Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 153020 |
| ensemblid | ENSG00000138670.19 |
| hgncid | 24881 |
| symbol | RASGEF1B |
| name | RasGEF domain family member 1B |
| refseq_nuc | NM_152545.3 |
| refseq_prot | NP_689758.1 |
| ensembl_nuc | ENST00000264400.7 |
| ensembl_prot | ENSP00000264400.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 81426393 |
| end | 81471907 |
| strand | - |
| ver | v1.2 |
| region | chr4:81426393-81471907 |
| region5000 | chr4:81421393-81476907 |
| regionname0 | RASGEF1B_chr4_81426393_81471907 |
| regionname5000 | RASGEF1B_chr4_81421393_81476907 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 473 | 313 | 88 | 60 | 108 | 16 | 39 | 78 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | MPQTP others(468): Show |
chr4 | 81421393 | 81476907 |
| a0002 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | MPQTP others(468): Show |
chr4 | 81421393 | 81476907 |
| a0003 | 0/0 | 473 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | MPQTP others(468): Show |
chr4 | 81421393 | 81476907 |
| a0004 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | MPQTP others(468): Show |
chr4 | 81421393 | 81476907 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1419 | 311 | 87 | 60 | 108 | 16 | 38 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | ATGCC others(1414): Show |
chr4 | 81421393 | 81476907 | ||
| a0001c0002 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | ATGCC others(1414): Show |
chr4 | 81421393 | 81476907 | ||
| a0001c0005 | 0/0 | 1419 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | ATGCC others(1414): Show |
chr4 | 81421393 | 81476907 | ||
| a0002c0006 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | ATGCC others(1414): Show |
chr4 | 81421393 | 81476907 | ||
| a0003c0004 | 0/0 | 1419 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | ATGCC others(1414): Show |
chr4 | 81421393 | 81476907 | ||
| a0004c0003 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | ATGCC others(1414): Show |
chr4 | 81421393 | 81476907 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2941 | 121 | 13 | 35 | 46 | 13 | 13 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2936): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0002 | 0/1 | 2939 | 52 | 15 | 4 | 22 | 1 | 9 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2934): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0003 | 0/0 | 2940 | 35 | 7 | 5 | 15 | 0 | 8 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2935): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0004 | 0/0 | 2942 | 24 | 3 | 4 | 16 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2937): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0005 | 0/0 | 2937 | 20 | 9 | 5 | 0 | 2 | 4 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2932): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0006 | 0/0 | 2938 | 23 | 16 | 3 | 3 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2933): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0007 | 0/0 | 2938 | 6 | 6 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2933): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0008 | 0/0 | 2936 | 6 | 0 | 0 | 4 | 0 | 2 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2931): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0009 | 0/0 | 2941 | 5 | 5 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2936): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0010 | 0/0 | 2939 | 4 | 2 | 2 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2934): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0011 | 0/0 | 2942 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2937): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0012 | 0/0 | 2939 | 2 | 0 | 0 | 2 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2934): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0013 | 0/0 | 2941 | 2 | 2 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2936): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0014 | 0/0 | 2941 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2936): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0015 | 0/0 | 2938 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2933): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0016 | 0/0 | 2939 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2934): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0017 | 0/0 | 2939 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2934): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0018 | 0/0 | 2939 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2934): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0019 | 0/0 | 2940 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2935): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0020 | 0/0 | 2941 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2936): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0021 | 0/0 | 2942 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2937): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0022 | 0/0 | 2941 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2936): Show |
chr4 | 81421393 | 81476907 |
| a0001c0001t0023 | 0/0 | 2942 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2937): Show |
chr4 | 81421393 | 81476907 |
| a0001c0002t0005 | 0/0 | 2937 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2932): Show |
chr4 | 81421393 | 81476907 |
| a0001c0005t0001 | 0/0 | 2941 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2936): Show |
chr4 | 81421393 | 81476907 |
| a0002c0006t0011 | 0/0 | 2942 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2937): Show |
chr4 | 81421393 | 81476907 |
| a0003c0004t0005 | 0/0 | 2937 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2932): Show |
chr4 | 81421393 | 81476907 |
| a0004c0003t0005 | 0/0 | 2937 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | AGTAT others(2932): Show |
chr4 | 81421393 | 81476907 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 8 | 1 | 1 | 4 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0007g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0008g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0008g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0009g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0010g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0010g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0011g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0012g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0012g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0013g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0014g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0015g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0016g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0017g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0018g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0019g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0020g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0021g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0022g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0001t0023g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0002t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0001c0005t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0002c0006t0011g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0003c0004t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| a0004c0003t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | GBR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | GBR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0064 | EUR | FIN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | FIN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | CHS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0247 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0248 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0194 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0118 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01106 | hp2 | a0001 | c0001 | t0014 | g0024 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0041 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0104 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0226 | AMR | PUR | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0074 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0111 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01346 | hp2 | a0001 | c0001 | t0020 | g0177 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0101 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0263 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0262 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0196 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0216 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02155 | hp2 | a0001 | c0001 | t0008 | g0015 | EAS | CDX | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02258 | hp1 | a0001 | c0001 | t0019 | g0042 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0244 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02572 | hp2 | a0001 | c0001 | t0018 | g0251 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0277 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0270 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0274 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0043 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0099 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02886 | hp2 | a0001 | c0001 | t0017 | g0279 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0264 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0023 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02897 | hp1 | a0001 | c0001 | t0013 | g0023 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0259 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0252 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0276 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0034 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03130 | hp2 | a0001 | c0002 | t0005 | g0275 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0094 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0192 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0236 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03490 | hp1 | a0001 | c0005 | t0001 | g0191 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03516 | hp1 | a0001 | c0001 | t0022 | g0109 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03516 | hp2 | a0002 | c0006 | t0011 | g0232 | AFR | ESN | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0273 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0103 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03688 | hp1 | a0001 | c0001 | t0008 | g0136 | SAS | STU | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0249 | SAS | STU | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0069 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0184 | SAS | BEB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0197 | SAS | BEB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0154 | SAS | BEB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | STU | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG04115 | hp2 | a0003 | c0004 | t0005 | g0170 | SAS | STU | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | STU | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0257 | SAS | STU | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | STU | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG04228 | hp2 | a0001 | c0001 | t0008 | g0261 | SAS | STU | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0228 | AFR | YRI | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | CHB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0227 | AFR | YRI | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | YRI | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18950 | hp1 | a0001 | c0001 | t0012 | g0127 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18956 | hp2 | a0001 | c0001 | t0012 | g0121 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0070 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18989 | hp1 | a0001 | c0001 | t0008 | g0195 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18990 | hp1 | a0001 | c0001 | t0008 | g0122 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18997 | hp1 | a0001 | c0001 | t0006 | g0129 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | LWK | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | LWK | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | LWK | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19043 | hp2 | a0001 | c0001 | t0023 | g0229 | AFR | LWK | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19083 | hp1 | a0001 | c0001 | t0008 | g0015 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19240 | hp1 | a0004 | c0003 | t0005 | g0231 | AFR | YRI | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | YRI | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | ASW | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ASW | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0112 | EUR | TSI | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | TSI | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | TSI | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0171 | SAS | GIH | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0230 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02109 | hp1 | a0001 | c0001 | t0021 | g0219 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0271 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0254 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0237 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | MSL | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | USA | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0096 | AFR | USA | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | USA | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | USA | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | LWK | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | LWK | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0213 | REF | REF | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | RASGEF1B_chr4_81421393_81476907 | RASGEF1B | chr4 | 81421393 | 81476907 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:81426394 | C | A | 1 | a0001 | 2 | NA18950.hp1 NA18956.hp2 |
splice_region_variant | LOW | c.*1374G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | chr4 | 81426394 | |||||||
| chr4:81445823 | G | A | 1 | a0004 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.745C>T | p.Arg249Trp | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 7/14 | 889/2941 | 745/1422 | 249/473 | chr4 | 81445823 | |||
| chr4:81448145 | T | C | 1 | a0003 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.578A>G | p.Gln193Arg | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 5/14 | 722/2941 | 578/1422 | 193/473 | chr4 | 81448145 | |||
| chr4:81459443 | C | A | 1 | a0002 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.66G>T | p.Gln22His | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/14 | 210/2941 | 66/1422 | 22/473 | chr4 | 81459443 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:81442336 | A | C | 1 | a0001c0002 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.969T>G | p.Thr323Thr | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/14 | 1113/2941 | 969/1422 | 323/473 | chr4 | 81442336 | |||
| chr4:81456657 | G | A | 1 | a0001c0005 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.432C>T | p.Gly144Gly | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/14 | 576/2941 | 432/1422 | 144/473 | chr4 | 81456657 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:81426439 | C | G | 3 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0019 |
6 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1329G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 1329 | chr4 | 81426439 | ||||||
| chr4:81426477 | A | G | 1 | a0001c0001t0015 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1291T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 1291 | chr4 | 81426477 | ||||||
| chr4:81426504 | C | A | 5 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0013 others(2): Show |
10 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1264G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 1264 | chr4 | 81426504 | ||||||
