Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51306 |
| ensemblid | ENSG00000031003.11 |
| hgncid | 1335 |
| symbol | FAM13B |
| name | family with sequence similarity 13 member B |
| refseq_nuc | NM_001385994.1 |
| refseq_prot | NP_001372923.1 |
| ensembl_nuc | ENST00000689681.1 |
| ensembl_prot | ENSP00000509788.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 137937960 |
| end | 138033079 |
| strand | - |
| ver | v1.2 |
| region | chr5:137937960-138033079 |
| region5000 | chr5:137932960-138038079 |
| regionname0 | FAM13B_chr5_137937960_138033079 |
| regionname5000 | FAM13B_chr5_137932960_138038079 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 937 | 314 | 92 | 74 | 106 | 12 | 28 | 78 | FAM13B_chr5_137932960_138038079 | FAM13B | MRKSS others(932): Show |
chr5 | 137932960 | 138038079 |
| a0002 | 0/0 | 937 | 6 | 2 | 1 | 0 | 2 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | MRKSS others(932): Show |
chr5 | 137932960 | 138038079 |
| a0003 | 0/0 | 937 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | MRKSS others(932): Show |
chr5 | 137932960 | 138038079 |
| a0004 | 0/0 | 937 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | MRKSS others(932): Show |
chr5 | 137932960 | 138038079 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2811 | 302 | 83 | 72 | 106 | 12 | 28 | FAM13B_chr5_137932960_138038079 | FAM13B | ATGAG others(2806): Show |
chr5 | 137932960 | 138038079 | ||
| a0001c0002 | 1/0 | 2811 | 10 | 9 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | ATGAG others(2806): Show |
chr5 | 137932960 | 138038079 | ||
| a0001c0004 | 0/0 | 2811 | 2 | 0 | 2 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | ATGAG others(2806): Show |
chr5 | 137932960 | 138038079 | ||
| a0002c0003 | 0/0 | 2811 | 5 | 2 | 1 | 0 | 1 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | ATGAG others(2806): Show |
chr5 | 137932960 | 138038079 | ||
| a0002c0006 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | ATGAG others(2806): Show |
chr5 | 137932960 | 138038079 | ||
| a0003c0005 | 0/0 | 2811 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | ATGAG others(2806): Show |
chr5 | 137932960 | 138038079 | ||
| a0004c0007 | 0/0 | 2811 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | ATGAG others(2806): Show |
chr5 | 137932960 | 138038079 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5579 | 201 | 43 | 51 | 80 | 6 | 20 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0002 | 0/0 | 5579 | 66 | 29 | 19 | 7 | 6 | 5 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0003 | 0/0 | 5579 | 16 | 0 | 1 | 14 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0004 | 0/0 | 5579 | 6 | 6 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0005 | 0/0 | 5601 | 2 | 0 | 0 | 2 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5596): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0006 | 0/0 | 5579 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0008 | 0/0 | 5579 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0009 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0010 | 0/0 | 5579 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0011 | 0/0 | 5579 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0012 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0013 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0014 | 0/0 | 5579 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0001t0015 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0002t0002 | 1/0 | 5579 | 10 | 9 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0001c0004t0007 | 0/0 | 5579 | 2 | 0 | 2 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0002c0003t0002 | 0/0 | 5579 | 5 | 2 | 1 | 0 | 1 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0002c0006t0002 | 0/0 | 5579 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0003c0005t0001 | 0/0 | 5579 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| a0004c0007t0001 | 0/0 | 5579 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | AGCCG others(5574): Show |
chr5 | 137932960 | 138038079 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0002 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0010g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0011g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0012g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0013g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0014g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0015g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0004t0007g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0004t0007g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0003t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0003t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0003t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0003t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0003t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0006t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0003c0005t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0004c0007t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | GBR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00280 | hp1 | a0002 | c0006 | t0002 | g0008 | EUR | FIN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00323 | hp1 | a0002 | c0003 | t0002 | g0007 | EUR | FIN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | FIN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00738 | hp2 | a0001 | c0004 | t0007 | g0183 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00741 | hp2 | a0003 | c0005 | t0001 | g0244 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01192 | hp1 | a0001 | c0004 | t0007 | g0187 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01433 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0058 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0262 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0261 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0153 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01943 | hp2 | a0001 | c0001 | t0011 | g0016 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02129 | hp2 | a0001 | c0001 | t0012 | g0218 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | CDX | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0282 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0292 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0281 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0290 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0283 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0284 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0254 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0255 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0108 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02976 | hp1 | a0002 | c0003 | t0002 | g0010 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03017 | hp2 | a0002 | c0003 | t0002 | g0009 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0289 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03579 | hp1 | a0002 | c0003 | t0002 | g0011 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03710 | hp1 | a0004 | c0007 | t0001 | g0186 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0260 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0313 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03927 | hp2 | a0001 | c0001 | t0014 | g0029 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0258 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18969 | hp1 | a0001 | c0001 | t0015 | g0301 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18978 | hp1 | a0001 | c0001 | t0013 | g0229 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | GIH | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0287 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0286 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | USA | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | USA | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | USA | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0164 | REF | REF | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0288 | REF | REF | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137940279 | C | G | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.2760G>C | p.Lys920Asn | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 3260/5579 | 2760/2814 | 920/937 | chr5 | 137940279 | |||
| chr5:137942993 | T | C | 1 | a0002 | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
missense_variant | MODERATE | c.2470A>G | p.Met824Val | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/24 | 2970/5579 | 2470/2814 | 824/937 | chr5 | 137942993 | |||
| chr5:137960194 | T | C | 1 | a0004 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1265A>G | p.Asp422Gly | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 12/24 | 1765/5579 | 1265/2814 | 422/937 | chr5 | 137960194 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137940237 | T | G | 1 | a0001c0004 | 2 | HG00738.hp2 HG01192.hp1 |
synonymous_variant | LOW | c.2802A>C | p.Ser934Ser | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 3302/5579 | 2802/2814 | 934/937 | chr5 | 137940237 | |||
| chr5:137945986 | T | C | 1 | a0002c0006 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.2256A>G | p.Glu752Glu | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/24 | 2756/5579 | 2256/2814 | 752/937 | chr5 | 137945986 | |||
| chr5:138011809 | G | A | 6 | a0001c0001 a0001c0004 a0002c0003 others(3): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
synonymous_variant | LOW | c.507C>T | p.Ser169Ser | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 5/24 | 1007/5579 | 507/2814 | 169/937 | chr5 | 138011809 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137938043 | A | G | 1 | a0001c0001t0011 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2182T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 2182 | chr5 | 137938043 | ||||||
| chr5:137938089 | C | T | 1 | a0001c0001t0008 | 2 | HG02895.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2136G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 2136 | chr5 | 137938089 | ||||||
| chr5:137938090 | A | T | 2 | a0001c0001t0004 a0001c0001t0006 |
8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2135T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 2135 | chr5 | 137938090 | ||||||
| chr5:137938192 | T | C | 1 | a0001c0001t0012 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2033A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 2033 | chr5 | 137938192 | ||||||
| chr5:137938342 | A | C | 2 | a0001c0001t0004 a0001c0001t0006 |
8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1883T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 1883 | chr5 | 137938342 | ||||||
| chr5:137938528 | T | C | 1 | a0001c0001t0013 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1697A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 1697 | chr5 | 137938528 | ||||||
| chr5:137938692 | G | A | 1 | a0001c0001t0015 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1533C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 1533 | chr5 | 137938692 | ||||||
| chr5:137938781 | C | G | 1 | a0001c0004t0007 | 2 | HG00738.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1444G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 1444 | chr5 | 137938781 | ||||||
| chr5:137938797 | G | T | 1 | a0001c0001t0010 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1428C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 1428 | chr5 | 137938797 | ||||||
| chr5:137939426 | G | A | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(13): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*799C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 799 | chr5 | 137939426 | ||||||
| chr5:137939510 | T | C | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(12): Show |
237 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*715A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 715 | chr5 | 137939510 | ||||||
| chr5:137939518 | G | A | 1 | a0001c0001t0008 | 2 | HG02895.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*707C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 707 | chr5 | 137939518 | ||||||
| chr5:137939701 | C | T | 1 | a0001c0001t0009 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 524 | chr5 | 137939701 | ||||||
| chr5:137939952 | G | A | 1 | a0001c0001t0014 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*273C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 273 | chr5 | 137939952 | ||||||
| chr5:138032801 | C | A | 2 | a0001c0001t0003 a0001c0001t0015 |
17 | HG00544.hp1 HG01433.hp2 HG02071.hp1 others(14): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-222G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/24 | chr5 | 138032801 | |||||||
| chr5:138033062 | A | AGCGGGAG others(15): Show |
1 | a0001c0001t0005 | 2 | HG00408.hp2 NA18980.hp2 |
5_prime_UTR_variant | MODIFIER | c.-505_-484dupCCGCCA others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/24 | 13952 | chr5 | 138033062 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137940443 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2691-95A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137940443 | |||||||
| chr5:137940469 | TA | T | 7 | a0001c0001t0001g0098 a0001c0001t0001g0241 a0001c0001t0002g0261 others(4): Show |
7 | HG01516.hp1 HG01517.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.2691-122delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137940469 | |||||||
| chr5:137940710 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0149 |
2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2691-362C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137940710 | |||||||
| chr5:137940903 | T | C | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2691-555A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137940903 | |||||||
| chr5:137940979 | C | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
123 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.2691-631G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137940979 | |||||||
| chr5:137941031 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2691-683C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941031 | |||||||
| chr5:137941049 | G | A | 5 | a0001c0001t0001g0208 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG00597.hp2 HG02135.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.2691-701C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941049 | |||||||
| chr5:137941063 | G | A | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2691-715C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941063 | |||||||
| chr5:137941077 | T | A | 1 | a0001c0001t0010g0260 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2691-729A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941077 | |||||||
| chr5:137941126 | T | C | 2 | a0002c0003t0002g0010 a0002c0003t0002g0011 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2691-778A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941126 | |||||||
| chr5:137941692 | A | C | 4 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.2690+252T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941692 | |||||||
| chr5:137942286 | A | AAG | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2589-243_2589-242d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/23 | chr5 | 137942286 | |||||||
| chr5:137942320 | A | T | 1 | a0001c0001t0001g0247 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2589-275T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/23 | chr5 | 137942320 | |||||||
| chr5:137942443 | C | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2589-398G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/23 | chr5 | 137942443 | |||||||
| chr5:137942729 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2588+146A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/23 | chr5 | 137942729 | |||||||
| chr5:137942832 | T | G | 1 | a0001c0001t0001g0151 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2588+43A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/23 | chr5 | 137942832 | |||||||
| chr5:137943044 | A | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | HG00733.hp2 HG01168.hp1 |
splice_region_variant&intron_variant | LOW | c.2425-6T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 21/23 | chr5 | 137943044 | |||||||
| chr5:137943058 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2425-20C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 21/23 | chr5 | 137943058 | |||||||
| chr5:137943082 | G | T | 1 | a0001c0001t0002g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2425-44C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 21/23 | chr5 | 137943082 | |||||||
| chr5:137943301 | T | C | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2341-85A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943301 | |||||||
| chr5:137943737 | T | A | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.2341-521A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943737 | |||||||
| chr5:137943740 | G | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0128 |
2 | NA19009.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2341-524C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943740 | |||||||
| chr5:137943744 | C | CA | 52 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(49): Show |
52 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2341-529dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943744 | |||||||
| chr5:137943841 | A | G | 2 | a0001c0001t0001g0157 a0001c0002t0002g0283 |
2 | HG01358.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2341-625T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943841 | |||||||
| chr5:137943921 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2341-705A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943921 | |||||||
| chr5:137943961 | C | T | 19 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(16): Show |
19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.2341-745G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943961 | |||||||
| chr5:137944017 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.2341-801A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944017 | |||||||
| chr5:137944173 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.2341-957G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944173 | |||||||
| chr5:137944232 | G | A | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.2341-1016C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944232 | |||||||
| chr5:137944276 | C | A | 1 | a0001c0001t0002g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2341-1060G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944276 | |||||||
| chr5:137944486 | G | A | 1 | a0001c0001t0004g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2341-1270C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944486 | |||||||
| chr5:137944671 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2340+1231A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944671 | |||||||
| chr5:137944763 | CA | C | 71 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0185 others(68): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2340+1138delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944763 | |||||||
| chr5:137944763 | CAA | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
235 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.2340+1137_2340+113 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944763 | |||||||
| chr5:137944768 | A | C | 4 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.2340+1134T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944768 | |||||||
| chr5:137944769 | A | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2340+1133T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944769 | |||||||
| chr5:137944777 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.2340+1125T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944777 | |||||||
| chr5:137944955 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02027.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2340+947C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944955 | |||||||
| chr5:137945075 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0095 |
2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2340+827G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137945075 | |||||||
| chr5:137945287 | A | G | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2340+615T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137945287 | |||||||
| chr5:137945438 | TAA | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0274 |
3 | HG02055.hp2 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2340+462_2340+463d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137945438 | |||||||
| chr5:137945511 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(106): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.2340+391G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137945511 | |||||||
| chr5:137946019 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.2245-22T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 19/23 | chr5 | 137946019 | |||||||
| chr5:137946069 | T | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG01952.hp2 HG02004.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2245-72A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 19/23 | chr5 | 137946069 | |||||||
| chr5:137946074 | G | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0201 a0001c0001t0001g0232 |
3 | NA18957.hp2 NA18961.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2245-77C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 19/23 | chr5 | 137946074 | |||||||
| chr5:137946342 | C | CA | 8 | a0001c0001t0001g0198 a0001c0001t0001g0273 a0001c0001t0002g0161 others(5): Show |
8 | HG01167.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.2161-32dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137946342 | |||||||
| chr5:137946350 | A | C | 1 | a0001c0001t0002g0077 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2161-39T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137946350 | |||||||
| chr5:137946436 | G | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.2161-125C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137946436 | |||||||
| chr5:137946899 | T | C | 64 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.2161-588A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137946899 | |||||||
| chr5:137947105 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.2161-794G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947105 | |||||||
| chr5:137947117 | G | A | 32 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2161-806C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947117 | |||||||
| chr5:137947255 | A | T | 64 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.2161-944T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947255 | |||||||
| chr5:137947361 | A | G | 1 | a0001c0001t0002g0067 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2161-1050T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947361 | |||||||
| chr5:137947398 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2161-1087G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947398 | |||||||
| chr5:137947511 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2161-1200T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947511 | |||||||
| chr5:137948080 | T | C | 1 | a0001c0001t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2160+875A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948080 | |||||||
| chr5:137948083 | TC | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2160+871delG | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948083 | |||||||
| chr5:137948123 | T | C | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.2160+832A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948123 | |||||||
| chr5:137948180 | CA | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(223): Show |
232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.2160+774delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948180 | |||||||
| chr5:137948401 | CTTTA | C | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2160+550_2160+553d others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948401 | |||||||
| chr5:137948605 | G | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0250 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2160+350C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948605 | |||||||
| chr5:137948819 | T | C | 1 | a0001c0001t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2160+136A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948819 | |||||||
| chr5:137948855 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2160+100C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948855 | |||||||
| chr5:137948879 | CTACCCTG others(15): Show |
C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2160+54_2160+75del others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948879 | |||||||
| chr5:137949212 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1931-28C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949212 | |||||||
| chr5:137949321 | T | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1931-137A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949321 | |||||||
