Item | Value |
---|---|
geneid | 100271927 |
ensemblid | ENSG00000170667.16 |
hgncid | 35202 |
symbol | RASA4B |
name | RAS p21 protein activator 4B |
refseq_nuc | NM_001367767.2 |
refseq_prot | NP_001354696.1 |
ensembl_nuc | ENST00000465829.6 |
ensembl_prot | ENSP00000417895.1 |
mane_status | MANE Select |
chr | chr7 |
start | 102479976 |
end | 102517777 |
strand | - |
ver | v1.2 |
region | chr7:102479976-102517777 |
region5000 | chr7:102474976-102522777 |
regionname0 | RASA4B_chr7_102479976_102517777 |
regionname5000 | RASA4B_chr7_102474976_102522777 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 803 | 19 | 3 | 5 | 8 | 1 | 2 | 2 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0002 | 0/0 | 803 | 9 | 4 | 1 | 3 | 1 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0003 | 1/0 | 803 | 7 | 2 | 2 | 1 | 0 | 1 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0004 | 0/0 | 803 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0005 | 0/0 | 803 | 4 | 0 | 1 | 1 | 0 | 2 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0006 | 0/0 | 803 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0007 | 0/0 | 803 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0008 | 0/0 | 803 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0009 | 0/0 | 803 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0010 | 0/0 | 803 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0011 | 0/0 | 379 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(374): Show |
chr7 | 102474976 | 102522777 |
a0012 | 0/0 | 803 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0013 | 0/0 | 803 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
a0014 | 0/0 | 803 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | MAKRS others(798): Show |
chr7 | 102474976 | 102522777 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2409 | 15 | 0 | 5 | 7 | 1 | 2 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0001c0007 | 0/0 | 2409 | 2 | 1 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0001c0012 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0001c0022 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0002c0002 | 0/0 | 2409 | 7 | 2 | 1 | 3 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0002c0011 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0002c0023 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0003c0004 | 1/0 | 2409 | 4 | 2 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0003c0006 | 0/0 | 2409 | 2 | 0 | 0 | 1 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0003c0020 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0004c0005 | 0/0 | 2409 | 4 | 4 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0004c0008 | 0/0 | 2409 | 2 | 0 | 2 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0005c0014 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0005c0015 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0005c0016 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0005c0021 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0006c0003 | 0/0 | 2409 | 4 | 4 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0007c0017 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0007c0018 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0008c0009 | 0/0 | 2409 | 2 | 0 | 2 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0009c0026 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0010c0019 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0011c0024 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0012c0025 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0013c0010 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 | ||
a0014c0013 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | ATGGC others(2404): Show |
chr7 | 102474976 | 102522777 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6097 | 10 | 0 | 4 | 5 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6092): Show |
chr7 | 102474976 | 102522777 |
a0001c0001t0005 | 0/0 | 6096 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6091): Show |
chr7 | 102474976 | 102522777 |
a0001c0001t0006 | 0/0 | 6098 | 2 | 0 | 0 | 2 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6093): Show |
chr7 | 102474976 | 102522777 |
a0001c0001t0014 | 0/0 | 6097 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6092): Show |
chr7 | 102474976 | 102522777 |
a0001c0001t0020 | 0/0 | 6098 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6093): Show |
chr7 | 102474976 | 102522777 |
a0001c0007t0013 | 0/0 | 6097 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6092): Show |
chr7 | 102474976 | 102522777 |
a0001c0007t0021 | 0/0 | 6110 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6105): Show |
chr7 | 102474976 | 102522777 |
a0001c0012t0009 | 0/0 | 6086 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6081): Show |
chr7 | 102474976 | 102522777 |
a0001c0022t0006 | 0/0 | 6098 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6093): Show |
chr7 | 102474976 | 102522777 |
a0002c0002t0003 | 0/0 | 6116 | 3 | 0 | 1 | 1 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6111): Show |
chr7 | 102474976 | 102522777 |
a0002c0002t0010 | 0/0 | 6116 | 2 | 2 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6111): Show |
chr7 | 102474976 | 102522777 |
a0002c0002t0012 | 0/0 | 6116 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6111): Show |
chr7 | 102474976 | 102522777 |
a0002c0002t0023 | 0/0 | 6115 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6110): Show |
chr7 | 102474976 | 102522777 |
a0002c0011t0022 | 0/0 | 6114 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6109): Show |
chr7 | 102474976 | 102522777 |
a0002c0023t0003 | 0/0 | 6116 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6111): Show |
chr7 | 102474976 | 102522777 |
a0003c0004t0002 | 0/0 | 6095 | 2 | 2 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6090): Show |
chr7 | 102474976 | 102522777 |
a0003c0004t0007 | 1/0 | 6095 | 1 | 0 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6090): Show |
chr7 | 102474976 | 102522777 |
a0003c0004t0019 | 0/0 | 6096 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6091): Show |
chr7 | 102474976 | 102522777 |
a0003c0006t0002 | 0/0 | 6095 | 2 | 0 | 0 | 1 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6090): Show |
chr7 | 102474976 | 102522777 |
a0003c0020t0011 | 0/0 | 6095 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6090): Show |
chr7 | 102474976 | 102522777 |
a0004c0005t0004 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6106): Show |
chr7 | 102474976 | 102522777 |
a0004c0005t0017 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6106): Show |
