Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55095 |
| ensemblid | ENSG00000179134.16 |
| hgncid | 25492 |
| symbol | SAMD4B |
| name | sterile alpha motif domain containing 4B |
| refseq_nuc | NM_001384574.2 |
| refseq_prot | NP_001371503.1 |
| ensembl_nuc | ENST00000610417.5 |
| ensembl_prot | ENSP00000484229.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 39342421 |
| end | 39385700 |
| strand | + |
| ver | v1.2 |
| region | chr19:39342421-39385700 |
| region5000 | chr19:39337421-39390700 |
| regionname0 | SAMD4B_chr19_39342421_39385700 |
| regionname5000 | SAMD4B_chr19_39337421_39390700 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 694 | 230 | 78 | 38 | 82 | 12 | 18 | 62 | SAMD4B_chr19_39337421_39390700 | SAMD4B | MMFRD others(689): Show |
chr19 | 39337421 | 39390700 |
| a0002 | 0/0 | 694 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | MMFRD others(689): Show |
chr19 | 39337421 | 39390700 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2082 | 222 | 73 | 38 | 81 | 10 | 18 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ATGAT others(2077): Show |
chr19 | 39337421 | 39390700 | ||
| a0001c0002 | 0/0 | 2082 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ATGAT others(2077): Show |
chr19 | 39337421 | 39390700 | ||
| a0001c0004 | 0/0 | 2082 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ATGAT others(2077): Show |
chr19 | 39337421 | 39390700 | ||
| a0001c0005 | 0/0 | 2082 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ATGAT others(2077): Show |
chr19 | 39337421 | 39390700 | ||
| a0001c0006 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ATGAT others(2077): Show |
chr19 | 39337421 | 39390700 | ||
| a0002c0003 | 0/0 | 2082 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ATGAT others(2077): Show |
chr19 | 39337421 | 39390700 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4680 | 98 | 7 | 25 | 44 | 8 | 13 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0002 | 0/0 | 4680 | 78 | 41 | 6 | 27 | 2 | 2 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0003 | 0/0 | 4680 | 16 | 14 | 2 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0004 | 0/0 | 4680 | 5 | 0 | 0 | 4 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0005 | 0/0 | 4680 | 4 | 4 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0008 | 0/0 | 4680 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0009 | 0/0 | 4681 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4676): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0010 | 0/0 | 4680 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0011 | 1/0 | 4680 | 2 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0012 | 0/0 | 4681 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4676): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0013 | 0/0 | 4680 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0014 | 0/0 | 4683 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4678): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0015 | 0/0 | 4683 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4678): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0016 | 0/0 | 4680 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0017 | 0/0 | 4680 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0018 | 0/0 | 4680 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0019 | 0/0 | 4680 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0020 | 0/0 | 4680 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0021 | 0/0 | 4680 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0001t0022 | 0/0 | 4680 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0002t0006 | 0/0 | 4680 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0004t0002 | 0/0 | 4680 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0005t0007 | 0/0 | 4680 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0001c0006t0001 | 0/0 | 4680 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| a0002c0003t0001 | 0/0 | 4680 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD4B_chr19_39337421_39390700 | SAMD4B | ACGGC others(4675): Show |
chr19 | 39337421 | 39390700 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 1 | 2 | 7 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 2 | 2 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0012 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0009g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0010g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0011g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0011g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0013g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0014g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0015g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0016g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0017g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0018g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0019g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0020g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0021g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0001t0022g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0002t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0002t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0002t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0004t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0004t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0005t0007g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0001c0006t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| a0002c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | GBR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00140 | hp2 | a0001 | c0005 | t0007 | g0029 | EUR | GBR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00558 | hp1 | a0001 | c0001 | t0015 | g0071 | EAS | CHS | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01070 | hp1 | a0001 | c0001 | t0017 | g0145 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01109 | hp2 | a0001 | c0001 | t0020 | g0006 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01192 | hp2 | a0001 | c0001 | t0010 | g0019 | AMR | PUR | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01255 | hp1 | a0001 | c0001 | t0011 | g0054 | AMR | CLM | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01496 | hp2 | a0001 | c0001 | t0010 | g0019 | AMR | CLM | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0048 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | KHV | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02165 | hp2 | a0001 | c0006 | t0001 | g0061 | EAS | CDX | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02818 | hp2 | a0001 | c0002 | t0006 | g0153 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0133 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0146 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03195 | hp2 | a0001 | c0002 | t0006 | g0120 | AFR | ESN | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03486 | hp1 | a0001 | c0004 | t0002 | g0100 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03540 | hp1 | a0001 | c0002 | t0006 | g0152 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0139 | SAS | STU | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03710 | hp1 | a0001 | c0001 | t0021 | g0038 | SAS | PJL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03834 | hp2 | a0002 | c0003 | t0001 | g0013 | SAS | BEB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | BEB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG04115 | hp2 | a0001 | c0001 | t0016 | g0123 | SAS | STU | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0013 | SAS | BEB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0025 | AFR | YRI | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | CHB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18956 | hp1 | a0001 | c0001 | t0009 | g0017 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18993 | hp1 | a0001 | c0001 | t0013 | g0009 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19009 | hp1 | a0001 | c0001 | t0009 | g0099 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19030 | hp1 | a0001 | c0001 | t0022 | g0104 | AFR | LWK | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0032 | AFR | LWK | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | LWK | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | LWK | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19087 | hp1 | a0001 | c0001 | t0019 | g0073 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0025 | AFR | YRI | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0101 | AFR | YRI | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | TSI | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA20805 | hp1 | a0001 | c0005 | t0007 | g0029 | EUR | TSI | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | CLM | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | MSL | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | USA | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18955 | hp1 | a0001 | c0001 | t0013 | g0009 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | LWK | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| NA21309 | hp2 | a0001 | c0001 | t0018 | g0121 | AFR | LWK | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0012 | REF | REF | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0011 | g0014 | REF | REF | SAMD4B_chr19_39337421_39390700 | SAMD4B | chr19 | 39337421 | 39390700 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:39377629 | G | A | 1 | a0002 | 2 | HG03834.hp2 HG04184.hp1 |
missense_variant | MODERATE | c.1249G>A | p.Glu417Lys | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 8/14 | 1671/4680 | 1249/2085 | 417/694 | chr19 | 39377629 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:39369659 | C | T | 1 | a0001c0005 | 2 | HG00140.hp2 NA20805.hp1 |
synonymous_variant | LOW | c.201C>T | p.Ile67Ile | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/14 | 623/4680 | 201/2085 | 67/694 | chr19 | 39369659 | |||
| chr19:39375735 | G | A | 1 | a0001c0002 | 3 | HG02818.hp2 HG03195.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.753G>A | p.Pro251Pro | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 5/14 | 1175/4680 | 753/2085 | 251/694 | chr19 | 39375735 | |||
| chr19:39376710 | C | T | 1 | a0001c0004 | 2 | HG03486.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1023C>T | p.Val341Val | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 7/14 | 1445/4680 | 1023/2085 | 341/694 | chr19 | 39376710 | |||
| chr19:39381082 | G | A | 1 | a0001c0006 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.1941G>A | p.Ser647Ser | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/14 | 2363/4680 | 1941/2085 | 647/694 | chr19 | 39381082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:39342442 | A | ACGG | 2 | a0001c0001t0014 a0001c0001t0015 |
2 | HG00558.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-379_-377dupCGG | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/14 | 14427 | INFO_REALIGN_3_PRIME | chr19 | 39342442 | |||||
| chr19:39342449 | C | T | 1 | a0001c0001t0013 | 2 | NA18955.hp1 NA18993.hp1 |
5_prime_UTR_variant | MODIFIER | c.-394C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/14 | 14445 | chr19 | 39342449 | ||||||
| chr19:39342550 | G | A | 1 | a0001c0005t0007 | 2 | HG00140.hp2 NA20805.hp1 |
5_prime_UTR_variant | MODIFIER | c.-293G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/14 | 14344 | chr19 | 39342550 | ||||||