| chr5:137949473 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1931-289T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949473 | |||||||
| chr5:137949554 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1931-370A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949554 | |||||||
| chr5:137949567 | G | C | 2 | a0001c0001t0002g0058 a0001c0001t0002g0060 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1931-383C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949567 | |||||||
| chr5:137949660 | C | T | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1931-476G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949660 | |||||||
| chr5:137949798 | CA | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(293): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1931-615delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949798 | |||||||
| chr5:137949864 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0167 |
2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1931-680C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949864 | |||||||
| chr5:137950176 | T | A | 2 | a0001c0001t0008g0108 a0001c0001t0008g0111 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1931-992A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950176 | |||||||
| chr5:137950176 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1931-992A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950176 | |||||||
| chr5:137950208 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1931-1024G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950208 | |||||||
| chr5:137950251 | G | A | 32 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1931-1067C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950251 | |||||||
| chr5:137950407 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1931-1223T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950407 | |||||||
| chr5:137950431 | G | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
242 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.1931-1247C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950431 | |||||||
| chr5:137950675 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1931-1491C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950675 | |||||||
| chr5:137950841 | T | C | 2 | a0001c0001t0002g0036 a0001c0001t0002g0065 |
2 | NA18945.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1931-1657A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950841 | |||||||
| chr5:137951124 | C | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1930+1504G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951124 | |||||||
| chr5:137951156 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0245 |
2 | HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1930+1472C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951156 | |||||||
| chr5:137951209 | C | CA | 68 | a0001c0001t0001g0103 a0001c0001t0001g0120 a0001c0001t0001g0129 others(65): Show |
68 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.1930+1418dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951209 | |||||||
| chr5:137951209 | C | CAA | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(107): Show |
116 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1930+1417_1930+141 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951209 | |||||||
| chr5:137951209 | C | CAAA | 10 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0115 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1930+1416_1930+141 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951209 | |||||||
| chr5:137951209 | CA | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0171 a0001c0001t0002g0261 others(9): Show |
12 | HG01516.hp1 HG01517.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1930+1418delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951209 | |||||||
| chr5:137951213 | A | C | 1 | a0003c0005t0001g0244 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1930+1415T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951213 | |||||||
| chr5:137951233 | A | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0188 a0001c0004t0007g0183 others(1): Show |
4 | HG00738.hp2 HG01192.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1930+1395T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951233 | |||||||
| chr5:137951234 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1930+1394C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951234 | |||||||
| chr5:137951235 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1930+1393C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951235 | |||||||
| chr5:137951236 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1930+1392T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951236 | |||||||
| chr5:137951977 | G | A | 8 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0176 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.1930+651C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951977 | |||||||
| chr5:137952124 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1930+504A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137952124 | |||||||
| chr5:137952296 | C | G | 6 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG01978.hp1 HG02109.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1930+332G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137952296 | |||||||
| chr5:137952530 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0093 |
2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1930+98T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137952530 | |||||||
| chr5:137952931 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0002g0069 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1849-222G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137952931 | |||||||
| chr5:137953027 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1848+309G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137953027 | |||||||
| chr5:137953059 | A | G | 8 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1848+277T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137953059 | |||||||
| chr5:137953105 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1848+231G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137953105 | |||||||
| chr5:137953195 | C | T | 2 | a0001c0001t0002g0279 a0001c0001t0002g0280 |
2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1848+141G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137953195 | |||||||
| chr5:137953323 | G | A | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1848+13C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137953323 | |||||||
| chr5:137953505 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1719-40C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137953505 | |||||||
| chr5:137953526 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1719-61A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137953526 | |||||||
| chr5:137953664 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1719-199G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137953664 | |||||||
| chr5:137953720 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1719-255G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137953720 | |||||||
| chr5:137953901 | A | G | 4 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(1): Show |
4 | HG01978.hp1 HG02735.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1718+265T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137953901 | |||||||
| chr5:137954041 | C | CT | 74 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(71): Show |
74 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1718+124dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137954041 | |||||||
| chr5:137954505 | T | TAC | 20 | a0001c0001t0001g0096 a0001c0001t0001g0109 a0001c0001t0001g0134 others(17): Show |
20 | HG01243.hp2 HG01515.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.1508-131_1508-130d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954505 | |||||||
| chr5:137954525 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
221 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.1508-149A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954525 | |||||||
| chr5:137954527 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
216 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1508-151G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954527 | |||||||
| chr5:137954528 | ATG | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0212 a0001c0001t0001g0233 |
3 | NA18982.hp1 NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1508-154_1508-153d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954528 | |||||||
| chr5:137954529 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
217 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1508-153A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954529 | |||||||
| chr5:137954529 | T | TAC | 4 | a0001c0001t0001g0080 a0001c0001t0001g0095 a0001c0001t0003g0300 others(1): Show |
4 | HG01081.hp2 HG01123.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1508-154_1508-153i others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954529 | |||||||
| chr5:137954530 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
221 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.1508-154C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954530 | |||||||
| chr5:137954536 | GTGTA | G | 67 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(64): Show |
67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1508-164_1508-161d others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954536 | |||||||
| chr5:137954538 | G | A | 17 | a0001c0001t0001g0096 a0001c0001t0001g0109 a0001c0001t0001g0234 others(14): Show |
17 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.1508-162C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954538 | |||||||
| chr5:137954601 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1508-225A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954601 | |||||||
| chr5:137954619 | AT | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
238 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.1508-244delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954619 | |||||||
| chr5:137954644 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1508-268G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954644 | |||||||
| chr5:137954673 | T | C | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1508-297A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954673 | |||||||
| chr5:137954692 | T | G | 1 | a0001c0001t0008g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1508-316A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954692 | |||||||
| chr5:137954700 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1508-324G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954700 | |||||||
| chr5:137954868 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1508-492G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954868 | |||||||
| chr5:137954983 | T | C | 17 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(14): Show |
17 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1508-607A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954983 | |||||||
| chr5:137955008 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1508-632A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955008 | |||||||
| chr5:137955072 | T | TA | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1508-697dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955072 | |||||||
| chr5:137955118 | T | G | 1 | a0002c0003t0002g0006 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1508-742A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955118 | |||||||
| chr5:137955161 | T | C | 3 | a0001c0001t0002g0055 a0001c0001t0002g0072 a0001c0001t0002g0074 |
3 | HG01891.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1508-785A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955161 | |||||||
| chr5:137955172 | CCTCA | C | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1508-800_1508-797d others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955172 | |||||||
| chr5:137955362 | TATAATAT others(8): Show |
T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1508-1001_1508-987 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955362 | |||||||
| chr5:137955507 | AT | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1507+969delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955507 | |||||||
| chr5:137955633 | A | G | 1 | a0001c0001t0013g0229 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1507+844T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955633 | |||||||
| chr5:137955900 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1507+577T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955900 | |||||||
| chr5:137955928 | G | A | 1 | a0001c0001t0015g0301 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1507+549C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955928 | |||||||
| chr5:137956146 | A | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1507+331T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137956146 | |||||||
| chr5:137956184 | A | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1507+293T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137956184 | |||||||
| chr5:137956406 | G | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1507+71C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137956406 | |||||||
| chr5:137956444 | C | CA | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1507+32dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137956444 | |||||||
| chr5:137956706 | A | AT | 73 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1442-165dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956706 | |||||||
| chr5:137956748 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0166 others(3): Show |
7 | HG00140.hp1 HG00642.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1442-206T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956748 | |||||||
| chr5:137956757 | A | AG | 18 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0002g0068 others(15): Show |
18 | HG00280.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1442-216dupC | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956757 | |||||||
| chr5:137956757 | A | AGG | 42 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(39): Show |
42 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1442-217_1442-216d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956757 | |||||||
| chr5:137956757 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1442-215T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956757 | |||||||
| chr5:137956766 | A | G | 53 | a0001c0001t0001g0171 a0001c0001t0001g0196 a0001c0001t0002g0022 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1442-224T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956766 | |||||||
| chr5:137956767 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1442-225T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956767 | |||||||
| chr5:137956878 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0184 |
2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1442-336A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956878 | |||||||
| chr5:137957264 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1442-722C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957264 | |||||||
| chr5:137957332 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1442-790C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957332 | |||||||
| chr5:137957398 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1442-856C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957398 | |||||||
| chr5:137957453 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0002g0078 |
2 | HG02818.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1442-911A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957453 | |||||||
| chr5:137957540 | C | CA | 50 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0091 others(47): Show |
50 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1442-999dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957540 | |||||||
| chr5:137957540 | CA | C | 25 | a0001c0001t0001g0018 a0001c0001t0001g0079 a0001c0001t0001g0083 others(22): Show |
25 | HG00741.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1442-999delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957540 | |||||||
| chr5:137957682 | G | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0225 a0001c0001t0001g0237 |
3 | HG01074.hp1 HG04204.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1442-1140C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957682 | |||||||
| chr5:137957924 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1442-1382C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957924 | |||||||
| chr5:137957927 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1442-1385C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957927 | |||||||
| chr5:137957929 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1442-1387G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957929 | |||||||
| chr5:137958230 | T | G | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1441+1386A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137958230 | |||||||
| chr5:137958874 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1441+742A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137958874 | |||||||
| chr5:137959013 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1441+603T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137959013 | |||||||
| chr5:137959219 | T | C | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0230 others(1): Show |
4 | NA19009.hp2 NA19010.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441+397A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137959219 | |||||||
| chr5:137959230 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1441+386T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137959230 | |||||||
| chr5:137959291 | G | A | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441+325C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137959291 | |||||||
| chr5:137959529 | G | C | 1 | a0001c0001t0001g0227 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1441+87C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137959529 | |||||||
| chr5:137959827 | C | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1294-64G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 12/23 | chr5 | 137959827 | |||||||
| chr5:137959829 | T | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1294-66A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 12/23 | chr5 | 137959829 | |||||||
| chr5:137959940 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1294-177A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 12/23 | chr5 | 137959940 | |||||||
| chr5:137960134 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1293+32A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 12/23 | chr5 | 137960134 | |||||||
| chr5:137960400 | A | G | 3 | a0001c0001t0002g0055 a0001c0001t0002g0072 a0001c0001t0002g0074 |
3 | HG01891.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1245-186T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137960400 | |||||||
| chr5:137960422 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1245-208A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137960422 | |||||||
| chr5:137960837 | C | T | 4 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1245-623G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137960837 | |||||||
| chr5:137960876 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1245-662G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137960876 | |||||||
| chr5:137961314 | A | AAACAAC | 21 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(18): Show |
21 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1244+1085_1244+109 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961314 | |||||||
| chr5:137961314 | A | AAACAACA others(2): Show |
3 | a0001c0001t0001g0083 a0001c0001t0001g0239 a0001c0001t0004g0258 |
3 | HG01175.hp2 HG01975.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1244+1082_1244+109 others(13): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961314 | |||||||
| chr5:137961314 | A | AAACAACA others(5): Show |
3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1244+1079_1244+109 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961314 | |||||||
| chr5:137961314 | AAAC | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1244+1088_1244+109 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961314 | |||||||
| chr5:137961314 | AAACAAC | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1244+1085_1244+109 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961314 | |||||||
| chr5:137961708 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1244+697G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961708 | |||||||
| chr5:137961867 | C | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1244+538G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961867 | |||||||
| chr5:137961879 | ACT | A | 64 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1244+524_1244+525d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961879 | |||||||
| chr5:137962120 | A | T | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1244+285T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137962120 | |||||||
| chr5:137962150 | G | C | 1 | a0001c0001t0002g0075 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1244+255C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137962150 | |||||||
| chr5:137962152 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1244+253A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137962152 | |||||||
| chr5:137962234 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
242 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.1244+171G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137962234 | |||||||
| chr5:137962765 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0194 a0001c0001t0001g0200 |
3 | HG02895.hp2 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1180-296C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137962765 | |||||||
| chr5:137962810 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1180-341T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137962810 | |||||||
| chr5:137962948 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1180-479C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137962948 | |||||||
| chr5:137962975 | T | C | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1180-506A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137962975 | |||||||
| chr5:137963052 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(80): Show |
84 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1180-583A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963052 | |||||||
| chr5:137963122 | A | T | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1180-653T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963122 | |||||||
| chr5:137963155 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-686C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963155 | |||||||
| chr5:137963201 | T | C | 19 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(16): Show |
19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1180-732A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963201 | |||||||
| chr5:137963481 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1180-1012A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963481 | |||||||
| chr5:137963532 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1180-1063A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963532 | |||||||
| chr5:137963588 | A | C | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1180-1119T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963588 | |||||||
| chr5:137963625 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1180-1156A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963625 | |||||||
| chr5:137963658 | G | A | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1180-1189C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963658 | |||||||
| chr5:137963663 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0079 |
2 | NA18948.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1180-1194G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963663 | |||||||
| chr5:137963749 | G | A | 32 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1180-1280C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963749 | |||||||
| chr5:137963751 | G | A | 2 | a0001c0001t0002g0293 a0001c0001t0002g0297 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1180-1282C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963751 | |||||||
| chr5:137963858 | T | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-1389A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963858 | |||||||
| chr5:137963903 | C | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-1434G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963903 | |||||||