| chr4:81426624 | C | T | 1 | a0001c0001t0020 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1144G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 1144 | chr4 | 81426624 | ||||||
| chr4:81426962 | T | C | 1 | a0001c0001t0018 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 806 | chr4 | 81426962 | ||||||
| chr4:81426981 | C | CA | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0021 others(2): Show |
28 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*786dupT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 786 | chr4 | 81426981 | ||||||
| chr4:81426981 | CA | C | 2 | a0001c0001t0003 a0001c0001t0019 |
36 | HG01106.hp1 HG01167.hp2 HG01257.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*786delT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 786 | chr4 | 81426981 | ||||||
| chr4:81426981 | CAA | C | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(2): Show |
59 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*785_*786delTT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 785 | chr4 | 81426981 | ||||||
| chr4:81426981 | CAAA | C | 1 | a0001c0001t0006 | 23 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*784_*786delTTT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 784 | chr4 | 81426981 | ||||||
| chr4:81426981 | CAAAA | C | 5 | a0001c0001t0005 a0001c0001t0016 a0001c0002t0005 others(2): Show |
24 | HG00280.hp1 HG00733.hp2 HG01099.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*783_*786delTTTT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 783 | chr4 | 81426981 | ||||||
| chr4:81426981 | CAAAAA | C | 3 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0015 |
13 | HG01884.hp1 HG02155.hp2 HG02486.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*782_*786delTTTTT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 782 | chr4 | 81426981 | ||||||
| chr4:81427250 | C | G | 1 | a0001c0001t0017 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*518G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 518 | chr4 | 81427250 | ||||||
| chr4:81427350 | A | G | 4 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0013 others(1): Show |
9 | HG02809.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*418T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 418 | chr4 | 81427350 | ||||||
| chr4:81427426 | A | AAC | 3 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0016 |
8 | HG01884.hp1 HG01891.hp2 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*340_*341dupGT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 341 | chr4 | 81427426 | ||||||
| chr4:81427682 | G | A | 2 | a0001c0001t0022 a0001c0001t0023 |
2 | HG03516.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*86C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 14/14 | 86 | chr4 | 81427682 | ||||||
| chr4:81471823 | A | G | 1 | a0001c0001t0014 | 1 | HG01106.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-60T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/14 | chr4 | 81471823 | |||||||
| chr4:81471902 | T | C | 1 | a0001c0001t0013 | 2 | HG02896.hp2 HG02897.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-139A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/14 | chr4 | 81471902 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:81427950 | A | G | 1 | a0001c0001t0006g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1398-158T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81427950 | |||||||
| chr4:81427982 | A | G | 1 | a0001c0001t0003g0106 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1398-190T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81427982 | |||||||
| chr4:81428045 | G | A | 45 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(42): Show |
54 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1398-253C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81428045 | |||||||
| chr4:81428110 | G | A | 11 | a0001c0001t0001g0105 a0001c0001t0001g0144 a0001c0001t0001g0145 others(8): Show |
11 | HG01167.hp2 HG01168.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1398-318C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81428110 | |||||||
| chr4:81428407 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0004g0206 |
2 | HG02080.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1398-615G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81428407 | |||||||
| chr4:81428438 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1398-646T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81428438 | |||||||
| chr4:81428610 | T | C | 6 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0010g0103 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1398-818A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81428610 | |||||||
| chr4:81428666 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1398-874C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81428666 | |||||||
| chr4:81428859 | C | T | 1 | a0001c0001t0003g0048 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1398-1067G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81428859 | |||||||
| chr4:81428909 | G | A | 60 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0050 others(57): Show |
64 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.1398-1117C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81428909 | |||||||
| chr4:81428930 | T | C | 1 | a0001c0001t0021g0219 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1398-1138A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81428930 | |||||||
| chr4:81429060 | G | C | 1 | a0001c0001t0019g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1398-1268C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429060 | |||||||
| chr4:81429217 | C | A | 19 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0272 others(16): Show |
20 | HG00738.hp1 HG01167.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1398-1425G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429217 | |||||||
| chr4:81429218 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0258 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1398-1426C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429218 | |||||||
| chr4:81429239 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1398-1447A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429239 | |||||||
| chr4:81429279 | CAG | C | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1398-1489_1398-148 others(6): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429279 | |||||||
| chr4:81429333 | T | A | 1 | a0001c0001t0001g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1398-1541A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429333 | |||||||
| chr4:81429364 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1398-1572A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429364 | |||||||
| chr4:81429465 | T | G | 2 | a0001c0001t0007g0108 a0001c0001t0015g0259 |
2 | HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1398-1673A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429465 | |||||||
| chr4:81429576 | C | A | 2 | a0001c0001t0001g0202 a0001c0001t0004g0206 |
2 | HG02080.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1398-1784G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429576 | |||||||
| chr4:81429580 | C | T | 1 | a0001c0001t0005g0260 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1398-1788G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429580 | |||||||
| chr4:81429625 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1398-1833G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429625 | |||||||
| chr4:81429698 | T | C | 4 | a0001c0001t0001g0224 a0001c0001t0003g0102 a0001c0001t0003g0222 others(1): Show |
4 | HG01243.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-1906A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429698 | |||||||
| chr4:81429862 | C | T | 1 | a0001c0001t0003g0011 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1398-2070G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429862 | |||||||
| chr4:81429869 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0005t0001g0191 |
3 | HG01516.hp1 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1398-2077G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429869 | |||||||
| chr4:81429952 | T | C | 9 | a0001c0001t0001g0037 a0001c0001t0009g0018 a0001c0001t0009g0032 others(6): Show |
11 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1398-2160A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81429952 | |||||||
| chr4:81430014 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0005t0001g0191 |
3 | HG01516.hp1 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1398-2222G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430014 | |||||||
| chr4:81430170 | G | C | 25 | a0001c0001t0005g0022 a0001c0001t0005g0064 a0001c0001t0005g0069 others(22): Show |
27 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1397+2129C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430170 | |||||||
| chr4:81430227 | G | C | 1 | a0001c0001t0001g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1397+2072C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430227 | |||||||
| chr4:81430238 | C | T | 2 | a0001c0001t0005g0236 a0001c0001t0006g0237 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1397+2061G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430238 | |||||||
| chr4:81430356 | C | T | 4 | a0001c0001t0002g0036 a0001c0001t0006g0096 a0001c0001t0006g0192 others(1): Show |
4 | HG00738.hp1 HG02055.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+1943G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430356 | |||||||
| chr4:81430447 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1397+1852G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430447 | |||||||
| chr4:81430451 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1397+1848T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430451 | |||||||
| chr4:81430620 | C | G | 2 | a0001c0001t0022g0109 a0001c0001t0023g0229 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1397+1679G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430620 | |||||||
| chr4:81430721 | C | T | 43 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(40): Show |
52 | HG00140.hp1 HG00423.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1397+1578G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430721 | |||||||
| chr4:81430750 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1397+1549A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430750 | |||||||
| chr4:81430950 | C | T | 5 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0010g0103 others(2): Show |
5 | HG01109.hp2 HG01243.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1397+1349G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81430950 | |||||||
| chr4:81431186 | G | A | 2 | a0001c0001t0022g0109 a0001c0001t0023g0229 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1397+1113C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81431186 | |||||||
| chr4:81431250 | A | AAT | 13 | a0001c0001t0001g0035 a0001c0001t0002g0265 a0001c0001t0002g0266 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1397+1047_1397+104 others(6): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81431250 | |||||||
| chr4:81431250 | AAT | A | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1397+1047_1397+104 others(6): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81431250 | |||||||
| chr4:81431904 | C | T | 1 | a0001c0001t0010g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1397+395G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81431904 | |||||||
| chr4:81431939 | C | G | 53 | a0001c0001t0001g0113 a0001c0001t0002g0002 a0001c0001t0002g0003 others(50): Show |
62 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1397+360G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81431939 | |||||||
| chr4:81432020 | A | AT | 9 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0007g0021 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1397+278dupA | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81432020 | |||||||
| chr4:81432192 | G | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0224 a0001c0001t0003g0102 others(2): Show |
5 | HG00741.hp1 HG01243.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1397+107C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 13/13 | chr4 | 81432192 | |||||||
| chr4:81432433 | A | C | 1 | a0001c0001t0004g0152 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1325-62T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81432433 | |||||||
| chr4:81432446 | G | A | 1 | a0001c0001t0003g0159 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1325-75C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81432446 | |||||||
| chr4:81432561 | A | G | 1 | a0001c0001t0001g0007 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1325-190T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81432561 | |||||||
| chr4:81432608 | G | T | 134 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(131): Show |
148 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1325-237C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81432608 | |||||||
| chr4:81432626 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1325-255T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81432626 | |||||||
| chr4:81432632 | T | G | 3 | a0001c0001t0001g0095 a0001c0001t0004g0094 a0001c0001t0004g0250 |
3 | HG02280.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1325-261A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81432632 | |||||||
| chr4:81432697 | T | TGGGA | 31 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0095 others(28): Show |
32 | HG00738.hp1 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1325-330_1325-327d others(6): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81432697 | |||||||
| chr4:81432717 | T | C | 115 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(112): Show |
127 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1325-346A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81432717 | |||||||
| chr4:81433064 | A | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0157 |
2 | NA18975.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1325-693T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433064 | |||||||
| chr4:81433079 | A | G | 2 | a0001c0001t0022g0109 a0001c0001t0023g0229 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1325-708T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433079 | |||||||
| chr4:81433140 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1324+700C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433140 | |||||||
| chr4:81433171 | G | A | 4 | a0001c0001t0002g0036 a0001c0001t0006g0096 a0001c0001t0006g0192 others(1): Show |
4 | HG00738.hp1 HG02055.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+669C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433171 | |||||||
| chr4:81433206 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1324+634C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433206 | |||||||
| chr4:81433223 | T | A | 8 | a0001c0001t0001g0031 a0001c0001t0001g0119 a0001c0001t0001g0135 others(5): Show |
8 | HG00741.hp1 HG01243.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1324+617A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433223 | |||||||
| chr4:81433228 | T | TA | 26 | a0001c0001t0001g0135 a0001c0001t0001g0224 a0001c0001t0002g0029 others(23): Show |
26 | HG00738.hp1 HG00741.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1324+611dupT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433228 | |||||||
| chr4:81433228 | TA | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0004g0152 others(8): Show |
12 | HG01099.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1324+611delT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433228 | |||||||
| chr4:81433263 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1324+577T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433263 | |||||||
| chr4:81433343 | T | C | 1 | a0001c0001t0013g0023 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1324+497A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433343 | |||||||
| chr4:81433456 | C | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0067 a0001c0001t0002g0193 |
4 | HG02630.hp2 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+384G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433456 | |||||||
