
40 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2224dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2224 | chr16 | 74621703 | ||||||
| chr16:74621703 | G | T | 43 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0006 others(40): Show |
263 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*2225C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2225 | chr16 | 74621703 | ||||||
| chr16:74621707 | T | G | 7 | a0002c0001t0012 a0003c0003t0005 a0003c0003t0012 others(4): Show |
24 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2221A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2221 | chr16 | 74621707 | ||||||
| chr16:74621736 | G | C | 57 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0006 others(54): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*2192C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2192 | chr16 | 74621736 | ||||||
| chr16:74621754 | C | T | 12 | a0001c0002t0031 a0001c0004t0004 a0001c0004t0009 others(9): Show |
40 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2174G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2174 | chr16 | 74621754 | ||||||
| chr16:74621755 | G | A | 1 | a0001c0002t0033 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2173C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2173 | chr16 | 74621755 | ||||||
| chr16:74621844 | G | A | 3 | a0001c0002t0006 a0001c0002t0013 a0002c0001t0039 |
15 | HG00673.hp1 HG00738.hp1 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2084C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2084 | chr16 | 74621844 | ||||||
| chr16:74621883 | G | C | 1 | a0001c0002t0034 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2045C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2045 | chr16 | 74621883 | ||||||
| chr16:74621926 | T | C | 1 | a0003c0003t0020 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2002A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2002 | chr16 | 74621926 | ||||||
| chr16:74621950 | G | A | 57 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0006 others(54): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*1978C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1978 | chr16 | 74621950 | ||||||
| chr16:74622024 | C | A | 2 | a0001c0004t0017 a0001c0004t0051 |
3 | HG00558.hp2 NA18982.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1904G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1904 | chr16 | 74622024 | ||||||
| chr16:74622034 | A | G | 1 | a0001c0002t0030 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1894T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1894 | chr16 | 74622034 | ||||||
| chr16:74622101 | T | A | 3 | a0002c0001t0012 a0003c0003t0012 a0010c0017t0012 |
3 | HG01109.hp2 HG01169.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1827A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1827 | chr16 | 74622101 | ||||||
| chr16:74622462 | CA | C | 55 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0006 others(52): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*1465delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1465 | chr16 | 74622462 | ||||||
| chr16:74622509 | G | A | 2 | a0001c0005t0007 a0001c0008t0046 |
9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1419C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1419 | chr16 | 74622509 | ||||||
| chr16:74622624 | A | G | 8 | a0001c0002t0006 a0001c0002t0013 a0001c0002t0014 others(5): Show |
22 | HG00673.hp1 HG00738.hp1 HG02451.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1304T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1304 | chr16 | 74622624 | ||||||
| chr16:74622626 | A | G | 1 | a0001c0002t0029 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1302T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1302 | chr16 | 74622626 | ||||||
| chr16:74622883 | T | C | 1 | a0001c0002t0035 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1045A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1045 | chr16 | 74622883 | ||||||
| chr16:74622897 | G | C | 1 | a0001c0004t0023 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1031C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1031 | chr16 | 74622897 | ||||||
| chr16:74622951 | G | T | 1 | a0001c0002t0044 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*977C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 977 | chr16 | 74622951 | ||||||
| chr16:74622979 | T | C | 1 | a0001c0002t0042 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*949A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 949 | chr16 | 74622979 | ||||||
| chr16:74623014 | T | A | 1 | a0002c0001t0043 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 914 | chr16 | 74623014 | ||||||
| chr16:74623051 | G | T | 2 | a0001c0005t0007 a0001c0008t0046 |
9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*877C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 877 | chr16 | 74623051 | ||||||
| chr16:74623140 | T | C | 1 | a0009c0013t0045 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*788A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 788 | chr16 | 74623140 | ||||||
| chr16:74623147 | G | T | 1 | a0001c0002t0016 | 2 | HG02738.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*781C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 781 | chr16 | 74623147 | ||||||
| chr16:74623174 | G | A | 1 | a0003c0003t0022 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*754C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 754 | chr16 | 74623174 | ||||||
| chr16:74623350 | C | A | 2 | a0001c0002t0044 a0009c0013t0045 |
2 | HG02258.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*578G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 578 | chr16 | 74623350 | ||||||
| chr16:74623394 | C | T | 1 | a0001c0002t0026 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*534G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 534 | chr16 | 74623394 | ||||||
| chr16:74623523 | T | C | 58 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0006 others(55): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 405 | chr16 | 74623523 | ||||||
| chr16:74623587 | A | T | 46 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0006 others(43): Show |
268 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*341T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 341 | chr16 | 74623587 | ||||||
| chr16:74623603 | G | C | 1 | a0001c0002t0047 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 325 | chr16 | 74623603 | ||||||
| chr16:74623874 | C | T | 1 | a0003c0003t0020 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 54 | chr16 | 74623874 | ||||||
| chr16:74623885 | A | G | 3 | a0002c0001t0012 a0003c0003t0012 a0010c0017t0012 |
3 | HG01109.hp2 HG01169.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*43T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 43 | chr16 | 74623885 | ||||||
| chr16:74666819 | C | CCCGCCGA others(17): Show |
19 | a0001c0002t0001 a0001c0002t0006 a0001c0002t0014 others(16): Show |
144 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
5_prime_UTR_variant | MODIFIER | c.-60_-37dupAGGTAACT others(16): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5371 | chr16 | 74666819 | ||||||
| chr16:74666819 | C | CCCGCCGA others(41): Show |
20 | a0001c0002t0002 a0001c0002t0013 a0001c0002t0016 others(17): Show |
112 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(109): Show |
5_prime_UTR_variant | MODIFIER | c.-37_-36insAGGTAACT others(40): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5371 | chr16 | 74666819 | ||||||
| chr16:74666819 | C | CCCGCCGA others(62): Show |
1 | a0001c0004t0051 | 1 | NA18982.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37_-36insTAACTACC others(61): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5371 | chr16 | 74666819 | ||||||
| chr16:74666819 | C | CCCGCCGA others(65): Show |
6 | a0001c0002t0008 a0001c0002t0026 a0001c0004t0028 others(3): Show |
11 | HG01256.hp2 HG01993.hp1 HG02027.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-37_-36insAGGTAACT others(64): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5371 | chr16 | 74666819 | ||||||
| chr16:74666819 | C | CCCGCCGA others(89): Show |
2 | a0001c0002t0015 a0001c0004t0025 |
3 | HG00673.hp2 HG01261.hp1 HG02027.hp1 |
5_prime_UTR_variant | MODIFIER | c.-37_-36insAGGTAACT others(88): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5371 | chr16 | 74666819 | ||||||
| chr16:74666825 | G | GAAGACTC others(17): Show |
1 | a0002c0001t0024 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43_-42insAGGCGGAG others(16): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5377 | chr16 | 74666825 | ||||||
| chr16:74666843 | T | TCCGCCGA others(17): Show |
2 | a0002c0001t0018 a0002c0001t0052 |
3 | HG01109.hp1 HG02615.hp1 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-61_-60insCGGTAACT others(16): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5395 | chr16 | 74666843 | ||||||
| chr16:74666844 | C | CCGCCGAA others(41): Show |
1 | a0001c0002t0053 | 1 | HG00408.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62_-61insTAGGTAAC others(40): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5396 | chr16 | 74666844 | ||||||
| chr16:74666845 | G | C | 55 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0006 others(52): Show |
279 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(276): Show |
5_prime_UTR_variant | MODIFIER | c.-62C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5396 | chr16 | 74666845 | ||||||
| chr16:74666857 | A | G | 1 | a0004c0006t0019 | 1 | HG03942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5408 | chr16 | 74666857 | ||||||
| chr16:74666865 | T | C | 1 | a0001c0002t0054 | 1 | NA19062.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5416 | chr16 | 74666865 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74624199 | C | G | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2182-128G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624199 | |||||||
| chr16:74624285 | C | T | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-214G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624285 | |||||||
| chr16:74624286 | T | G | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-215A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624286 | |||||||
| chr16:74624287 | G | T | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-216C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624287 | |||||||
| chr16:74624420 | A | T | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-349T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624420 | |||||||
| chr16:74624532 | A | T | 111 | a0001c0002t0002g0201 a0001c0002t0002g0202 a0001c0002t0002g0211 others(108): Show |
122 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2182-461T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624532 | |||||||
| chr16:74624686 | C | G | 1 | a0003c0003t0003g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2182-615G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624686 | |||||||
| chr16:74624689 | G | A | 3 | a0001c0002t0002g0176 a0001c0002t0002g0177 a0001c0002t0002g0178 |
3 | HG01099.hp1 HG01261.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2182-618C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624689 | |||||||
| chr16:74624692 | T | C | 4 | a0002c0001t0001g0264 a0002c0001t0001g0273 a0002c0001t0001g0289 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2182-621A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624692 | |||||||
| chr16:74624719 | G | T | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-648C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624719 | |||||||
| chr16:74624821 | A | T | 292 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(289): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2182-750T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624821 | |||||||
| chr16:74624825 | A | C | 292 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(289): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2182-754T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624825 | |||||||
| chr16:74624902 | T | C | 1 | a0002c0001t0001g0280 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2182-831A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624902 | |||||||
| chr16:74624969 | G | A | 251 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(248): Show |
268 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.2182-898C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624969 | |||||||
| chr16:74624994 | A | C | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-923T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624994 | |||||||
| chr16:74625157 | A | G | 1 | a0001c0002t0033g0171 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2182-1086T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625157 | |||||||
| chr16:74625199 | C | CA | 166 | a0001c0002t0002g0189 a0001c0002t0002g0210 a0001c0002t0006g0355 others(163): Show |
178 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.2182-1129dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625199 | |||||||
| chr16:74625199 | C | CAA | 81 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(78): Show |
86 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.2182-1130_2182-112 others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625199 | |||||||
| chr16:74625215 | T | C | 8 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(5): Show |
9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2181+1128A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625215 | |||||||
| chr16:74625239 | T | TA | 3 | a0001c0004t0004g0131 a0001c0004t0004g0132 a0001c0004t0023g0130 |
3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2181+1103dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625239 | |||||||
| chr16:74625241 | G | C | 20 | a0001c0002t0006g0355 a0001c0002t0006g0356 a0001c0002t0006g0357 others(17): Show |
20 | HG00673.hp1 HG00738.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.2181+1102C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625241 | |||||||
| chr16:74625251 | T | C | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2181+1092A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625251 | |||||||
| chr16:74625331 | G | A | 1 | a0001c0008t0046g0348 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2181+1012C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625331 | |||||||
| chr16:74625470 | C | A | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2181+873G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625470 | |||||||
| chr16:74625514 | G | GA | 252 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(249): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.2181+828dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625514 | |||||||
| chr16:74625545 | T | C | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2181+798A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625545 | |||||||
| chr16:74625632 | C | T | 1 | a0002c0001t0040g0286 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2181+711G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625632 | |||||||
| chr16:74625796 | A | G | 2 | a0003c0003t0003g0022 a0003c0003t0003g0023 |
2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2181+547T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625796 | |||||||
| chr16:74625894 | A | T | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2181+449T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625894 | |||||||
| chr16:74625934 | C | T | 6 | a0001c0004t0004g0116 a0001c0004t0004g0131 a0001c0004t0004g0132 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2181+409G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625934 | |||||||
| chr16:74626042 | C | T | 4 | a0002c0001t0001g0253 a0002c0001t0001g0325 a0002c0001t0001g0326 others(1): Show |
4 | NA18964.hp1 NA18967.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2181+301G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74626042 | |||||||
| chr16:74626199 | C | T | 1 | a0002c0001t0001g0288 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2181+144G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74626199 | |||||||
| chr16:74626263 | A | G | 4 | a0002c0001t0001g0264 a0002c0001t0001g0273 a0002c0001t0001g0289 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2181+80T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74626263 | |||||||
| chr16:74626276 | G | A | 140 | a0002c0001t0001g0005 a0002c0001t0001g0018 a0002c0001t0001g0019 others(137): Show |
152 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.2181+67C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74626276 | |||||||
| chr16:74626287 | C | T | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2181+56G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74626287 | |||||||
| chr16:74626707 | A | G | 1 | a0002c0001t0040g0286 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1970-153T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626707 | |||||||
| chr16:74626818 | T | A | 27 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0117 others(24): Show |
33 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1970-264A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626818 | |||||||
| chr16:74626831 | C | T | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1970-277G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626831 | |||||||
| chr16:74626832 | T | G | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1970-278A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626832 | |||||||
| chr16:74626833 | G | C | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1970-279C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626833 | |||||||
| chr16:74626912 | T | C | 1 | a0002c0001t0001g0295 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1970-358A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626912 | |||||||
| chr16:74626913 | T | C | 1 | a0002c0001t0001g0295 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1970-359A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626913 | |||||||
| chr16:74627095 | C | A | 281 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(278): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1970-541G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627095 | |||||||
| chr16:74627224 | T | A | 1 | a0001c0002t0002g0195 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1970-670A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627224 | |||||||