| chr5:137963931 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-1462C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963931 | |||||||
| chr5:137963932 | T | C | 32 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1180-1463A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963932 | |||||||
| chr5:137964076 | T | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1180-1607A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964076 | |||||||
| chr5:137964160 | C | T | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-1691G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964160 | |||||||
| chr5:137964182 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1180-1713G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964182 | |||||||
| chr5:137964213 | G | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1180-1744C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964213 | |||||||
| chr5:137964262 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1180-1793A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964262 | |||||||
| chr5:137964392 | A | C | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1180-1923T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964392 | |||||||
| chr5:137964597 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1180-2128A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964597 | |||||||
| chr5:137964622 | G | A | 2 | a0002c0003t0002g0010 a0002c0003t0002g0011 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1180-2153C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964622 | |||||||
| chr5:137964716 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0155 |
2 | HG00438.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.1180-2247C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964716 | |||||||
| chr5:137964899 | G | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-2430C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964899 | |||||||
| chr5:137965101 | G | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-2632C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965101 | |||||||
| chr5:137965102 | C | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
242 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.1180-2633G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965102 | |||||||
| chr5:137965110 | G | A | 3 | a0001c0001t0002g0055 a0001c0001t0002g0072 a0001c0001t0002g0074 |
3 | HG01891.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1180-2641C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965110 | |||||||
| chr5:137965178 | T | C | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1180-2709A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965178 | |||||||
| chr5:137965449 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1180-2980G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965449 | |||||||
| chr5:137965495 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0059 |
2 | HG01081.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1180-3026C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965495 | |||||||
| chr5:137965515 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1180-3046A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965515 | |||||||
| chr5:137965547 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1180-3078C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965547 | |||||||
| chr5:137965571 | A | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0191 a0001c0001t0001g0194 others(6): Show |
9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1180-3102T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965571 | |||||||
| chr5:137965776 | A | T | 2 | a0001c0001t0002g0042 a0001c0001t0002g0044 |
2 | NA18957.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1180-3307T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965776 | |||||||
| chr5:137965979 | C | CA | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1180-3511dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965979 | |||||||
| chr5:137966006 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1180-3537G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966006 | |||||||
| chr5:137966100 | TA | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1180-3632delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966100 | |||||||
| chr5:137966100 | TAA | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(106): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1180-3633_1180-363 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966100 | |||||||
| chr5:137966231 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-3762C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966231 | |||||||
| chr5:137966257 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0152 a0001c0001t0002g0295 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-3788G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966257 | |||||||
| chr5:137966428 | G | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-3959C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966428 | |||||||
| chr5:137966459 | T | TTA | 5 | a0001c0001t0001g0015 a0001c0001t0001g0205 a0001c0001t0001g0210 others(2): Show |
5 | HG01891.hp1 HG02004.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-3992_1180-399 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | |||||||
| chr5:137966459 | T | TTATA | 3 | a0001c0001t0001g0154 a0001c0001t0002g0297 a0001c0002t0002g0286 |
3 | HG01346.hp2 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1180-3994_1180-399 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | |||||||
| chr5:137966459 | T | TTATATAT others(3): Show |
1 | a0001c0001t0010g0260 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1180-4000_1180-399 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | |||||||
| chr5:137966459 | T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0079 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1180-4002_1180-399 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | |||||||
| chr5:137966459 | TTA | T | 25 | a0001c0001t0001g0124 a0001c0001t0001g0203 a0001c0001t0001g0204 others(22): Show |
25 | HG00544.hp1 HG01891.hp2 HG02293.hp2 others(22): Show |
intron_variant | MODIFIER | c.1180-3992_1180-399 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | |||||||
| chr5:137966459 | TTATA | T | 6 | a0001c0001t0001g0273 a0001c0001t0002g0023 a0001c0001t0002g0037 others(3): Show |
6 | HG01167.hp2 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-3994_1180-399 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | |||||||
| chr5:137966459 | TTATATA | T | 5 | a0001c0001t0002g0032 a0001c0001t0002g0040 a0001c0001t0002g0049 others(2): Show |
5 | HG01257.hp1 HG01258.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-3996_1180-399 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | |||||||
| chr5:137966474 | TATATATA others(11): Show |
T | 1 | a0001c0001t0004g0253 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180-4023_1180-400 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966474 | |||||||
| chr5:137966476 | TATATATA others(11): Show |
T | 3 | a0001c0001t0004g0258 a0001c0001t0006g0254 a0001c0001t0006g0255 |
3 | HG02896.hp2 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1180-4025_1180-400 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966476 | |||||||
| chr5:137966480 | T | G | 1 | a0001c0001t0001g0025 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1180-4011A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966480 | |||||||
| chr5:137966480 | T | TAGAGAGA others(5): Show |
1 | a0001c0001t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1180-4012_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966480 | |||||||
| chr5:137966480 | TATATATA others(3): Show |
T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0073 |
2 | HG01081.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1180-4021_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966480 | |||||||
| chr5:137966480 | TATATATA others(5): Show |
T | 1 | a0001c0001t0002g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1180-4023_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966480 | |||||||
| chr5:137966480 | TATATATA others(9): Show |
T | 2 | a0001c0001t0004g0251 a0001c0001t0004g0256 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1180-4027_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966480 | |||||||
| chr5:137966482 | T | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0114 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-4013A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | |||||||
| chr5:137966482 | T | TAGAGAGA others(3): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0137 |
2 | HG00558.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1180-4014_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | |||||||
| chr5:137966482 | T | TAGAGAGA others(5): Show |
3 | a0001c0001t0001g0102 a0001c0001t0001g0142 a0001c0001t0001g0233 |
3 | HG02148.hp2 NA19067.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1180-4014_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | |||||||
| chr5:137966482 | T | TAGAGAGA others(7): Show |
1 | a0001c0001t0003g0315 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1180-4014_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | |||||||
| chr5:137966482 | T | TAGAGAGA others(19): Show |
1 | a0001c0001t0001g0151 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1180-4014_1180-401 others(30): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | |||||||
| chr5:137966482 | TATATATA others(3): Show |
T | 1 | a0001c0001t0002g0059 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1180-4023_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | |||||||
| chr5:137966482 | TATATATA others(9): Show |
T | 1 | a0001c0001t0004g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1180-4029_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | |||||||
| chr5:137966482 | TATATATA others(11): Show |
T | 1 | a0001c0001t0004g0257 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1180-4031_1180-401 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | |||||||
| chr5:137966484 | T | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0025 others(18): Show |
21 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1180-4015A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | |||||||
| chr5:137966484 | T | TAGAGAGA others(1): Show |
5 | a0001c0001t0001g0028 a0001c0001t0001g0126 a0001c0001t0001g0176 others(2): Show |
5 | HG01106.hp2 HG01243.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-4016_1180-401 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | |||||||
| chr5:137966484 | T | TAGAGAGA others(3): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0112 others(3): Show |
6 | HG01952.hp2 HG02257.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-4016_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | |||||||
| chr5:137966484 | T | TAGAGAGA others(5): Show |
3 | a0001c0001t0001g0103 a0001c0001t0001g0217 a0001c0004t0007g0187 |
3 | HG01192.hp1 HG02735.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1180-4016_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | |||||||
| chr5:137966484 | T | TAGAGAGA others(7): Show |
3 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0242 |
3 | HG03139.hp1 NA18945.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1180-4016_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | |||||||
| chr5:137966484 | T | TAGAGAGA others(9): Show |
3 | a0001c0001t0001g0120 a0001c0001t0001g0130 a0001c0001t0001g0185 |
3 | HG01255.hp2 NA19068.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1180-4016_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | |||||||
| chr5:137966484 | TATATAG | T | 18 | a0001c0001t0001g0226 a0001c0001t0002g0022 a0001c0001t0002g0031 others(15): Show |
18 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1180-4021_1180-401 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | |||||||
| chr5:137966484 | TATATAGA others(3): Show |
T | 1 | a0001c0001t0002g0046 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1180-4025_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | |||||||
| chr5:137966484 | TATATAGA others(5): Show |
T | 2 | a0001c0001t0002g0261 a0001c0001t0002g0262 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1180-4027_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | |||||||
| chr5:137966486 | T | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(49): Show |
52 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1180-4017A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | |||||||
| chr5:137966486 | T | TAGAG | 8 | a0001c0001t0001g0081 a0001c0001t0001g0240 a0001c0001t0001g0241 others(5): Show |
8 | HG02055.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-4018_1180-401 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | |||||||
| chr5:137966486 | T | TAGAGAGA others(1): Show |
5 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0115 others(2): Show |
5 | HG00741.hp2 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-4018_1180-401 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | |||||||
| chr5:137966486 | T | TAGAGAGA others(3): Show |
7 | a0001c0001t0001g0136 a0001c0001t0001g0152 a0001c0001t0001g0177 others(4): Show |
7 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-4018_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | |||||||
| chr5:137966486 | T | TAGAGAGA others(7): Show |
1 | a0001c0001t0001g0134 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1180-4018_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | |||||||
| chr5:137966486 | T | TAGAGAGA others(9): Show |
1 | a0001c0001t0001g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1180-4018_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | |||||||
| chr5:137966486 | T | TAGAGAGA others(11): Show |
1 | a0001c0001t0001g0101 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1180-4018_1180-401 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | |||||||
| chr5:137966486 | TATAG | T | 6 | a0001c0001t0001g0167 a0001c0001t0001g0209 a0001c0001t0001g0235 others(3): Show |
6 | HG02683.hp2 HG03041.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-4021_1180-401 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | |||||||
| chr5:137966486 | TATAGAG | T | 5 | a0001c0001t0002g0036 a0001c0001t0002g0052 a0001c0001t0002g0065 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-4023_1180-401 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | |||||||
| chr5:137966488 | T | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(93): Show |
96 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.1180-4019A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TAGAG | 4 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-4023_1180-402 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TAGAGAGA others(3): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0140 others(2): Show |
5 | HG02273.hp1 HG02965.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-4029_1180-402 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TAGAGAGA others(5): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0141 a0001c0001t0001g0145 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-4031_1180-402 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TAGAGAGA others(7): Show |
7 | a0001c0001t0001g0133 a0001c0001t0001g0147 a0001c0001t0001g0173 others(4): Show |
7 | HG00423.hp2 HG01515.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-4033_1180-402 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TAGAGAGA others(11): Show |
1 | a0001c0001t0001g0117 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1180-4037_1180-402 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATAG | 3 | a0001c0001t0002g0285 a0001c0001t0002g0293 a0001c0002t0002g0292 |
3 | HG02451.hp2 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATAGAG | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0132 |
3 | HG01123.hp1 HG03017.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATAGAGA others(1): Show |
5 | a0001c0001t0001g0024 a0001c0001t0001g0096 a0001c0001t0001g0098 others(2): Show |
5 | HG04228.hp2 NA18957.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATAGAGA others(3): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0148 a0001c0001t0001g0163 |
3 | HG00280.hp2 HG03225.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATAGAGA others(5): Show |
1 | a0001c0001t0001g0246 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATAGAGA others(7): Show |
1 | a0004c0007t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATAG | 4 | a0001c0001t0001g0080 a0001c0001t0001g0090 a0001c0001t0001g0276 others(1): Show |
4 | HG00642.hp2 HG01081.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATAGA others(1): Show |
3 | a0001c0001t0001g0116 a0001c0001t0001g0156 a0002c0003t0002g0011 |
3 | HG03579.hp1 NA18978.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATAGA others(3): Show |
2 | a0001c0001t0001g0160 a0001c0001t0001g0267 |
2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATAGA others(5): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0155 |
3 | HG00408.hp1 HG00438.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATAGA others(11): Show |
1 | a0001c0001t0001g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATAGA others(13): Show |
2 | a0001c0001t0001g0181 a0001c0001t0001g0245 |
2 | HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(24): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0201 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0127 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(13): Show |
1 | a0001c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(24): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(9): Show |
2 | a0001c0001t0001g0092 a0001c0001t0001g0189 |
2 | HG00558.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(11): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0194 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(15): Show |
1 | a0002c0003t0002g0007 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(26): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(19): Show |
1 | a0002c0003t0002g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(30): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(25): Show |
1 | a0002c0003t0002g0006 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(36): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(7): Show |
2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(13): Show |
1 | a0001c0001t0001g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(24): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(19): Show |
1 | a0002c0003t0002g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(30): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | T | TATATATA others(37): Show |
1 | a0002c0006t0002g0008 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(48): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | TAG | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(31): Show |
34 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1180-4021_1180-402 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | TAGAG | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0212 others(6): Show |
9 | HG00323.hp2 HG00741.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180-4023_1180-402 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | TAGAGAG | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG00738.hp1 HG01074.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-4025_1180-402 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966488 | TAGAGAGA others(5): Show |
T | 2 | a0001c0001t0002g0054 a0001c0001t0002g0056 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1180-4031_1180-402 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | |||||||
| chr5:137966490 | G | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0165 others(13): Show |
16 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.1180-4021C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966490 | |||||||
| chr5:137966492 | G | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(25): Show |
28 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1180-4023C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966492 | |||||||
| chr5:137966494 | G | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0157 others(12): Show |
15 | HG00438.hp2 HG01074.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1180-4025C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966494 | |||||||
| chr5:137966496 | G | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0157 others(3): Show |
6 | HG00438.hp2 HG00738.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-4027C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966496 | |||||||
| chr5:137966498 | G | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0219 |
2 | HG00738.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1180-4029C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966498 | |||||||
| chr5:137966500 | G | T | 1 | a0001c0001t0001g0219 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1180-4031C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966500 | |||||||
| chr5:137966524 | G | GAGAGAGA others(4): Show |
2 | a0001c0001t0001g0097 a0001c0004t0007g0183 |
2 | HG00738.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1180-4056_1180-405 others(15): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966524 | |||||||
| chr5:137966525 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0079 |
2 | NA18948.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1180-4056C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966525 | |||||||
| chr5:137966636 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1180-4167A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966636 | |||||||
| chr5:137966674 | A | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-4205T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966674 | |||||||
| chr5:137967051 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0154 |
2 | HG01346.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1180-4582G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967051 | |||||||
| chr5:137967085 | T | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-4616A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967085 | |||||||
| chr5:137967200 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1180-4731A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967200 | |||||||
| chr5:137967241 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1180-4772A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967241 | |||||||
| chr5:137967522 | CA | C | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1180-5054delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967522 | |||||||
| chr5:137967595 | G | A | 2 | a0001c0001t0005g0004 a0001c0001t0005g0005 |
2 | HG00408.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1180-5126C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967595 | |||||||
| chr5:137967606 | G | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-5137C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967606 | |||||||
| chr5:137967664 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(106): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1180-5195C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967664 | |||||||
| chr5:137967705 | C | A | 2 | a0001c0001t0002g0285 a0001c0001t0002g0291 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1180-5236G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967705 | |||||||
| chr5:137967833 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0188 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1180-5364G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967833 | |||||||
| chr5:137967837 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1180-5368C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967837 | |||||||
| chr5:137968082 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1180-5613G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968082 | |||||||
| chr5:137968099 | A | G | 19 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(16): Show |
19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1180-5630T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968099 | |||||||
| chr5:137968109 | C | T | 1 | a0001c0001t0002g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1180-5640G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968109 | |||||||
| chr5:137968146 | C | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-5677G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968146 | |||||||
| chr5:137968219 | C | CA | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1180-5751dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968219 | |||||||
| chr5:137968219 | C | CAA | 52 | a0001c0001t0001g0103 a0001c0001t0001g0222 a0001c0001t0001g0223 others(49): Show |
52 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1180-5752_1180-575 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968219 | |||||||
| chr5:137968266 | T | C | 8 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-5797A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968266 | |||||||
| chr5:137968438 | C | CA | 16 | a0001c0001t0001g0019 a0001c0001t0001g0091 a0001c0001t0001g0155 others(13): Show |