| chr4:81433539 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1324+301A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 12/13 | chr4 | 81433539 | |||||||
| chr4:81434001 | T | TA | 18 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0253 others(15): Show |
18 | HG00738.hp1 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1201-39dupT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 11/13 | chr4 | 81434001 | |||||||
| chr4:81434076 | G | T | 1 | a0001c0001t0004g0152 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1201-113C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 11/13 | chr4 | 81434076 | |||||||
| chr4:81434114 | A | ATCATAGC others(4): Show |
1 | a0001c0001t0005g0069 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1201-162_1201-152d others(13): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 11/13 | chr4 | 81434114 | |||||||
| chr4:81434439 | G | A | 110 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(107): Show |
122 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1200+200C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 11/13 | chr4 | 81434439 | |||||||
| chr4:81434544 | G | T | 6 | a0001c0001t0002g0115 a0001c0001t0002g0207 a0001c0001t0002g0239 others(3): Show |
6 | HG01928.hp2 NA18747.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+95C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 11/13 | chr4 | 81434544 | |||||||
| chr4:81434547 | T | A | 1 | a0001c0001t0005g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1200+92A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 11/13 | chr4 | 81434547 | |||||||
| chr4:81434572 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0005t0001g0191 |
3 | HG01516.hp1 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1200+67A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 11/13 | chr4 | 81434572 | |||||||
| chr4:81434969 | A | G | 12 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0095 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1105-235T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81434969 | |||||||
| chr4:81434991 | T | A | 1 | a0001c0001t0002g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1105-257A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81434991 | |||||||
| chr4:81435178 | A | G | 149 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(146): Show |
163 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1105-444T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435178 | |||||||
| chr4:81435260 | A | C | 1 | a0001c0001t0001g0201 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1105-526T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435260 | |||||||
| chr4:81435268 | A | G | 1 | a0001c0001t0005g0260 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1105-534T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435268 | |||||||
| chr4:81435271 | T | C | 1 | a0001c0001t0005g0260 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1105-537A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435271 | |||||||
| chr4:81435273 | T | C | 4 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105-539A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435273 | |||||||
| chr4:81435284 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0119 |
2 | HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1105-550C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435284 | |||||||
| chr4:81435303 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0004g0078 |
2 | NA18950.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1105-569G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435303 | |||||||
| chr4:81435359 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0119 a0001c0001t0001g0208 |
3 | HG02970.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1105-625G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435359 | |||||||
| chr4:81435396 | C | G | 1 | a0001c0001t0005g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1105-662G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435396 | |||||||
| chr4:81435417 | C | CA | 12 | a0001c0001t0001g0037 a0001c0001t0001g0107 a0001c0001t0001g0160 others(9): Show |
12 | HG00544.hp2 HG01109.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1105-684dupT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435417 | |||||||
| chr4:81435417 | CA | C | 107 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(104): Show |
120 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1105-684delT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435417 | |||||||
| chr4:81435417 | CAA | C | 12 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0002g0214 others(9): Show |
13 | HG01516.hp1 HG01517.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1105-685_1105-684d others(4): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435417 | |||||||
| chr4:81435427 | A | C | 2 | a0001c0001t0002g0036 a0001c0001t0006g0096 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1105-693T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435427 | |||||||
| chr4:81435432 | A | C | 19 | a0001c0001t0002g0036 a0001c0001t0002g0272 a0001c0001t0003g0221 others(16): Show |
19 | HG00738.hp1 HG01109.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1105-698T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435432 | |||||||
| chr4:81435459 | ACCGATT | A | 3 | a0001c0001t0001g0095 a0001c0001t0004g0094 a0001c0001t0004g0250 |
3 | HG02280.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1105-731_1105-726d others(8): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435459 | |||||||
| chr4:81435463 | A | AT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(45): Show |
50 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1105-730dupA | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435463 | |||||||
| chr4:81435463 | A | ATT | 11 | a0001c0001t0002g0036 a0001c0001t0003g0215 a0001c0001t0003g0221 others(8): Show |
11 | HG00738.hp1 HG01243.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1105-731_1105-730d others(4): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435463 | |||||||
| chr4:81435463 | AT | A | 23 | a0001c0001t0001g0031 a0001c0001t0001g0119 a0001c0001t0002g0003 others(20): Show |
25 | HG00408.hp1 HG00423.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1105-730delA | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435463 | |||||||
| chr4:81435463 | ATT | A | 72 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0148 others(69): Show |
83 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.1105-731_1105-730d others(4): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435463 | |||||||
| chr4:81435466 | T | G | 3 | a0001c0001t0001g0095 a0001c0001t0004g0094 a0001c0001t0004g0250 |
3 | HG02280.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1105-732A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435466 | |||||||
| chr4:81435531 | C | A | 1 | a0001c0001t0005g0249 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1105-797G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435531 | |||||||
| chr4:81435538 | T | G | 1 | a0001c0001t0003g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1105-804A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435538 | |||||||
| chr4:81435629 | C | T | 1 | a0001c0001t0003g0080 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1105-895G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435629 | |||||||
| chr4:81435630 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1105-896C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435630 | |||||||
| chr4:81435650 | AT | A | 15 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0147 others(12): Show |
15 | HG00423.hp1 HG01167.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1105-917delA | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435650 | |||||||
| chr4:81435666 | A | G | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(12): Show |
15 | HG01433.hp2 HG02280.hp1 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.1105-932T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435666 | |||||||
| chr4:81435668 | G | T | 1 | a0001c0001t0004g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1105-934C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435668 | |||||||
| chr4:81435721 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1105-987G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435721 | |||||||
| chr4:81435763 | A | C | 151 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0030 others(148): Show |
167 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1105-1029T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435763 | |||||||
| chr4:81435774 | C | CT | 120 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0053 others(117): Show |
137 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1105-1041dupA | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435774 | |||||||
| chr4:81435774 | C | CTT | 34 | a0001c0001t0001g0037 a0001c0001t0001g0050 a0001c0001t0001g0211 others(31): Show |
34 | HG00280.hp1 HG00423.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1105-1042_1105-104 others(6): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435774 | |||||||
| chr4:81435774 | C | CTTT | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(8): Show |
12 | HG01346.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1105-1043_1105-104 others(7): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81435774 | |||||||
| chr4:81436012 | G | A | 31 | a0001c0001t0001g0135 a0001c0001t0001g0224 a0001c0001t0003g0102 others(28): Show |
33 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1105-1278C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81436012 | |||||||
| chr4:81436184 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0004g0094 a0001c0001t0004g0250 |
3 | HG02280.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1105-1450G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81436184 | |||||||
| chr4:81436360 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1105-1626G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81436360 | |||||||
| chr4:81436580 | A | T | 1 | a0001c0001t0001g0278 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1105-1846T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81436580 | |||||||
| chr4:81436935 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1105-2201G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81436935 | |||||||
| chr4:81437016 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1105-2282C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81437016 | |||||||
| chr4:81437063 | T | C | 11 | a0001c0001t0001g0037 a0001c0001t0002g0036 a0001c0001t0006g0096 others(8): Show |
12 | HG02055.hp1 HG02109.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1105-2329A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81437063 | |||||||
| chr4:81437206 | G | A | 52 | a0001c0001t0001g0095 a0001c0001t0001g0186 a0001c0001t0001g0187 others(49): Show |
61 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1105-2472C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81437206 | |||||||
| chr4:81437770 | C | T | 64 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0095 others(61): Show |
75 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1105-3036G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81437770 | |||||||
| chr4:81437992 | G | C | 1 | a0001c0001t0003g0132 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1104+2842C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81437992 | |||||||
| chr4:81438006 | G | A | 6 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0010g0103 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1104+2828C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438006 | |||||||
| chr4:81438323 | G | A | 1 | a0001c0001t0003g0059 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1104+2511C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438323 | |||||||
| chr4:81438370 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1104+2464C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438370 | |||||||
| chr4:81438502 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0119 |
2 | HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1104+2332G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438502 | |||||||
| chr4:81438505 | C | T | 126 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(123): Show |
140 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1104+2329G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438505 | |||||||
| chr4:81438508 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1104+2326C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438508 | |||||||
| chr4:81438729 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1104+2105G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438729 | |||||||
| chr4:81438779 | GTTCTCAT others(4): Show |
G | 2 | a0001c0001t0009g0018 a0002c0006t0011g0232 |
3 | HG03041.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1104+2044_1104+205 others(15): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438779 | |||||||
| chr4:81438794 | C | T | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1104+2040G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438794 | |||||||
| chr4:81438921 | C | T | 1 | a0001c0001t0003g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1104+1913G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438921 | |||||||
| chr4:81438933 | T | C | 11 | a0001c0001t0001g0105 a0001c0001t0001g0144 a0001c0001t0001g0145 others(8): Show |
11 | HG01167.hp2 HG01168.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1104+1901A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438933 | |||||||
| chr4:81438978 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1104+1856C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81438978 | |||||||
| chr4:81439151 | C | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0038 others(25): Show |
32 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1104+1683G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81439151 | |||||||
| chr4:81439234 | T | C | 1 | a0001c0001t0018g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1104+1600A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81439234 | |||||||
| chr4:81439282 | T | C | 1 | a0001c0001t0022g0109 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1104+1552A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81439282 | |||||||
| chr4:81439316 | A | G | 6 | a0001c0001t0001g0113 a0001c0001t0002g0003 a0001c0001t0002g0057 others(3): Show |
9 | HG02165.hp2 NA18947.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.1104+1518T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81439316 | |||||||
| chr4:81439400 | G | A | 1 | a0001c0001t0003g0151 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1104+1434C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81439400 | |||||||
| chr4:81439547 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1104+1287C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81439547 | |||||||
| chr4:81439651 | A | T | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1104+1183T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81439651 | |||||||
| chr4:81439718 | A | AT | 3 | a0001c0001t0002g0003 a0001c0001t0002g0057 a0001c0001t0003g0051 |
6 | HG02165.hp2 NA18947.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.1104+1115dupA | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81439718 | |||||||
| chr4:81439919 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1104+915A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81439919 | |||||||
| chr4:81439933 | C | T | 6 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0010g0103 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1104+901G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81439933 | |||||||
| chr4:81440042 | T | G | 1 | a0001c0001t0003g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1104+792A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81440042 | |||||||
| chr4:81440142 | A | G | 140 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(137): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1104+692T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81440142 | |||||||
| chr4:81440231 | C | G | 7 | a0001c0001t0002g0029 a0001c0001t0005g0270 a0001c0001t0006g0263 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1104+603G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81440231 | |||||||