| chr16:74627261 | T | C | 145 | a0001c0002t0002g0188 a0002c0001t0001g0005 a0002c0001t0001g0018 others(142): Show |
157 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1970-707A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627261 | |||||||
| chr16:74627357 | C | T | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1970-803G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627357 | |||||||
| chr16:74627359 | T | C | 1 | a0013c0012t0009g0219 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1970-805A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627359 | |||||||
| chr16:74627521 | G | A | 1 | a0003c0003t0003g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1969+931C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627521 | |||||||
| chr16:74627575 | C | A | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1969+877G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627575 | |||||||
| chr16:74627702 | G | A | 1 | a0001c0004t0021g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1969+750C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627702 | |||||||
| chr16:74627746 | G | A | 1 | a0003c0003t0003g0076 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1969+706C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627746 | |||||||
| chr16:74627840 | C | A | 8 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(5): Show |
9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1969+612G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627840 | |||||||
| chr16:74627927 | C | T | 1 | a0002c0001t0001g0324 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1969+525G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627927 | |||||||
| chr16:74628014 | G | C | 1 | a0002c0001t0001g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1969+438C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628014 | |||||||
| chr16:74628123 | T | C | 1 | a0001c0002t0002g0233 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1969+329A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628123 | |||||||
| chr16:74628149 | A | G | 4 | a0001c0002t0011g0025 a0001c0002t0011g0026 a0001c0002t0011g0029 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1969+303T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628149 | |||||||
| chr16:74628208 | G | A | 1 | a0002c0001t0001g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1969+244C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628208 | |||||||
| chr16:74628222 | C | A | 1 | a0001c0004t0004g0125 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1969+230G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628222 | |||||||
| chr16:74628340 | G | A | 1 | a0002c0001t0039g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1969+112C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628340 | |||||||
| chr16:74628354 | G | A | 1 | a0003c0003t0003g0030 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1969+98C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628354 | |||||||
| chr16:74628699 | C | T | 141 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(138): Show |
152 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1755-33G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74628699 | |||||||
| chr16:74628816 | C | A | 2 | a0003c0003t0003g0027 a0003c0003t0003g0028 |
2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1755-150G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74628816 | |||||||
| chr16:74628955 | A | G | 1 | a0002c0001t0001g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1755-289T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74628955 | |||||||
| chr16:74628991 | TAAGAA | T | 23 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(20): Show |
28 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1755-330_1755-326d others(7): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74628991 | |||||||
| chr16:74629058 | C | T | 2 | a0002c0001t0001g0261 a0002c0001t0001g0263 |
2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1755-392G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629058 | |||||||
| chr16:74629397 | G | A | 1 | a0003c0003t0003g0077 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1755-731C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629397 | |||||||
| chr16:74629401 | G | A | 3 | a0001c0002t0006g0357 a0001c0002t0006g0358 a0001c0002t0006g0363 |
3 | NA18954.hp1 NA19002.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1755-735C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629401 | |||||||
| chr16:74629422 | G | C | 1 | a0002c0001t0001g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1755-756C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629422 | |||||||
| chr16:74629478 | G | T | 3 | a0001c0002t0002g0201 a0001c0002t0002g0202 a0001c0002t0002g0212 |
3 | NA18959.hp1 NA18969.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1755-812C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629478 | |||||||
| chr16:74629665 | C | CA | 6 | a0001c0002t0002g0216 a0001c0002t0042g0339 a0002c0001t0001g0244 others(3): Show |
6 | HG02040.hp1 HG02040.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1755-1000dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629665 | |||||||
| chr16:74629665 | CA | C | 23 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(20): Show |
28 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1755-1000delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629665 | |||||||
| chr16:74629768 | G | C | 1 | a0002c0001t0012g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1754+1013C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629768 | |||||||
| chr16:74629965 | C | G | 23 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(20): Show |
28 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1754+816G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629965 | |||||||
| chr16:74629978 | T | C | 8 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(5): Show |
9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1754+803A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629978 | |||||||
| chr16:74630147 | G | C | 1 | a0002c0001t0001g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1754+634C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630147 | |||||||
| chr16:74630271 | T | C | 1 | a0001c0005t0007g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1754+510A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630271 | |||||||
| chr16:74630345 | G | T | 28 | a0001c0002t0006g0355 a0001c0002t0006g0356 a0001c0002t0006g0357 others(25): Show |
29 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1754+436C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630345 | |||||||
| chr16:74630362 | T | G | 1 | a0001c0004t0004g0123 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1754+419A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630362 | |||||||
| chr16:74630463 | G | C | 1 | a0008c0016t0036g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1754+318C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630463 | |||||||
| chr16:74630567 | T | TACTTGTA others(23): Show |
1 | a0001c0002t0002g0195 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1754+184_1754+213d others(32): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630567 | |||||||
| chr16:74630716 | G | A | 1 | a0003c0003t0003g0076 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1754+65C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630716 | |||||||
| chr16:74631064 | C | G | 1 | a0001c0002t0042g0339 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1578-107G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631064 | |||||||
| chr16:74631071 | T | A | 285 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(282): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.1578-114A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631071 | |||||||
| chr16:74631133 | A | G | 5 | a0002c0001t0001g0018 a0002c0001t0001g0270 a0002c0001t0001g0278 others(2): Show |
6 | HG01884.hp1 HG02280.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1578-176T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631133 | |||||||
| chr16:74631158 | G | T | 1 | a0001c0002t0002g0195 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1578-201C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631158 | |||||||
| chr16:74631424 | G | A | 1 | a0007c0018t0005g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1578-467C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631424 | |||||||
| chr16:74631463 | A | ACTCTCT | 23 | a0001c0002t0006g0357 a0001c0002t0006g0358 a0001c0002t0006g0359 others(20): Show |
23 | HG00673.hp1 HG00738.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1578-512_1578-507d others(8): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631463 | |||||||
| chr16:74631463 | A | ACTCTCTC others(1): Show |
222 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(219): Show |
237 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1578-514_1578-507d others(10): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631463 | |||||||
| chr16:74631463 | A | ACTCTCTC others(3): Show |
110 | a0001c0004t0004g0001 a0001c0004t0004g0116 a0001c0004t0004g0117 others(107): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1578-516_1578-507d others(12): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631463 | |||||||
| chr16:74631463 | A | ACTCTCTC others(5): Show |
14 | a0001c0004t0004g0010 a0001c0004t0004g0119 a0001c0004t0004g0123 others(11): Show |
15 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1578-518_1578-507d others(14): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631463 | |||||||
| chr16:74631463 | A | ACTCTCTC others(7): Show |
8 | a0001c0005t0007g0009 a0001c0005t0007g0091 a0001c0005t0007g0092 others(5): Show |
9 | HG01192.hp2 HG01257.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1578-520_1578-507d others(16): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631463 | |||||||
| chr16:74631734 | T | C | 8 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(5): Show |
9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1578-777A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631734 | |||||||
| chr16:74631905 | C | T | 1 | a0001c0004t0004g0127 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1577+618G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631905 | |||||||
| chr16:74632004 | G | A | 2 | a0001c0002t0002g0224 a0001c0002t0002g0225 |
2 | NA18957.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1577+519C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632004 | |||||||
| chr16:74632044 | A | G | 3 | a0002c0001t0001g0255 a0002c0001t0001g0256 a0002c0001t0001g0298 |
3 | NA18953.hp1 NA18963.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1577+479T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632044 | |||||||
| chr16:74632099 | A | G | 1 | a0003c0003t0005g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1577+424T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632099 | |||||||
| chr16:74632299 | G | C | 1 | a0001c0002t0029g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1577+224C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632299 | |||||||
| chr16:74632426 | C | A | 1 | a0001c0002t0006g0356 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1577+97G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632426 | |||||||
| chr16:74632456 | C | T | 1 | a0002c0001t0001g0242 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1577+67G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632456 | |||||||
| chr16:74632474 | A | C | 3 | a0002c0001t0001g0245 a0002c0001t0001g0246 a0002c0001t0001g0248 |
3 | NA18978.hp2 NA18982.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1577+49T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632474 | |||||||
| chr16:74632736 | G | C | 287 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(284): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1427-63C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74632736 | |||||||
| chr16:74632821 | C | G | 1 | a0003c0003t0003g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1427-148G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74632821 | |||||||
| chr16:74633097 | T | C | 1 | a0001c0004t0004g0126 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1427-424A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633097 | |||||||
| chr16:74633191 | C | T | 1 | a0001c0002t0031g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1427-518G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633191 | |||||||
| chr16:74633210 | G | C | 9 | a0003c0003t0003g0030 a0003c0003t0003g0051 a0003c0003t0003g0056 others(6): Show |
9 | NA18972.hp2 NA18981.hp2 NA18993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1427-537C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633210 | |||||||
| chr16:74633212 | G | A | 3 | a0001c0002t0008g0150 a0006c0009t0008g0148 a0006c0009t0008g0149 |
3 | NA18946.hp2 NA19065.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1427-539C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633212 | |||||||
| chr16:74633217 | T | C | 1 | a0001c0002t0002g0209 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1427-544A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633217 | |||||||
| chr16:74633271 | C | G | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1427-598G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633271 | |||||||
| chr16:74633279 | G | GA | 247 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(244): Show |
264 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.1427-607dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633279 | |||||||
| chr16:74633334 | A | G | 1 | a0002c0001t0048g0374 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1427-661T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633334 | |||||||
| chr16:74633439 | G | A | 1 | a0001c0005t0007g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1427-766C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633439 | |||||||
| chr16:74633487 | G | A | 3 | a0002c0001t0001g0019 a0002c0001t0001g0297 a0002c0001t0001g0316 |
4 | NA18960.hp2 NA18971.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1427-814C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633487 | |||||||
| chr16:74633536 | G | A | 1 | a0001c0002t0031g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1427-863C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633536 | |||||||
| chr16:74633565 | G | A | 1 | a0001c0002t0015g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1427-892C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633565 | |||||||
| chr16:74633881 | C | T | 82 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(79): Show |
87 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.1427-1208G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633881 | |||||||
| chr16:74633928 | C | T | 9 | a0001c0002t0002g0170 a0001c0002t0002g0175 a0001c0002t0002g0205 others(6): Show |
9 | HG00642.hp1 HG02135.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1427-1255G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633928 | |||||||
| chr16:74633929 | G | A | 13 | a0003c0003t0003g0024 a0003c0003t0003g0048 a0003c0003t0003g0049 others(10): Show |
13 | HG00597.hp2 HG00621.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1427-1256C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633929 | |||||||
| chr16:74633966 | C | T | 285 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(282): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.1427-1293G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633966 | |||||||
| chr16:74633984 | C | CA | 11 | a0001c0002t0002g0170 a0001c0002t0002g0205 a0001c0002t0002g0206 others(8): Show |
11 | HG00642.hp1 HG02155.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1427-1312dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633984 | |||||||
| chr16:74634033 | G | T | 3 | a0002c0001t0001g0366 a0002c0001t0001g0367 a0002c0001t0001g0368 |
3 | NA18946.hp1 NA18947.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1427-1360C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634033 | |||||||
| chr16:74634051 | A | G | 1 | a0001c0002t0011g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1427-1378T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634051 | |||||||
| chr16:74634080 | G | A | 1 | a0001c0002t0002g0207 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1427-1407C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634080 | |||||||
| chr16:74634221 | A | C | 1 | a0002c0001t0001g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1427-1548T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634221 | |||||||
| chr16:74634376 | C | A | 5 | a0001c0004t0004g0131 a0001c0004t0004g0132 a0001c0004t0023g0130 others(2): Show |
5 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1427-1703G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634376 | |||||||
| chr16:74634378 | T | TTATA | 4 | a0003c0003t0003g0075 a0003c0003t0003g0090 a0003c0003t0003g0098 others(1): Show |
4 | HG02818.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1427-1709_1427-170 others(8): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634378 | |||||||
| chr16:74634378 | TTA | T | 218 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(215): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1427-1707_1427-170 others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634378 | |||||||
| chr16:74634548 | C | T | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1426+1798G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634548 | |||||||
| chr16:74634575 | G | A | 252 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(249): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1426+1771C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634575 | |||||||
| chr16:74634635 | C | T | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1426+1711G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634635 | |||||||
| chr16:74634644 | C | T | 246 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(243): Show |
263 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.1426+1702G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634644 | |||||||