16 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.1180-5970dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968438 | |||||||
| chr5:137968438 | CA | C | 7 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0125 others(4): Show |
7 | HG01070.hp1 HG01168.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-5970delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968438 | |||||||
| chr5:137968498 | T | A | 2 | a0001c0001t0002g0036 a0001c0001t0002g0065 |
2 | NA18945.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1180-6029A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968498 | |||||||
| chr5:137968542 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1180-6073T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968542 | |||||||
| chr5:137968634 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0066 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1180-6165C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968634 | |||||||
| chr5:137968644 | C | T | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1180-6175G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968644 | |||||||
| chr5:137968649 | C | G | 7 | a0001c0001t0002g0050 a0001c0001t0002g0052 a0001c0001t0002g0058 others(4): Show |
7 | HG01069.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-6180G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968649 | |||||||
| chr5:137968650 | G | A | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-6181C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968650 | |||||||
| chr5:137968652 | G | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-6183C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968652 | |||||||
| chr5:137968719 | T | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-6250A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968719 | |||||||
| chr5:137968760 | C | T | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-6291G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968760 | |||||||
| chr5:137968902 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1180-6433C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968902 | |||||||
| chr5:137968971 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1180-6502A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968971 | |||||||
| chr5:137969034 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1180-6565T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969034 | |||||||
| chr5:137969043 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1180-6574C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969043 | |||||||
| chr5:137969071 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1180-6602T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969071 | |||||||
| chr5:137969089 | T | G | 1 | a0001c0001t0001g0225 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1180-6620A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969089 | |||||||
| chr5:137969188 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
123 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1180-6719G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969188 | |||||||
| chr5:137969397 | G | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1180-6928C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969397 | |||||||
| chr5:137969439 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
123 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1180-6970G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969439 | |||||||
| chr5:137969478 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1180-7009C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969478 | |||||||
| chr5:137969517 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1180-7048C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969517 | |||||||
| chr5:137969573 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1180-7104C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969573 | |||||||
| chr5:137969662 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1180-7193T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969662 | |||||||
| chr5:137969668 | C | T | 1 | a0002c0003t0002g0006 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1180-7199G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969668 | |||||||
| chr5:137969709 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1180-7240A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969709 | |||||||
| chr5:137969776 | T | G | 57 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(54): Show |
57 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1180-7307A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969776 | |||||||
| chr5:137969854 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1180-7385C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969854 | |||||||
| chr5:137969871 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-7402A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969871 | |||||||
| chr5:137969901 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0066 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1180-7432C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969901 | |||||||
| chr5:137969996 | C | A | 1 | a0001c0001t0001g0193 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1180-7527G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969996 | |||||||
| chr5:137970057 | C | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG00423.hp1 NA18950.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1180-7588G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970057 | |||||||
| chr5:137970085 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1180-7616C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970085 | |||||||
| chr5:137970103 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1180-7634G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970103 | |||||||
| chr5:137970167 | C | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02717.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-7698G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970167 | |||||||
| chr5:137970179 | C | T | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1180-7710G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970179 | |||||||
| chr5:137970280 | G | C | 1 | a0001c0001t0004g0253 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180-7811C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970280 | |||||||
| chr5:137970281 | G | C | 58 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(55): Show |
58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1180-7812C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970281 | |||||||
| chr5:137970315 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1180-7846A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970315 | |||||||
| chr5:137970319 | C | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0231 |
2 | HG03516.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1180-7850G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970319 | |||||||
| chr5:137970419 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1180-7950G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970419 | |||||||
| chr5:137970462 | G | A | 65 | a0001c0001t0001g0265 a0001c0001t0002g0022 a0001c0001t0002g0023 others(62): Show |
65 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1180-7993C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970462 | |||||||
| chr5:137970544 | T | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-8075A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970544 | |||||||
| chr5:137970555 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1180-8086T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970555 | |||||||
| chr5:137970762 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0012g0218 |
2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1180-8293C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970762 | |||||||
| chr5:137970806 | C | A | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1180-8337G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970806 | |||||||
| chr5:137970902 | A | T | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1180-8433T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970902 | |||||||
| chr5:137970946 | C | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1180-8477G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970946 | |||||||
| chr5:137970950 | G | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1180-8481C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970950 | |||||||
| chr5:137970954 | C | G | 1 | a0002c0003t0002g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1180-8485G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970954 | |||||||
| chr5:137971039 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-8570A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971039 | |||||||
| chr5:137971107 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-8638C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971107 | |||||||
| chr5:137971137 | C | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1180-8668G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971137 | |||||||
| chr5:137971193 | T | C | 64 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1180-8724A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971193 | |||||||
| chr5:137971204 | G | C | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1180-8735C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971204 | |||||||
| chr5:137971319 | G | A | 2 | a0001c0001t0002g0054 a0001c0001t0002g0056 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1180-8850C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971319 | |||||||
| chr5:137971333 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1180-8864G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971333 | |||||||
| chr5:137971375 | A | G | 9 | a0001c0001t0001g0099 a0001c0001t0001g0191 a0001c0001t0001g0194 others(6): Show |
9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1180-8906T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971375 | |||||||
| chr5:137971429 | A | G | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-8960T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971429 | |||||||
| chr5:137971434 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-8965G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971434 | |||||||
| chr5:137971477 | T | A | 2 | a0001c0001t0002g0054 a0001c0001t0002g0056 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1180-9008A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971477 | |||||||
| chr5:137971518 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-9049A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971518 | |||||||
| chr5:137971646 | C | T | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1180-9177G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971646 | |||||||
| chr5:137971667 | C | T | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-9198G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971667 | |||||||
| chr5:137971709 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-9240G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971709 | |||||||
| chr5:137971756 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-9287C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971756 | |||||||
| chr5:137971789 | A | G | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1180-9320T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971789 | |||||||
| chr5:137971796 | C | A | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-9327G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971796 | |||||||
| chr5:137971796 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1180-9327G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971796 | |||||||
| chr5:137971940 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1180-9471C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971940 | |||||||
| chr5:137972078 | C | T | 19 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(16): Show |
19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1180-9609G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972078 | |||||||
| chr5:137972100 | T | G | 1 | a0001c0001t0001g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1180-9631A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972100 | |||||||
| chr5:137972110 | T | G | 19 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(16): Show |
19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1180-9641A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972110 | |||||||
| chr5:137972127 | C | T | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-9658G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972127 | |||||||
| chr5:137972147 | GAGACACA others(25): Show |
G | 1 | a0001c0001t0001g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1180-9710_1180-967 others(36): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972147 | |||||||
| chr5:137972447 | A | T | 1 | a0001c0001t0002g0057 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1180-9978T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972447 | |||||||
| chr5:137972478 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180-10009G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972478 | |||||||
| chr5:137972618 | G | C | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1180-10149C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972618 | |||||||
| chr5:137972674 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-10205G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972674 | |||||||
| chr5:137972675 | G | T | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-10206C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972675 | |||||||
| chr5:137972714 | T | C | 1 | a0001c0001t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180-10245A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972714 | |||||||
| chr5:137972882 | C | T | 7 | a0001c0001t0002g0050 a0001c0001t0002g0052 a0001c0001t0002g0058 others(4): Show |
7 | HG01069.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-10413G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972882 | |||||||
| chr5:137972893 | A | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-10424T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972893 | |||||||
| chr5:137972915 | C | T | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1180-10446G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972915 | |||||||
| chr5:137972980 | C | G | 1 | a0001c0001t0002g0070 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1180-10511G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972980 | |||||||
| chr5:137973007 | C | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-10538G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973007 | |||||||
| chr5:137973012 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1180-10543A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973012 | |||||||
| chr5:137973214 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1180-10745A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973214 | |||||||
| chr5:137973239 | T | C | 2 | a0001c0001t0006g0254 a0001c0001t0006g0255 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1180-10770A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973239 | |||||||
| chr5:137973284 | T | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1180-10815A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973284 | |||||||
| chr5:137973340 | C | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0149 |
2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1180-10871G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973340 | |||||||
| chr5:137973395 | A | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(72): Show |
76 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1180-10926T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973395 | |||||||
| chr5:137973519 | T | C | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(2): Show |
5 | HG02809.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-11050A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973519 | |||||||
| chr5:137973582 | C | A | 9 | a0001c0001t0001g0099 a0001c0001t0001g0191 a0001c0001t0001g0194 others(6): Show |
9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1180-11113G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973582 | |||||||
| chr5:137973610 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0129 others(3): Show |
6 | NA18612.hp2 NA18959.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-11141C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973610 | |||||||
| chr5:137973675 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0066 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1180-11206C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973675 | |||||||
| chr5:137973791 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1180-11322T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973791 | |||||||
| chr5:137973795 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1180-11326C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973795 | |||||||
| chr5:137973843 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(4): Show |
7 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-11374G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973843 | |||||||
| chr5:137973847 | T | C | 58 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(55): Show |
58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1180-11378A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973847 | |||||||
| chr5:137973861 | C | T | 4 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-11392G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973861 | |||||||
| chr5:137973901 | T | G | 1 | a0001c0001t0001g0238 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1179+11356A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973901 | |||||||
| chr5:137973912 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1179+11345A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973912 | |||||||
| chr5:137973939 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1179+11318T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973939 | |||||||
| chr5:137974011 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1179+11246A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974011 | |||||||
| chr5:137974048 | G | A | 1 | a0001c0001t0001g0298 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1179+11209C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974048 | |||||||
| chr5:137974457 | T | G | 1 | a0001c0001t0001g0259 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1179+10800A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974457 | |||||||
| chr5:137974465 | G | C | 1 | a0001c0001t0001g0259 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1179+10792C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974465 | |||||||
| chr5:137974471 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1179+10786T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974471 | |||||||
| chr5:137974481 | G | C | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG01975.hp1 HG01978.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+10776C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974481 | |||||||
| chr5:137974599 | T | TA | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1179+10657dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974599 | |||||||
| chr5:137974623 | A | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(106): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1179+10634T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974623 | |||||||
| chr5:137974628 | G | GA | 73 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1179+10628dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974628 | |||||||
| chr5:137974663 | C | CA | 7 | a0001c0001t0001g0020 a0001c0001t0001g0113 a0001c0001t0001g0122 others(4): Show |
7 | HG00423.hp1 HG02145.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+10593dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974663 | |||||||
| chr5:137974663 | C | CAA | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+10592_1179+10 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974663 | |||||||
| chr5:137974663 | CA | C | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01175.hp2 HG01255.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+10593delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974663 | |||||||
| chr5:137974761 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1179+10496C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974761 | |||||||
| chr5:137974868 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0095 |
2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1179+10389G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974868 | |||||||
| chr5:137974975 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1179+10282C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974975 | |||||||
| chr5:137975128 | T | C | 1 | a0001c0001t0002g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1179+10129A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975128 | |||||||
| chr5:137975147 | A | G | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+10110T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975147 | |||||||
| chr5:137975294 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1179+9963A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975294 | |||||||
| chr5:137975309 | G | A | 1 | a0001c0001t0010g0260 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1179+9948C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975309 | |||||||
| chr5:137975314 | C | T | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(2): Show |
5 | HG02809.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+9943G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975314 | |||||||
| chr5:137975493 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1179+9764A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975493 | |||||||
| chr5:137975537 | CCA | C | 32 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1179+9718_1179+971 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975537 | |||||||
| chr5:137975670 | T | TA | 9 | a0001c0001t0001g0156 a0001c0001t0004g0251 a0001c0001t0004g0252 others(6): Show |
9 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+9586dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975670 | |||||||
| chr5:137975677 | AT | A | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+9579delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975677 | |||||||
| chr5:137975819 | G | GT | 7 | a0001c0001t0001g0233 a0001c0001t0002g0052 a0001c0001t0002g0261 others(4): Show |
7 | HG01109.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+9437dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975819 | |||||||
| chr5:137975902 | T | TA | 12 | a0001c0001t0001g0096 a0001c0001t0001g0103 a0001c0001t0001g0104 others(9): Show |
12 | HG01106.hp1 HG01978.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1179+9354dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975902 | |||||||
| chr5:137975979 | C | CT | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0250 |
3 | HG01243.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1179+9277_1179+927 others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975979 | |||||||
| chr5:137975980 | C | CTTTTT | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
220 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.1179+9272_1179+927 others(9): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | |||||||
| chr5:137975980 | C | CTTTTTT | 10 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0113 others(7): Show |
10 | HG01175.hp2 HG01256.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1179+9271_1179+927 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | |||||||
| chr5:137975980 | C | CTTTTTTT others(6): Show |
9 | a0001c0001t0002g0047 a0001c0001t0002g0063 a0001c0001t0002g0078 others(6): Show |
9 | HG01070.hp2 HG01243.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+9264_1179+927 others(17): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | |||||||
| chr5:137975980 | C | CTTTTTTT others(7): Show |
42 | a0001c0001t0002g0023 a0001c0001t0002g0031 a0001c0001t0002g0035 others(39): Show |
42 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1179+9263_1179+927 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | |||||||
| chr5:137975980 | C | CTTTTTTT others(8): Show |
10 | a0001c0001t0002g0022 a0001c0001t0002g0032 a0001c0001t0002g0033 others(7): Show |
10 | HG00741.hp1 HG01192.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1179+9262_1179+927 others(19): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | |||||||
| chr5:137975980 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0162 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1179+9276_1179+927 others(21): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | |||||||
| chr5:137975980 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0002g0161 a0001c0001t0002g0243 |
2 | HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+9276_1179+927 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | |||||||