| chr4:81440246 | A | G | 3 | a0001c0001t0006g0008 a0001c0001t0006g0044 a0001c0001t0006g0104 |
4 | HG01167.hp1 HG03453.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1104+588T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81440246 | |||||||
| chr4:81440331 | C | T | 6 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0010g0103 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1104+503G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81440331 | |||||||
| chr4:81440478 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(10): Show |
14 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1104+356G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81440478 | |||||||
| chr4:81440490 | G | A | 1 | a0001c0001t0007g0254 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1104+344C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 10/13 | chr4 | 81440490 | |||||||
| chr4:81441128 | G | A | 14 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(11): Show |
16 | HG01167.hp1 HG02109.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.1009-199C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441128 | |||||||
| chr4:81441129 | A | G | 4 | a0001c0001t0001g0224 a0001c0001t0003g0102 a0001c0001t0003g0222 others(1): Show |
4 | HG01243.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009-200T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441129 | |||||||
| chr4:81441268 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1009-339C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441268 | |||||||
| chr4:81441304 | G | T | 7 | a0001c0001t0001g0037 a0001c0001t0009g0032 a0001c0001t0009g0099 others(4): Show |
8 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1009-375C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441304 | |||||||
| chr4:81441457 | T | C | 47 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0002g0002 others(44): Show |
56 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.1009-528A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441457 | |||||||
| chr4:81441540 | A | AT | 27 | a0001c0001t0001g0037 a0001c0001t0001g0076 a0001c0001t0001g0085 others(24): Show |
28 | HG00738.hp2 HG01243.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.1009-612dupA | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441540 | |||||||
| chr4:81441540 | A | ATT | 10 | a0001c0001t0001g0135 a0001c0001t0001g0224 a0001c0001t0003g0102 others(7): Show |
11 | HG00741.hp1 HG01167.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1009-613_1009-612d others(4): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441540 | |||||||
| chr4:81441540 | ATT | A | 48 | a0001c0001t0001g0063 a0001c0001t0001g0186 a0001c0001t0001g0187 others(45): Show |
57 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.1009-613_1009-612d others(4): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441540 | |||||||
| chr4:81441732 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG01975.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1008+565C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441732 | |||||||
| chr4:81441740 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1008+557C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441740 | |||||||
| chr4:81441834 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1008+463G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81441834 | |||||||
| chr4:81442179 | T | C | 1 | a0001c0001t0005g0022 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1008+118A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 9/13 | chr4 | 81442179 | |||||||
| chr4:81442447 | A | G | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.929-71T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81442447 | |||||||
| chr4:81442481 | T | C | 1 | a0001c0001t0002g0046 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.929-105A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81442481 | |||||||
| chr4:81442791 | C | T | 3 | a0001c0001t0005g0270 a0001c0001t0006g0263 a0001c0001t0006g0271 |
3 | HG01884.hp2 HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.929-415G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81442791 | |||||||
| chr4:81442962 | C | T | 2 | a0001c0001t0009g0018 a0002c0006t0011g0232 |
3 | HG03041.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.929-586G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81442962 | |||||||
| chr4:81443219 | C | T | 1 | a0001c0001t0003g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.929-843G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81443219 | |||||||
| chr4:81443260 | C | A | 7 | a0001c0001t0002g0029 a0001c0001t0005g0270 a0001c0001t0006g0263 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.929-884G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81443260 | |||||||
| chr4:81443516 | T | A | 1 | a0001c0001t0022g0109 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.929-1140A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81443516 | |||||||
| chr4:81443755 | A | C | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.929-1379T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81443755 | |||||||
| chr4:81443808 | T | C | 60 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(57): Show |
64 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.929-1432A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81443808 | |||||||
| chr4:81443989 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.928+1537A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81443989 | |||||||
| chr4:81444116 | C | CT | 7 | a0001c0001t0002g0272 a0001c0001t0005g0227 a0001c0001t0006g0025 others(4): Show |
7 | HG02723.hp2 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.928+1409dupA | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81444116 | |||||||
| chr4:81444146 | A | G | 6 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0010g0103 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+1380T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81444146 | |||||||
| chr4:81444248 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.928+1278A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81444248 | |||||||
| chr4:81444264 | C | G | 137 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(134): Show |
152 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.928+1262G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81444264 | |||||||
| chr4:81444342 | A | G | 137 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(134): Show |
152 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.928+1184T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81444342 | |||||||
| chr4:81444361 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.928+1165T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81444361 | |||||||
| chr4:81444397 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0005t0001g0191 |
3 | HG01516.hp1 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.928+1129T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81444397 | |||||||
| chr4:81444561 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0001g0114 others(8): Show |
14 | HG00558.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.928+965C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81444561 | |||||||
| chr4:81444688 | C | T | 19 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(16): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.928+838G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81444688 | |||||||
| chr4:81444795 | A | G | 1 | a0001c0001t0003g0143 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.928+731T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81444795 | |||||||
| chr4:81445066 | T | C | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.928+460A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81445066 | |||||||
| chr4:81445101 | C | G | 1 | a0001c0001t0002g0207 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.928+425G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81445101 | |||||||
| chr4:81445164 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.928+362A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81445164 | |||||||
| chr4:81445258 | T | A | 6 | a0001c0001t0001g0037 a0001c0001t0009g0032 a0001c0001t0009g0099 others(3): Show |
7 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.928+268A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81445258 | |||||||
| chr4:81445261 | A | G | 42 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0002g0002 others(39): Show |
51 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.928+265T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81445261 | |||||||
| chr4:81445358 | C | T | 1 | a0001c0001t0002g0057 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.928+168G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 8/13 | chr4 | 81445358 | |||||||
| chr4:81445634 | C | T | 61 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(58): Show |
65 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
splice_region_variant&intron_variant | LOW | c.826-6G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 7/13 | chr4 | 81445634 | |||||||
| chr4:81445971 | G | C | 5 | a0001c0001t0009g0032 a0001c0001t0009g0099 a0001c0001t0011g0034 others(2): Show |
6 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.730-133C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81445971 | |||||||
| chr4:81445977 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.730-139C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81445977 | |||||||
| chr4:81445991 | T | C | 2 | a0001c0001t0007g0108 a0001c0001t0022g0109 |
2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.730-153A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81445991 | |||||||
| chr4:81446172 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.730-334G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81446172 | |||||||
| chr4:81446232 | T | G | 1 | a0001c0001t0011g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.730-394A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81446232 | |||||||
| chr4:81446243 | G | GC | 3 | a0001c0001t0006g0008 a0001c0001t0006g0044 a0001c0001t0006g0104 |
4 | HG01167.hp1 HG03453.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-406dupG | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81446243 | |||||||
| chr4:81446286 | A | G | 61 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(58): Show |
65 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.730-448T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81446286 | |||||||
| chr4:81446482 | C | T | 3 | a0001c0001t0005g0270 a0001c0001t0006g0263 a0001c0001t0006g0271 |
3 | HG01884.hp2 HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.730-644G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81446482 | |||||||
| chr4:81446497 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.730-659C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81446497 | |||||||
| chr4:81446539 | A | G | 3 | a0001c0001t0006g0008 a0001c0001t0006g0044 a0001c0001t0006g0104 |
4 | HG01167.hp1 HG03453.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-701T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81446539 | |||||||
| chr4:81446751 | C | T | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.729+753G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81446751 | |||||||
| chr4:81447082 | T | C | 144 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(141): Show |
159 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.729+422A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81447082 | |||||||
| chr4:81447200 | T | A | 1 | a0001c0001t0001g0245 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.729+304A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81447200 | |||||||
| chr4:81447236 | G | C | 7 | a0001c0001t0002g0029 a0001c0001t0005g0270 a0001c0001t0006g0263 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.729+268C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81447236 | |||||||
| chr4:81447237 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG01975.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.729+267G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81447237 | |||||||
| chr4:81447419 | C | T | 1 | a0001c0001t0004g0124 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.729+85G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81447419 | |||||||
| chr4:81447479 | G | T | 37 | a0001c0001t0001g0211 a0001c0001t0001g0258 a0001c0001t0002g0052 others(34): Show |
39 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.729+25C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 6/13 | chr4 | 81447479 | |||||||
| chr4:81447737 | C | T | 7 | a0001c0001t0001g0148 a0001c0001t0002g0265 a0001c0001t0002g0266 others(4): Show |
7 | HG01168.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-159G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 5/13 | chr4 | 81447737 | |||||||
| chr4:81448006 | C | T | 140 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(137): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.654+63G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 5/13 | chr4 | 81448006 | |||||||
| chr4:81448007 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0169 |
2 | NA18981.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.654+62C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 5/13 | chr4 | 81448007 | |||||||
| chr4:81448051 | T | A | 140 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(137): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.654+18A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 5/13 | chr4 | 81448051 | |||||||
| chr4:81448321 | G | A | 1 | a0001c0001t0004g0209 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.439-37C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81448321 | |||||||
| chr4:81448340 | G | T | 134 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(131): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.439-56C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81448340 | |||||||
| chr4:81448793 | C | G | 1 | a0001c0001t0004g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.439-509G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81448793 | |||||||
| chr4:81448794 | G | A | 6 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0010g0103 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-510C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81448794 | |||||||
| chr4:81449191 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0119 |
2 | HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.439-907T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81449191 | |||||||
| chr4:81449192 | C | A | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.439-908G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81449192 | |||||||
| chr4:81449398 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0005t0001g0191 |
3 | HG01516.hp1 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.439-1114T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81449398 | |||||||
| chr4:81449631 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.439-1347A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81449631 | |||||||
| chr4:81449665 | T | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0224 a0001c0001t0003g0102 others(2): Show |
5 | HG00741.hp1 HG01243.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-1381A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81449665 | |||||||
| chr4:81449705 | T | C | 1 | a0001c0001t0003g0059 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.439-1421A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81449705 | |||||||
| chr4:81449800 | C | A | 2 | a0001c0001t0001g0040 a0001c0001t0004g0039 |
2 | HG00423.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.439-1516G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81449800 | |||||||
| chr4:81449839 | T | A | 59 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0113 others(56): Show |
68 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.439-1555A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81449839 | |||||||
| chr4:81449936 | C | T | 6 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0010g0103 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-1652G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81449936 | |||||||