| chr16:74634667 | T | G | 314 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(311): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1426+1679A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634667 | |||||||
| chr16:74634815 | A | AG | 3 | a0001c0004t0004g0118 a0001c0004t0004g0135 a0001c0004t0021g0124 |
3 | HG01496.hp2 HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1426+1530_1426+153 others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634815 | |||||||
| chr16:74634816 | A | G | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1426+1530T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634816 | |||||||
| chr16:74634823 | A | G | 317 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(314): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1426+1523T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634823 | |||||||
| chr16:74634962 | T | C | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1426+1384A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634962 | |||||||
| chr16:74635003 | G | A | 1 | a0002c0001t0001g0324 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1426+1343C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635003 | |||||||
| chr16:74635004 | G | C | 252 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(249): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1426+1342C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635004 | |||||||
| chr16:74635055 | C | T | 21 | a0003c0003t0003g0022 a0003c0003t0003g0023 a0003c0003t0005g0006 others(18): Show |
23 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1426+1291G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635055 | |||||||
| chr16:74635136 | T | C | 253 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(250): Show |
270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1426+1210A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635136 | |||||||
| chr16:74635169 | A | T | 3 | a0002c0001t0001g0019 a0002c0001t0001g0297 a0002c0001t0001g0316 |
4 | NA18960.hp2 NA18971.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1426+1177T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635169 | |||||||
| chr16:74635253 | G | A | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1426+1093C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635253 | |||||||
| chr16:74635331 | G | A | 1 | a0001c0002t0011g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1426+1015C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635331 | |||||||
| chr16:74635343 | C | T | 292 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(289): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1426+1003G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635343 | |||||||
| chr16:74635443 | C | T | 1 | a0003c0003t0003g0024 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1426+903G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635443 | |||||||
| chr16:74635466 | C | T | 1 | a0003c0003t0003g0080 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1426+880G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635466 | |||||||
| chr16:74635471 | GA | G | 250 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(247): Show |
267 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.1426+874delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635471 | |||||||
| chr16:74635481 | A | T | 1 | a0001c0004t0023g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1426+865T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635481 | |||||||
| chr16:74635562 | CGGACTGG others(3): Show |
C | 1 | a0002c0001t0002g0172 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1426+774_1426+783d others(12): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635562 | |||||||
| chr16:74635568 | G | A | 1 | a0003c0003t0003g0082 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1426+778C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635568 | |||||||
| chr16:74635929 | C | A | 3 | a0002c0001t0001g0366 a0002c0001t0001g0367 a0002c0001t0001g0368 |
3 | NA18946.hp1 NA18947.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1426+417G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635929 | |||||||
| chr16:74636034 | C | G | 1 | a0001c0002t0002g0193 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1426+312G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74636034 | |||||||
| chr16:74636094 | C | T | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1426+252G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74636094 | |||||||
| chr16:74636149 | T | C | 2 | a0002c0001t0001g0240 a0002c0001t0001g0241 |
2 | NA18972.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1426+197A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74636149 | |||||||
| chr16:74636285 | AAGGAAAT others(4): Show |
A | 1 | a0001c0002t0044g0373 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1426+50_1426+60del others(11): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74636285 | |||||||
| chr16:74636677 | T | C | 2 | a0001c0004t0004g0118 a0001c0004t0004g0120 |
2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1195-100A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74636677 | |||||||
| chr16:74636707 | C | T | 1 | a0001c0002t0047g0349 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1195-130G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74636707 | |||||||
| chr16:74636714 | G | C | 1 | a0001c0004t0004g0123 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1195-137C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74636714 | |||||||
| chr16:74636779 | T | C | 6 | a0002c0001t0001g0269 a0002c0001t0001g0344 a0002c0001t0001g0345 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195-202A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74636779 | |||||||
| chr16:74636923 | G | A | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1195-346C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74636923 | |||||||
| chr16:74637122 | T | TA | 50 | a0001c0002t0001g0371 a0001c0002t0002g0198 a0001c0002t0002g0210 others(47): Show |
56 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1195-546dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | |||||||
| chr16:74637122 | T | TAA | 147 | a0001c0002t0002g0201 a0001c0002t0002g0202 a0001c0002t0002g0211 others(144): Show |
158 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1195-547_1195-546d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | |||||||
| chr16:74637122 | T | TAAA | 19 | a0001c0002t0006g0360 a0001c0002t0006g0363 a0001c0002t0011g0029 others(16): Show |
20 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1195-548_1195-546d others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | |||||||
| chr16:74637122 | T | TAAAAAAA others(6): Show |
1 | a0001c0005t0007g0110 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1195-558_1195-546d others(15): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | |||||||
| chr16:74637122 | T | TAAAAAAA others(7): Show |
2 | a0001c0005t0007g0009 a0001c0005t0007g0091 |
3 | HG03017.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1195-559_1195-546d others(16): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | |||||||
| chr16:74637122 | T | TAAAAAAA others(8): Show |
4 | a0001c0005t0007g0047 a0001c0005t0007g0092 a0001c0005t0007g0111 others(1): Show |
4 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-560_1195-546d others(17): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | |||||||
| chr16:74637122 | TA | T | 15 | a0001c0002t0002g0203 a0001c0002t0002g0229 a0001c0002t0002g0231 others(12): Show |
15 | HG01081.hp2 HG01256.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1195-546delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | |||||||
| chr16:74637146 | C | A | 6 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0092 others(3): Show |
7 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195-569G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637146 | |||||||
| chr16:74637201 | G | T | 1 | a0001c0004t0004g0129 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1195-624C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637201 | |||||||
| chr16:74637423 | T | C | 1 | a0003c0003t0005g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1194+433A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637423 | |||||||
| chr16:74637443 | A | G | 1 | a0002c0001t0010g0262 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1194+413T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637443 | |||||||
| chr16:74637501 | C | T | 15 | a0001c0002t0006g0355 a0001c0002t0006g0356 a0001c0002t0006g0357 others(12): Show |
15 | HG00673.hp1 HG00738.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.1194+355G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637501 | |||||||
| chr16:74637750 | A | C | 1 | a0001c0004t0023g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1194+106T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637750 | |||||||
| chr16:74637976 | G | A | 1 | a0003c0003t0003g0100 | 1 | NA18948.hp1 | splice_region_variant&intron_variant | LOW | c.1080-6C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74637976 | |||||||
| chr16:74638013 | A | G | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1080-43T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638013 | |||||||
| chr16:74638022 | T | A | 3 | a0001c0002t0013g0152 a0001c0002t0013g0153 a0001c0002t0013g0164 |
3 | HG00738.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1080-52A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638022 | |||||||
| chr16:74638033 | G | A | 5 | a0001c0004t0004g0131 a0001c0004t0004g0132 a0001c0004t0023g0130 others(2): Show |
5 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1080-63C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638033 | |||||||
| chr16:74638125 | G | A | 3 | a0002c0001t0001g0252 a0002c0001t0001g0304 a0002c0001t0001g0307 |
3 | HG01070.hp1 HG01071.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1080-155C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638125 | |||||||
| chr16:74638170 | C | G | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1080-200G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638170 | |||||||
| chr16:74638218 | A | T | 3 | a0001c0002t0002g0205 a0001c0002t0002g0206 a0001c0002t0002g0207 |
3 | NA18943.hp2 NA18945.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1080-248T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638218 | |||||||
| chr16:74638243 | C | T | 4 | a0002c0001t0001g0330 a0002c0001t0001g0341 a0002c0001t0001g0342 others(1): Show |
4 | NA18943.hp1 NA18950.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080-273G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638243 | |||||||
| chr16:74638244 | G | C | 1 | a0001c0002t0002g0170 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1080-274C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638244 | |||||||
| chr16:74638303 | G | A | 293 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(290): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1080-333C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638303 | |||||||
| chr16:74638329 | G | A | 1 | a0001c0002t0047g0349 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1080-359C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638329 | |||||||
| chr16:74638343 | A | G | 4 | a0001c0002t0011g0025 a0001c0002t0011g0026 a0001c0002t0011g0029 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080-373T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638343 | |||||||
| chr16:74638346 | TA | T | 3 | a0001c0002t0013g0152 a0001c0002t0013g0153 a0001c0002t0013g0164 |
3 | HG00738.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1080-377delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638346 | |||||||
| chr16:74638450 | T | C | 1 | a0001c0002t0002g0193 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1080-480A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638450 | |||||||
| chr16:74638453 | C | T | 1 | a0002c0001t0001g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1080-483G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638453 | |||||||
| chr16:74638592 | T | C | 2 | a0005c0007t0002g0167 a0005c0007t0002g0168 |
2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1080-622A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638592 | |||||||
| chr16:74638593 | TGGAAAAG others(4): Show |
T | 1 | a0003c0003t0003g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1080-634_1080-624d others(13): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638593 | |||||||
| chr16:74638605 | A | T | 1 | a0003c0003t0003g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1080-635T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638605 | |||||||
| chr16:74638606 | G | T | 1 | a0003c0003t0003g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1080-636C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638606 | |||||||
| chr16:74638607 | C | T | 1 | a0003c0003t0003g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1080-637G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638607 | |||||||
| chr16:74638663 | T | A | 3 | a0001c0002t0013g0152 a0001c0002t0013g0153 a0001c0002t0013g0164 |
3 | HG00738.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1080-693A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638663 | |||||||
| chr16:74638997 | T | C | 1 | a0002c0001t0001g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1080-1027A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638997 | |||||||
| chr16:74639002 | C | A | 253 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(250): Show |
270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1080-1032G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639002 | |||||||
| chr16:74639003 | T | A | 253 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(250): Show |
270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1080-1033A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639003 | |||||||
| chr16:74639036 | C | CT | 8 | a0001c0004t0009g0184 a0003c0003t0003g0027 a0003c0003t0003g0052 others(5): Show |
8 | HG00741.hp1 HG01243.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1080-1067dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639036 | |||||||
| chr16:74639036 | CT | C | 7 | a0001c0002t0002g0187 a0001c0002t0002g0237 a0001c0002t0002g0238 others(4): Show |
7 | HG00408.hp2 NA18747.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080-1067delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639036 | |||||||
| chr16:74639036 | CTT | C | 95 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(92): Show |
100 | HG00642.hp1 HG00673.hp2 HG01099.hp1 others(97): Show |
intron_variant | MODIFIER | c.1080-1068_1080-106 others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639036 | |||||||
| chr16:74639036 | CTTT | C | 152 | a0001c0002t0002g0202 a0001c0002t0006g0356 a0001c0002t0006g0357 others(149): Show |
164 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1080-1069_1080-106 others(7): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639036 | |||||||
| chr16:74639041 | T | C | 2 | a0002c0001t0001g0306 a0002c0001t0001g0308 |
2 | HG00558.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1080-1071A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639041 | |||||||
| chr16:74639063 | G | A | 1 | a0002c0001t0001g0336 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1080-1093C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639063 | |||||||
| chr16:74639127 | C | G | 3 | a0001c0002t0013g0152 a0001c0002t0013g0153 a0001c0002t0013g0164 |
3 | HG00738.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1080-1157G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639127 | |||||||
| chr16:74639161 | C | T | 10 | a0001c0002t0001g0370 a0001c0002t0001g0371 a0001c0002t0001g0372 others(7): Show |
10 | NA18946.hp2 NA18952.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1080-1191G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639161 | |||||||
| chr16:74639282 | C | G | 4 | a0001c0002t0011g0025 a0001c0002t0011g0026 a0001c0002t0011g0029 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080-1312G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639282 | |||||||
| chr16:74639634 | A | C | 1 | a0002c0001t0001g0334 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1080-1664T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639634 | |||||||
| chr16:74639662 | G | A | 1 | a0001c0008t0046g0348 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1080-1692C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639662 | |||||||
| chr16:74639724 | T | C | 1 | a0001c0002t0002g0186 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1080-1754A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639724 | |||||||
| chr16:74639908 | T | C | 2 | a0002c0001t0018g0378 a0002c0001t0018g0379 |
2 | HG01109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1080-1938A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639908 | |||||||
| chr16:74639963 | T | C | 2 | a0001c0002t0002g0189 a0001c0002t0033g0171 |
2 | HG01168.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1080-1993A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639963 | |||||||
| chr16:74639982 | A | AT | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1080-2013dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639982 | |||||||
| chr16:74640002 | G | A | 1 | a0003c0003t0003g0067 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1080-2032C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640002 | |||||||
| chr16:74640109 | G | C | 32 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(29): Show |
38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1080-2139C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640109 | |||||||
| chr16:74640110 | G | A | 52 | a0002c0001t0001g0005 a0002c0001t0001g0019 a0002c0001t0001g0020 others(49): Show |
62 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1080-2140C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640110 | |||||||
| chr16:74640145 | AT | A | 278 | a0001c0002t0001g0369 a0001c0002t0001g0371 a0001c0002t0001g0372 others(275): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1080-2176delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640145 | |||||||
| chr16:74640145 | ATT | A | 7 | a0001c0002t0001g0370 a0001c0002t0002g0239 a0001c0002t0006g0365 others(4): Show |