| chr5:137975980 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+9276_1179+927 others(23): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | |||||||
| chr5:137975980 | C | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0250 |
3 | HG01243.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1179+9277G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | |||||||
| chr5:137975994 | T | TTTTTTTT others(8): Show |
1 | a0002c0006t0002g0008 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1179+9262_1179+926 others(19): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975994 | |||||||
| chr5:137976145 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1179+9112A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976145 | |||||||
| chr5:137976145 | T | G | 1 | a0001c0001t0001g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1179+9112A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976145 | |||||||
| chr5:137976191 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0066 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1179+9066C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976191 | |||||||
| chr5:137976216 | A | C | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+9041T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976216 | |||||||
| chr5:137976380 | C | G | 2 | a0001c0001t0002g0293 a0001c0001t0002g0297 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1179+8877G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976380 | |||||||
| chr5:137976486 | T | A | 9 | a0001c0001t0001g0099 a0001c0001t0001g0191 a0001c0001t0001g0194 others(6): Show |
9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+8771A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976486 | |||||||
| chr5:137976486 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1179+8771A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976486 | |||||||
| chr5:137976759 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1179+8498G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976759 | |||||||
| chr5:137976788 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1179+8469A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976788 | |||||||
| chr5:137976814 | A | T | 1 | a0001c0001t0001g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1179+8443T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976814 | |||||||
| chr5:137976815 | T | A | 1 | a0001c0001t0001g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1179+8442A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976815 | |||||||
| chr5:137976839 | T | C | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+8418A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976839 | |||||||
| chr5:137977014 | T | G | 1 | a0001c0001t0001g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1179+8243A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977014 | |||||||
| chr5:137977026 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0002g0054 a0001c0001t0002g0056 |
3 | HG01167.hp1 HG01169.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1179+8231G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977026 | |||||||
| chr5:137977027 | G | A | 2 | a0001c0002t0002g0282 a0001c0002t0002g0283 |
2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1179+8230C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977027 | |||||||
| chr5:137977460 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(106): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1179+7797G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977460 | |||||||
| chr5:137977603 | C | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+7654G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977603 | |||||||
| chr5:137977700 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1179+7557T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977700 | |||||||
| chr5:137977707 | A | G | 16 | a0001c0001t0001g0122 a0001c0001t0003g0299 a0001c0001t0003g0300 others(13): Show |
16 | HG00544.hp1 HG01433.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1179+7550T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977707 | |||||||
| chr5:137977889 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1179+7368A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977889 | |||||||
| chr5:137978266 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1179+6991G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978266 | |||||||
| chr5:137978377 | A | G | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1179+6880T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978377 | |||||||
| chr5:137978490 | C | T | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+6767G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978490 | |||||||
| chr5:137978711 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1179+6546T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978711 | |||||||
| chr5:137978723 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1179+6534A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978723 | |||||||
| chr5:137978780 | T | C | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1179+6477A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978780 | |||||||
| chr5:137978826 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0201 a0001c0001t0001g0232 |
3 | NA18957.hp2 NA18961.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1179+6431G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978826 | |||||||
| chr5:137979114 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1179+6143C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979114 | |||||||
| chr5:137979233 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1179+6024C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979233 | |||||||
| chr5:137979373 | C | T | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+5884G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979373 | |||||||
| chr5:137979725 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1179+5532A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979725 | |||||||
| chr5:137979845 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1179+5412G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979845 | |||||||
| chr5:137979878 | T | A | 9 | a0001c0001t0001g0096 a0001c0001t0001g0103 a0001c0001t0001g0104 others(6): Show |
9 | HG01106.hp1 HG01978.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+5379A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979878 | |||||||
| chr5:137979999 | TA | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1179+5257delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979999 | |||||||
| chr5:137979999 | TAA | T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0117 a0001c0001t0001g0119 others(4): Show |
7 | HG00733.hp2 HG01168.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+5256_1179+525 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979999 | |||||||
| chr5:137980029 | C | T | 2 | a0001c0001t0002g0293 a0001c0001t0002g0297 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1179+5228G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980029 | |||||||
| chr5:137980116 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1179+5141A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980116 | |||||||
| chr5:137980146 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1179+5111G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980146 | |||||||
| chr5:137980152 | G | T | 1 | a0001c0001t0002g0037 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1179+5105C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980152 | |||||||
| chr5:137980155 | A | G | 1 | a0001c0002t0002g0287 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1179+5102T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980155 | |||||||
| chr5:137980168 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1179+5089G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980168 | |||||||
| chr5:137980176 | G | GAA | 19 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(16): Show |
19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1179+5079_1179+508 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980176 | |||||||
| chr5:137980272 | T | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1179+4985A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980272 | |||||||
| chr5:137980440 | CT | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1179+4816delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980440 | |||||||
| chr5:137980440 | CTT | C | 9 | a0001c0001t0001g0141 a0001c0001t0001g0148 a0001c0001t0001g0234 others(6): Show |
9 | HG01069.hp2 HG01243.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+4815_1179+481 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980440 | |||||||
| chr5:137980454 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1179+4803A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980454 | |||||||
| chr5:137980458 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1179+4799A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980458 | |||||||
| chr5:137980583 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1179+4674G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980583 | |||||||
| chr5:137980847 | C | T | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+4410G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980847 | |||||||
| chr5:137980951 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1179+4306G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980951 | |||||||
| chr5:137981017 | T | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+4240A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981017 | |||||||
| chr5:137981077 | A | AT | 11 | a0001c0001t0002g0043 a0001c0001t0002g0053 a0001c0001t0002g0057 others(8): Show |
11 | HG00323.hp2 HG01192.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1179+4179dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981077 | |||||||
| chr5:137981077 | AT | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(105): Show |
111 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.1179+4179delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981077 | |||||||
| chr5:137981077 | ATT | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0024 others(110): Show |
117 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1179+4178_1179+417 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981077 | |||||||
| chr5:137981077 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1179+4170_1179+417 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981077 | |||||||
| chr5:137981077 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0277 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1179+4166_1179+417 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981077 | |||||||
| chr5:137981177 | A | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+4080T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981177 | |||||||
| chr5:137981218 | A | G | 2 | a0002c0003t0002g0007 a0002c0006t0002g0008 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1179+4039T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981218 | |||||||
| chr5:137981432 | G | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(14): Show |
17 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1179+3825C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981432 | |||||||
| chr5:137981614 | C | T | 3 | a0001c0001t0002g0051 a0001c0001t0002g0069 a0001c0001t0002g0073 |
3 | HG00639.hp2 HG00735.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1179+3643G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981614 | |||||||
| chr5:137981771 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1179+3486C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981771 | |||||||
| chr5:137981859 | G | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0130 |
2 | NA18950.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1179+3398C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981859 | |||||||
| chr5:137981871 | G | A | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+3386C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981871 | |||||||
| chr5:137982092 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1179+3165C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982092 | |||||||
| chr5:137982351 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1179+2906C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982351 | |||||||
| chr5:137982355 | C | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+2902G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982355 | |||||||
| chr5:137982507 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1179+2750G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982507 | |||||||
| chr5:137982523 | A | AAAC | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(106): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1179+2731_1179+273 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982523 | |||||||
| chr5:137982545 | A | AACC | 123 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1179+2709_1179+271 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982545 | |||||||
| chr5:137982662 | T | TTTA | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1179+2592_1179+259 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982662 | |||||||
| chr5:137982697 | G | C | 1 | a0001c0001t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1179+2560C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982697 | |||||||
| chr5:137982765 | T | G | 1 | a0001c0001t0004g0251 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1179+2492A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982765 | |||||||
| chr5:137982989 | G | A | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+2268C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982989 | |||||||
| chr5:137983176 | T | TA | 7 | a0001c0001t0002g0296 a0001c0002t0002g0281 a0001c0002t0002g0284 others(4): Show |
7 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1179+2080dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | |||||||
| chr5:137983176 | TAAAAAAA others(3): Show |
T | 4 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0074 others(1): Show |
4 | HG00323.hp1 HG01891.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+2071_1179+208 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | |||||||
| chr5:137983176 | TAAAAAAA others(4): Show |
T | 5 | a0001c0001t0002g0055 a0001c0001t0002g0072 a0001c0001t0002g0279 others(2): Show |
5 | HG01433.hp1 HG02559.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+2070_1179+208 others(15): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | |||||||
| chr5:137983176 | TAAAAAAA others(5): Show |
T | 4 | a0001c0001t0002g0036 a0001c0001t0002g0038 a0001c0001t0002g0065 others(1): Show |
4 | HG00140.hp2 HG03225.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+2069_1179+208 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | |||||||
| chr5:137983176 | TAAAAAAA others(6): Show |
T | 3 | a0001c0001t0002g0285 a0001c0001t0002g0291 a0001c0001t0002g0293 |
3 | HG02451.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1179+2068_1179+208 others(17): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | |||||||
| chr5:137983176 | TAAAAAAA others(7): Show |
T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0059 |
2 | HG01081.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1179+2067_1179+208 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | |||||||
| chr5:137983176 | TAAAAAAA others(8): Show |
T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0149 a0001c0001t0001g0156 others(16): Show |
19 | HG00423.hp1 HG00597.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1179+2066_1179+208 others(19): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | |||||||
| chr5:137983176 | TAAAAAAA others(9): Show |
T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1179+2065_1179+208 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | |||||||
| chr5:137983176 | TAAAAAAA others(10): Show |
T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(92): Show |
101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1179+2064_1179+208 others(21): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | |||||||
| chr5:137983194 | A | T | 1 | a0001c0001t0001g0146 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1179+2063T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983194 | |||||||
| chr5:137983205 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1179+2052T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983205 | |||||||
| chr5:137983213 | A | AAAAAAAA others(38): Show |
1 | a0001c0001t0002g0062 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(49): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | |||||||
| chr5:137983213 | A | AAAAAAAA others(37): Show |
1 | a0001c0001t0002g0077 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(48): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | |||||||
| chr5:137983213 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0002g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(30): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | |||||||
| chr5:137983213 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0002g0041 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(28): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | |||||||
| chr5:137983213 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0057 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(25): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | |||||||
| chr5:137983213 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0002g0043 a0001c0001t0002g0052 |
2 | HG01109.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1179+2043_1179+204 others(24): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | |||||||
| chr5:137983213 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0002g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | |||||||
| chr5:137983213 | A | AAAAAAAA others(3): Show |
2 | a0001c0001t0002g0058 a0001c0001t0002g0063 |
2 | HG01070.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1179+2043_1179+204 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | |||||||
| chr5:137983213 | A | AAAAAC | 6 | a0001c0001t0002g0022 a0001c0001t0002g0034 a0001c0001t0002g0068 others(3): Show |
6 | HG00735.hp2 HG02027.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+2043_1179+204 others(9): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | |||||||
| chr5:137983213 | A | C | 16 | a0001c0001t0002g0023 a0001c0001t0002g0035 a0001c0001t0002g0036 others(13): Show |
16 | HG00140.hp2 HG00741.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1179+2044T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | |||||||
| chr5:137983312 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1179+1945A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983312 | |||||||
| chr5:137983402 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1179+1855A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983402 | |||||||
| chr5:137983760 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1179+1497G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983760 | |||||||
| chr5:137983900 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1179+1357G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983900 | |||||||
| chr5:137984086 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1179+1171G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984086 | |||||||
| chr5:137984106 | C | T | 1 | a0001c0001t0002g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1179+1151G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984106 | |||||||
| chr5:137984113 | G | A | 64 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1179+1144C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984113 | |||||||
| chr5:137984199 | GATTATTT others(7): Show |
G | 1 | a0001c0001t0002g0076 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1179+1044_1179+105 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984199 | |||||||
| chr5:137984228 | T | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+1029A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984228 | |||||||
| chr5:137984255 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1179+1002A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984255 | |||||||
| chr5:137984512 | T | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0250 |
3 | HG01243.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1179+745A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984512 | |||||||
| chr5:137984594 | C | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(4): Show |
7 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+663G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984594 | |||||||
| chr5:137984633 | C | T | 1 | a0002c0003t0002g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1179+624G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984633 | |||||||
| chr5:137984634 | CT | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
234 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1179+622delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984634 | |||||||
| chr5:137984736 | G | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1179+521C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984736 | |||||||
| chr5:137984765 | T | C | 14 | a0001c0001t0002g0042 a0001c0001t0002g0044 a0001c0001t0002g0050 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1179+492A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984765 | |||||||
| chr5:137984766 | GT | G | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1179+490delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984766 | |||||||
| chr5:137984766 | GTTT | G | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+488_1179+490d others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984766 | |||||||
| chr5:137984821 | T | C | 1 | a0001c0001t0002g0036 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1179+436A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984821 | |||||||
| chr5:137984963 | G | A | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1179+294C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984963 | |||||||
| chr5:137984999 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0246 |
3 | HG03130.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1179+258C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984999 | |||||||
| chr5:137985226 | A | T | 1 | a0001c0001t0002g0041 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1179+31T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137985226 | |||||||
| chr5:137985658 | G | A | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1047-269C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137985658 | |||||||
| chr5:137985693 | CATA | C | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1047-307_1047-305d others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137985693 | |||||||
| chr5:137985713 | C | T | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047-324G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137985713 | |||||||
| chr5:137986001 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1047-612A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986001 | |||||||
| chr5:137986010 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
245 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.1047-621G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986010 | |||||||
| chr5:137986029 | C | T | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-640G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986029 | |||||||
| chr5:137986076 | C | CT | 58 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(55): Show |
58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1047-688dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986076 | |||||||
| chr5:137986134 | G | C | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-745C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986134 | |||||||
| chr5:137986341 | T | TA | 11 | a0001c0001t0002g0059 a0001c0001t0002g0073 a0001c0001t0002g0261 others(8): Show |
11 | HG00280.hp1 HG00323.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1047-953dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986341 | |||||||
| chr5:137986426 | T | TCC | 46 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 others(43): Show |
46 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1046+1033_1046+103 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986426 | |||||||
| chr5:137986435 | CA | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1046+1025delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986435 | |||||||
| chr5:137986436 | A | C | 70 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1046+1025T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986436 | |||||||
| chr5:137986449 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1046+1012T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986449 | |||||||
| chr5:137986554 | T | C | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1046+907A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986554 | |||||||