| chr4:81449989 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.439-1705G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81449989 | |||||||
| chr4:81450046 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.439-1762G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450046 | |||||||
| chr4:81450085 | T | C | 1 | a0001c0001t0004g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.439-1801A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450085 | |||||||
| chr4:81450315 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.439-2031G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450315 | |||||||
| chr4:81450388 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.439-2104G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450388 | |||||||
| chr4:81450388 | CAG | C | 62 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(59): Show |
66 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.439-2106_439-2105d others(4): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450388 | |||||||
| chr4:81450390 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.439-2106C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450390 | |||||||
| chr4:81450469 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.439-2185C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450469 | |||||||
| chr4:81450476 | G | A | 63 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(60): Show |
67 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.439-2192C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450476 | |||||||
| chr4:81450487 | T | C | 6 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(3): Show |
6 | HG02647.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-2203A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450487 | |||||||
| chr4:81450496 | G | C | 1 | a0001c0001t0001g0012 | 2 | HG00544.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.439-2212C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450496 | |||||||
| chr4:81450533 | T | TTTG | 138 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(135): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.439-2252_439-2250d others(5): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450533 | |||||||
| chr4:81450533 | T | TTTGTTG | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.439-2255_439-2250d others(8): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450533 | |||||||
| chr4:81450558 | C | A | 2 | a0001c0001t0005g0230 a0001c0001t0006g0274 |
2 | HG01123.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.439-2274G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450558 | |||||||
| chr4:81450580 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.439-2296C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450580 | |||||||
| chr4:81450699 | C | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0224 a0001c0001t0003g0102 others(2): Show |
5 | HG00741.hp1 HG01243.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-2415G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450699 | |||||||
| chr4:81450804 | G | C | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.439-2520C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450804 | |||||||
| chr4:81450931 | A | C | 1 | a0001c0001t0010g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.439-2647T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81450931 | |||||||
| chr4:81451000 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.439-2716T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81451000 | |||||||
| chr4:81451419 | A | G | 1 | a0001c0001t0002g0137 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.439-3135T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81451419 | |||||||
| chr4:81451456 | T | C | 143 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(140): Show |
158 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.439-3172A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81451456 | |||||||
| chr4:81451510 | G | A | 19 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(16): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.439-3226C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81451510 | |||||||
| chr4:81451675 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0061 others(4): Show |
9 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.439-3391C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81451675 | |||||||
| chr4:81451729 | T | G | 1 | a0001c0001t0005g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.439-3445A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81451729 | |||||||
| chr4:81451743 | C | G | 11 | a0001c0001t0001g0105 a0001c0001t0001g0144 a0001c0001t0001g0145 others(8): Show |
11 | HG01167.hp2 HG01168.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.439-3459G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81451743 | |||||||
| chr4:81452228 | A | C | 1 | a0001c0001t0003g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.439-3944T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81452228 | |||||||
| chr4:81452299 | G | A | 1 | a0001c0001t0003g0117 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.439-4015C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81452299 | |||||||
| chr4:81452311 | T | C | 4 | a0001c0001t0001g0224 a0001c0001t0003g0102 a0001c0001t0003g0222 others(1): Show |
4 | HG01243.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.439-4027A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81452311 | |||||||
| chr4:81452400 | G | A | 2 | a0001c0001t0007g0108 a0001c0001t0022g0109 |
2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.439-4116C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81452400 | |||||||
| chr4:81452416 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0246 others(1): Show |
4 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(1): Show |
intron_variant | MODIFIER | c.439-4132C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81452416 | |||||||
| chr4:81452758 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.438+3893A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81452758 | |||||||
| chr4:81452899 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+3752C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81452899 | |||||||
| chr4:81452906 | A | G | 19 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(16): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.438+3745T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81452906 | |||||||
| chr4:81452967 | T | C | 60 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0113 others(57): Show |
69 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.438+3684A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81452967 | |||||||
| chr4:81453004 | G | GA | 57 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0113 others(54): Show |
66 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.438+3646dupT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453004 | |||||||
| chr4:81453022 | T | G | 1 | a0001c0001t0005g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.438+3629A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453022 | |||||||
| chr4:81453424 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0003g0182 a0001c0001t0004g0181 |
3 | NA18966.hp2 NA18988.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.438+3227G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453424 | |||||||
| chr4:81453556 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+3095C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453556 | |||||||
| chr4:81453578 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+3073G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453578 | |||||||
| chr4:81453628 | A | C | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+3023T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453628 | |||||||
| chr4:81453643 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+3008T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453643 | |||||||
| chr4:81453672 | G | A | 5 | a0001c0001t0009g0032 a0001c0001t0009g0099 a0001c0001t0011g0034 others(2): Show |
6 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.438+2979C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453672 | |||||||
| chr4:81453672 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2979C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453672 | |||||||
| chr4:81453693 | A | G | 146 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(143): Show |
161 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.438+2958T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453693 | |||||||
| chr4:81453724 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2927T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453724 | |||||||
| chr4:81453765 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2886C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453765 | |||||||
| chr4:81453766 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2885T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453766 | |||||||
| chr4:81453863 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2788C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453863 | |||||||
| chr4:81453876 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2775G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81453876 | |||||||
| chr4:81454068 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2583T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454068 | |||||||
| chr4:81454070 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2581G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454070 | |||||||
| chr4:81454075 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2576A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454075 | |||||||
| chr4:81454076 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2575C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454076 | |||||||
| chr4:81454080 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2571A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454080 | |||||||
| chr4:81454087 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.438+2564C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454087 | |||||||
| chr4:81454089 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2562A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454089 | |||||||
| chr4:81454102 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+2549A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454102 | |||||||
| chr4:81454261 | C | A | 1 | a0001c0001t0003g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.438+2390G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454261 | |||||||
| chr4:81454340 | T | G | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.438+2311A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454340 | |||||||
| chr4:81454409 | T | C | 1 | a0001c0001t0002g0243 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.438+2242A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454409 | |||||||
| chr4:81454493 | G | A | 3 | a0001c0001t0009g0032 a0001c0001t0011g0034 a0001c0001t0013g0023 |
4 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+2158C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454493 | |||||||
| chr4:81454564 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0005t0001g0191 |
3 | HG01516.hp1 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.438+2087G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454564 | |||||||
| chr4:81454605 | C | T | 1 | a0001c0001t0007g0021 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.438+2046G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454605 | |||||||
| chr4:81454698 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.438+1953G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454698 | |||||||
| chr4:81454782 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0009g0032 a0001c0001t0009g0099 others(3): Show |
7 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.438+1869A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454782 | |||||||
| chr4:81454804 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+1847T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454804 | |||||||
| chr4:81454805 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+1846C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454805 | |||||||
| chr4:81454809 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+1842T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454809 | |||||||
| chr4:81454810 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+1841T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454810 | |||||||
| chr4:81454811 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+1840A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454811 | |||||||
| chr4:81454812 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+1839C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454812 | |||||||
| chr4:81454815 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+1836A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454815 | |||||||
| chr4:81454818 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+1833A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454818 | |||||||
| chr4:81454819 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+1832G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454819 | |||||||
| chr4:81454851 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.438+1800G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454851 | |||||||
| chr4:81454926 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.438+1725T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454926 | |||||||
| chr4:81454987 | GAAGTAAA others(7): Show |
G | 1 | a0001c0001t0001g0131 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.438+1650_438+1663d others(16): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81454987 | |||||||
| chr4:81455065 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.438+1586C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81455065 | |||||||
| chr4:81455144 | C | T | 1 | a0001c0001t0010g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.438+1507G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81455144 | |||||||
| chr4:81455289 | C | A | 6 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0010g0103 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.438+1362G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81455289 | |||||||
| chr4:81455292 | G | T | 1 | a0001c0001t0006g0192 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.438+1359C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81455292 | |||||||
| chr4:81455375 | A | C | 77 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0063 others(74): Show |
88 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.438+1276T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81455375 | |||||||
| chr4:81455443 | A | G | 18 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0002g0036 others(15): Show |
20 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.438+1208T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81455443 | |||||||
| chr4:81455467 | C | T | 64 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(61): Show |
68 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.438+1184G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81455467 | |||||||
| chr4:81455784 | C | A | 139 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(136): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.438+867G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81455784 | |||||||
| chr4:81455987 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0005t0001g0191 |
3 | HG01516.hp1 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.438+664G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81455987 | |||||||
| chr4:81456084 | T | C | 2 | a0001c0001t0003g0045 a0001c0001t0003g0049 |
2 | NA18975.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.438+567A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81456084 | |||||||
| chr4:81456133 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.438+518G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81456133 | |||||||
| chr4:81456175 | G | A | 63 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
68 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.438+476C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81456175 | |||||||