7 | HG01168.hp1 HG01256.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1080-2177_1080-217 others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640145 | |||||||
| chr16:74640229 | G | A | 1 | a0005c0007t0002g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1080-2259C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640229 | |||||||
| chr16:74640336 | C | G | 284 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(281): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1080-2366G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640336 | |||||||
| chr16:74640344 | T | C | 1 | a0001c0002t0011g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1080-2374A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640344 | |||||||
| chr16:74640373 | C | T | 291 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(288): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1080-2403G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640373 | |||||||
| chr16:74640644 | A | T | 1 | a0002c0001t0001g0334 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1080-2674T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640644 | |||||||
| chr16:74640665 | C | T | 1 | a0002c0001t0052g0380 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1080-2695G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640665 | |||||||
| chr16:74640677 | T | A | 3 | a0003c0003t0003g0057 a0003c0003t0003g0072 a0003c0003t0003g0088 |
3 | NA18977.hp1 NA19001.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1080-2707A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640677 | |||||||
| chr16:74640774 | C | A | 1 | a0001c0002t0011g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1080-2804G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640774 | |||||||
| chr16:74640822 | T | C | 313 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(310): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1080-2852A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640822 | |||||||
| chr16:74640955 | A | G | 370 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(367): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.1080-2985T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640955 | |||||||
| chr16:74640985 | C | CT | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1080-3016dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640985 | |||||||
| chr16:74641028 | G | C | 1 | a0002c0001t0052g0380 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1080-3058C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641028 | |||||||
| chr16:74641212 | G | C | 3 | a0002c0001t0018g0378 a0002c0001t0018g0379 a0002c0001t0052g0380 |
3 | HG01109.hp1 HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1079+3150C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641212 | |||||||
| chr16:74641221 | G | A | 3 | a0001c0004t0004g0127 a0001c0004t0004g0128 a0001c0004t0004g0129 |
3 | HG00099.hp2 HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1079+3141C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641221 | |||||||
| chr16:74641259 | T | A | 1 | a0004c0006t0001g0274 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1079+3103A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641259 | |||||||
| chr16:74641288 | G | A | 1 | a0001c0002t0002g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1079+3074C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641288 | |||||||
| chr16:74641295 | T | G | 1 | a0002c0001t0001g0334 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1079+3067A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641295 | |||||||
| chr16:74641306 | G | A | 1 | a0002c0001t0052g0380 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1079+3056C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641306 | |||||||
| chr16:74641351 | T | A | 1 | a0001c0004t0009g0174 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1079+3011A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641351 | |||||||
| chr16:74641385 | A | C | 252 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(249): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1079+2977T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641385 | |||||||
| chr16:74641469 | GATTA | G | 252 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(249): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1079+2889_1079+289 others(8): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641469 | |||||||
| chr16:74641655 | T | C | 1 | a0002c0001t0008g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1079+2707A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641655 | |||||||
| chr16:74641706 | C | T | 32 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(29): Show |
38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079+2656G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641706 | |||||||
| chr16:74641769 | A | C | 1 | a0001c0002t0002g0232 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1079+2593T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641769 | |||||||
| chr16:74641810 | C | T | 26 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0118 others(23): Show |
32 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1079+2552G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641810 | |||||||
| chr16:74641928 | C | CA | 39 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(36): Show |
41 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.1079+2433dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641928 | |||||||
| chr16:74641928 | CA | C | 80 | a0001c0002t0002g0169 a0001c0002t0002g0180 a0001c0002t0002g0186 others(77): Show |
84 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1079+2433delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641928 | |||||||
| chr16:74641928 | CAA | C | 145 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0372 others(142): Show |
158 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1079+2432_1079+243 others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641928 | |||||||
| chr16:74641928 | CAAA | C | 30 | a0001c0002t0002g0195 a0001c0002t0002g0196 a0001c0002t0006g0355 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1079+2431_1079+243 others(7): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641928 | |||||||
| chr16:74641928 | CAAAA | C | 25 | a0001c0002t0014g0353 a0001c0002t0014g0354 a0001c0004t0004g0001 others(22): Show |
31 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.1079+2430_1079+243 others(8): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641928 | |||||||
| chr16:74642017 | A | T | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079+2345T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642017 | |||||||
| chr16:74642135 | A | T | 284 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(281): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1079+2227T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642135 | |||||||
| chr16:74642143 | C | G | 291 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(288): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1079+2219G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642143 | |||||||
| chr16:74642160 | T | C | 1 | a0003c0003t0003g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1079+2202A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642160 | |||||||
| chr16:74642209 | G | A | 1 | a0001c0002t0001g0369 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1079+2153C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642209 | |||||||
| chr16:74642272 | A | G | 1 | a0001c0005t0007g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1079+2090T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642272 | |||||||
| chr16:74642283 | C | T | 1 | a0009c0013t0045g0319 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1079+2079G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642283 | |||||||
| chr16:74642361 | C | T | 1 | a0003c0003t0003g0024 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1079+2001G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642361 | |||||||
| chr16:74642398 | T | G | 2 | a0003c0003t0005g0042 a0003c0003t0005g0043 |
2 | HG00280.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1079+1964A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642398 | |||||||
| chr16:74642502 | T | C | 1 | a0001c0002t0002g0233 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1079+1860A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642502 | |||||||
| chr16:74642525 | G | A | 1 | a0001c0002t0011g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1079+1837C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642525 | |||||||
| chr16:74642652 | C | T | 291 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(288): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1079+1710G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642652 | |||||||
| chr16:74642672 | T | C | 1 | a0001c0002t0002g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1079+1690A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642672 | |||||||
| chr16:74642705 | C | T | 1 | a0001c0004t0050g0375 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1079+1657G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642705 | |||||||
| chr16:74642740 | G | C | 4 | a0002c0001t0002g0003 a0002c0001t0002g0011 a0002c0001t0002g0013 others(1): Show |
9 | NA18941.hp2 NA18985.hp1 NA19004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1079+1622C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642740 | |||||||
| chr16:74642788 | C | T | 1 | a0001c0002t0002g0173 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1079+1574G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642788 | |||||||
| chr16:74642970 | A | T | 1 | a0001c0002t0013g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1079+1392T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642970 | |||||||
| chr16:74643066 | T | C | 148 | a0001c0002t0002g0201 a0001c0002t0002g0202 a0001c0002t0002g0211 others(145): Show |
160 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1079+1296A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643066 | |||||||
| chr16:74643112 | C | G | 3 | a0001c0002t0002g0176 a0001c0002t0002g0177 a0001c0002t0002g0178 |
3 | HG01099.hp1 HG01261.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1079+1250G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643112 | |||||||
| chr16:74643249 | G | A | 1 | a0001c0002t0001g0372 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1079+1113C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643249 | |||||||
| chr16:74643414 | T | C | 6 | a0001c0004t0004g0116 a0001c0004t0004g0131 a0001c0004t0004g0132 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079+948A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643414 | |||||||
| chr16:74643669 | G | GC | 218 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0372 others(215): Show |
233 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1079+692_1079+693i others(3): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643669 | |||||||
| chr16:74643669 | G | GCT | 43 | a0001c0002t0001g0371 a0001c0002t0002g0017 a0001c0002t0002g0176 others(40): Show |
45 | HG00597.hp1 HG01070.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.1079+692_1079+693i others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643669 | |||||||
| chr16:74643669 | G | GCTT | 3 | a0001c0002t0002g0224 a0002c0001t0001g0341 a0002c0001t0001g0343 |
3 | NA18950.hp2 NA18981.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1079+692_1079+693i others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643669 | |||||||
| chr16:74643669 | GT | G | 20 | a0001c0004t0004g0116 a0001c0004t0004g0131 a0001c0004t0023g0130 others(17): Show |
21 | HG00140.hp1 HG00280.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1079+692delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643669 | |||||||
| chr16:74643669 | GTTTTTTT others(6): Show |
G | 26 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0118 others(23): Show |
32 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1079+680_1079+692d others(15): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643669 | |||||||
| chr16:74643670 | T | C | 69 | a0001c0002t0002g0202 a0001c0002t0006g0364 a0001c0004t0004g0117 others(66): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1079+692A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643670 | |||||||
| chr16:74643671 | T | C | 20 | a0001c0004t0004g0116 a0001c0004t0004g0131 a0001c0004t0023g0130 others(17): Show |
21 | HG00140.hp1 HG00280.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1079+691A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643671 | |||||||
| chr16:74643672 | T | C | 1 | a0001c0004t0004g0132 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1079+690A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643672 | |||||||
| chr16:74643683 | T | C | 26 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0118 others(23): Show |
32 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1079+679A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643683 | |||||||
| chr16:74643699 | G | A | 251 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(248): Show |
268 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.1079+663C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643699 | |||||||
| chr16:74643822 | T | C | 2 | a0001c0002t0002g0181 a0001c0002t0002g0222 |
2 | HG03927.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1079+540A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643822 | |||||||
| chr16:74643837 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1079+525C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643837 | |||||||
| chr16:74643852 | AT | A | 6 | a0001c0002t0002g0210 a0001c0002t0035g0228 a0001c0002t0054g0382 others(3): Show |
6 | HG04199.hp2 NA18948.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079+509delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643852 | |||||||
| chr16:74643878 | C | T | 1 | a0002c0001t0001g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1079+484G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643878 | |||||||
| chr16:74643898 | T | C | 9 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(6): Show |
10 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079+464A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643898 | |||||||
| chr16:74643912 | T | C | 1 | a0002c0001t0001g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1079+450A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643912 | |||||||
| chr16:74643965 | C | T | 1 | a0001c0002t0011g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1079+397G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643965 | |||||||
| chr16:74643987 | T | C | 1 | a0003c0003t0003g0064 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1079+375A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643987 | |||||||
| chr16:74644165 | C | T | 26 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0118 others(23): Show |
32 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1079+197G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74644165 | |||||||
| chr16:74644260 | T | A | 20 | a0001c0002t0006g0355 a0001c0002t0006g0356 a0001c0002t0006g0357 others(17): Show |
20 | HG00673.hp1 HG00738.hp1 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.1079+102A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74644260 | |||||||
| chr16:74644823 | CA | C | 88 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(85): Show |
93 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.793-89delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74644823 | |||||||
| chr16:74645184 | G | A | 1 | a0002c0001t0052g0380 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.793-449C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645184 | |||||||
| chr16:74645248 | A | G | 1 | a0001c0004t0004g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.793-513T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645248 | |||||||
| chr16:74645346 | C | A | 114 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(111): Show |
119 | HG00408.hp2 HG00642.hp1 HG00673.hp1 others(116): Show |
intron_variant | MODIFIER | c.793-611G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645346 | |||||||
| chr16:74645364 | A | T | 3 | a0001c0004t0009g0182 a0001c0004t0009g0185 a0013c0012t0009g0219 |
3 | NA18945.hp1 NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.793-629T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645364 | |||||||
| chr16:74645418 | C | T | 19 | a0003c0003t0005g0006 a0003c0003t0005g0007 a0003c0003t0005g0032 others(16): Show |
21 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.793-683G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645418 | |||||||
| chr16:74645501 | T | G | 1 | a0003c0003t0003g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.793-766A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645501 | |||||||
| chr16:74645554 | T | C | 1 | a0001c0002t0016g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.793-819A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645554 | |||||||
| chr16:74645644 | C | T | 1 | a0004c0006t0019g0021 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.793-909G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645644 | |||||||
| chr16:74645726 | T | G | 15 | a0001c0002t0006g0355 a0001c0002t0006g0356 a0001c0002t0006g0357 others(12): Show |
15 | HG00673.hp1 HG00738.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.793-991A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645726 | |||||||
| chr16:74645745 | C | CT | 32 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0117 others(29): Show |
38 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.793-1011dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645745 | |||||||
| chr16:74645745 | C | CTT | 10 | a0001c0004t0004g0120 a0001c0004t0004g0121 a0001c0004t0004g0131 others(7): Show |
10 | HG01358.hp1 HG01978.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-1012_793-1011d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645745 | |||||||
| chr16:74645745 | CT | C | 228 | a0001c0002t0001g0369 a0001c0002t0001g0372 a0001c0002t0002g0004 others(225): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.793-1011delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645745 | |||||||
| chr16:74645745 | CTT | C | 9 | a0001c0002t0001g0370 a0001c0002t0002g0189 a0001c0002t0002g0234 others(6): Show |