| chr5:137986746 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1046+715A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986746 | |||||||
| chr5:137986813 | C | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0195 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1046+648G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986813 | |||||||
| chr5:137986965 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1046+496A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986965 | |||||||
| chr5:137987428 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1046+33T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137987428 | |||||||
| chr5:137988054 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.890+220T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 8/23 | chr5 | 137988054 | |||||||
| chr5:137988055 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.890+219C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 8/23 | chr5 | 137988055 | |||||||
| chr5:137988431 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.849-116C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137988431 | |||||||
| chr5:137988627 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.849-312C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137988627 | |||||||
| chr5:137988650 | T | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0250 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.849-335A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137988650 | |||||||
| chr5:137988885 | T | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.849-570A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137988885 | |||||||
| chr5:137988974 | C | T | 6 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 others(3): Show |
6 | HG01516.hp1 HG01517.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.849-659G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137988974 | |||||||
| chr5:137989004 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0003g0311 |
3 | NA19009.hp2 NA19085.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.849-689A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989004 | |||||||
| chr5:137989078 | C | G | 2 | a0001c0001t0006g0254 a0001c0001t0006g0255 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.849-763G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989078 | |||||||
| chr5:137989118 | G | A | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-803C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989118 | |||||||
| chr5:137989251 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.849-936A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989251 | |||||||
| chr5:137989369 | CAGTA | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.849-1058_849-1055d others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989369 | |||||||
| chr5:137989405 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0130 |
2 | NA18950.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.849-1090G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989405 | |||||||
| chr5:137989896 | G | GA | 48 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(45): Show |
48 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.849-1582dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989896 | |||||||
| chr5:137989925 | G | T | 1 | a0001c0001t0001g0264 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.849-1610C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989925 | |||||||
| chr5:137989954 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.849-1639G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989954 | |||||||
| chr5:137990429 | G | C | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-2114C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137990429 | |||||||
| chr5:137990715 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.849-2400C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137990715 | |||||||
| chr5:137990775 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.849-2460G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137990775 | |||||||
| chr5:137990991 | C | G | 1 | a0001c0001t0001g0225 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.849-2676G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137990991 | |||||||
| chr5:137991241 | T | C | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.849-2926A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137991241 | |||||||
| chr5:137992112 | A | G | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(2): Show |
5 | HG02809.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-3797T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992112 | |||||||
| chr5:137992159 | G | A | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849-3844C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992159 | |||||||
| chr5:137992239 | T | G | 1 | a0001c0001t0002g0043 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.849-3924A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992239 | |||||||
| chr5:137992299 | G | GA | 27 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(24): Show |
27 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.849-3985dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992299 | |||||||
| chr5:137992365 | G | A | 2 | a0001c0001t0002g0293 a0001c0001t0002g0297 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.849-4050C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992365 | |||||||
| chr5:137992378 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849-4063C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992378 | |||||||
| chr5:137992451 | G | A | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849-4136C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992451 | |||||||
| chr5:137992551 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA18961.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.849-4236C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992551 | |||||||
| chr5:137992634 | A | G | 32 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.849-4319T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992634 | |||||||
| chr5:137992908 | A | C | 64 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.849-4593T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992908 | |||||||
| chr5:137992948 | G | A | 4 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0236 others(1): Show |
4 | HG00621.hp1 NA18961.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-4633C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992948 | |||||||
| chr5:137992949 | TCCA | T | 4 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0236 others(1): Show |
4 | HG00621.hp1 NA18961.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-4637_849-4635d others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992949 | |||||||
| chr5:137992965 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.849-4650A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992965 | |||||||
| chr5:137993001 | T | TACA | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.849-4689_849-4687d others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137993001 | |||||||
| chr5:137993454 | G | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.849-5139C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137993454 | |||||||
| chr5:137993506 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.849-5191T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137993506 | |||||||
| chr5:137993781 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0057 |
2 | HG00323.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.849-5466G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137993781 | |||||||
| chr5:137994104 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG01975.hp1 HG01978.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.849-5789G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994104 | |||||||
| chr5:137994278 | C | CT | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(51): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.849-5964dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994278 | |||||||
| chr5:137994507 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.849-6192A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994507 | |||||||
| chr5:137994665 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.849-6350G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994665 | |||||||
| chr5:137994742 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0041 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.849-6427T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994742 | |||||||
| chr5:137994892 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.849-6577G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994892 | |||||||
| chr5:137994954 | C | T | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849-6639G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994954 | |||||||
| chr5:137995016 | A | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.849-6701T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137995016 | |||||||
| chr5:137995152 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0250 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.849-6837C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137995152 | |||||||
| chr5:137995403 | A | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.849-7088T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137995403 | |||||||
| chr5:137996069 | C | T | 8 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.849-7754G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996069 | |||||||
| chr5:137996292 | C | T | 64 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.849-7977G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996292 | |||||||
| chr5:137996329 | C | T | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.849-8014G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996329 | |||||||
| chr5:137996473 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.849-8158A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996473 | |||||||
| chr5:137996636 | A | G | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.849-8321T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996636 | |||||||
| chr5:137996717 | G | A | 2 | a0001c0001t0003g0299 a0001c0001t0003g0314 |
2 | HG01433.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.849-8402C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996717 | |||||||
| chr5:137996829 | C | T | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.849-8514G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996829 | |||||||
| chr5:137996884 | A | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.849-8569T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996884 | |||||||
| chr5:137996965 | G | A | 1 | a0001c0001t0002g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.849-8650C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996965 | |||||||
| chr5:137996997 | G | A | 1 | a0001c0001t0004g0253 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849-8682C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996997 | |||||||
| chr5:137997003 | G | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA18961.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.849-8688C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997003 | |||||||
| chr5:137997049 | C | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(14): Show |
17 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.849-8734G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997049 | |||||||
| chr5:137997193 | G | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.849-8878C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997193 | |||||||
| chr5:137997270 | G | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.849-8955C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997270 | |||||||
| chr5:137997393 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0237 |
2 | HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.849-9078G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997393 | |||||||
| chr5:137997400 | C | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.849-9085G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997400 | |||||||
| chr5:137997411 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.849-9096C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997411 | |||||||
| chr5:137997424 | G | A | 1 | a0002c0003t0002g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.849-9109C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997424 | |||||||
| chr5:137997444 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.849-9129C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997444 | |||||||
| chr5:137997474 | A | AAT | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849-9161_849-9160d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997474 | |||||||
| chr5:137997476 | T | A | 6 | a0001c0001t0002g0051 a0001c0001t0002g0069 a0001c0001t0002g0073 others(3): Show |
6 | HG00639.hp2 HG00735.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.849-9161A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997476 | |||||||
| chr5:137997482 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.849-9167A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997482 | |||||||
| chr5:137997700 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(106): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.848+9290G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997700 | |||||||
| chr5:137997982 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02109.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.848+9008A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997982 | |||||||
| chr5:137998386 | C | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(106): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.848+8604G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998386 | |||||||
| chr5:137998714 | A | T | 2 | a0002c0003t0002g0010 a0002c0003t0002g0011 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.848+8276T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998714 | |||||||
| chr5:137998752 | T | C | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+8238A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998752 | |||||||
| chr5:137998759 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.848+8231C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998759 | |||||||
| chr5:137998866 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+8124G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998866 | |||||||
| chr5:137998924 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.848+8066C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998924 | |||||||
| chr5:137999102 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(80): Show |
84 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.848+7888C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999102 | |||||||
| chr5:137999104 | C | CT | 80 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(77): Show |
81 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.848+7885dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999104 | |||||||
| chr5:137999118 | G | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.848+7872C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999118 | |||||||
| chr5:137999120 | C | T | 1 | a0001c0001t0010g0260 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.848+7870G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999120 | |||||||
| chr5:137999126 | T | C | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.848+7864A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999126 | |||||||
| chr5:137999133 | A | G | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.848+7857T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999133 | |||||||
| chr5:137999433 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.848+7557T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999433 | |||||||
| chr5:137999445 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.848+7545T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999445 | |||||||
| chr5:137999787 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.848+7203A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999787 | |||||||
| chr5:137999912 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.848+7078C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999912 | |||||||
| chr5:138000088 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.848+6902G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000088 | |||||||
| chr5:138000169 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0167 |
2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.848+6821A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000169 | |||||||
| chr5:138000201 | T | C | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0250 |
3 | HG01243.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.848+6789A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000201 | |||||||
| chr5:138000293 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.848+6697A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000293 | |||||||
| chr5:138000524 | G | T | 8 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
8 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+6466C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000524 | |||||||
| chr5:138000728 | C | T | 2 | a0002c0003t0002g0010 a0002c0003t0002g0011 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.848+6262G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000728 | |||||||
| chr5:138000836 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0233 |
2 | NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.848+6154G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000836 | |||||||
| chr5:138000936 | C | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
238 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.848+6054G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000936 | |||||||
| chr5:138000943 | C | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(93): Show |
102 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.848+6047G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000943 | |||||||
| chr5:138000943 | CA | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(196): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.848+6046delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000943 | |||||||
| chr5:138000944 | A | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(90): Show |
99 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.848+6046T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000944 | |||||||
| chr5:138000948 | A | C | 1 | a0001c0001t0009g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.848+6042T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000948 | |||||||
| chr5:138001120 | C | CAA | 6 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0180 others(3): Show |
6 | HG01257.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+5868_848+5869d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001120 | |||||||
| chr5:138001134 | A | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+5856T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001134 | |||||||
| chr5:138001455 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.848+5535G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001455 | |||||||
| chr5:138001740 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(106): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.848+5250C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001740 | |||||||
| chr5:138001769 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.848+5221T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001769 | |||||||
| chr5:138001952 | G | A | 8 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+5038C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001952 | |||||||
| chr5:138002477 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0003g0311 |
3 | NA19009.hp2 NA19085.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.848+4513G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002477 | |||||||
| chr5:138002530 | T | C | 6 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
6 | HG01167.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+4460A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002530 | |||||||
| chr5:138002664 | A | AT | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.848+4325dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002664 | |||||||
| chr5:138002664 | A | ATT | 14 | a0001c0001t0001g0100 a0001c0001t0001g0129 a0001c0001t0001g0149 others(11): Show |
14 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.848+4324_848+4325d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002664 | |||||||
| chr5:138002737 | C | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+4253G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002737 | |||||||
| chr5:138002832 | AT | A | 60 | a0001c0001t0001g0118 a0001c0001t0002g0022 a0001c0001t0002g0023 others(57): Show |
60 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.848+4157delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002832 | |||||||
| chr5:138002963 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+4027G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002963 | |||||||
| chr5:138003054 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+3936G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003054 | |||||||
| chr5:138003161 | A | G | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.848+3829T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003161 | |||||||
| chr5:138003358 | A | G | 64 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.848+3632T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003358 | |||||||
| chr5:138003458 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.848+3532A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003458 | |||||||
| chr5:138003483 | G | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+3507C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003483 | |||||||
| chr5:138003488 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.848+3502C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003488 | |||||||
| chr5:138003644 | C | A | 1 | a0001c0001t0001g0233 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.848+3346G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003644 | |||||||
| chr5:138003775 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.848+3215T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003775 | |||||||
| chr5:138003977 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.848+3013G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003977 | |||||||
| chr5:138004304 | C | CAATGAAT others(8): Show |
302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.848+2685_848+2686i others(17): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004304 | |||||||
| chr5:138004378 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.848+2612A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004378 | |||||||
| chr5:138004480 | G | C | 4 | a0001c0001t0002g0022 a0001c0001t0002g0031 a0001c0001t0002g0032 others(1): Show |
4 | HG02451.hp1 HG02486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+2510C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004480 | |||||||
| chr5:138004513 | T | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0191 a0001c0001t0001g0194 others(6): Show |
9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.848+2477A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004513 | |||||||
| chr5:138004529 | C | A | 53 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.848+2461G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004529 | |||||||
| chr5:138004532 | G | A | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+2458C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004532 | |||||||
| chr5:138004608 | G | A | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.848+2382C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004608 | |||||||
| chr5:138004749 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.848+2241C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004749 | |||||||
| chr5:138004754 | C | T | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.848+2236G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004754 | |||||||
| chr5:138004898 | C | T | 2 | a0001c0002t0002g0282 a0001c0002t0002g0283 |
2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.848+2092G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004898 | |||||||
| chr5:138004909 | A | G | 1 | a0001c0001t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.848+2081T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004909 | |||||||
| chr5:138005020 | T | C | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.848+1970A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005020 | |||||||
| chr5:138005126 | A | G | 32 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.848+1864T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005126 | |||||||
| chr5:138005127 | C | G | 1 | a0001c0001t0002g0078 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.848+1863G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005127 | |||||||