| chr19:39356694 | T | C | 2 | a0001c0001t0008 a0001c0001t0014 |
3 | HG02970.hp1 NA18522.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-200T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/14 | 200 | chr19 | 39356694 | ||||||
| chr19:39383948 | C | T | 2 | a0001c0001t0003 a0001c0001t0022 |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*421C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 421 | chr19 | 39383948 | ||||||
| chr19:39384305 | T | C | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(13): Show |
123 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*778T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 778 | chr19 | 39384305 | ||||||
| chr19:39384407 | C | T | 1 | a0001c0001t0021 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*880C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 880 | chr19 | 39384407 | ||||||
| chr19:39384422 | G | A | 1 | a0001c0001t0016 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*895G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 895 | chr19 | 39384422 | ||||||
| chr19:39384439 | C | G | 1 | a0001c0002t0006 | 3 | HG02818.hp2 HG03195.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*912C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 912 | chr19 | 39384439 | ||||||
| chr19:39384546 | C | T | 1 | a0001c0001t0020 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1019C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 1019 | chr19 | 39384546 | ||||||
| chr19:39384719 | G | T | 1 | a0001c0001t0018 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1192G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 1192 | chr19 | 39384719 | ||||||
| chr19:39384911 | A | AC | 2 | a0001c0001t0009 a0001c0001t0012 |
4 | HG02055.hp2 NA18956.hp1 NA19009.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1385dupC | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 1386 | INFO_REALIGN_3_PRIME | chr19 | 39384911 | |||||
| chr19:39384911 | A | C | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(19): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*1384A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 1384 | chr19 | 39384911 | ||||||
| chr19:39385046 | G | A | 1 | a0001c0001t0017 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1519G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 1519 | chr19 | 39385046 | ||||||
| chr19:39385373 | A | C | 1 | a0001c0001t0010 | 2 | HG01192.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1846A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 1846 | chr19 | 39385373 | ||||||
| chr19:39385375 | T | A | 1 | a0001c0001t0022 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1848T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 1848 | chr19 | 39385375 | ||||||
| chr19:39385565 | G | A | 1 | a0001c0001t0005 | 4 | HG02723.hp1 HG02886.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2038G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 2038 | chr19 | 39385565 | ||||||
| chr19:39385684 | C | A | 1 | a0001c0001t0001 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2157C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 2157 | chr19 | 39385684 | ||||||
| chr19:39385688 | C | A | 2 | a0001c0001t0004 a0001c0001t0019 |
6 | HG02056.hp2 HG03688.hp1 NA18612.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2161C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 14/14 | 2161 | chr19 | 39385688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:39342613 | A | G | 95 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0002g0002 others(92): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-267+37A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39342613 | |||||||
| chr19:39342778 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-267+202C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39342778 | |||||||
| chr19:39342820 | C | G | 1 | a0001c0001t0002g0171 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-267+244C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39342820 | |||||||
| chr19:39342878 | C | T | 12 | a0001c0001t0002g0030 a0001c0001t0002g0160 a0001c0001t0002g0161 others(9): Show |
13 | HG02145.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-267+302C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39342878 | |||||||
| chr19:39342966 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-267+390C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39342966 | |||||||
| chr19:39343003 | A | C | 1 | a0001c0001t0001g0095 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-267+427A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343003 | |||||||
| chr19:39343013 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG01975.hp1 HG02293.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-267+437C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343013 | |||||||
| chr19:39343022 | C | T | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-267+446C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343022 | |||||||
| chr19:39343364 | T | A | 2 | a0001c0001t0002g0098 a0001c0001t0009g0099 |
2 | NA19009.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-267+788T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343364 | |||||||
| chr19:39343367 | T | C | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-267+791T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343367 | |||||||
| chr19:39343491 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-267+915A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343491 | |||||||
| chr19:39343521 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-267+945C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343521 | |||||||
| chr19:39343556 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-267+980C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343556 | |||||||
| chr19:39343733 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0102 a0001c0001t0010g0019 |
5 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-267+1157T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343733 | |||||||
| chr19:39343784 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0009g0017 |
2 | NA18956.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-267+1208C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343784 | |||||||
| chr19:39343843 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-267+1267C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343843 | |||||||
| chr19:39343958 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-267+1382C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343958 | |||||||
| chr19:39343982 | A | AC | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(20): Show |
37 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.-267+1418dupC | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 39343982 | ||||||
| chr19:39343982 | A | ACC | 14 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG00741.hp2 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-267+1417_-267+141 others(6): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 39343982 | ||||||
| chr19:39343982 | AC | A | 20 | a0001c0001t0002g0022 a0001c0001t0002g0111 a0001c0001t0002g0113 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.-267+1418delC | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 39343982 | ||||||
| chr19:39343989 | C | CA | 3 | a0001c0001t0002g0103 a0001c0001t0002g0160 a0001c0001t0002g0161 |
3 | HG02896.hp1 HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-267+1413_-267+141 others(5): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343989 | |||||||
| chr19:39343990 | C | A | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-267+1414C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343990 | |||||||
| chr19:39343991 | C | A | 6 | a0001c0001t0002g0103 a0001c0001t0002g0160 a0001c0001t0002g0161 others(3): Show |
8 | HG00140.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-267+1415C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343991 | |||||||
| chr19:39343991 | C | CA | 15 | a0001c0001t0001g0031 a0001c0001t0002g0002 a0001c0001t0002g0021 others(12): Show |
24 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-267+1415_-267+141 others(5): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343991 | |||||||
| chr19:39343991 | C | CACA | 2 | a0001c0001t0002g0018 a0001c0001t0002g0102 |
3 | HG00733.hp2 HG01433.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-267+1415_-267+141 others(7): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343991 | |||||||
| chr19:39343993 | C | A | 52 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0002g0002 others(49): Show |
69 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.-267+1417C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343993 | |||||||
| chr19:39343993 | C | CA | 32 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(29): Show |
36 | HG00323.hp1 HG00323.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.-267+1417_-267+141 others(5): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343993 | |||||||
| chr19:39343993 | C | CCA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0049 others(17): Show |
27 | HG00408.hp2 HG00544.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.-267+1430_-267+143 others(6): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 39343993 | ||||||
| chr19:39343995 | A | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0002g0085 others(1): Show |
4 | HG03041.hp1 NA18941.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.-267+1419A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39343995 | |||||||
| chr19:39344479 | C | T | 1 | a0001c0001t0003g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-267+1903C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39344479 | |||||||
| chr19:39344529 | G | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(23): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.-267+1953G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39344529 | |||||||
| chr19:39344744 | T | C | 1 | a0001c0001t0003g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-267+2168T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39344744 | |||||||
| chr19:39344817 | A | G | 1 | a0001c0001t0002g0109 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-267+2241A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39344817 | |||||||
| chr19:39344858 | A | G | 96 | a0001c0001t0001g0066 a0001c0001t0002g0002 a0001c0001t0002g0008 others(93): Show |
121 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.-267+2282A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39344858 | |||||||
| chr19:39344931 | C | T | 3 | a0001c0001t0002g0151 a0001c0001t0002g0156 a0001c0001t0002g0170 |
3 | HG02145.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-267+2355C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39344931 | |||||||
| chr19:39345158 | C | G | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.-267+2582C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39345158 | |||||||
| chr19:39345424 | C | A | 3 | a0001c0001t0002g0151 a0001c0001t0002g0156 a0001c0001t0002g0170 |
3 | HG02145.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-267+2848C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39345424 | |||||||
| chr19:39346065 | T | C | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(21): Show |
37 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.-267+3489T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39346065 | |||||||