9 | HG00323.hp2 HG01168.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.793-1012_793-1011d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645745 | |||||||
| chr16:74645746 | T | C | 1 | a0003c0003t0003g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.793-1011A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645746 | |||||||
| chr16:74645751 | T | C | 1 | a0009c0013t0045g0319 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.793-1016A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645751 | |||||||
| chr16:74645754 | T | C | 1 | a0002c0001t0001g0299 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.793-1019A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645754 | |||||||
| chr16:74645789 | G | A | 1 | a0001c0002t0006g0365 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.793-1054C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645789 | |||||||
| chr16:74645813 | C | G | 2 | a0003c0003t0003g0078 a0003c0003t0003g0079 |
2 | HG01255.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.793-1078G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645813 | |||||||
| chr16:74645815 | G | C | 319 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(316): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.793-1080C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645815 | |||||||
| chr16:74645837 | C | T | 1 | a0002c0001t0001g0266 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.793-1102G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645837 | |||||||
| chr16:74645913 | C | T | 1 | a0001c0002t0002g0177 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.793-1178G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645913 | |||||||
| chr16:74645939 | G | A | 2 | a0003c0003t0003g0051 a0003c0003t0003g0076 |
2 | NA18966.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.793-1204C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645939 | |||||||
| chr16:74645985 | C | T | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.793-1250G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645985 | |||||||
| chr16:74645987 | A | C | 1 | a0002c0001t0001g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.793-1252T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645987 | |||||||
| chr16:74646069 | T | C | 1 | a0001c0002t0002g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.793-1334A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646069 | |||||||
| chr16:74646081 | A | T | 1 | a0001c0002t0030g0190 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.793-1346T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646081 | |||||||
| chr16:74646162 | C | A | 1 | a0001c0004t0004g0117 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.793-1427G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646162 | |||||||
| chr16:74646176 | A | G | 65 | a0002c0001t0001g0005 a0002c0001t0001g0019 a0002c0001t0001g0020 others(62): Show |
75 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.793-1441T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646176 | |||||||
| chr16:74646180 | G | A | 1 | a0001c0002t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.793-1445C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646180 | |||||||
| chr16:74646207 | C | T | 286 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(283): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.793-1472G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646207 | |||||||
| chr16:74646354 | G | A | 1 | a0003c0003t0003g0077 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.793-1619C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646354 | |||||||
| chr16:74646388 | T | C | 1 | a0002c0001t0001g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.793-1653A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646388 | |||||||
| chr16:74646408 | G | C | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.793-1673C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646408 | |||||||
| chr16:74646454 | G | A | 3 | a0001c0002t0002g0017 a0001c0002t0002g0238 a0001c0002t0002g0239 |
4 | NA18949.hp1 NA18968.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-1719C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646454 | |||||||
| chr16:74646569 | T | C | 1 | a0003c0003t0005g0042 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.793-1834A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646569 | |||||||
| chr16:74646602 | A | C | 3 | a0001c0002t0002g0176 a0001c0002t0002g0177 a0001c0002t0002g0178 |
3 | HG01099.hp1 HG01261.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.793-1867T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646602 | |||||||
| chr16:74646614 | C | T | 1 | a0001c0002t0011g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.793-1879G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646614 | |||||||
| chr16:74646615 | G | A | 2 | a0001c0002t0015g0138 a0001c0008t0046g0348 |
2 | HG00673.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.793-1880C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646615 | |||||||
| chr16:74646659 | G | A | 1 | a0001c0002t0011g0133 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.793-1924C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646659 | |||||||
| chr16:74646774 | T | C | 1 | a0002c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.793-2039A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646774 | |||||||
| chr16:74646794 | C | G | 87 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(84): Show |
92 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.793-2059G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646794 | |||||||
| chr16:74646847 | C | T | 1 | a0001c0002t0008g0142 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.793-2112G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646847 | |||||||
| chr16:74646903 | TCAA | T | 31 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(28): Show |
37 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.793-2171_793-2169d others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646903 | |||||||
| chr16:74646903 | TCAACAA | T | 3 | a0003c0003t0003g0078 a0003c0003t0003g0079 a0003c0003t0003g0109 |
3 | HG01255.hp2 HG02258.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.793-2174_793-2169d others(8): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646903 | |||||||
| chr16:74646903 | TCAACAAC others(5): Show |
T | 254 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(251): Show |
271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.793-2180_793-2169d others(14): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646903 | |||||||
| chr16:74646903 | TCAACAAC others(8): Show |
T | 1 | a0002c0001t0001g0303 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.793-2183_793-2169d others(17): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646903 | |||||||
| chr16:74646994 | G | C | 3 | a0001c0002t0014g0254 a0001c0002t0014g0353 a0001c0002t0014g0354 |
3 | HG02886.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.792+2138C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646994 | |||||||
| chr16:74647085 | C | CA | 10 | a0001c0002t0002g0207 a0001c0002t0013g0164 a0001c0002t0014g0254 others(7): Show |
11 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.792+2046dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647085 | |||||||
| chr16:74647100 | A | C | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+2032T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647100 | |||||||
| chr16:74647232 | G | A | 1 | a0001c0002t0042g0339 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.792+1900C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647232 | |||||||
| chr16:74647554 | C | G | 2 | a0003c0003t0003g0067 a0003c0003t0003g0095 |
2 | NA18969.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.792+1578G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647554 | |||||||
| chr16:74647580 | G | A | 1 | a0001c0002t0002g0188 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.792+1552C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647580 | |||||||
| chr16:74647583 | C | T | 3 | a0001c0004t0004g0131 a0001c0004t0004g0132 a0001c0004t0023g0130 |
3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.792+1549G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647583 | |||||||
| chr16:74647584 | GGCC | G | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+1545_792+1547d others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647584 | |||||||
| chr16:74647609 | T | C | 4 | a0001c0002t0002g0203 a0001c0002t0002g0218 a0001c0002t0015g0139 others(1): Show |
4 | HG00642.hp1 HG01261.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+1523A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647609 | |||||||
| chr16:74647652 | C | T | 2 | a0003c0003t0003g0078 a0003c0003t0003g0079 |
2 | HG01255.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.792+1480G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647652 | |||||||
| chr16:74647683 | C | T | 1 | a0001c0002t0002g0220 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.792+1449G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647683 | |||||||
| chr16:74647734 | T | G | 254 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(251): Show |
271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.792+1398A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647734 | |||||||
| chr16:74647737 | G | A | 1 | a0002c0001t0001g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.792+1395C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647737 | |||||||
| chr16:74647756 | TA | T | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+1375delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647756 | |||||||
| chr16:74647779 | A | G | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.792+1353T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647779 | |||||||
| chr16:74647788 | C | T | 1 | a0002c0001t0002g0172 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.792+1344G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647788 | |||||||
| chr16:74647793 | T | C | 1 | a0002c0001t0001g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.792+1339A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647793 | |||||||
| chr16:74647822 | C | A | 1 | a0001c0002t0006g0360 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.792+1310G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647822 | |||||||
| chr16:74647945 | T | C | 1 | a0001c0008t0046g0348 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.792+1187A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647945 | |||||||
| chr16:74648046 | A | C | 6 | a0001c0004t0004g0116 a0001c0004t0004g0131 a0001c0004t0004g0132 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+1086T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648046 | |||||||
| chr16:74648071 | A | G | 6 | a0001c0004t0004g0116 a0001c0004t0004g0131 a0001c0004t0004g0132 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+1061T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648071 | |||||||
| chr16:74648528 | T | C | 3 | a0002c0001t0001g0264 a0002c0001t0001g0279 a0002c0001t0048g0374 |
3 | HG01358.hp2 HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.792+604A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648528 | |||||||
| chr16:74648539 | G | A | 1 | a0001c0002t0002g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.792+593C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648539 | |||||||
| chr16:74648546 | G | A | 1 | a0003c0003t0005g0043 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.792+586C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648546 | |||||||
| chr16:74648598 | C | T | 253 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(250): Show |
270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.792+534G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648598 | |||||||
| chr16:74648645 | G | C | 1 | a0001c0004t0004g0116 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.792+487C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648645 | |||||||
| chr16:74648711 | A | G | 293 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(290): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.792+421T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648711 | |||||||
| chr16:74648784 | G | A | 1 | a0001c0002t0001g0371 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.792+348C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648784 | |||||||
| chr16:74648792 | A | G | 1 | a0001c0002t0011g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.792+340T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648792 | |||||||
| chr16:74648837 | A | G | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.792+295T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648837 | |||||||
| chr16:74648851 | C | T | 3 | a0003c0003t0003g0052 a0003c0003t0003g0094 a0003c0003t0020g0066 |
3 | HG00741.hp1 HG01243.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.792+281G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648851 | |||||||
| chr16:74648854 | G | A | 12 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0117 others(9): Show |
17 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+278C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648854 | |||||||
| chr16:74648883 | C | T | 3 | a0001c0004t0004g0127 a0001c0004t0004g0128 a0001c0004t0004g0129 |
3 | HG00099.hp2 HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.792+249G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648883 | |||||||
| chr16:74649104 | G | A | 6 | a0001c0002t0002g0170 a0001c0002t0002g0205 a0001c0002t0002g0206 others(3): Show |
6 | HG02155.hp2 NA18943.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+28C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74649104 | |||||||
| chr16:74649112 | T | A | 1 | a0003c0003t0003g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.792+20A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74649112 | |||||||
| chr16:74649113 | A | T | 1 | a0006c0009t0008g0148 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.792+19T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74649113 | |||||||
| chr16:74649205 | G | A | 1 | a0001c0002t0002g0218 | 1 | HG00642.hp1 | splice_region_variant&intron_variant | LOW | c.722-3C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649205 | |||||||
| chr16:74649206 | C | A | 1 | a0001c0002t0002g0218 | 1 | HG00642.hp1 | splice_region_variant&intron_variant | LOW | c.722-4G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649206 | |||||||
| chr16:74649255 | T | C | 1 | a0003c0003t0005g0044 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.722-53A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649255 | |||||||
| chr16:74649335 | G | C | 1 | a0001c0002t0002g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.722-133C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649335 | |||||||
| chr16:74649468 | A | G | 1 | a0002c0001t0001g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.722-266T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649468 | |||||||
| chr16:74649839 | T | C | 253 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(250): Show |
270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.722-637A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649839 | |||||||
| chr16:74649839 | T | G | 1 | a0002c0001t0001g0302 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.722-637A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649839 | |||||||
| chr16:74649884 | G | T | 1 | a0002c0001t0001g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.722-682C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649884 | |||||||
| chr16:74650039 | C | G | 1 | a0002c0001t0001g0301 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.722-837G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650039 | |||||||
| chr16:74650098 | G | A | 3 | a0001c0002t0013g0152 a0001c0002t0013g0153 a0001c0002t0013g0164 |
3 | HG00738.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.722-896C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650098 | |||||||
| chr16:74650117 | G | T | 1 | a0002c0001t0018g0378 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.722-915C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650117 | |||||||
| chr16:74650296 | C | T | 1 | a0001c0002t0016g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.722-1094G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650296 | |||||||
| chr16:74650356 | T | C | 2 | a0002c0001t0001g0351 a0002c0001t0001g0352 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.722-1154A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650356 | |||||||
| chr16:74650420 | G | T | 11 | a0001c0002t0006g0355 a0001c0002t0006g0356 a0001c0002t0006g0357 others(8): Show |
11 | HG00673.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.722-1218C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650420 | |||||||
| chr16:74650628 | G | A | 1 | a0002c0001t0001g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.721+1292C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650628 | |||||||
| chr16:74650792 | G | A | 25 | a0002c0001t0001g0242 a0002c0001t0001g0243 a0002c0001t0001g0244 others(22): Show |
26 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.721+1128C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650792 | |||||||
| chr16:74650904 | C | A | 1 | a0001c0002t0002g0170 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.721+1016G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650904 | |||||||
| chr16:74650998 | G | GT | 254 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(251): Show |
271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.721+921dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650998 | |||||||
| chr16:74651016 | T | C | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.721+904A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651016 | |||||||
| chr16:74651061 | A | T | 2 | a0004c0006t0001g0257 a0004c0006t0001g0258 |
2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.721+859T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651061 | |||||||
| chr16:74651254 | A | G | 2 | a0002c0001t0001g0281 a0002c0001t0001g0282 |
2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.721+666T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651254 | |||||||