| chr4:81456385 | T | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(8): Show |
12 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.438+266A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81456385 | |||||||
| chr4:81456388 | T | G | 1 | a0004c0003t0005g0231 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.438+263A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81456388 | |||||||
| chr4:81456512 | C | A | 1 | a0001c0001t0010g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.438+139G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 4/13 | chr4 | 81456512 | |||||||
| chr4:81456897 | G | A | 3 | a0001c0001t0002g0137 a0001c0001t0002g0188 a0001c0001t0003g0117 |
3 | NA18944.hp1 NA18979.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.301-109C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 3/13 | chr4 | 81456897 | |||||||
| chr4:81456982 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.301-194C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 3/13 | chr4 | 81456982 | |||||||
| chr4:81457037 | G | T | 1 | a0001c0001t0003g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.301-249C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 3/13 | chr4 | 81457037 | |||||||
| chr4:81457078 | G | A | 64 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(61): Show |
69 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.301-290C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 3/13 | chr4 | 81457078 | |||||||
| chr4:81457120 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.301-332C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 3/13 | chr4 | 81457120 | |||||||
| chr4:81457287 | G | A | 10 | a0001c0001t0001g0208 a0001c0001t0002g0029 a0001c0001t0005g0236 others(7): Show |
11 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.300+212C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 3/13 | chr4 | 81457287 | |||||||
| chr4:81457315 | A | G | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.300+184T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 3/13 | chr4 | 81457315 | |||||||
| chr4:81457759 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0009g0032 a0001c0001t0009g0099 others(3): Show |
7 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-138A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81457759 | |||||||
| chr4:81457864 | T | A | 12 | a0001c0001t0001g0037 a0001c0001t0003g0221 a0001c0001t0006g0008 others(9): Show |
14 | HG01167.hp1 HG02109.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.178-243A>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81457864 | |||||||
| chr4:81457963 | T | C | 65 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(62): Show |
70 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.178-342A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81457963 | |||||||
| chr4:81458064 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.178-443T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458064 | |||||||
| chr4:81458127 | T | C | 53 | a0001c0001t0001g0113 a0001c0001t0001g0135 a0001c0001t0001g0186 others(50): Show |
62 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.178-506A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458127 | |||||||
| chr4:81458144 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0009g0032 a0001c0001t0009g0099 others(3): Show |
7 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-523C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458144 | |||||||
| chr4:81458157 | T | C | 2 | a0001c0001t0007g0108 a0001c0001t0022g0109 |
2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.178-536A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458157 | |||||||
| chr4:81458166 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.178-545A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458166 | |||||||
| chr4:81458335 | G | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(8): Show |
12 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178-714C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458335 | |||||||
| chr4:81458359 | C | G | 2 | a0001c0001t0007g0108 a0001c0001t0022g0109 |
2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.178-738G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458359 | |||||||
| chr4:81458471 | T | G | 1 | a0001c0001t0007g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178-850A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458471 | |||||||
| chr4:81458486 | C | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.177+846G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458486 | |||||||
| chr4:81458494 | A | G | 25 | a0001c0001t0001g0020 a0001c0001t0001g0199 a0001c0001t0001g0211 others(22): Show |
27 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.177+838T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458494 | |||||||
| chr4:81458553 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0005t0001g0191 |
3 | HG01516.hp1 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.177+779A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458553 | |||||||
| chr4:81458745 | G | A | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.177+587C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458745 | |||||||
| chr4:81458902 | T | C | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.177+430A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81458902 | |||||||
| chr4:81459048 | T | C | 3 | a0001c0001t0006g0008 a0001c0001t0006g0044 a0001c0001t0006g0104 |
4 | HG01167.hp1 HG03453.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+284A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81459048 | |||||||
| chr4:81459214 | T | C | 12 | a0001c0001t0001g0037 a0001c0001t0003g0221 a0001c0001t0006g0008 others(9): Show |
14 | HG01167.hp1 HG02109.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.177+118A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81459214 | |||||||
| chr4:81459321 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0256 |
2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.177+11A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 2/13 | chr4 | 81459321 | |||||||
| chr4:81459609 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-6-95C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81459609 | |||||||
| chr4:81459699 | T | C | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0020g0177 |
3 | HG01346.hp2 HG01928.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-6-185A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81459699 | |||||||
| chr4:81459779 | C | A | 1 | a0001c0001t0005g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-265G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81459779 | |||||||
| chr4:81459900 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-6-386C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81459900 | |||||||
| chr4:81460159 | G | A | 64 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0135 others(61): Show |
75 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-6-645C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460159 | |||||||
| chr4:81460164 | G | A | 2 | a0001c0001t0002g0188 a0001c0001t0003g0117 |
2 | NA18944.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-6-650C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460164 | |||||||
| chr4:81460212 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-6-698T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460212 | |||||||
| chr4:81460298 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-6-784G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460298 | |||||||
| chr4:81460473 | C | T | 136 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(133): Show |
152 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.-6-959G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460473 | |||||||
| chr4:81460604 | A | T | 1 | a0001c0001t0001g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-6-1090T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460604 | |||||||
| chr4:81460654 | T | C | 1 | a0001c0001t0004g0138 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-6-1140A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460654 | |||||||
| chr4:81460705 | A | T | 56 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0113 others(53): Show |
65 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-6-1191T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460705 | |||||||
| chr4:81460838 | T | C | 1 | a0001c0001t0002g0185 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-6-1324A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460838 | |||||||
| chr4:81460840 | G | T | 7 | a0001c0001t0002g0272 a0001c0001t0005g0227 a0001c0001t0006g0025 others(4): Show |
7 | HG02723.hp2 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-1326C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460840 | |||||||
| chr4:81460847 | A | C | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-6-1333T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460847 | |||||||
| chr4:81460950 | T | G | 134 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(131): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.-6-1436A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81460950 | |||||||
| chr4:81461025 | TCTGCA | T | 64 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(61): Show |
70 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.-6-1516_-6-1512del others(5): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461025 | |||||||
| chr4:81461142 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-6-1628T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461142 | |||||||
| chr4:81461167 | C | T | 1 | a0001c0001t0004g0138 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-6-1653G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461167 | |||||||
| chr4:81461185 | G | A | 3 | a0001c0001t0006g0008 a0001c0001t0006g0044 a0001c0001t0006g0104 |
4 | HG01167.hp1 HG03453.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-1671C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461185 | |||||||
| chr4:81461207 | C | T | 28 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(25): Show |
31 | HG01109.hp2 HG01167.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-6-1693G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461207 | |||||||
| chr4:81461245 | ACTCATAG others(4): Show |
A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0061 others(4): Show |
9 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6-1742_-6-1732del others(11): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461245 | |||||||
| chr4:81461250 | T | C | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-1736A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461250 | |||||||
| chr4:81461372 | T | G | 95 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0030 others(92): Show |
102 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.-6-1858A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461372 | |||||||
| chr4:81461423 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-6-1909C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461423 | |||||||
| chr4:81461628 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG01975.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-6-2114G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461628 | |||||||
| chr4:81461648 | A | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0001c0001t0009g0099 others(2): Show |
6 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-2134T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461648 | |||||||
| chr4:81461663 | G | T | 95 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0030 others(92): Show |
102 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.-6-2149C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461663 | |||||||
| chr4:81461673 | C | A | 1 | a0001c0001t0002g0014 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-6-2159G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461673 | |||||||
| chr4:81461710 | C | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0033 |
2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-6-2196G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461710 | |||||||
| chr4:81461742 | A | C | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-2228T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461742 | |||||||
| chr4:81461919 | G | C | 47 | a0001c0001t0001g0020 a0001c0001t0001g0135 a0001c0001t0001g0199 others(44): Show |
50 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.-6-2405C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81461919 | |||||||
| chr4:81462295 | C | T | 104 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0030 others(101): Show |
112 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(109): Show |
intron_variant | MODIFIER | c.-6-2781G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81462295 | |||||||
| chr4:81462592 | A | T | 1 | a0001c0001t0003g0051 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-6-3078T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81462592 | |||||||
| chr4:81462593 | G | T | 1 | a0001c0001t0003g0051 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-6-3079C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81462593 | |||||||
| chr4:81462877 | A | C | 1 | a0001c0001t0001g0113 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-6-3363T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81462877 | |||||||
| chr4:81462959 | T | C | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-3445A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81462959 | |||||||
| chr4:81463041 | C | T | 1 | a0001c0001t0005g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-6-3527G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81463041 | |||||||
| chr4:81463091 | G | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-3577C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81463091 | |||||||
| chr4:81463231 | A | G | 1 | a0001c0001t0002g0185 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-6-3717T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81463231 | |||||||
| chr4:81463498 | G | A | 7 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0002g0137 others(4): Show |
8 | HG00323.hp2 NA18944.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-3984C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81463498 | |||||||
| chr4:81463635 | C | T | 5 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 others(2): Show |
5 | HG02258.hp2 HG03139.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-4121G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81463635 | |||||||
| chr4:81463762 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0005t0001g0191 |
3 | HG01516.hp1 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-6-4248G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81463762 | |||||||
| chr4:81464103 | T | G | 6 | a0001c0001t0001g0135 a0001c0001t0001g0224 a0001c0001t0003g0102 others(3): Show |
6 | HG00741.hp1 HG01243.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-4589A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464103 | |||||||
| chr4:81464157 | C | T | 1 | a0001c0001t0005g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-4643G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464157 | |||||||
| chr4:81464203 | C | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-4689G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464203 | |||||||
| chr4:81464492 | T | G | 2 | a0001c0001t0005g0236 a0001c0001t0006g0237 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-6-4978A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464492 | |||||||
| chr4:81464715 | A | G | 1 | a0001c0001t0002g0255 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-6-5201T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464715 | |||||||
| chr4:81464740 | C | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-5226G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464740 | |||||||
| chr4:81464748 | G | A | 5 | a0001c0001t0005g0236 a0001c0001t0005g0270 a0001c0001t0006g0237 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-5234C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464748 | |||||||
| chr4:81464787 | C | A | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-5273G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464787 | |||||||