| chr19:39346160 | A | G | 13 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(10): Show |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-267+3584A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39346160 | |||||||
| chr19:39346208 | T | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0087 |
2 | NA18941.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-267+3632T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39346208 | |||||||
| chr19:39346220 | A | G | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-267+3644A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39346220 | |||||||
| chr19:39346387 | G | C | 1 | a0001c0001t0002g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-267+3811G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39346387 | |||||||
| chr19:39346608 | C | T | 1 | a0001c0001t0003g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-267+4032C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39346608 | |||||||
| chr19:39346700 | A | G | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0147 others(1): Show |
4 | HG02055.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-267+4124A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39346700 | |||||||
| chr19:39346927 | A | T | 14 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(11): Show |
15 | HG01070.hp2 HG02056.hp2 HG02970.hp1 others(12): Show |
intron_variant | MODIFIER | c.-267+4351A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39346927 | |||||||
| chr19:39347039 | T | G | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-267+4463T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39347039 | |||||||
| chr19:39347199 | A | G | 2 | a0001c0001t0002g0113 a0001c0001t0002g0135 |
2 | HG01070.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-267+4623A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39347199 | |||||||
| chr19:39347278 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-267+4702G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39347278 | |||||||
| chr19:39347285 | A | C | 1 | a0001c0001t0003g0007 | 3 | HG02630.hp2 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-267+4709A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39347285 | |||||||
| chr19:39347468 | C | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0102 a0001c0001t0010g0019 |
5 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-267+4892C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39347468 | |||||||
| chr19:39347504 | C | G | 1 | a0001c0001t0002g0137 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-267+4928C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39347504 | |||||||
| chr19:39347592 | C | G | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-267+5016C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39347592 | |||||||
| chr19:39348127 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-267+5551C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39348127 | |||||||
| chr19:39348234 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-267+5658A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39348234 | |||||||
| chr19:39348242 | A | G | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-267+5666A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39348242 | |||||||
| chr19:39348314 | C | G | 19 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(16): Show |
20 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-266-5692C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39348314 | |||||||
| chr19:39348384 | G | T | 8 | a0001c0001t0002g0022 a0001c0001t0002g0113 a0001c0001t0002g0135 others(5): Show |
9 | HG01070.hp2 HG02056.hp2 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.-266-5622G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39348384 | |||||||
| chr19:39348555 | A | G | 15 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(12): Show |
16 | HG01070.hp2 HG02056.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.-266-5451A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39348555 | |||||||
| chr19:39348763 | A | G | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-266-5243A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39348763 | |||||||
| chr19:39348830 | A | T | 1 | a0001c0001t0002g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-266-5176A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39348830 | |||||||
| chr19:39348847 | G | T | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-266-5159G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39348847 | |||||||
| chr19:39349206 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-266-4800G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39349206 | |||||||
| chr19:39349366 | T | G | 1 | a0001c0001t0003g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-266-4640T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39349366 | |||||||
| chr19:39349386 | C | T | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-266-4620C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39349386 | |||||||
| chr19:39349402 | T | C | 1 | a0001c0001t0002g0137 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-266-4604T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39349402 | |||||||
| chr19:39349535 | A | G | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-266-4471A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39349535 | |||||||
| chr19:39349584 | TATAAG | T | 4 | a0001c0001t0001g0095 a0001c0001t0002g0018 a0001c0001t0002g0102 others(1): Show |
6 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-266-4420_-266-441 others(9): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 39349584 | ||||||
| chr19:39349909 | C | G | 95 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
120 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.-266-4097C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39349909 | |||||||
| chr19:39349976 | T | G | 1 | a0001c0001t0002g0128 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-266-4030T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39349976 | |||||||
| chr19:39349979 | A | G | 56 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(53): Show |
74 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-266-4027A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39349979 | |||||||
| chr19:39350061 | T | A | 95 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
120 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.-266-3945T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39350061 | |||||||
| chr19:39350214 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-266-3792C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39350214 | |||||||
| chr19:39350582 | G | A | 2 | a0001c0001t0002g0086 a0001c0001t0002g0122 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-266-3424G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39350582 | |||||||
| chr19:39350735 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-266-3271C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39350735 | |||||||
| chr19:39350838 | G | C | 1 | a0001c0001t0002g0137 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-266-3168G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39350838 | |||||||
| chr19:39350898 | G | A | 3 | a0001c0001t0002g0111 a0001c0001t0002g0128 a0001c0001t0002g0134 |
3 | HG02896.hp2 HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-266-3108G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39350898 | |||||||
| chr19:39350914 | G | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.-266-3092G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39350914 | |||||||
| chr19:39351093 | C | T | 13 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(10): Show |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-266-2913C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39351093 | |||||||
| chr19:39351145 | C | CTAATTTT others(4): Show |
1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-266-2852_-266-284 others(15): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 39351145 | ||||||
| chr19:39351220 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0102 a0001c0001t0010g0019 |
5 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-266-2786G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39351220 | |||||||
| chr19:39351253 | G | T | 1 | a0001c0001t0016g0123 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-266-2753G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39351253 | |||||||
| chr19:39351402 | C | T | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-266-2604C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39351402 | |||||||
| chr19:39351570 | G | A | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-266-2436G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39351570 | |||||||
| chr19:39351692 | T | C | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-266-2314T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39351692 | |||||||
| chr19:39351756 | G | A | 7 | a0001c0001t0002g0010 a0001c0001t0002g0026 a0001c0001t0002g0027 others(4): Show |
11 | HG00099.hp2 HG01070.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.-266-2250G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39351756 | |||||||
| chr19:39351845 | A | G | 1 | a0001c0001t0005g0164 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-266-2161A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39351845 | |||||||
| chr19:39352211 | G | A | 3 | a0001c0002t0006g0120 a0001c0002t0006g0152 a0001c0002t0006g0153 |
3 | HG02818.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-266-1795G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352211 | |||||||
| chr19:39352489 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-266-1517G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352489 | |||||||
| chr19:39352489 | G | GAA | 17 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(14): Show |
27 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.-266-1499_-266-149 others(6): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 39352489 | ||||||
| chr19:39352489 | GA | G | 22 | a0001c0001t0001g0052 a0001c0001t0001g0089 a0001c0001t0001g0090 others(19): Show |
29 | HG00140.hp2 HG00733.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.-266-1498delA | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 39352489 | ||||||
| chr19:39352505 | A | AC | 2 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-266-1501_-266-150 others(5): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352505 | |||||||
| chr19:39352505 | A | C | 1 | a0001c0001t0002g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-266-1501A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352505 | |||||||
| chr19:39352591 | G | A | 3 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0147 |
3 | HG02055.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-266-1415G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352591 | |||||||
| chr19:39352645 | C | G | 13 | a0001c0001t0002g0010 a0001c0001t0002g0026 a0001c0001t0002g0027 others(10): Show |
18 | HG00099.hp2 HG01070.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-266-1361C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352645 | |||||||
| chr19:39352684 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-266-1322C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352684 | |||||||