| chr16:74651425 | C | T | 1 | a0002c0001t0001g0251 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.721+495G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651425 | |||||||
| chr16:74651426 | G | A | 1 | a0002c0001t0001g0285 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.721+494C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651426 | |||||||
| chr16:74651691 | C | T | 292 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(289): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.721+229G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651691 | |||||||
| chr16:74651909 | A | G | 2 | a0002c0001t0001g0292 a0002c0001t0001g0300 |
2 | NA19066.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.721+11T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651909 | |||||||
| chr16:74652192 | T | C | 1 | a0001c0004t0004g0116 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.519-70A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652192 | |||||||
| chr16:74652268 | G | A | 252 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(249): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.519-146C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652268 | |||||||
| chr16:74652335 | C | A | 1 | a0002c0001t0001g0343 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.519-213G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652335 | |||||||
| chr16:74652626 | G | A | 2 | a0003c0003t0003g0078 a0003c0003t0003g0079 |
2 | HG01255.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.519-504C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652626 | |||||||
| chr16:74652788 | A | G | 1 | a0001c0002t0001g0372 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.519-666T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652788 | |||||||
| chr16:74652789 | C | T | 1 | a0001c0002t0029g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.519-667G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652789 | |||||||
| chr16:74652792 | G | A | 285 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(282): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.519-670C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652792 | |||||||
| chr16:74652877 | T | C | 1 | a0001c0002t0011g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.519-755A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652877 | |||||||
| chr16:74652923 | C | T | 3 | a0001c0004t0004g0131 a0001c0004t0004g0132 a0001c0004t0023g0130 |
3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.519-801G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652923 | |||||||
| chr16:74653129 | A | C | 3 | a0001c0002t0014g0254 a0001c0002t0014g0353 a0001c0002t0014g0354 |
3 | HG02886.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.519-1007T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653129 | |||||||
| chr16:74653151 | T | G | 88 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(85): Show |
93 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.519-1029A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653151 | |||||||
| chr16:74653226 | C | T | 2 | a0003c0003t0003g0049 a0003c0003t0003g0065 |
2 | NA19056.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.519-1104G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653226 | |||||||
| chr16:74653353 | A | G | 6 | a0002c0001t0001g0323 a0002c0001t0001g0324 a0002c0001t0001g0341 others(3): Show |
6 | HG00423.hp2 HG03927.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.519-1231T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653353 | |||||||
| chr16:74653490 | CA | C | 32 | a0001c0002t0002g0189 a0001c0004t0004g0001 a0001c0004t0004g0010 others(29): Show |
38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.519-1369delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653490 | |||||||
| chr16:74653704 | T | C | 93 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(90): Show |
98 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.519-1582A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653704 | |||||||
| chr16:74653816 | T | C | 1 | a0002c0001t0001g0330 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.519-1694A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653816 | |||||||
| chr16:74653906 | C | T | 284 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(281): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.519-1784G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653906 | |||||||
| chr16:74653909 | A | T | 1 | a0002c0001t0002g0160 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.519-1787T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653909 | |||||||
| chr16:74654008 | A | G | 253 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(250): Show |
270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.519-1886T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654008 | |||||||
| chr16:74654024 | T | C | 2 | a0002c0001t0001g0255 a0002c0001t0001g0256 |
2 | NA18963.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.519-1902A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654024 | |||||||
| chr16:74654028 | G | GT | 9 | a0002c0001t0001g0253 a0002c0001t0001g0255 a0002c0001t0001g0256 others(6): Show |
9 | HG01074.hp2 NA18953.hp1 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.519-1907dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654028 | |||||||
| chr16:74654096 | T | C | 2 | a0003c0003t0005g0045 a0003c0003t0005g0046 |
2 | HG00738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.519-1974A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654096 | |||||||
| chr16:74654111 | A | G | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.519-1989T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654111 | |||||||
| chr16:74654171 | T | C | 1 | a0001c0002t0013g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.519-2049A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654171 | |||||||
| chr16:74654260 | C | G | 1 | a0001c0002t0014g0354 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.519-2138G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654260 | |||||||
| chr16:74654321 | C | T | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.519-2199G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654321 | |||||||
| chr16:74654379 | T | C | 1 | a0001c0002t0011g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.519-2257A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654379 | |||||||
| chr16:74654433 | T | A | 1 | a0001c0002t0033g0171 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.519-2311A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654433 | |||||||
| chr16:74654542 | A | G | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-2420T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654542 | |||||||
| chr16:74654585 | A | G | 4 | a0002c0001t0001g0287 a0002c0001t0001g0288 a0002c0001t0024g0136 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.519-2463T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654585 | |||||||
| chr16:74654610 | G | C | 2 | a0001c0004t0049g0376 a0001c0004t0050g0375 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.519-2488C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654610 | |||||||
| chr16:74654755 | A | G | 4 | a0002c0001t0002g0157 a0002c0001t0002g0158 a0002c0001t0002g0161 others(1): Show |
4 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.519-2633T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654755 | |||||||
| chr16:74654796 | T | C | 1 | a0001c0008t0046g0348 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.519-2674A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654796 | |||||||
| chr16:74654925 | G | A | 1 | a0002c0001t0002g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.519-2803C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654925 | |||||||
| chr16:74654939 | T | C | 3 | a0001c0004t0004g0131 a0001c0004t0004g0132 a0001c0004t0023g0130 |
3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.519-2817A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654939 | |||||||
| chr16:74655050 | T | G | 254 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(251): Show |
271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.519-2928A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655050 | |||||||
| chr16:74655155 | G | T | 1 | a0002c0001t0001g0323 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.519-3033C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655155 | |||||||
| chr16:74655284 | G | A | 32 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(29): Show |
38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.519-3162C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655284 | |||||||
| chr16:74655364 | C | T | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.519-3242G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655364 | |||||||
| chr16:74655388 | C | T | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-3266G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655388 | |||||||
| chr16:74655494 | G | A | 2 | a0003c0003t0003g0090 a0003c0003t0003g0107 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.519-3372C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655494 | |||||||
| chr16:74655506 | C | T | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.519-3384G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655506 | |||||||
| chr16:74655619 | GCTCT | G | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-3501_519-3498d others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655619 | |||||||
| chr16:74655626 | CTCTT | C | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.519-3508_519-3505d others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655626 | |||||||
| chr16:74655921 | T | C | 1 | a0002c0001t0010g0262 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.519-3799A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655921 | |||||||
| chr16:74656164 | G | C | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-4042C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656164 | |||||||
| chr16:74656213 | G | A | 27 | a0003c0003t0003g0008 a0003c0003t0003g0030 a0003c0003t0003g0053 others(24): Show |
28 | HG00544.hp1 HG00609.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.519-4091C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656213 | |||||||
| chr16:74656305 | T | C | 293 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(290): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.519-4183A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656305 | |||||||
| chr16:74656308 | C | CA | 110 | a0001c0002t0002g0181 a0001c0002t0002g0208 a0001c0002t0002g0209 others(107): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.519-4187dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656308 | |||||||
| chr16:74656308 | C | CAA | 21 | a0001c0002t0011g0029 a0001c0002t0054g0382 a0001c0005t0007g0009 others(18): Show |
22 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.519-4188_519-4187d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656308 | |||||||
| chr16:74656308 | CA | C | 34 | a0001c0002t0002g0188 a0001c0004t0004g0001 a0001c0004t0004g0010 others(31): Show |
40 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.519-4187delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656308 | |||||||
| chr16:74656308 | CAAAAAAA others(4): Show |
C | 1 | a0002c0001t0001g0251 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.519-4197_519-4187d others(13): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656308 | |||||||
| chr16:74656324 | A | G | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-4202T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656324 | |||||||
| chr16:74656327 | A | G | 2 | a0001c0002t0002g0223 a0001c0002t0006g0357 |
2 | NA18947.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.519-4205T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656327 | |||||||
| chr16:74656328 | A | G | 1 | a0001c0002t0002g0230 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.519-4206T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656328 | |||||||
| chr16:74656457 | T | C | 2 | a0002c0001t0001g0281 a0002c0001t0001g0282 |
2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.519-4335A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656457 | |||||||
| chr16:74656534 | G | A | 1 | a0002c0001t0001g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.518+4398C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656534 | |||||||
| chr16:74656536 | G | A | 1 | a0002c0001t0001g0336 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.518+4396C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656536 | |||||||
| chr16:74656661 | T | C | 1 | a0001c0002t0029g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.518+4271A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656661 | |||||||
| chr16:74656716 | C | G | 1 | a0009c0013t0045g0319 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.518+4216G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656716 | |||||||
| chr16:74656733 | T | C | 117 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(114): Show |
122 | HG00408.hp2 HG00642.hp1 HG00673.hp1 others(119): Show |
intron_variant | MODIFIER | c.518+4199A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656733 | |||||||
| chr16:74656771 | T | C | 1 | a0003c0003t0003g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.518+4161A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656771 | |||||||
| chr16:74656933 | T | C | 3 | a0003c0003t0003g0088 a0003c0003t0005g0006 a0003c0003t0005g0007 |
5 | NA18977.hp1 NA18977.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.518+3999A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656933 | |||||||
| chr16:74657046 | GA | G | 5 | a0001c0005t0007g0009 a0001c0005t0007g0092 a0001c0005t0007g0110 others(2): Show |
6 | HG01192.hp2 HG01257.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.518+3885delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657046 | |||||||
| chr16:74657100 | G | C | 1 | a0001c0002t0011g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.518+3832C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657100 | |||||||
| chr16:74657137 | A | G | 2 | a0001c0004t0049g0376 a0001c0004t0050g0375 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.518+3795T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657137 | |||||||
| chr16:74657149 | C | A | 1 | a0002c0001t0001g0315 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.518+3783G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657149 | |||||||
| chr16:74657294 | T | C | 1 | a0002c0001t0001g0247 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.518+3638A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657294 | |||||||
| chr16:74657366 | T | C | 253 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(250): Show |
270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.518+3566A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657366 | |||||||
| chr16:74657464 | C | T | 253 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(250): Show |
270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.518+3468G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657464 | |||||||
| chr16:74657474 | TTTTC | T | 27 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0117 others(24): Show |
32 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.518+3454_518+3457d others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657474 | |||||||
| chr16:74657478 | C | CTT | 237 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(234): Show |
253 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.518+3452_518+3453d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657478 | |||||||
| chr16:74657478 | C | CTTT | 15 | a0001c0002t0006g0359 a0001c0002t0047g0349 a0002c0001t0001g0314 others(12): Show |
15 | HG00323.hp2 HG00639.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.518+3451_518+3453d others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657478 | |||||||
| chr16:74657498 | C | T | 1 | a0002c0001t0001g0344 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518+3434G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657498 | |||||||
| chr16:74657559 | T | C | 12 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0117 others(9): Show |
17 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.518+3373A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657559 | |||||||
| chr16:74657636 | C | T | 2 | a0002c0001t0001g0297 a0002c0001t0001g0316 |
2 | NA18960.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.518+3296G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657636 | |||||||
| chr16:74657758 | G | A | 1 | a0001c0004t0004g0116 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.518+3174C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657758 | |||||||
| chr16:74657763 | T | C | 8 | a0003c0003t0005g0032 a0003c0003t0005g0033 a0003c0003t0005g0034 others(5): Show |
8 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.518+3169A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657763 | |||||||
| chr16:74657791 | A | G | 1 | a0001c0004t0004g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.518+3141T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657791 | |||||||
| chr16:74657894 | T | G | 2 | a0003c0003t0012g0058 a0010c0017t0012g0060 |
2 | HG01169.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.518+3038A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657894 | |||||||
| chr16:74657930 | C | T | 1 | a0001c0002t0002g0173 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.518+3002G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657930 | |||||||
| chr16:74657940 | T | C | 6 | a0001c0002t0006g0357 a0001c0002t0006g0358 a0001c0002t0006g0359 others(3): Show |
6 | HG00673.hp1 HG01993.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.518+2992A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657940 | |||||||
| chr16:74658207 | G | C | 3 | a0001c0002t0002g0217 a0001c0002t0016g0214 a0001c0002t0016g0215 |
3 | HG02738.hp2 HG03017.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.518+2725C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658207 | |||||||
| chr16:74658320 | G | A | 3 | a0002c0001t0010g0250 a0002c0001t0037g0283 a0002c0001t0038g0284 |