| chr4:81464797 | C | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-5283G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464797 | |||||||
| chr4:81464813 | G | A | 27 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(24): Show |
30 | HG01109.hp2 HG01167.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-6-5299C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464813 | |||||||
| chr4:81464842 | C | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-5328G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464842 | |||||||
| chr4:81464859 | C | A | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-5345G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464859 | |||||||
| chr4:81464940 | C | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-5426G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81464940 | |||||||
| chr4:81465015 | C | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-5501G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465015 | |||||||
| chr4:81465016 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6-5502C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465016 | |||||||
| chr4:81465084 | CA | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0119 others(8): Show |
12 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6-5571delT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465084 | |||||||
| chr4:81465086 | A | G | 5 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 others(2): Show |
5 | HG02258.hp2 HG03139.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-5572T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465086 | |||||||
| chr4:81465096 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-5583_-6-5582ins others(13): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465096 | |||||||
| chr4:81465096 | A | G | 1 | a0001c0001t0002g0137 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-6-5582T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465096 | |||||||
| chr4:81465125 | G | A | 1 | a0001c0001t0019g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-6-5611C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465125 | |||||||
| chr4:81465140 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0003g0051 |
5 | HG02165.hp2 NA18947.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-5626T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465140 | |||||||
| chr4:81465161 | G | T | 1 | a0001c0001t0008g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-6-5647C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465161 | |||||||
| chr4:81465310 | A | C | 80 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0037 others(77): Show |
85 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.-6-5796T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465310 | |||||||
| chr4:81465316 | G | A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0038 others(28): Show |
35 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.-6-5802C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465316 | |||||||
| chr4:81465563 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-6-6049G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465563 | |||||||
| chr4:81465888 | C | T | 5 | a0001c0001t0005g0236 a0001c0001t0005g0270 a0001c0001t0006g0237 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+5882G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465888 | |||||||
| chr4:81465930 | G | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-7+5840C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465930 | |||||||
| chr4:81465934 | A | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-7+5836T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81465934 | |||||||
| chr4:81466112 | T | C | 75 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(72): Show |
82 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.-7+5658A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466112 | |||||||
| chr4:81466384 | T | C | 2 | a0001c0001t0007g0108 a0001c0001t0022g0109 |
2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-7+5386A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466384 | |||||||
| chr4:81466521 | A | C | 1 | a0001c0001t0001g0133 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-7+5249T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466521 | |||||||
| chr4:81466556 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0199 |
2 | HG04115.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-7+5214C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466556 | |||||||
| chr4:81466560 | C | G | 1 | a0001c0001t0003g0049 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-7+5210G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466560 | |||||||
| chr4:81466562 | A | G | 1 | a0001c0001t0002g0239 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-7+5208T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466562 | |||||||
| chr4:81466607 | A | C | 15 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0002g0253 others(12): Show |
16 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-7+5163T>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466607 | |||||||
| chr4:81466631 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0092 others(2): Show |
6 | HG01175.hp2 HG01975.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+5139A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466631 | |||||||
| chr4:81466633 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0004g0098 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-7+5137G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466633 | |||||||
| chr4:81466707 | T | C | 1 | a0001c0001t0010g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-7+5063A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466707 | |||||||
| chr4:81466754 | A | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0116 a0001c0001t0001g0125 others(16): Show |
20 | HG00558.hp1 HG02056.hp1 NA18943.hp1 others(17): Show |
intron_variant | MODIFIER | c.-7+5016T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466754 | |||||||
| chr4:81466758 | C | A | 2 | a0001c0001t0009g0018 a0002c0006t0011g0232 |
3 | HG03041.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-7+5012G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466758 | |||||||
| chr4:81466758 | C | G | 6 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(3): Show |
6 | HG02647.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+5012G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466758 | |||||||
| chr4:81466758 | CA | C | 9 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0120 others(6): Show |
9 | HG00639.hp1 HG01099.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+5011delT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466758 | |||||||
| chr4:81466761 | A | AGAAAGAA others(173): Show |
1 | a0001c0001t0002g0269 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7+5008_-7+5009ins others(180): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466761 | |||||||
| chr4:81466761 | A | AGAAAGAA others(161): Show |
2 | a0001c0001t0002g0265 a0001c0001t0006g0264 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-7+5008_-7+5009ins others(168): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466761 | |||||||
| chr4:81466762 | A | G | 3 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0003g0268 |
3 | HG02647.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-7+5008T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466762 | |||||||
| chr4:81466765 | A | AGAAAGAA others(161): Show |
1 | a0001c0001t0002g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-7+5004_-7+5005ins others(168): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466765 | |||||||
| chr4:81466765 | A | AGAAAGAA others(157): Show |
1 | a0001c0001t0002g0267 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-7+5004_-7+5005ins others(164): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466765 | |||||||
| chr4:81466765 | A | AGAAAGAA others(153): Show |
1 | a0001c0001t0003g0268 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-7+5004_-7+5005ins others(160): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466765 | |||||||
| chr4:81466765 | A | G | 3 | a0001c0001t0002g0265 a0001c0001t0002g0269 a0001c0001t0006g0264 |
3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-7+5005T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466765 | |||||||
| chr4:81466766 | A | AAAAGAAA others(5): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18988.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-7+5003_-7+5004ins others(12): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466766 | |||||||
| chr4:81466766 | A | AAAAGAAA others(29): Show |
1 | a0001c0001t0002g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-7+5003_-7+5004ins others(36): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466766 | |||||||
| chr4:81466766 | A | AAAAGAAA others(285): Show |
1 | a0001c0001t0002g0067 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-7+5003_-7+5004ins others(292): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466766 | |||||||
| chr4:81466766 | A | AAAGAAAG others(4): Show |
1 | a0001c0001t0005g0112 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-7+5003_-7+5004ins others(11): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466766 | |||||||
| chr4:81466766 | A | AAAGAAAG others(12): Show |
1 | a0001c0001t0004g0073 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-7+5003_-7+5004ins others(19): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466766 | |||||||
| chr4:81466766 | A | AAAGAAAG others(160): Show |
1 | a0001c0001t0001g0072 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-7+5003_-7+5004ins others(167): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466766 | |||||||
| chr4:81466766 | A | AGAAAGAA others(6): Show |
1 | a0001c0001t0005g0111 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-7+5003_-7+5004ins others(13): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466766 | |||||||
| chr4:81466766 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7+5004T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466766 | |||||||
| chr4:81466769 | A | G | 5 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+5001T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466769 | |||||||
| chr4:81466769 | AAAAAG | A | 8 | a0001c0001t0001g0202 a0001c0001t0001g0205 a0001c0001t0001g0208 others(5): Show |
8 | HG00558.hp1 HG01891.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7+4996_-7+5000del others(5): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466769 | |||||||
| chr4:81466770 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0008g0261 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(12): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0005g0270 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(16): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAAG others(4): Show |
8 | a0001c0001t0001g0020 a0001c0001t0001g0278 a0001c0001t0002g0272 others(5): Show |
8 | HG01515.hp2 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(11): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAAG others(8): Show |
9 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0001c0001t0003g0004 others(6): Show |
9 | HG01123.hp1 HG02630.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(15): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAAG others(12): Show |
3 | a0001c0001t0004g0094 a0001c0001t0006g0104 a0001c0001t0006g0276 |
3 | HG01167.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(19): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAAG others(16): Show |
1 | a0001c0001t0007g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(23): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAGA others(3): Show |
2 | a0001c0001t0001g0050 a0001c0001t0009g0018 |
2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(10): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAGA others(7): Show |
6 | a0001c0001t0001g0007 a0001c0001t0002g0240 a0001c0001t0003g0004 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(14): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAGA others(11): Show |
2 | a0001c0001t0001g0235 a0001c0001t0004g0250 |
2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(18): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAGA others(15): Show |
3 | a0001c0001t0001g0082 a0001c0001t0001g0095 a0001c0001t0003g0071 |
3 | HG02155.hp1 HG02280.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(22): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAGA others(19): Show |
2 | a0001c0001t0001g0093 a0001c0001t0004g0074 |
2 | HG01255.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(26): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAGA others(23): Show |
2 | a0001c0001t0001g0030 a0001c0001t0006g0263 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(30): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAGA others(27): Show |
1 | a0001c0001t0001g0092 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(34): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAAGA others(43): Show |
1 | a0001c0001t0001g0090 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(50): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAGAA others(6): Show |
1 | a0001c0001t0006g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(13): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAGAA others(10): Show |
3 | a0001c0001t0001g0163 a0001c0001t0002g0003 a0001c0001t0002g0057 |
3 | HG02738.hp1 NA18973.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(17): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAGAA others(14): Show |
2 | a0001c0001t0002g0058 a0001c0002t0005g0275 |
2 | HG03130.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(21): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAAGAA others(9): Show |
1 | a0001c0001t0006g0271 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(16): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAGAAA others(1): Show |
9 | a0001c0001t0001g0053 a0001c0001t0001g0199 a0001c0001t0001g0233 others(6): Show |
9 | HG00621.hp1 HG00621.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+4992_-7+4999dup others(8): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAGAAA others(5): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0054 others(14): Show |
19 | HG01099.hp1 HG01243.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7+4988_-7+4999dup others(12): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAGAAA others(9): Show |
14 | a0001c0001t0001g0083 a0001c0001t0001g0225 a0001c0001t0002g0002 others(11): Show |
14 | HG00423.hp1 HG00423.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+4984_-7+4999dup others(16): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAGAAA others(13): Show |
10 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0002g0046 others(7): Show |
10 | HG00280.hp1 HG01081.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7+4980_-7+4999dup others(20): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAGAAA others(17): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0033 others(5): Show |
9 | HG00408.hp1 HG00639.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+4976_-7+4999dup others(24): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAGAAA others(21): Show |
3 | a0001c0001t0001g0031 a0001c0001t0002g0002 a0001c0001t0003g0059 |
3 | HG02132.hp1 HG02602.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-7+4972_-7+4999dup others(28): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAGAAA others(25): Show |
1 | a0001c0001t0001g0201 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-7+4968_-7+4999dup others(32): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAAGAAA others(41): Show |
1 | a0001c0001t0001g0091 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-7+4952_-7+4999dup others(48): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAG | 21 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(18): Show |
23 | HG00323.hp2 HG00544.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(3): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAGAAAG | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0110 others(10): Show |
16 | HG00438.hp2 HG00741.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(7): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAGAAAG others(4): Show |
23 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0140 others(20): Show |