| chr19:39352685 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-266-1321G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352685 | |||||||
| chr19:39352700 | A | G | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-266-1306A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352700 | |||||||
| chr19:39352913 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0150 others(2): Show |
8 | HG00544.hp2 HG00621.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.-266-1093C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352913 | |||||||
| chr19:39352983 | G | A | 95 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
120 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.-266-1023G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39352983 | |||||||
| chr19:39353006 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-266-1000C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353006 | |||||||
| chr19:39353022 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-266-984A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353022 | |||||||
| chr19:39353048 | A | G | 1 | a0001c0001t0015g0071 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-266-958A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353048 | |||||||
| chr19:39353338 | A | C | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-266-668A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353338 | |||||||
| chr19:39353468 | A | G | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.-266-538A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353468 | |||||||
| chr19:39353536 | G | A | 95 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
120 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.-266-470G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353536 | |||||||
| chr19:39353552 | C | T | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-266-454C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353552 | |||||||
| chr19:39353783 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-266-223G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353783 | |||||||
| chr19:39353884 | G | A | 3 | a0001c0001t0002g0111 a0001c0001t0002g0128 a0001c0001t0002g0134 |
3 | HG02896.hp2 HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-266-122G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353884 | |||||||
| chr19:39353894 | A | G | 56 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(53): Show |
74 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-266-112A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353894 | |||||||
| chr19:39353909 | G | C | 15 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(12): Show |
16 | HG01070.hp2 HG02056.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.-266-97G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353909 | |||||||
| chr19:39353927 | C | T | 56 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(53): Show |
74 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-266-79C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353927 | |||||||
| chr19:39353946 | G | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.-266-60G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 1/13 | chr19 | 39353946 | |||||||
| chr19:39354370 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-206+304G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39354370 | |||||||
| chr19:39354472 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-206+406G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39354472 | |||||||
| chr19:39354496 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-206+430A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39354496 | |||||||
| chr19:39354605 | C | CAT | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
191 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-206+540_-206+541i others(4): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 39354605 | ||||||
| chr19:39354683 | G | A | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-206+617G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39354683 | |||||||
| chr19:39354904 | T | G | 95 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
120 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.-206+838T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39354904 | |||||||
| chr19:39354910 | T | G | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-206+844T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39354910 | |||||||
| chr19:39355034 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-206+968G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355034 | |||||||
| chr19:39355095 | ACTC | A | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-206+1032_-206+103 others(7): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 39355095 | ||||||
| chr19:39355198 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-206+1132T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355198 | |||||||
| chr19:39355207 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-206+1141A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355207 | |||||||
| chr19:39355413 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-205-1276C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355413 | |||||||
| chr19:39355575 | G | A | 4 | a0001c0001t0003g0110 a0001c0001t0003g0114 a0001c0001t0003g0115 others(1): Show |
4 | HG02615.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205-1114G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355575 | |||||||
| chr19:39355608 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0096 |
2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-205-1081G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355608 | |||||||
| chr19:39355658 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-205-1031A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355658 | |||||||
| chr19:39355668 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-205-1021G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355668 | |||||||
| chr19:39355688 | A | G | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(20): Show |
35 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.-205-1001A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355688 | |||||||
| chr19:39355782 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-205-907A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355782 | |||||||
| chr19:39355821 | G | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0102 a0001c0001t0010g0019 |
5 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205-868G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355821 | |||||||
| chr19:39355902 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-205-787T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39355902 | |||||||
| chr19:39356030 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-205-659C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356030 | |||||||
| chr19:39356054 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-205-635A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356054 | |||||||
| chr19:39356167 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-205-522A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356167 | |||||||
| chr19:39356168 | C | A | 1 | a0001c0001t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-205-521C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356168 | |||||||
| chr19:39356315 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-205-374G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356315 | |||||||
| chr19:39356322 | C | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(20): Show |
35 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.-205-367C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356322 | |||||||
| chr19:39356411 | C | T | 14 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(11): Show |
15 | HG01070.hp2 HG02056.hp2 HG02970.hp1 others(12): Show |
intron_variant | MODIFIER | c.-205-278C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356411 | |||||||
| chr19:39356412 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-205-277G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356412 | |||||||
| chr19:39356451 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-205-238C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356451 | |||||||
| chr19:39356458 | T | C | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-205-231T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356458 | |||||||
| chr19:39356492 | C | T | 13 | a0001c0001t0002g0010 a0001c0001t0002g0026 a0001c0001t0002g0027 others(10): Show |
18 | HG00099.hp2 HG01070.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-205-197C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356492 | |||||||
| chr19:39356573 | G | A | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-205-116G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 2/13 | chr19 | 39356573 | |||||||
| chr19:39357576 | C | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(20): Show |
35 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.196+487C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39357576 | |||||||
| chr19:39357786 | A | T | 15 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(12): Show |
16 | HG01070.hp2 HG02056.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.196+697A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39357786 | |||||||
| chr19:39357848 | C | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.196+759C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39357848 | |||||||
| chr19:39357901 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.196+812C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39357901 | |||||||
| chr19:39358069 | G | A | 7 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(4): Show |
11 | HG01123.hp2 HG02630.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+980G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358069 | |||||||
| chr19:39358102 | G | C | 56 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(53): Show |
74 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.196+1013G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358102 | |||||||
| chr19:39358203 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.196+1114G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358203 | |||||||
| chr19:39358393 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.196+1304T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358393 | |||||||
| chr19:39358393 | T | G | 1 | a0001c0001t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.196+1304T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358393 | |||||||
| chr19:39358400 | C | T | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.196+1311C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358400 | |||||||
| chr19:39358405 | C | T | 32 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(29): Show |
37 | HG01070.hp2 HG01109.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.196+1316C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358405 | |||||||
| chr19:39358519 | G | A | 32 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(29): Show |
37 | HG01070.hp2 HG01109.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.196+1430G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358519 | |||||||
| chr19:39358540 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.196+1451G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358540 | |||||||