3 | HG02809.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.518+2612C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658320 | |||||||
| chr16:74658446 | T | C | 1 | a0001c0002t0047g0349 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.518+2486A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658446 | |||||||
| chr16:74658528 | C | T | 286 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(283): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.518+2404G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658528 | |||||||
| chr16:74658555 | C | T | 286 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(283): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.518+2377G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658555 | |||||||
| chr16:74658694 | C | T | 2 | a0002c0001t0001g0242 a0002c0001t0001g0328 |
2 | HG00733.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.518+2238G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658694 | |||||||
| chr16:74658698 | C | G | 2 | a0001c0004t0009g0182 a0013c0012t0009g0219 |
2 | NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.518+2234G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658698 | |||||||
| chr16:74658702 | T | C | 10 | a0001c0004t0009g0174 a0001c0004t0009g0182 a0001c0004t0009g0183 others(7): Show |
11 | HG00558.hp2 HG02027.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.518+2230A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658702 | |||||||
| chr16:74658724 | C | T | 4 | a0002c0001t0001g0293 a0002c0001t0001g0294 a0002c0001t0001g0295 others(1): Show |
4 | HG00621.hp1 HG03831.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.518+2208G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658724 | |||||||
| chr16:74658766 | A | AT | 13 | a0001c0002t0002g0187 a0001c0002t0011g0025 a0002c0001t0001g0264 others(10): Show |
13 | HG01358.hp2 HG01515.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.518+2165dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658766 | |||||||
| chr16:74658766 | AT | A | 15 | a0001c0002t0002g0173 a0001c0002t0002g0175 a0001c0002t0002g0216 others(12): Show |
15 | HG01106.hp2 HG01192.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.518+2165delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658766 | |||||||
| chr16:74658766 | ATT | A | 32 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(29): Show |
38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.518+2164_518+2165d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658766 | |||||||
| chr16:74658800 | T | G | 1 | a0001c0004t0009g0174 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.518+2132A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658800 | |||||||
| chr16:74658817 | G | T | 1 | a0002c0001t0001g0335 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.518+2115C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658817 | |||||||
| chr16:74658834 | C | A | 1 | a0002c0001t0001g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.518+2098G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658834 | |||||||
| chr16:74658863 | G | A | 6 | a0001c0002t0006g0357 a0001c0002t0006g0358 a0001c0002t0006g0359 others(3): Show |
6 | HG00673.hp1 HG01993.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.518+2069C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658863 | |||||||
| chr16:74658924 | C | G | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.518+2008G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658924 | |||||||
| chr16:74658939 | T | C | 1 | a0002c0001t0008g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.518+1993A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658939 | |||||||
| chr16:74658979 | C | T | 5 | a0001c0004t0004g0131 a0001c0004t0004g0132 a0001c0004t0023g0130 others(2): Show |
5 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.518+1953G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658979 | |||||||
| chr16:74658980 | G | A | 2 | a0003c0003t0003g0056 a0003c0003t0003g0114 |
2 | NA18981.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.518+1952C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658980 | |||||||
| chr16:74659032 | T | C | 5 | a0001c0005t0007g0009 a0001c0005t0007g0092 a0001c0005t0007g0110 others(2): Show |
6 | HG01192.hp2 HG01257.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.518+1900A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659032 | |||||||
| chr16:74659040 | G | T | 1 | a0001c0002t0029g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.518+1892C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659040 | |||||||
| chr16:74659171 | T | C | 1 | a0003c0003t0003g0115 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.518+1761A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659171 | |||||||
| chr16:74659197 | G | A | 1 | a0001c0002t0002g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.518+1735C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659197 | |||||||
| chr16:74659209 | C | T | 1 | a0001c0002t0042g0339 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.518+1723G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659209 | |||||||
| chr16:74659510 | G | A | 2 | a0002c0001t0001g0285 a0002c0001t0001g0322 |
2 | HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.518+1422C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659510 | |||||||
| chr16:74659577 | A | G | 1 | a0003c0003t0003g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.518+1355T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659577 | |||||||
| chr16:74659590 | T | A | 1 | a0002c0001t0052g0380 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.518+1342A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659590 | |||||||
| chr16:74659601 | C | CA | 247 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(244): Show |
264 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.518+1330dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659601 | |||||||
| chr16:74659703 | T | A | 2 | a0001c0002t0006g0361 a0001c0002t0006g0362 |
2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.518+1229A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659703 | |||||||
| chr16:74659791 | T | C | 1 | a0001c0002t0001g0372 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.518+1141A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659791 | |||||||
| chr16:74659818 | C | T | 3 | a0002c0001t0001g0293 a0002c0001t0001g0294 a0002c0001t0001g0295 |
3 | HG03831.hp2 NA18965.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.518+1114G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659818 | |||||||
| chr16:74660010 | G | C | 10 | a0002c0001t0001g0242 a0002c0001t0001g0243 a0002c0001t0001g0244 others(7): Show |
10 | HG00733.hp1 HG01516.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.518+922C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660010 | |||||||
| chr16:74660029 | T | TG | 33 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(30): Show |
39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.518+902dupC | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660029 | |||||||
| chr16:74660075 | C | G | 288 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(285): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.518+857G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660075 | |||||||
| chr16:74660160 | T | G | 254 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(251): Show |
271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.518+772A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660160 | |||||||
| chr16:74660577 | A | G | 2 | a0001c0002t0011g0025 a0001c0002t0011g0133 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.518+355T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660577 | |||||||
| chr16:74660686 | C | G | 294 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(291): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.518+246G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660686 | |||||||
| chr16:74660794 | T | C | 135 | a0002c0001t0001g0005 a0002c0001t0001g0018 a0002c0001t0001g0019 others(132): Show |
147 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.518+138A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660794 | |||||||
| chr16:74660817 | G | T | 1 | a0001c0002t0029g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.518+115C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660817 | |||||||
| chr16:74660833 | C | A | 32 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0116 others(29): Show |
38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.518+99G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660833 | |||||||
| chr16:74660849 | C | T | 1 | a0002c0001t0001g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.518+83G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660849 | |||||||
| chr16:74660876 | A | G | 2 | a0002c0001t0002g0165 a0002c0001t0002g0179 |
2 | NA19067.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.518+56T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660876 | |||||||
| chr16:74660880 | T | G | 4 | a0002c0001t0001g0287 a0002c0001t0001g0288 a0002c0001t0024g0136 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.518+52A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660880 | |||||||
| chr16:74661660 | C | T | 1 | a0002c0001t0001g0292 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-2-209G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74661660 | |||||||
| chr16:74661691 | G | A | 1 | a0001c0004t0050g0375 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-2-240C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74661691 | |||||||
| chr16:74661701 | G | A | 1 | a0001c0004t0009g0185 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-2-250C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74661701 | |||||||
| chr16:74661887 | GATAA | G | 3 | a0001c0002t0014g0254 a0001c0002t0014g0353 a0001c0002t0014g0354 |
3 | HG02886.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-2-440_-2-437delTT others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74661887 | |||||||
| chr16:74661915 | C | A | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-464G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74661915 | |||||||
| chr16:74662007 | T | A | 2 | a0002c0001t0001g0289 a0002c0001t0001g0290 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-2-556A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662007 | |||||||
| chr16:74662027 | CCAT | C | 71 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(68): Show |
76 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.-2-579_-2-577delAT others(1): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662027 | |||||||
| chr16:74662101 | T | C | 1 | a0001c0002t0015g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-2-650A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662101 | |||||||
| chr16:74662147 | AAAT | A | 19 | a0002c0001t0001g0242 a0002c0001t0001g0243 a0002c0001t0001g0244 others(16): Show |
20 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2-699_-2-697delAT others(1): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662147 | |||||||
| chr16:74662279 | G | A | 1 | a0002c0001t0010g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2-828C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662279 | |||||||
| chr16:74662374 | T | C | 1 | a0002c0001t0001g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-2-923A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662374 | |||||||
| chr16:74662463 | A | C | 1 | a0001c0002t0006g0363 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-2-1012T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662463 | |||||||
| chr16:74662491 | A | C | 1 | a0003c0003t0012g0058 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-2-1040T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662491 | |||||||
| chr16:74662549 | T | C | 1 | a0009c0013t0045g0319 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-2-1098A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662549 | |||||||
| chr16:74662575 | G | C | 2 | a0004c0006t0001g0257 a0004c0006t0001g0258 |
2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-2-1124C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662575 | |||||||
| chr16:74662627 | G | A | 3 | a0001c0002t0006g0361 a0001c0002t0006g0362 a0001c0002t0006g0365 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-2-1176C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662627 | |||||||
| chr16:74662903 | GCTT | G | 5 | a0002c0001t0001g0344 a0002c0001t0001g0345 a0002c0001t0001g0346 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-1455_-2-1453del others(3): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662903 | |||||||
| chr16:74662904 | C | T | 1 | a0001c0002t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-2-1453G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662904 | |||||||
| chr16:74662907 | C | CT | 6 | a0002c0001t0001g0320 a0002c0001t0001g0337 a0003c0003t0003g0093 others(3): Show |
6 | HG01981.hp2 HG02293.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-1457dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662907 | |||||||
| chr16:74662907 | CT | C | 8 | a0001c0002t0002g0220 a0001c0002t0047g0349 a0002c0001t0001g0242 others(5): Show |
8 | HG00323.hp2 HG01168.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-1457delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662907 | |||||||
| chr16:74662932 | T | C | 1 | a0001c0002t0029g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2-1481A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662932 | |||||||
| chr16:74662943 | T | C | 3 | a0001c0004t0004g0127 a0001c0004t0004g0128 a0001c0004t0004g0129 |
3 | HG00099.hp2 HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.-2-1492A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662943 | |||||||
| chr16:74663061 | C | T | 260 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(257): Show |
278 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.-2-1610G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663061 | |||||||
| chr16:74663068 | C | A | 1 | a0002c0001t0002g0221 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-2-1617G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663068 | |||||||
| chr16:74663072 | T | C | 1 | a0003c0003t0003g0109 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-2-1621A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663072 | |||||||
| chr16:74663121 | G | C | 13 | a0002c0001t0012g0059 a0003c0003t0005g0006 a0003c0003t0005g0007 others(10): Show |
15 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-1670C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663121 | |||||||
| chr16:74663281 | A | G | 1 | a0001c0002t0002g0176 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-2-1830T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663281 | |||||||
| chr16:74663290 | G | C | 1 | a0001c0002t0029g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2-1839C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663290 | |||||||
| chr16:74663340 | T | C | 24 | a0001c0002t0011g0133 a0001c0004t0004g0001 a0001c0004t0004g0010 others(21): Show |
29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2-1889A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663340 | |||||||
| chr16:74663377 | G | A | 4 | a0002c0001t0001g0240 a0002c0001t0001g0241 a0002c0001t0001g0337 others(1): Show |
4 | NA18970.hp1 NA18972.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1926C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663377 | |||||||
| chr16:74663406 | T | C | 1 | a0002c0001t0001g0318 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-2-1955A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663406 | |||||||
| chr16:74663523 | C | T | 293 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(290): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-2-2072G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663523 | |||||||
| chr16:74663674 | C | T | 3 | a0002c0001t0001g0291 a0002c0001t0002g0155 a0002c0001t0002g0156 |
3 | HG02083.hp2 NA18989.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-2-2223G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663674 | |||||||
| chr16:74663774 | A | T | 24 | a0001c0002t0011g0133 a0001c0004t0004g0001 a0001c0004t0004g0010 others(21): Show |
29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2-2323T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663774 | |||||||
| chr16:74663884 | A | G | 1 | a0009c0013t0045g0319 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-2-2433T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663884 | |||||||
| chr16:74663984 | G | A | 1 | a0001c0008t0046g0348 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2-2533C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663984 | |||||||
| chr16:74664101 | ATGTGAGA others(86): Show |
A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2592_-2-2651del others(93): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664101 | |||||||
| chr16:74664153 | G | A | 1 | a0002c0001t0001g0302 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-3+2633C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664153 | |||||||
| chr16:74664198 | G | C | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2588C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664198 | |||||||
| chr16:74664199 | C | T | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2587G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664199 | |||||||
| chr16:74664204 | G | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2582C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664204 | |||||||
| chr16:74664206 | C | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2580G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664206 | |||||||
| chr16:74664207 | T | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2579A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664207 | |||||||
| chr16:74664209 | C | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2577G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664209 | |||||||
| chr16:74664213 | A | C | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2573T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664213 | |||||||
| chr16:74664215 | T | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2571A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664215 | |||||||