24 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(11): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAGAAAG others(8): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0035 others(7): Show |
10 | HG00408.hp2 HG02451.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(15): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAGAAAG others(12): Show |
4 | a0001c0001t0001g0081 a0001c0001t0001g0105 a0001c0001t0001g0133 others(1): Show |
4 | HG01943.hp1 HG01978.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(19): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAGAAAG others(16): Show |
2 | a0001c0001t0001g0006 a0001c0001t0022g0109 |
2 | HG03516.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(23): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAGAAAG others(20): Show |
2 | a0001c0001t0001g0148 a0001c0005t0001g0191 |
2 | HG01168.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(27): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAAGAAAG others(36): Show |
1 | a0001c0001t0001g0175 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(43): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAGAAAGA others(3): Show |
5 | a0001c0001t0001g0027 a0001c0001t0001g0086 a0001c0001t0003g0159 others(2): Show |
5 | HG00140.hp2 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(10): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAGAAAGA others(7): Show |
1 | a0001c0001t0002g0002 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(14): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAGAAAGA others(11): Show |
2 | a0001c0001t0001g0087 a0001c0001t0002g0065 |
2 | HG01261.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(18): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAGAAAGA others(15): Show |
2 | a0001c0001t0001g0164 a0001c0001t0001g0190 |
2 | HG01123.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(22): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAGAAAGA others(19): Show |
1 | a0001c0001t0001g0084 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(26): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAGAAAGA others(23): Show |
1 | a0001c0001t0001g0079 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(30): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AAGAAAGA others(27): Show |
3 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0014g0024 |
3 | HG01106.hp2 HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(34): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AGAAAGAA others(6): Show |
2 | a0001c0001t0001g0211 a0001c0001t0003g0146 |
2 | HG01167.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(13): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AGAAAGAA others(10): Show |
3 | a0001c0001t0001g0166 a0001c0001t0002g0055 a0001c0001t0003g0167 |
3 | HG01106.hp1 HG02132.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(17): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AGAAAGAA others(14): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0168 |
2 | HG00558.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(21): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AGAAAGAA others(18): Show |
2 | a0001c0001t0001g0145 a0001c0001t0001g0172 |
2 | HG01081.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(25): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AGAAAGAA others(22): Show |
2 | a0001c0001t0001g0165 a0001c0001t0011g0034 |
2 | HG03130.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(29): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AGAAAGAA others(26): Show |
2 | a0001c0001t0002g0214 a0001c0001t0003g0215 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(33): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | AGAAAGAA others(30): Show |
1 | a0001c0001t0002g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-7+4999_-7+5000ins others(37): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0113 others(16): Show |
19 | HG00140.hp1 HG00544.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7+5000T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | AAAAGAAA others(5): Show |
A | 1 | a0001c0001t0002g0003 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-7+4988_-7+4999del others(12): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466770 | AAAAGAAA others(13): Show |
A | 1 | a0001c0001t0006g0192 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-7+4980_-7+4999del others(20): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466770 | |||||||
| chr4:81466773 | A | G | 3 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0003g0268 |
3 | HG02647.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-7+4997T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466773 | |||||||
| chr4:81466774 | G | A | 1 | a0001c0001t0006g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-7+4996C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466774 | |||||||
| chr4:81466805 | A | AGAAAGAA others(94): Show |
1 | a0001c0001t0005g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-7+4964_-7+4965ins others(101): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466805 | |||||||
| chr4:81466805 | A | AGAAAGAA others(86): Show |
1 | a0001c0001t0006g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-7+4964_-7+4965ins others(93): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466805 | |||||||
| chr4:81466813 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7+4957T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466813 | |||||||
| chr4:81466817 | A | AG | 3 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0003g0215 |
3 | HG02258.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-7+4952dupC | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466817 | |||||||
| chr4:81466915 | G | A | 3 | a0001c0001t0005g0270 a0001c0001t0006g0263 a0001c0001t0006g0271 |
3 | HG01884.hp2 HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-7+4855C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466915 | |||||||
| chr4:81466937 | T | TA | 38 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(35): Show |
43 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.-7+4832dupT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466937 | |||||||
| chr4:81466937 | TA | T | 8 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0107 others(5): Show |
8 | HG00738.hp2 HG01516.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+4832delT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466937 | |||||||
| chr4:81466948 | A | G | 1 | a0001c0001t0003g0045 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-7+4822T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466948 | |||||||
| chr4:81466952 | A | AG | 17 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0095 others(14): Show |
18 | HG01109.hp2 HG01167.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-7+4817_-7+4818ins others(1): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466952 | |||||||
| chr4:81466954 | A | G | 2 | a0001c0001t0009g0018 a0002c0006t0011g0232 |
3 | HG03041.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-7+4816T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466954 | |||||||
| chr4:81466955 | AG | A | 2 | a0001c0001t0009g0018 a0002c0006t0011g0232 |
3 | HG03041.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-7+4814delC | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466955 | |||||||
| chr4:81466956 | G | A | 32 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(29): Show |
37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-7+4814C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81466956 | |||||||
| chr4:81467086 | C | T | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-7+4684G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81467086 | |||||||
| chr4:81467120 | G | GA | 55 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(52): Show |
61 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-7+4649dupT | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81467120 | |||||||
| chr4:81467404 | A | G | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0245 others(6): Show |
11 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+4366T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81467404 | |||||||
| chr4:81467406 | T | C | 7 | a0001c0001t0002g0214 a0001c0001t0003g0215 a0001c0001t0005g0236 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+4364A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81467406 | |||||||
| chr4:81467415 | G | A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0095 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+4355C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81467415 | |||||||
| chr4:81467477 | C | A | 1 | a0001c0001t0006g0216 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-7+4293G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81467477 | |||||||
| chr4:81467675 | A | T | 1 | a0001c0001t0009g0099 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-7+4095T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81467675 | |||||||
| chr4:81467780 | T | C | 1 | a0001c0001t0006g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-7+3990A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81467780 | |||||||
| chr4:81468279 | A | G | 27 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0033 others(24): Show |
29 | HG00639.hp2 HG00733.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-7+3491T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81468279 | |||||||
| chr4:81468399 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-7+3371A>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81468399 | |||||||
| chr4:81468895 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0004g0098 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-7+2875T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81468895 | |||||||
| chr4:81469078 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-7+2692A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469078 | |||||||
| chr4:81469179 | T | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0095 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+2591A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469179 | |||||||
| chr4:81469235 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG00639.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.-7+2535C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469235 | |||||||
| chr4:81469252 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-7+2518A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469252 | |||||||
| chr4:81469311 | A | T | 104 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0019 others(101): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-7+2459T>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469311 | |||||||
| chr4:81469629 | A | G | 51 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(48): Show |
57 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-7+2141T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469629 | |||||||
| chr4:81469654 | T | TACAC | 27 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0224 others(24): Show |
29 | HG01123.hp1 HG01168.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-7+2112_-7+2115dup others(4): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469654 | |||||||
| chr4:81469654 | T | TACACAC | 4 | a0001c0001t0001g0027 a0001c0001t0001g0233 a0001c0001t0002g0029 others(1): Show |
4 | HG02723.hp2 HG02818.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+2110_-7+2115dup others(6): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469654 | |||||||
| chr4:81469654 | T | TACACACA others(3): Show |
1 | a0001c0001t0002g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-7+2106_-7+2115dup others(10): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469654 | |||||||
| chr4:81469654 | TAC | T | 52 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(49): Show |
58 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.-7+2114_-7+2115del others(2): Show |
RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469654 | |||||||
| chr4:81469656 | C | T | 1 | a0001c0001t0004g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-7+2114G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469656 | |||||||
| chr4:81469674 | T | C | 35 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0033 others(32): Show |
38 | HG00639.hp2 HG00733.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.-7+2096A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469674 | |||||||
| chr4:81469773 | C | T | 46 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0053 others(43): Show |
54 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-7+1997G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81469773 | |||||||
| chr4:81470092 | C | T | 1 | a0001c0001t0002g0238 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-7+1678G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81470092 | |||||||
| chr4:81470484 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-7+1286G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81470484 | |||||||
| chr4:81470559 | G | C | 2 | a0001c0001t0005g0236 a0001c0001t0006g0237 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-7+1211C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81470559 | |||||||
| chr4:81470560 | A | G | 3 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0019g0042 |
3 | HG01109.hp2 HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-7+1210T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81470560 | |||||||
| chr4:81470574 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0004g0039 |
2 | HG00423.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-7+1196G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81470574 | |||||||
| chr4:81470794 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-7+976G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81470794 | |||||||
| chr4:81470828 | G | C | 2 | a0001c0001t0005g0026 a0001c0001t0006g0025 |
2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-7+942C>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81470828 | |||||||
| chr4:81470832 | G | A | 6 | a0001c0001t0002g0238 a0001c0001t0002g0239 a0001c0001t0002g0240 others(3): Show |
6 | HG00423.hp1 HG01928.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+938C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81470832 | |||||||
| chr4:81470852 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-7+918C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81470852 | |||||||
| chr4:81470956 | T | C | 29 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0245 others(26): Show |
32 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-7+814A>G | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81470956 | |||||||
| chr4:81471115 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-7+655G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81471115 | |||||||
| chr4:81471467 | C | A | 2 | a0001c0001t0005g0270 a0001c0001t0006g0271 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-7+303G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81471467 | |||||||
| chr4:81471558 | G | A | 8 | a0001c0001t0001g0278 a0001c0001t0002g0272 a0001c0001t0005g0022 others(5): Show |
9 | HG02630.hp1 HG02717.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+212C>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81471558 | |||||||
| chr4:81471612 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-7+158C>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81471612 | |||||||
| chr4:81471651 | C | A | 1 | a0001c0001t0017g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-7+119G>T | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81471651 | |||||||
| chr4:81471666 | C | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(2): Show |
5 | HG02622.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+104G>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81471666 | |||||||
| chr4:81471682 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0002g0029 a0001c0001t0006g0028 |
3 | HG02723.hp2 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-7+88T>C | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81471682 | |||||||
| chr4:81471714 | C | T | 2 | a0001c0001t0005g0026 a0001c0001t0006g0025 |
2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-7+56G>A | RASGEF1B | ENSG00000138670.19 | transcript | ENST00000264400.7 | protein_coding | 1/13 | chr4 | 81471714 |