| chr19:39358602 | T | TA | 13 | a0001c0001t0002g0010 a0001c0001t0002g0026 a0001c0001t0002g0027 others(10): Show |
18 | HG00099.hp2 HG01070.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.196+1526dupA | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 39358602 | ||||||
| chr19:39358692 | G | A | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(21): Show |
37 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.196+1603G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358692 | |||||||
| chr19:39358781 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.196+1692G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39358781 | |||||||
| chr19:39359118 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.196+2029T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39359118 | |||||||
| chr19:39359149 | A | G | 95 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
120 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.196+2060A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39359149 | |||||||
| chr19:39359182 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.196+2093G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39359182 | |||||||
| chr19:39359315 | C | T | 56 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(53): Show |
74 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.196+2226C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39359315 | |||||||
| chr19:39359462 | T | C | 98 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(95): Show |
123 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.196+2373T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39359462 | |||||||
| chr19:39359741 | C | G | 1 | a0001c0001t0002g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196+2652C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39359741 | |||||||
| chr19:39359744 | T | G | 1 | a0001c0006t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.196+2655T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39359744 | |||||||
| chr19:39359879 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.196+2790A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39359879 | |||||||
| chr19:39359913 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0083 |
2 | HG02080.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.196+2824C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39359913 | |||||||
| chr19:39360192 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.196+3103A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360192 | |||||||
| chr19:39360193 | A | T | 1 | a0001c0001t0021g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.196+3104A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360193 | |||||||
| chr19:39360194 | A | T | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.196+3105A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360194 | |||||||
| chr19:39360195 | A | T | 1 | a0001c0006t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.196+3106A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360195 | |||||||
| chr19:39360196 | A | T | 55 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(52): Show |
73 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.196+3107A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360196 | |||||||
| chr19:39360199 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196+3110T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360199 | |||||||
| chr19:39360245 | A | G | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.196+3156A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360245 | |||||||
| chr19:39360289 | A | G | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.196+3200A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360289 | |||||||
| chr19:39360342 | G | A | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(21): Show |
37 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.196+3253G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360342 | |||||||
| chr19:39360505 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.196+3416G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360505 | |||||||
| chr19:39360871 | G | A | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.196+3782G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360871 | |||||||
| chr19:39360897 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.196+3808C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360897 | |||||||
| chr19:39360907 | C | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(20): Show |
35 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.196+3818C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39360907 | |||||||
| chr19:39361346 | A | G | 13 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(10): Show |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.196+4257A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361346 | |||||||
| chr19:39361355 | A | G | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(21): Show |
37 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.196+4266A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361355 | |||||||
| chr19:39361392 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0102 a0001c0001t0010g0019 |
5 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+4303G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361392 | |||||||
| chr19:39361477 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.196+4388G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361477 | |||||||
| chr19:39361493 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.196+4404G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361493 | |||||||
| chr19:39361641 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.196+4552C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361641 | |||||||
| chr19:39361646 | G | A | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.196+4557G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361646 | |||||||
| chr19:39361706 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.196+4617G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361706 | |||||||
| chr19:39361781 | G | C | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.196+4692G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361781 | |||||||
| chr19:39361841 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0144 |
2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.196+4752G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361841 | |||||||
| chr19:39361922 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0012g0032 |
2 | HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.196+4833G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361922 | |||||||
| chr19:39361923 | T | C | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | NA18945.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.196+4834T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39361923 | |||||||
| chr19:39362214 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.196+5125A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39362214 | |||||||
| chr19:39362346 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.196+5257T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39362346 | |||||||
| chr19:39362535 | T | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.196+5446T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39362535 | |||||||
| chr19:39362887 | T | C | 11 | a0001c0001t0002g0010 a0001c0001t0002g0026 a0001c0001t0002g0027 others(8): Show |
15 | HG00099.hp2 HG01070.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.196+5798T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39362887 | |||||||
| chr19:39363020 | G | C | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(20): Show |
35 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.196+5931G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39363020 | |||||||
| chr19:39363039 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.196+5950C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39363039 | |||||||
| chr19:39363057 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.196+5968G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39363057 | |||||||
| chr19:39363126 | C | A | 1 | a0001c0001t0004g0112 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.196+6037C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39363126 | |||||||
| chr19:39363248 | A | C | 1 | a0001c0001t0002g0137 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.196+6159A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39363248 | |||||||
| chr19:39363298 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0115 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.196+6209G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39363298 | |||||||
| chr19:39363369 | A | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(20): Show |
35 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.196+6280A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39363369 | |||||||
| chr19:39363701 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.197-5954A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39363701 | |||||||
| chr19:39363702 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.197-5953T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39363702 | |||||||
| chr19:39363853 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.197-5802C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39363853 | |||||||
| chr19:39364309 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.197-5346A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39364309 | |||||||
| chr19:39364502 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.197-5153A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39364502 | |||||||
| chr19:39364567 | T | A | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.197-5088T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39364567 | |||||||
| chr19:39364568 | T | A | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.197-5087T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39364568 | |||||||
| chr19:39364817 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197-4838A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39364817 | |||||||
| chr19:39365083 | C | CA | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.197-4563dupA | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 39365083 | ||||||
| chr19:39365097 | T | G | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.197-4558T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365097 | |||||||
| chr19:39365103 | G | A | 1 | a0002c0003t0001g0013 | 2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.197-4552G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365103 | |||||||
| chr19:39365105 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.197-4550G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365105 | |||||||
| chr19:39365242 | T | TA | 9 | a0001c0001t0001g0050 a0001c0001t0001g0069 a0001c0001t0001g0074 others(6): Show |
9 | HG01516.hp2 HG02818.hp2 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.197-4393dupA | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 39365242 | ||||||
| chr19:39365242 | TA | T | 33 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(30): Show |
47 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.197-4393delA | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 39365242 | ||||||
| chr19:39365243 | A | T | 1 | a0001c0001t0002g0128 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.197-4412A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365243 | |||||||