| chr16:74664216 | G | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2570C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664216 | |||||||
| chr16:74664217 | C | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2569G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664217 | |||||||
| chr16:74664218 | T | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2568A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664218 | |||||||
| chr16:74664219 | G | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2567C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664219 | |||||||
| chr16:74664223 | T | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2563A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664223 | |||||||
| chr16:74664224 | T | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2562A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664224 | |||||||
| chr16:74664226 | C | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2560G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664226 | |||||||
| chr16:74664228 | G | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2558C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664228 | |||||||
| chr16:74664232 | T | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2554A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664232 | |||||||
| chr16:74664235 | G | GATCTCTC others(4): Show |
1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2550_-3+2551ins others(11): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664235 | |||||||
| chr16:74664237 | T | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2549A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664237 | |||||||
| chr16:74664240 | T | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2546A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664240 | |||||||
| chr16:74664241 | G | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2545C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664241 | |||||||
| chr16:74664244 | G | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2542C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664244 | |||||||
| chr16:74664246 | T | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2540A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664246 | |||||||
| chr16:74664248 | C | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2538G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664248 | |||||||
| chr16:74664249 | C | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2537G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664249 | |||||||
| chr16:74664250 | T | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2536A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664250 | |||||||
| chr16:74664253 | C | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2533G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664253 | |||||||
| chr16:74664254 | T | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2532A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664254 | |||||||
| chr16:74664260 | C | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2526G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664260 | |||||||
| chr16:74664261 | T | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2525A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664261 | |||||||
| chr16:74664262 | T | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2524A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664262 | |||||||
| chr16:74664263 | T | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2523A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664263 | |||||||
| chr16:74664264 | T | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2522A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664264 | |||||||
| chr16:74664265 | A | G | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2521T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664265 | |||||||
| chr16:74664268 | G | C | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2518C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664268 | |||||||
| chr16:74664270 | T | C | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2516A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664270 | |||||||
| chr16:74664273 | T | TCTCATCA others(71): Show |
1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2512_-3+2513ins others(78): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664273 | |||||||
| chr16:74664277 | G | A | 1 | a0003c0003t0003g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2509C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664277 | |||||||
| chr16:74664354 | A | T | 49 | a0002c0001t0001g0018 a0002c0001t0001g0259 a0002c0001t0001g0260 others(46): Show |
50 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+2432T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664354 | |||||||
| chr16:74664365 | C | G | 135 | a0002c0001t0001g0005 a0002c0001t0001g0018 a0002c0001t0001g0019 others(132): Show |
147 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-3+2421G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664365 | |||||||
| chr16:74664426 | T | C | 1 | a0001c0002t0029g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3+2360A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664426 | |||||||
| chr16:74664489 | G | A | 24 | a0001c0002t0011g0133 a0001c0004t0004g0001 a0001c0004t0004g0010 others(21): Show |
29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-3+2297C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664489 | |||||||
| chr16:74664521 | C | A | 2 | a0003c0003t0005g0006 a0003c0003t0005g0007 |
4 | NA18977.hp2 NA19009.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+2265G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664521 | |||||||
| chr16:74664537 | A | G | 3 | a0001c0002t0002g0176 a0001c0002t0002g0177 a0001c0002t0002g0178 |
3 | HG01099.hp1 HG01261.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-3+2249T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664537 | |||||||
| chr16:74664549 | C | T | 2 | a0002c0001t0001g0255 a0002c0001t0001g0256 |
2 | NA18963.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-3+2237G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664549 | |||||||
| chr16:74664599 | A | T | 2 | a0001c0002t0002g0226 a0001c0002t0002g0227 |
2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-3+2187T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664599 | |||||||
| chr16:74664654 | C | A | 1 | a0001c0002t0002g0227 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-3+2132G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664654 | |||||||
| chr16:74664671 | C | T | 1 | a0003c0003t0003g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-3+2115G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664671 | |||||||
| chr16:74664678 | A | G | 286 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(283): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-3+2108T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664678 | |||||||
| chr16:74664755 | G | A | 1 | a0002c0001t0001g0242 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-3+2031C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664755 | |||||||
| chr16:74664755 | G | GAAA | 22 | a0002c0001t0012g0059 a0003c0003t0003g0022 a0003c0003t0003g0023 others(19): Show |
24 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3+2028_-3+2030dup others(3): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664755 | |||||||
| chr16:74664755 | G | GAAAA | 291 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(288): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-3+2027_-3+2030dup others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664755 | |||||||
| chr16:74664818 | A | C | 286 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(283): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-3+1968T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664818 | |||||||
| chr16:74664845 | G | C | 10 | a0002c0001t0001g0242 a0002c0001t0001g0243 a0002c0001t0001g0244 others(7): Show |
10 | HG00733.hp1 HG01516.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+1941C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664845 | |||||||
| chr16:74664864 | C | T | 3 | a0001c0004t0004g0131 a0001c0004t0004g0132 a0001c0004t0023g0130 |
3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-3+1922G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664864 | |||||||
| chr16:74664937 | A | G | 1 | a0001c0004t0009g0174 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-3+1849T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664937 | |||||||
| chr16:74664992 | T | C | 2 | a0003c0003t0005g0045 a0003c0003t0005g0046 |
2 | HG00738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-3+1794A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664992 | |||||||
| chr16:74665104 | G | A | 2 | a0002c0001t0010g0321 a0002c0001t0010g0340 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-3+1682C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665104 | |||||||
| chr16:74665203 | CTGAAATG others(29): Show |
C | 1 | a0001c0002t0002g0222 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-3+1547_-3+1582del others(36): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665203 | |||||||
| chr16:74665395 | T | C | 263 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(260): Show |
281 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.-3+1391A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665395 | |||||||
| chr16:74665421 | T | C | 3 | a0001c0002t0002g0223 a0001c0002t0002g0224 a0001c0002t0002g0225 |
3 | NA18947.hp1 NA18957.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-3+1365A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665421 | |||||||
| chr16:74665589 | G | A | 1 | a0001c0002t0047g0349 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-3+1197C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665589 | |||||||
| chr16:74665628 | G | A | 2 | a0001c0002t0002g0226 a0001c0002t0002g0227 |
2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-3+1158C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665628 | |||||||
| chr16:74665636 | G | T | 1 | a0001c0002t0008g0142 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-3+1150C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665636 | |||||||
| chr16:74665685 | G | A | 24 | a0001c0002t0011g0133 a0001c0004t0004g0001 a0001c0004t0004g0010 others(21): Show |
29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-3+1101C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665685 | |||||||
| chr16:74665707 | C | T | 11 | a0002c0001t0001g0323 a0002c0001t0001g0324 a0002c0001t0001g0341 others(8): Show |
12 | HG00423.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+1079G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665707 | |||||||
| chr16:74665749 | TTTC | T | 21 | a0001c0002t0006g0355 a0001c0002t0006g0356 a0001c0002t0006g0357 others(18): Show |
21 | HG00673.hp1 HG00738.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-3+1034_-3+1036del others(3): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665749 | |||||||
| chr16:74665752 | C | CT | 128 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(125): Show |
138 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-3+1033dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665752 | |||||||
| chr16:74665756 | C | T | 291 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(288): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-3+1030G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665756 | |||||||
| chr16:74665849 | C | G | 2 | a0001c0002t0002g0173 a0002c0001t0002g0172 |
2 | NA19056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-3+937G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665849 | |||||||
| chr16:74666082 | G | A | 25 | a0002c0001t0001g0242 a0002c0001t0001g0243 a0002c0001t0001g0244 others(22): Show |
26 | HG00423.hp2 HG00733.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3+704C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666082 | |||||||
| chr16:74666159 | CATAG | C | 7 | a0001c0005t0007g0009 a0001c0005t0007g0047 a0001c0005t0007g0091 others(4): Show |
8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+623_-3+626delCT others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666159 | |||||||
| chr16:74666182 | T | TTAGA | 22 | a0001c0005t0007g0009 a0001c0005t0007g0110 a0001c0005t0007g0111 others(19): Show |
24 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3+600_-3+603dupTC others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666182 | |||||||
| chr16:74666182 | T | TTAGATAG others(1): Show |
3 | a0003c0003t0003g0113 a0003c0003t0003g0114 a0003c0003t0003g0115 |
3 | HG02004.hp1 HG02273.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-3+596_-3+603dupTC others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666182 | |||||||
| chr16:74666182 | TTAGA | T | 43 | a0001c0002t0002g0015 a0001c0002t0002g0017 a0001c0002t0002g0169 others(40): Show |
45 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-3+600_-3+603delTC others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666182 | |||||||
| chr16:74666182 | TTAGATAG others(1): Show |
T | 20 | a0001c0004t0050g0375 a0001c0005t0007g0047 a0003c0003t0003g0030 others(17): Show |
22 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.-3+596_-3+603delTC others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666182 | |||||||
| chr16:74666182 | TTAGATAG others(5): Show |
T | 17 | a0001c0004t0004g0001 a0001c0004t0004g0010 a0001c0004t0004g0117 others(14): Show |
22 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.-3+592_-3+603delTC others(10): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666182 | |||||||
| chr16:74666212 | A | T | 6 | a0002c0001t0001g0243 a0002c0001t0001g0244 a0002c0001t0001g0245 others(3): Show |
6 | HG02040.hp2 NA18963.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+574T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666212 | |||||||
| chr16:74666216 | A | AGATT | 26 | a0001c0002t0013g0164 a0001c0002t0042g0339 a0002c0001t0001g0240 others(23): Show |
32 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-3+569_-3+570insAA others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666216 | |||||||
| chr16:74666216 | A | T | 112 | a0001c0002t0013g0152 a0001c0002t0013g0153 a0001c0002t0014g0254 others(109): Show |
118 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-3+570T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666216 | |||||||
| chr16:74666220 | A | AGATAGAT others(5): Show |
5 | a0001c0002t0001g0371 a0001c0002t0001g0372 a0001c0002t0002g0236 others(2): Show |
5 | NA18952.hp1 NA18967.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+565_-3+566insAA others(10): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | |||||||
| chr16:74666220 | A | AGATAGAT others(1): Show |
3 | a0001c0002t0011g0029 a0006c0009t0008g0148 a0006c0009t0008g0149 |
3 | HG03225.hp2 NA18946.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-3+565_-3+566insAA others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | |||||||
| chr16:74666220 | A | AGATAGAT others(5): Show |
2 | a0001c0002t0011g0025 a0001c0002t0011g0026 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-3+565_-3+566insAA others(10): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | |||||||
| chr16:74666220 | A | AGATT | 10 | a0001c0002t0001g0370 a0001c0002t0002g0229 a0001c0002t0002g0230 others(7): Show |
10 | HG00642.hp2 HG02258.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+562_-3+565dupAA others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | |||||||
| chr16:74666220 | A | AGATTGAT others(1): Show |
5 | a0001c0002t0047g0349 a0001c0008t0046g0348 a0002c0001t0001g0350 others(2): Show |
5 | HG02109.hp2 HG03453.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+558_-3+565dupAA others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | |||||||
| chr16:74666220 | A | T | 236 | a0001c0002t0001g0369 a0001c0002t0002g0004 a0001c0002t0002g0015 others(233): Show |
253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.-3+566T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | |||||||
| chr16:74666220 | AGATT | A | 3 | a0001c0004t0004g0131 a0001c0004t0004g0132 a0001c0004t0023g0130 |
3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-3+562_-3+565delAA others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | |||||||
| chr16:74666224 | T | A | 1 | a0001c0002t0011g0133 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-3+562A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666224 | |||||||
| chr16:74666238 | G | T | 1 | a0002c0001t0001g0242 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-3+548C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666238 | |||||||
| chr16:74666266 | TG | T | 3 | a0002c0001t0002g0003 a0002c0001t0002g0011 a0002c0001t0002g0151 |
7 | NA18941.hp2 NA18985.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+519delC | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666266 | |||||||
| chr16:74666267 | G | A | 1 | a0002c0001t0001g0336 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-3+519C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666267 | |||||||
| chr16:74666342 | C | A | 99 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(96): Show |
105 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.-3+444G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666342 | |||||||
| chr16:74666502 | G | A | 1 | a0001c0002t0044g0373 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-3+284C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666502 | |||||||
| chr16:74666548 | C | G | 1 | a0003c0003t0003g0024 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-3+238G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666548 | |||||||
| chr16:74666686 | G | A | 2 | a0001c0004t0004g0134 a0001c0004t0004g0135 |
2 | HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-3+100C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666686 | |||||||
| chr16:74666730 | G | A | 281 | a0001c0002t0001g0369 a0001c0002t0001g0370 a0001c0002t0001g0371 others(278): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.-3+56C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666730 | |||||||
| chr16:74666754 | A | G | 2 | a0003c0003t0003g0022 a0003c0003t0003g0023 |
2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-3+32T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666754 |