| chr5:138005221 | G | A | 2 | a0002c0003t0002g0010 a0002c0003t0002g0011 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.848+1769C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005221 | |||||||
| chr5:138005269 | A | G | 1 | a0001c0001t0013g0229 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.848+1721T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005269 | |||||||
| chr5:138005272 | TTAAAACA others(2): Show |
T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.848+1709_848+1717d others(11): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005272 | |||||||
| chr5:138005403 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.848+1587T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005403 | |||||||
| chr5:138005463 | AT | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(147): Show |
156 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.848+1526delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005463 | |||||||
| chr5:138005477 | G | A | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.848+1513C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005477 | |||||||
| chr5:138005653 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.848+1337T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005653 | |||||||
| chr5:138005670 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.848+1320C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005670 | |||||||
| chr5:138005845 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
241 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.848+1145A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005845 | |||||||
| chr5:138005922 | G | A | 2 | a0001c0001t0006g0254 a0001c0001t0006g0255 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.848+1068C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005922 | |||||||
| chr5:138005938 | G | A | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.848+1052C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005938 | |||||||
| chr5:138006045 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+945G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006045 | |||||||
| chr5:138006047 | C | T | 14 | a0001c0001t0002g0042 a0001c0001t0002g0044 a0001c0001t0002g0050 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.848+943G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006047 | |||||||
| chr5:138006139 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+851A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006139 | |||||||
| chr5:138006154 | C | G | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+836G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006154 | |||||||
| chr5:138006188 | C | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0191 a0001c0001t0001g0194 others(6): Show |
9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.848+802G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006188 | |||||||
| chr5:138006221 | C | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+769G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006221 | |||||||
| chr5:138006355 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0185 |
3 | HG00280.hp2 HG01255.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.848+635G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006355 | |||||||
| chr5:138006362 | G | A | 1 | a0001c0001t0004g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.848+628C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006362 | |||||||
| chr5:138006824 | A | T | 1 | a0001c0001t0001g0028 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.848+166T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006824 | |||||||
| chr5:138006887 | A | G | 1 | a0001c0001t0009g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.848+103T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006887 | |||||||
| chr5:138006900 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(107): Show |
116 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.848+90A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006900 | |||||||
| chr5:138007360 | A | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.691-213T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007360 | |||||||
| chr5:138007410 | T | C | 5 | a0001c0001t0001g0193 a0001c0001t0001g0202 a0001c0001t0001g0212 others(2): Show |
5 | HG00408.hp2 NA18612.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-263A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007410 | |||||||
| chr5:138007427 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.691-280T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007427 | |||||||
| chr5:138007574 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.691-427C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007574 | |||||||
| chr5:138007701 | CA | C | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.691-555delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007701 | |||||||
| chr5:138007752 | T | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02027.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.691-605A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007752 | |||||||
| chr5:138008066 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.691-919A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008066 | |||||||
| chr5:138008084 | C | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.691-937G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008084 | |||||||
| chr5:138008448 | A | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0128 |
2 | NA19009.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.691-1301T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008448 | |||||||
| chr5:138008498 | C | A | 50 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.691-1351G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008498 | |||||||
| chr5:138008624 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.691-1477A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008624 | |||||||
| chr5:138008658 | A | G | 1 | a0003c0005t0001g0244 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.691-1511T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008658 | |||||||
| chr5:138008739 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0237 |
2 | HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.691-1592A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008739 | |||||||
| chr5:138008999 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0202 a0001c0001t0005g0004 others(1): Show |
4 | HG00408.hp2 NA18612.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-1852G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008999 | |||||||
| chr5:138009344 | G | T | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.690+1664C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009344 | |||||||
| chr5:138009445 | G | A | 2 | a0002c0003t0002g0010 a0002c0003t0002g0011 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.690+1563C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009445 | |||||||
| chr5:138009488 | C | CA | 7 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(4): Show |
7 | HG01069.hp1 HG02735.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+1519dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009488 | |||||||
| chr5:138009778 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.690+1230A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009778 | |||||||
| chr5:138009784 | G | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.690+1224C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009784 | |||||||
| chr5:138009802 | C | CA | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(168): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.690+1205dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009802 | |||||||
| chr5:138009802 | C | CAA | 6 | a0001c0001t0001g0110 a0001c0001t0001g0239 a0001c0001t0002g0056 others(3): Show |
6 | HG01167.hp1 HG01175.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+1204_690+1205d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009802 | |||||||
| chr5:138009869 | G | A | 5 | a0001c0001t0001g0191 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+1139C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009869 | |||||||
| chr5:138010085 | A | G | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.690+923T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010085 | |||||||
| chr5:138010106 | C | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.690+902G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010106 | |||||||
| chr5:138010224 | AC | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.690+783delG | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010224 | |||||||
| chr5:138010556 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.690+452T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010556 | |||||||
| chr5:138010717 | A | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0059 |
2 | HG01081.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.690+291T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010717 | |||||||
| chr5:138010724 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.690+284A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010724 | |||||||
| chr5:138010854 | A | C | 2 | a0001c0001t0002g0279 a0001c0001t0002g0280 |
2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.690+154T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010854 | |||||||
| chr5:138010957 | T | TA | 176 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(173): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.690+50dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010957 | |||||||
| chr5:138010957 | T | TAA | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(95): Show |
104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.690+49_690+50dupTT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010957 | |||||||
| chr5:138011379 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.549-230A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 5/23 | chr5 | 138011379 | |||||||
| chr5:138011664 | C | T | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.548+104G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 5/23 | chr5 | 138011664 | |||||||
| chr5:138011714 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.548+54C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 5/23 | chr5 | 138011714 | |||||||
| chr5:138011751 | T | A | 1 | a0001c0001t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.548+17A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 5/23 | chr5 | 138011751 | |||||||
| chr5:138012028 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0237 |
2 | HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.371-83G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012028 | |||||||
| chr5:138012089 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.371-144G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012089 | |||||||
| chr5:138012117 | ATGGAGAA others(4): Show |
A | 1 | a0001c0002t0002g0286 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.371-183_371-173del others(11): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012117 | |||||||
| chr5:138012216 | C | CT | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.371-272dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012216 | |||||||
| chr5:138012216 | C | CTT | 11 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0203 others(8): Show |
11 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.371-273_371-272dup others(2): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012216 | |||||||
| chr5:138012216 | CTTTTTT | C | 50 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(47): Show |
50 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.371-277_371-272del others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012216 | |||||||
| chr5:138012224 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.371-279A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012224 | |||||||
| chr5:138012303 | A | G | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-358T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012303 | |||||||
| chr5:138012328 | G | C | 32 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.371-383C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012328 | |||||||
| chr5:138012508 | A | C | 58 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(55): Show |
58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.371-563T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012508 | |||||||
| chr5:138012527 | G | A | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-582C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012527 | |||||||
| chr5:138012608 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
241 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.371-663C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012608 | |||||||
| chr5:138012730 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.371-785G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012730 | |||||||
| chr5:138012905 | CA | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0175 a0001c0001t0002g0293 others(4): Show |
7 | HG01243.hp1 HG01256.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.371-961delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012905 | |||||||
| chr5:138013270 | G | C | 1 | a0001c0001t0002g0049 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.371-1325C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013270 | |||||||
| chr5:138013283 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.371-1338A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013283 | |||||||
| chr5:138013454 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.371-1509A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013454 | |||||||
| chr5:138013501 | C | CA | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.371-1557dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013501 | |||||||
| chr5:138013501 | C | CAA | 8 | a0001c0001t0001g0120 a0001c0001t0001g0142 a0001c0001t0001g0173 others(5): Show |
8 | HG01515.hp2 HG02559.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.371-1558_371-1557d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013501 | |||||||
| chr5:138013517 | A | T | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-1572T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013517 | |||||||
| chr5:138013694 | C | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | NA19003.hp2 NA19056.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.371-1749G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013694 | |||||||
| chr5:138014015 | C | G | 7 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(4): Show |
7 | HG00738.hp1 HG01074.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.371-2070G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014015 | |||||||
| chr5:138014031 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.371-2086C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014031 | |||||||
| chr5:138014050 | C | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.371-2105G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014050 | |||||||
| chr5:138014291 | G | A | 2 | a0002c0003t0002g0010 a0002c0003t0002g0011 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.371-2346C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014291 | |||||||
| chr5:138014599 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.371-2654C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014599 | |||||||
| chr5:138014789 | T | C | 32 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.371-2844A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014789 | |||||||
| chr5:138015273 | G | A | 2 | a0002c0003t0002g0010 a0002c0003t0002g0011 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.370+3029C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015273 | |||||||
| chr5:138015304 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.370+2998G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015304 | |||||||
| chr5:138015388 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.370+2914C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015388 | |||||||
| chr5:138015429 | G | C | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.370+2873C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015429 | |||||||
| chr5:138015459 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.370+2843G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015459 | |||||||
| chr5:138015470 | A | C | 32 | a0001c0001t0001g0099 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.370+2832T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015470 | |||||||
| chr5:138015478 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.370+2824T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015478 | |||||||
| chr5:138016148 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.370+2154A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138016148 | |||||||
| chr5:138016459 | T | C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0046 a0001c0001t0002g0075 others(1): Show |
4 | HG00741.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.370+1843A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138016459 | |||||||
| chr5:138016460 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0095 |
2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.370+1842T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138016460 | |||||||
| chr5:138016507 | G | A | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.370+1795C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138016507 | |||||||
| chr5:138016613 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(5): Show |
8 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.370+1689C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138016613 | |||||||
| chr5:138017343 | A | G | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.370+959T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138017343 | |||||||
| chr5:138017391 | T | C | 3 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0274 |
3 | HG02055.hp2 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.370+911A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138017391 | |||||||
| chr5:138017852 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.370+450A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138017852 | |||||||
| chr5:138017979 | C | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.370+323G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138017979 | |||||||
| chr5:138018278 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.370+24A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138018278 | |||||||
| chr5:138018792 | G | A | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+163C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 3/23 | chr5 | 138018792 | |||||||
| chr5:138019162 | C | CA | 62 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(59): Show |
62 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.-35-17dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019162 | |||||||
| chr5:138019162 | CA | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
238 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.-35-17delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019162 | |||||||
| chr5:138019247 | A | G | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-101T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019247 | |||||||
| chr5:138019440 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
2 | HG03490.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-35-294A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019440 | |||||||
| chr5:138019591 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-35-445C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019591 | |||||||
| chr5:138019682 | AT | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(259): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.-35-537delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019682 | |||||||
| chr5:138019813 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0250 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-35-667C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019813 | |||||||
| chr5:138019841 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0184 |
3 | HG00639.hp1 HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-35-695C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019841 | |||||||
| chr5:138019932 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-35-786C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019932 | |||||||
| chr5:138020196 | G | A | 1 | a0001c0001t0013g0229 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-36+835C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020196 | |||||||
| chr5:138020210 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-36+821C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020210 | |||||||
| chr5:138020287 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0120 a0001c0001t0001g0122 others(2): Show |
5 | NA18953.hp2 NA19011.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+744A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020287 | |||||||
| chr5:138020323 | C | T | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-36+708G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020323 | |||||||
| chr5:138020324 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-36+707C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020324 | |||||||
| chr5:138020663 | A | G | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-36+368T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020663 | |||||||
| chr5:138020850 | A | C | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(2): Show |
5 | HG02809.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+181T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020850 | |||||||
| chr5:138021523 | C | CATG | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-202-327_-202-326i others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138021523 | |||||||
| chr5:138021768 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0157 |
3 | HG00738.hp1 HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-202-571C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138021768 | |||||||
| chr5:138021846 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-202-649A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138021846 | |||||||
| chr5:138022087 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-202-890G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022087 | |||||||
| chr5:138022112 | CAAAAAAA others(2): Show |
C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
238 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.-202-924_-202-916d others(11): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022112 | |||||||
| chr5:138022294 | T | C | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-202-1097A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022294 | |||||||
| chr5:138022324 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-202-1127A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022324 | |||||||
| chr5:138022628 | C | T | 7 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0049 others(4): Show |
7 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-202-1431G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022628 | |||||||
| chr5:138022847 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-202-1650C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022847 | |||||||
| chr5:138022863 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-202-1666G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022863 | |||||||
| chr5:138022946 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-202-1749C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022946 | |||||||
| chr5:138022954 | A | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-1757T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022954 | |||||||
| chr5:138022993 | G | T | 64 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-202-1796C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022993 | |||||||
| chr5:138023065 | C | G | 5 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0062 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-1868G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023065 | |||||||
| chr5:138023235 | A | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-2038T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023235 | |||||||
| chr5:138023401 | C | A | 3 | a0001c0001t0002g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 |
3 | HG01243.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-202-2204G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023401 | |||||||
| chr5:138023404 | T | C | 64 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-202-2207A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023404 | |||||||
| chr5:138023551 | T | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0180 others(3): Show |
6 | HG01257.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-202-2354A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023551 | |||||||