| chr19:39365426 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0002g0022 a0001c0001t0004g0022 others(3): Show |
7 | HG01069.hp2 HG02056.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-4229C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365426 | |||||||
| chr19:39365428 | C | T | 7 | a0001c0001t0002g0010 a0001c0001t0002g0026 a0001c0001t0002g0027 others(4): Show |
11 | HG00099.hp2 HG01070.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-4227C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365428 | |||||||
| chr19:39365606 | C | T | 13 | a0001c0001t0002g0010 a0001c0001t0002g0026 a0001c0001t0002g0027 others(10): Show |
18 | HG00099.hp2 HG01070.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.197-4049C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365606 | |||||||
| chr19:39365702 | G | A | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.197-3953G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365702 | |||||||
| chr19:39365939 | G | T | 3 | a0001c0002t0006g0120 a0001c0002t0006g0152 a0001c0002t0006g0153 |
3 | HG02818.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.197-3716G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365939 | |||||||
| chr19:39365977 | A | C | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.197-3678A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365977 | |||||||
| chr19:39365978 | G | A | 56 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(53): Show |
74 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.197-3677G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39365978 | |||||||
| chr19:39366270 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.197-3385C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39366270 | |||||||
| chr19:39366309 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0096 |
3 | HG00323.hp1 HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.197-3346C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39366309 | |||||||
| chr19:39366313 | C | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0102 a0001c0001t0010g0019 |
5 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-3342C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39366313 | |||||||
| chr19:39366401 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.197-3254C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39366401 | |||||||
| chr19:39366505 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.197-3150C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39366505 | |||||||
| chr19:39366555 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.197-3100A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39366555 | |||||||
| chr19:39366702 | G | T | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.197-2953G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39366702 | |||||||
| chr19:39366778 | A | G | 24 | a0001c0001t0001g0036 a0001c0001t0002g0002 a0001c0001t0002g0008 others(21): Show |
36 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.197-2877A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39366778 | |||||||
| chr19:39366974 | A | T | 1 | a0001c0001t0018g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.197-2681A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39366974 | |||||||
| chr19:39367490 | G | GT | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(21): Show |
37 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.197-2155dupT | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 39367490 | ||||||
| chr19:39367507 | CT | C | 89 | a0001c0001t0001g0046 a0001c0001t0001g0084 a0001c0001t0002g0002 others(86): Show |
113 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.197-2128delT | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 39367507 | ||||||
| chr19:39367533 | G | A | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.197-2122G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39367533 | |||||||
| chr19:39367714 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.197-1941G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39367714 | |||||||
| chr19:39367794 | C | T | 2 | a0001c0001t0002g0163 a0001c0001t0002g0168 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.197-1861C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39367794 | |||||||
| chr19:39367800 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.197-1855C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39367800 | |||||||
| chr19:39367865 | C | G | 14 | a0001c0001t0002g0021 a0001c0001t0002g0030 a0001c0001t0002g0105 others(11): Show |
16 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.197-1790C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39367865 | |||||||
| chr19:39367913 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.197-1742G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39367913 | |||||||
| chr19:39367986 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.197-1669G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39367986 | |||||||
| chr19:39368030 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.197-1625C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368030 | |||||||
| chr19:39368066 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.197-1589A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368066 | |||||||
| chr19:39368070 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.197-1585T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368070 | |||||||
| chr19:39368071 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.197-1584G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368071 | |||||||
| chr19:39368075 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0102 a0001c0001t0010g0019 |
5 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-1580G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368075 | |||||||
| chr19:39368114 | T | A | 1 | a0001c0001t0001g0062 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.197-1541T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368114 | |||||||
| chr19:39368201 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197-1454G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368201 | |||||||
| chr19:39368477 | G | A | 1 | a0001c0004t0002g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.197-1178G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368477 | |||||||
| chr19:39368552 | G | C | 1 | a0001c0001t0001g0062 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.197-1103G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368552 | |||||||
| chr19:39368553 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.197-1102C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368553 | |||||||
| chr19:39368671 | C | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0102 a0001c0001t0010g0019 |
5 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-984C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368671 | |||||||
| chr19:39368913 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.197-742C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39368913 | |||||||
| chr19:39369029 | G | A | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.197-626G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39369029 | |||||||
| chr19:39369173 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.197-482G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39369173 | |||||||
| chr19:39369184 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.197-471T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39369184 | |||||||
| chr19:39369328 | G | A | 13 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(10): Show |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.197-327G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39369328 | |||||||
| chr19:39369371 | G | A | 3 | a0001c0001t0008g0025 a0001c0001t0008g0146 a0001c0001t0014g0025 |
3 | HG02970.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.197-284G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39369371 | |||||||
| chr19:39369527 | AGTTATGA others(10): Show |
A | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.197-114_197-98delA others(16): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 39369527 | ||||||
| chr19:39369579 | C | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.197-76C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39369579 | |||||||
| chr19:39369608 | G | C | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.197-47G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 3/13 | chr19 | 39369608 | |||||||
| chr19:39370136 | G | T | 5 | a0001c0001t0002g0098 a0001c0001t0002g0136 a0001c0001t0002g0137 others(2): Show |
5 | HG00621.hp2 NA18970.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+11G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39370136 | |||||||
| chr19:39370215 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.667+90A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39370215 | |||||||
| chr19:39370366 | T | G | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0147 others(1): Show |
4 | HG02055.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+241T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39370366 | |||||||
| chr19:39370440 | C | G | 2 | a0001c0001t0002g0136 a0001c0001t0002g0159 |
2 | HG00621.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.667+315C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39370440 | |||||||
| chr19:39370507 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.667+382C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39370507 | |||||||
| chr19:39370674 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.667+549A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39370674 | |||||||
| chr19:39370689 | C | T | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0147 others(1): Show |
4 | HG02055.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+564C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39370689 | |||||||
| chr19:39370792 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.667+667T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39370792 | |||||||
| chr19:39370842 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.667+717G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39370842 | |||||||
| chr19:39370874 | T | C | 96 | a0001c0001t0001g0082 a0001c0001t0002g0002 a0001c0001t0002g0008 others(93): Show |
121 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.667+749T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39370874 | |||||||
| chr19:39371274 | G | A | 1 | a0001c0002t0006g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.667+1149G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39371274 | |||||||
| chr19:39371309 | T | G | 14 | a0001c0001t0002g0030 a0001c0001t0002g0107 a0001c0001t0002g0111 others(11): Show |
15 | HG02145.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.667+1184T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39371309 | |||||||
| chr19:39371582 | C | T | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.667+1457C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39371582 | |||||||
| chr19:39371729 | G | A | 6 | a0001c0001t0002g0028 a0001c0001t0002g0131 a0001c0001t0002g0144 others(3): Show |
7 | HG02145.hp1 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.667+1604G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39371729 | |||||||
| chr19:39371766 | G | A | 5 | a0001c0001t0002g0098 a0001c0001t0002g0136 a0001c0001t0002g0137 others(2): Show |
5 | HG00621.hp2 NA18970.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+1641G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39371766 | |||||||
| chr19:39371816 | CA | C | 59 | a0001c0001t0001g0082 a0001c0001t0002g0018 a0001c0001t0002g0021 others(56): Show |
69 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.667+1704delA | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 39371816 | ||||||
| chr19:39372038 | T | G | 1 | a0001c0001t0002g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667+1913T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372038 | |||||||
| chr19:39372101 | A | G | 1 | a0001c0002t0006g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.667+1976A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372101 | |||||||
| chr19:39372225 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.667+2100C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372225 | |||||||
| chr19:39372241 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.667+2116C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372241 | |||||||
| chr19:39372274 | T | C | 3 | a0001c0001t0002g0111 a0001c0001t0002g0128 a0001c0001t0002g0134 |
3 | HG02896.hp2 HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.667+2149T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372274 | |||||||
| chr19:39372410 | C | T | 3 | a0001c0002t0006g0120 a0001c0002t0006g0152 a0001c0002t0006g0153 |
3 | HG02818.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.667+2285C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372410 | |||||||
| chr19:39372415 | C | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0102 a0001c0001t0010g0019 |
5 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+2290C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372415 | |||||||
| chr19:39372437 | C | G | 1 | a0001c0001t0001g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.667+2312C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372437 | |||||||
| chr19:39372570 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.667+2445C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372570 | |||||||
| chr19:39372687 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.667+2562G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372687 | |||||||
| chr19:39372803 | C | CA | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.667+2683dupA | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 39372803 | ||||||
| chr19:39372976 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.668-2674G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39372976 | |||||||
| chr19:39373051 | G | A | 3 | a0001c0001t0002g0151 a0001c0001t0002g0156 a0001c0001t0002g0170 |
3 | HG02145.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.668-2599G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373051 | |||||||
| chr19:39373176 | G | A | 8 | a0001c0001t0002g0022 a0001c0001t0002g0113 a0001c0001t0002g0135 others(5): Show |
9 | HG01070.hp2 HG02056.hp2 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.668-2474G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373176 | |||||||
| chr19:39373297 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0013g0009 |
3 | NA18955.hp1 NA18993.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.668-2353A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373297 | |||||||
| chr19:39373306 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.668-2344G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373306 | |||||||
| chr19:39373446 | TGCAAGAG others(24): Show |
T | 56 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(53): Show |
74 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.668-2170_668-2140d others(33): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 39373446 | ||||||
| chr19:39373511 | G | A | 1 | a0001c0006t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.668-2139G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373511 | |||||||
| chr19:39373533 | A | AG | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(20): Show |
35 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.668-2113dupG | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 39373533 | ||||||
| chr19:39373596 | G | A | 13 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(10): Show |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.668-2054G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373596 | |||||||
| chr19:39373648 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.668-2002C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373648 | |||||||
| chr19:39373724 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.668-1926G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373724 | |||||||
| chr19:39373737 | G | A | 15 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(12): Show |
16 | HG01070.hp2 HG02056.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.668-1913G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373737 | |||||||
| chr19:39373823 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.668-1827G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373823 | |||||||
| chr19:39373900 | G | A | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.668-1750G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373900 | |||||||
| chr19:39373971 | AT | A | 55 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(52): Show |
73 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.668-1678delT | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39373971 | |||||||
| chr19:39374139 | T | C | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(21): Show |
37 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.668-1511T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374139 | |||||||
| chr19:39374145 | C | T | 2 | a0001c0001t0002g0028 a0001c0001t0002g0154 |
3 | HG02257.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.668-1505C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374145 | |||||||
| chr19:39374186 | G | A | 1 | a0001c0001t0018g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668-1464G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374186 | |||||||
| chr19:39374186 | G | T | 1 | a0001c0001t0022g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.668-1464G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374186 | |||||||
| chr19:39374204 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.668-1446G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374204 | |||||||
| chr19:39374296 | A | G | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.668-1354A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374296 | |||||||
| chr19:39374372 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.668-1278C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374372 | |||||||
| chr19:39374431 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0102 a0001c0001t0010g0019 |
5 | HG00733.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.668-1219T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374431 | |||||||
| chr19:39374481 | T | A | 30 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(27): Show |
35 | HG01070.hp2 HG01109.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.668-1169T>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374481 | |||||||
| chr19:39374591 | C | T | 3 | a0001c0002t0006g0120 a0001c0002t0006g0152 a0001c0002t0006g0153 |
3 | HG02818.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.668-1059C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374591 | |||||||
| chr19:39374616 | C | T | 1 | a0001c0001t0005g0130 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.668-1034C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374616 | |||||||
| chr19:39374624 | G | A | 13 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(10): Show |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.668-1026G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374624 | |||||||
| chr19:39374733 | C | T | 1 | a0001c0001t0017g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.668-917C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374733 | |||||||
| chr19:39374760 | G | GAC | 3 | a0001c0001t0001g0046 a0001c0001t0001g0055 a0001c0001t0002g0085 |
3 | NA19063.hp2 NA19083.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.668-889_668-888ins others(2): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 39374760 | ||||||
| chr19:39374773 | A | G | 95 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
120 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.668-877A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374773 | |||||||
| chr19:39374805 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.668-845C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374805 | |||||||
| chr19:39374860 | A | T | 1 | a0001c0001t0001g0044 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.668-790A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39374860 | |||||||
| chr19:39375061 | A | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0105 |
3 | HG01891.hp1 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.668-589A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39375061 | |||||||
| chr19:39375096 | A | G | 15 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(12): Show |
16 | HG01070.hp2 HG02056.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.668-554A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39375096 | |||||||
| chr19:39375117 | A | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.668-533A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39375117 | |||||||
| chr19:39375329 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.668-321G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39375329 | |||||||
| chr19:39375424 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.668-226C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39375424 | |||||||
| chr19:39375590 | A | T | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.668-60A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39375590 | |||||||
| chr19:39375605 | T | G | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.668-45T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 4/13 | chr19 | 39375605 | |||||||
| chr19:39375900 | G | A | 15 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(12): Show |
16 | HG01070.hp2 HG02056.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.907+11G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 5/13 | chr19 | 39375900 | |||||||
| chr19:39376015 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.907+126G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 5/13 | chr19 | 39376015 | |||||||
| chr19:39376038 | A | G | 16 | a0001c0001t0002g0022 a0001c0001t0002g0086 a0001c0001t0002g0103 others(13): Show |
17 | HG01070.hp2 HG02056.hp2 HG02970.hp1 others(14): Show |
intron_variant | MODIFIER | c.907+149A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 5/13 | chr19 | 39376038 | |||||||
| chr19:39376081 | G | A | 13 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(10): Show |
23 | HG00544.hp2 HG00621.hp1 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.907+192G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 5/13 | chr19 | 39376081 | |||||||
| chr19:39376401 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.908-36A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 5/13 | chr19 | 39376401 | |||||||