| chr5:138023676 | C | G | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-202-2479G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023676 | |||||||
| chr5:138023765 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-202-2568C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023765 | |||||||
| chr5:138023856 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-202-2659C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023856 | |||||||
| chr5:138023894 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-202-2697G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023894 | |||||||
| chr5:138024068 | T | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-202-2871A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024068 | |||||||
| chr5:138024194 | A | C | 1 | a0001c0001t0001g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-202-2997T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024194 | |||||||
| chr5:138024314 | C | G | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-202-3117G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024314 | |||||||
| chr5:138024329 | G | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-3132C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024329 | |||||||
| chr5:138024359 | T | C | 2 | a0002c0003t0002g0010 a0002c0003t0002g0011 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-202-3162A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024359 | |||||||
| chr5:138024477 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(107): Show |
116 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-202-3280A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024477 | |||||||
| chr5:138024579 | T | TA | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.-202-3383dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024579 | |||||||
| chr5:138024632 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-202-3435A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024632 | |||||||
| chr5:138024683 | G | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(5): Show |
8 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.-202-3486C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024683 | |||||||
| chr5:138024786 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-202-3589T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024786 | |||||||
| chr5:138024810 | C | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-3613G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024810 | |||||||
| chr5:138024812 | C | G | 4 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 others(1): Show |
4 | HG01516.hp1 HG01517.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-202-3615G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024812 | |||||||
| chr5:138024812 | CAG | C | 68 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-202-3617_-202-361 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024812 | |||||||
| chr5:138024812 | CAGAG | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(113): Show |
122 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-202-3619_-202-361 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024812 | |||||||
| chr5:138024812 | CAGAGAG | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(111): Show |
115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-202-3621_-202-361 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024812 | |||||||
| chr5:138024816 | G | C | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02523.hp1 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-202-3619C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024816 | |||||||
| chr5:138024818 | G | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(117): Show |
126 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-202-3621C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024818 | |||||||
| chr5:138024820 | G | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0191 |
2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-202-3623C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024820 | |||||||
| chr5:138024834 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-202-3637C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024834 | |||||||
| chr5:138024836 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-202-3639T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024836 | |||||||
| chr5:138024902 | ACT | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-202-3707_-202-370 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024902 | |||||||
| chr5:138024922 | G | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0180 others(3): Show |
6 | HG01257.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-202-3725C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024922 | |||||||
| chr5:138025011 | T | C | 5 | a0001c0001t0001g0190 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
5 | HG00423.hp1 HG00438.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.-202-3814A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025011 | |||||||
| chr5:138025093 | C | G | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-3896G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025093 | |||||||
| chr5:138025093 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-202-3896G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025093 | |||||||
| chr5:138025288 | C | CATATAT | 5 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0060 others(2): Show |
5 | HG01069.hp1 HG01070.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-4097_-202-409 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | |||||||
| chr5:138025288 | C | CATATATA others(1): Show |
20 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0035 others(17): Show |
20 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-202-4099_-202-409 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | |||||||
| chr5:138025288 | C | CATATATA others(3): Show |
18 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0033 others(15): Show |
18 | HG01257.hp1 HG01258.hp2 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.-202-4101_-202-409 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | |||||||
| chr5:138025288 | C | CATATATA others(5): Show |
2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG00140.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-202-4103_-202-409 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | |||||||
| chr5:138025288 | CATAT | C | 16 | a0001c0001t0001g0191 a0001c0001t0001g0196 a0001c0001t0001g0197 others(13): Show |
16 | HG01192.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-202-4095_-202-409 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | |||||||
| chr5:138025288 | CATATAT | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0025 others(75): Show |
84 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-202-4097_-202-409 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | |||||||
| chr5:138025304 | TATATA | T | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0215 others(2): Show |
5 | HG00597.hp1 NA18948.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-4112_-202-410 others(9): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025304 | |||||||
| chr5:138025305 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(128): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.-202-4108T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025305 | |||||||
| chr5:138025306 | TATATG | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
115 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-202-4114_-202-411 others(9): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025306 | |||||||
| chr5:138025306 | TATATGTA | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0080 a0001c0001t0001g0081 others(14): Show |
17 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.-202-4116_-202-411 others(11): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025306 | |||||||
| chr5:138025307 | A | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-4110T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025307 | |||||||
| chr5:138025309 | A | G | 11 | a0001c0001t0001g0191 a0001c0001t0001g0196 a0001c0001t0001g0197 others(8): Show |
11 | HG01192.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-202-4112T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025309 | |||||||
| chr5:138025310 | T | G | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0215 others(2): Show |
5 | HG00597.hp1 NA18948.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-4113A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025310 | |||||||
| chr5:138025311 | G | A | 9 | a0001c0001t0002g0036 a0001c0001t0002g0062 a0001c0001t0002g0063 others(6): Show |
9 | HG00280.hp1 HG00323.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.-202-4114C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025311 | |||||||
| chr5:138025311 | G | T | 11 | a0001c0001t0001g0191 a0001c0001t0001g0196 a0001c0001t0001g0197 others(8): Show |
11 | HG01192.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-202-4114C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025311 | |||||||
| chr5:138025313 | A | AT | 7 | a0001c0001t0002g0161 a0001c0001t0002g0293 a0001c0001t0002g0294 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-202-4117dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025313 | |||||||
| chr5:138025313 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-202-4116T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025313 | |||||||
| chr5:138025313 | A | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
221 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-202-4116T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025313 | |||||||
| chr5:138025315 | T | A | 1 | a0002c0003t0002g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-202-4118A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025315 | |||||||
| chr5:138025319 | T | G | 1 | a0001c0001t0013g0229 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-202-4122A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025319 | |||||||
| chr5:138025322 | T | G | 78 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(75): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-202-4125A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025322 | |||||||
| chr5:138025516 | G | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-202-4319C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025516 | |||||||
| chr5:138025705 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-202-4508T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025705 | |||||||
| chr5:138025729 | C | T | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-202-4532G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025729 | |||||||
| chr5:138025775 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0120 |
2 | NA18953.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-202-4578G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025775 | |||||||
| chr5:138026009 | A | T | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-4812T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026009 | |||||||
| chr5:138026233 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-202-5036A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026233 | |||||||
| chr5:138026254 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-202-5057G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026254 | |||||||
| chr5:138026270 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-202-5073A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026270 | |||||||
| chr5:138026572 | T | C | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-5375A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026572 | |||||||
| chr5:138026628 | C | A | 1 | a0001c0001t0001g0151 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-202-5431G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026628 | |||||||
| chr5:138026628 | C | CA | 54 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0021 others(51): Show |
54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-202-5432dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026628 | |||||||
| chr5:138026628 | C | CAA | 45 | a0001c0001t0001g0230 a0001c0001t0001g0238 a0001c0001t0001g0275 others(42): Show |
45 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-202-5433_-202-543 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026628 | |||||||
| chr5:138026628 | C | CAAA | 9 | a0001c0001t0001g0273 a0001c0001t0002g0022 a0001c0001t0002g0066 others(6): Show |
9 | HG00735.hp2 HG01167.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-202-5434_-202-543 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026628 | |||||||
| chr5:138026628 | CA | C | 13 | a0001c0001t0001g0098 a0001c0001t0001g0117 a0001c0001t0001g0118 others(10): Show |
13 | HG00280.hp1 HG00323.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-202-5432delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026628 | |||||||
| chr5:138026655 | A | AC | 4 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-202-5459_-202-545 others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026655 | |||||||
| chr5:138026655 | A | C | 13 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.-202-5458T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026655 | |||||||
| chr5:138026689 | C | CA | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-202-5493dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026689 | |||||||
| chr5:138026742 | C | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-5545G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026742 | |||||||
| chr5:138026757 | T | A | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-202-5560A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026757 | |||||||
| chr5:138026858 | G | C | 1 | a0001c0001t0001g0116 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-202-5661C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026858 | |||||||
| chr5:138026938 | C | CAAAT | 23 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(20): Show |
23 | HG00280.hp2 HG00733.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-202-5745_-202-574 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | |||||||
| chr5:138026938 | C | CAAATAAA others(1): Show |
8 | a0001c0001t0001g0096 a0001c0001t0001g0173 a0001c0001t0001g0174 others(5): Show |
8 | HG00741.hp2 HG01515.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-202-5749_-202-574 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | |||||||
| chr5:138026938 | CAAAT | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0028 others(110): Show |
119 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-202-5745_-202-574 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | |||||||
| chr5:138026938 | CAAATAAA others(1): Show |
C | 15 | a0001c0001t0001g0094 a0001c0001t0001g0236 a0001c0001t0001g0237 others(12): Show |
15 | HG00621.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-202-5749_-202-574 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | |||||||
| chr5:138026938 | CAAATAAA others(5): Show |
C | 15 | a0001c0001t0002g0023 a0001c0001t0002g0075 a0001c0001t0002g0076 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-202-5753_-202-574 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | |||||||
| chr5:138026938 | CAAATAAA others(9): Show |
C | 1 | a0001c0001t0002g0077 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-202-5757_-202-574 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | |||||||
| chr5:138026938 | CAAATAAA others(13): Show |
C | 1 | a0001c0001t0002g0078 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-202-5761_-202-574 others(24): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | |||||||
| chr5:138026999 | G | A | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+5783C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026999 | |||||||
| chr5:138027383 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-203+5399A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027383 | |||||||
| chr5:138027484 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-203+5298A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027484 | |||||||
| chr5:138027496 | T | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-203+5286A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027496 | |||||||
| chr5:138027514 | G | A | 8 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+5268C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027514 | |||||||
| chr5:138027542 | T | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02258.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-203+5240A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027542 | |||||||
| chr5:138027589 | T | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-203+5193A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027589 | |||||||
| chr5:138027625 | C | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-203+5157G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027625 | |||||||
| chr5:138027785 | T | C | 8 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-203+4997A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027785 | |||||||
| chr5:138027969 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-203+4813T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027969 | |||||||
| chr5:138028408 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-203+4374A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028408 | |||||||
| chr5:138028494 | GA | G | 8 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+4287delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028494 | |||||||
| chr5:138028549 | G | A | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-203+4233C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028549 | |||||||
| chr5:138028592 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-203+4190C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028592 | |||||||
| chr5:138028607 | G | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-203+4175C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028607 | |||||||
| chr5:138028637 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-203+4145G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028637 | |||||||
| chr5:138028752 | T | C | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+4030A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028752 | |||||||
| chr5:138028800 | C | T | 2 | a0001c0002t0002g0282 a0001c0002t0002g0283 |
2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-203+3982G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028800 | |||||||
| chr5:138028968 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-203+3814C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028968 | |||||||
| chr5:138029029 | GA | G | 19 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 others(16): Show |
19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-203+3752delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029029 | |||||||
| chr5:138029106 | C | T | 19 | a0001c0001t0001g0163 a0001c0001t0001g0173 a0001c0001t0001g0174 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-203+3676G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029106 | |||||||
| chr5:138029133 | T | C | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+3649A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029133 | |||||||
| chr5:138029241 | T | C | 4 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-203+3541A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029241 | |||||||
| chr5:138029323 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-203+3459T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029323 | |||||||
| chr5:138029328 | T | C | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+3454A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029328 | |||||||
| chr5:138029432 | G | A | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-203+3350C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029432 | |||||||
| chr5:138030279 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-203+2503G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030279 | |||||||
| chr5:138030334 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-203+2448T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030334 | |||||||
| chr5:138030410 | C | CT | 12 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0165 others(9): Show |
13 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.-203+2371dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030410 | |||||||
| chr5:138030410 | CT | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(105): Show |
114 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-203+2371delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030410 | |||||||
| chr5:138030691 | G | C | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0243 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-203+2091C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030691 | |||||||
| chr5:138030711 | T | TC | 106 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(103): Show |
107 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-203+2070dupG | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030711 | |||||||
| chr5:138030711 | T | TCC | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0245 others(15): Show |
18 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.-203+2069_-203+207 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030711 | |||||||
| chr5:138030722 | C | CA | 8 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+2059dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030722 | |||||||
| chr5:138030723 | A | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(8): Show |
11 | HG00735.hp1 HG01516.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.-203+2059T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030723 | |||||||
| chr5:138030758 | G | A | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-203+2024C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030758 | |||||||
| chr5:138030837 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-203+1945G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030837 | |||||||
| chr5:138030893 | C | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-203+1889G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030893 | |||||||
| chr5:138030925 | C | A | 1 | a0001c0001t0001g0259 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-203+1857G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030925 | |||||||
| chr5:138030948 | G | A | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(2): Show |
5 | HG02809.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-203+1834C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030948 | |||||||
| chr5:138031030 | C | CA | 6 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 others(3): Show |
6 | HG01433.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+1751dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031030 | |||||||
| chr5:138031113 | C | A | 2 | a0002c0003t0002g0010 a0002c0003t0002g0011 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-203+1669G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031113 | |||||||
| chr5:138031232 | T | TA | 6 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(3): Show |
6 | HG01496.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-203+1549dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031232 | |||||||
| chr5:138031322 | C | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-203+1460G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031322 | |||||||
| chr5:138031426 | G | A | 6 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
6 | HG01167.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-203+1356C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031426 | |||||||
| chr5:138031451 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG00642.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-203+1331C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031451 | |||||||
| chr5:138031474 | G | A | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-203+1308C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031474 | |||||||
| chr5:138031742 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-203+1040G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031742 | |||||||
| chr5:138031908 | C | G | 1 | a0001c0001t0001g0012 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-203+874G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031908 | |||||||
| chr5:138032020 | T | C | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+762A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138032020 | |||||||
| chr5:138032479 | C | T | 6 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0009 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+303G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138032479 | |||||||
| chr5:138032714 | G | A | 5 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+68C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138032714 | |||||||
| chr5:138032732 | G | A | 1 | a0001c0001t0001g0298 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-203+50C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138032732 |