| chr19:39376921 | C | A | 13 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(10): Show |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1104+130C>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 7/13 | chr19 | 39376921 | |||||||
| chr19:39377093 | T | G | 2 | a0001c0001t0001g0043 a0001c0001t0011g0054 |
2 | HG01255.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1104+302T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 7/13 | chr19 | 39377093 | |||||||
| chr19:39377273 | C | T | 13 | a0001c0001t0002g0030 a0001c0001t0002g0107 a0001c0001t0002g0140 others(10): Show |
14 | HG02145.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1105-212C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 7/13 | chr19 | 39377273 | |||||||
| chr19:39377950 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1444+126A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 8/13 | chr19 | 39377950 | |||||||
| chr19:39378041 | G | A | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(21): Show |
37 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1444+217G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 8/13 | chr19 | 39378041 | |||||||
| chr19:39378071 | G | GA | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1444+247_1444+248i others(3): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 8/13 | chr19 | 39378071 | |||||||
| chr19:39378072 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1444+248G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 8/13 | chr19 | 39378072 | |||||||
| chr19:39378091 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1444+267A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 8/13 | chr19 | 39378091 | |||||||
| chr19:39378362 | A | G | 12 | a0001c0001t0002g0010 a0001c0001t0002g0026 a0001c0001t0002g0027 others(9): Show |
17 | HG00099.hp2 HG01070.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1445-142A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 8/13 | chr19 | 39378362 | |||||||
| chr19:39378403 | TGA | T | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0147 others(1): Show |
4 | HG02055.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1445-99_1445-98del others(2): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 39378403 | ||||||
| chr19:39378407 | T | G | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(20): Show |
35 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1445-97T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 8/13 | chr19 | 39378407 | |||||||
| chr19:39378678 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1530+89C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39378678 | |||||||
| chr19:39378797 | C | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(20): Show |
35 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1530+208C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39378797 | |||||||
| chr19:39378859 | G | A | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1530+270G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39378859 | |||||||
| chr19:39378883 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1530+294G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39378883 | |||||||
| chr19:39378900 | C | G | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(21): Show |
37 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1530+311C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39378900 | |||||||
| chr19:39378953 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG02074.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1530+364C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39378953 | |||||||
| chr19:39379043 | CCTCT | C | 16 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(13): Show |
26 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1530+465_1530+468d others(6): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 39379043 | ||||||
| chr19:39379056 | C | CT | 4 | a0001c0001t0001g0057 a0001c0001t0002g0128 a0001c0001t0002g0134 others(1): Show |
5 | HG00140.hp2 HG00738.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1530+481dupT | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 39379056 | ||||||
| chr19:39379058 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0051 |
2 | HG01081.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1530+469T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379058 | |||||||
| chr19:39379147 | CA | C | 3 | a0001c0002t0006g0120 a0001c0002t0006g0152 a0001c0002t0006g0153 |
3 | HG02818.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1530+561delA | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 39379147 | ||||||
| chr19:39379163 | C | T | 23 | a0001c0001t0002g0021 a0001c0001t0002g0030 a0001c0001t0002g0105 others(20): Show |
25 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1530+574C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379163 | |||||||
| chr19:39379225 | A | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1530+636A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379225 | |||||||
| chr19:39379634 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1531-332A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379634 | |||||||
| chr19:39379678 | C | G | 3 | a0001c0001t0002g0111 a0001c0001t0002g0128 a0001c0001t0002g0134 |
3 | HG02896.hp2 HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1531-288C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379678 | |||||||
| chr19:39379700 | A | G | 24 | a0001c0001t0002g0021 a0001c0001t0002g0030 a0001c0001t0002g0105 others(21): Show |
26 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.1531-266A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379700 | |||||||
| chr19:39379741 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1531-225T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379741 | |||||||
| chr19:39379832 | A | T | 1 | a0001c0001t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1531-134A>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379832 | |||||||
| chr19:39379846 | C | T | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(21): Show |
37 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1531-120C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379846 | |||||||
| chr19:39379862 | G | A | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1531-104G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379862 | |||||||
| chr19:39379888 | C | G | 13 | a0001c0001t0002g0010 a0001c0001t0002g0026 a0001c0001t0002g0027 others(10): Show |
18 | HG00099.hp2 HG01070.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1531-78C>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 9/13 | chr19 | 39379888 | |||||||
| chr19:39380146 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1649+62G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 10/13 | chr19 | 39380146 | |||||||
| chr19:39380194 | A | C | 12 | a0001c0001t0002g0030 a0001c0001t0002g0107 a0001c0001t0002g0160 others(9): Show |
13 | HG02145.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1649+110A>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 10/13 | chr19 | 39380194 | |||||||
| chr19:39380339 | A | G | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0127 others(6): Show |
12 | HG00544.hp2 HG00621.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1650-248A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 10/13 | chr19 | 39380339 | |||||||
| chr19:39380370 | T | C | 2 | a0001c0001t0003g0116 a0001c0001t0022g0104 |
2 | HG01123.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1650-217T>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 10/13 | chr19 | 39380370 | |||||||
| chr19:39380849 | A | G | 1 | a0001c0004t0002g0101 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1848+64A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 11/13 | chr19 | 39380849 | |||||||
| chr19:39380895 | G | A | 13 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(10): Show |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1849-95G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 11/13 | chr19 | 39380895 | |||||||
| chr19:39380921 | A | G | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1849-69A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 11/13 | chr19 | 39380921 | |||||||
| chr19:39380941 | T | G | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1849-49T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 11/13 | chr19 | 39380941 | |||||||
| chr19:39381184 | C | T | 1 | a0001c0002t0006g0153 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1972+71C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | chr19 | 39381184 | |||||||
| chr19:39381227 | A | G | 2 | a0001c0004t0002g0100 a0001c0004t0002g0101 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1972+114A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | chr19 | 39381227 | |||||||
| chr19:39381377 | A | G | 1 | a0001c0001t0003g0115 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1972+264A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | chr19 | 39381377 | |||||||
| chr19:39381590 | T | G | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1972+477T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | chr19 | 39381590 | |||||||
| chr19:39381909 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1972+796G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | chr19 | 39381909 | |||||||
| chr19:39382085 | TAG | T | 13 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(10): Show |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1972+979_1972+980d others(4): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 39382085 | ||||||
| chr19:39382155 | G | T | 1 | a0001c0005t0007g0029 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1972+1042G>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | chr19 | 39382155 | |||||||
| chr19:39382307 | C | T | 21 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(18): Show |
32 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1973-901C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | chr19 | 39382307 | |||||||
| chr19:39382323 | C | T | 13 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0024 others(10): Show |
17 | HG01109.hp1 HG01123.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1973-885C>T | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | chr19 | 39382323 | |||||||
| chr19:39382516 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0154 |
3 | HG02257.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1973-692G>A | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | chr19 | 39382516 | |||||||
| chr19:39382937 | CTG | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.1973-264_1973-263d others(4): Show |
SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 39382937 | ||||||
| chr19:39382972 | T | G | 5 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0150 others(2): Show |
8 | HG00544.hp2 HG00621.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.1973-236T>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 12/13 | chr19 | 39382972 | |||||||
| chr19:39383374 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2056+83A>G | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 13/13 | chr19 | 39383374 | |||||||
| chr19:39383460 | G | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(15): Show |
28 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.2057-39G>C | SAMD4B | ENSG00000179134.16 | transcript | ENST00000610417.5 | protein_coding | 13/13 | chr19 | 39383460 |