chr7 | 102474976 | 102522777 |
a0004c0005t0018 | 0/0 | 6112 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6107): Show |
chr7 | 102474976 | 102522777 |
a0004c0008t0004 | 0/0 | 6111 | 2 | 0 | 2 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6106): Show |
chr7 | 102474976 | 102522777 |
a0005c0014t0011 | 0/0 | 6095 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6090): Show |
chr7 | 102474976 | 102522777 |
a0005c0015t0008 | 0/0 | 6095 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6090): Show |
chr7 | 102474976 | 102522777 |
a0005c0016t0025 | 0/0 | 6096 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6091): Show |
chr7 | 102474976 | 102522777 |
a0005c0021t0008 | 0/0 | 6095 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6090): Show |
chr7 | 102474976 | 102522777 |
a0006c0003t0002 | 0/0 | 6095 | 3 | 3 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6090): Show |
chr7 | 102474976 | 102522777 |
a0006c0003t0007 | 0/0 | 6095 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6090): Show |
chr7 | 102474976 | 102522777 |
a0007c0017t0003 | 0/0 | 6116 | 1 | 0 | 0 | 0 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6111): Show |
chr7 | 102474976 | 102522777 |
a0007c0018t0003 | 0/0 | 6116 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6111): Show |
chr7 | 102474976 | 102522777 |
a0008c0009t0005 | 0/0 | 6096 | 2 | 0 | 2 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6091): Show |
chr7 | 102474976 | 102522777 |
a0009c0026t0016 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6106): Show |
chr7 | 102474976 | 102522777 |
a0010c0019t0024 | 0/0 | 6110 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6105): Show |
chr7 | 102474976 | 102522777 |
a0011c0024t0002 | 0/0 | 6095 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6090): Show |
chr7 | 102474976 | 102522777 |
a0012c0025t0009 | 0/0 | 6086 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6081): Show |
chr7 | 102474976 | 102522777 |
a0013c0010t0001 | 0/0 | 6097 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6092): Show |
chr7 | 102474976 | 102522777 |
a0014c0013t0015 | 0/0 | 6116 | 1 | 0 | 0 | 0 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | AGTCC others(6111): Show |
chr7 | 102474976 | 102522777 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0014g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0001t0020g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0007t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0007t0021g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0012t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0001c0022t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0002c0002t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0002c0002t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0002c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0002c0002t0010g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0002c0002t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0002c0002t0012g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0002c0002t0023g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0002c0011t0022g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0002c0023t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0003c0004t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0003c0004t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0003c0004t0007g0006 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0003c0004t0019g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0003c0006t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0003c0006t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0003c0020t0011g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0004c0005t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0004c0005t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0004c0005t0017g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0004c0005t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0004c0008t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0004c0008t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0005c0014t0011g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0005c0015t0008g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0005c0016t0025g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0005c0021t0008g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0006c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0006c0003t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0006c0003t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0006c0003t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0007c0017t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0007c0018t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0008c0009t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0008c0009t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0009c0026t0016g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0010c0019t0024g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0011c0024t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0012c0025t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0013c0010t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
a0014c0013t0015g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0002 | c0002 | t0003 | g0025 | EUR | FIN | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG00280 | hp2 | a0007 | c0017 | t0003 | g0010 | EUR | FIN | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG00438 | hp1 | a0001 | c0001 | t0006 | g0044 | EAS | CHS | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG00544 | hp2 | a0002 | c0002 | t0003 | g0013 | EAS | CHS | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01167 | hp1 | a0002 | c0002 | t0003 | g0008 | AMR | PUR | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0032 | AMR | PUR | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01175 | hp1 | a0004 | c0008 | t0004 | g0049 | AMR | PUR | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01175 | hp2 | a0005 | c0015 | t0008 | g0003 | AMR | PUR | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01243 | hp1 | a0003 | c0020 | t0011 | g0059 | AMR | PUR | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01243 | hp2 | a0003 | c0004 | t0019 | g0051 | AMR | PUR | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01258 | hp1 | a0007 | c0018 | t0003 | g0009 | AMR | CLM | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01258 | hp2 | a0004 | c0008 | t0004 | g0050 | AMR | CLM | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01891 | hp1 | a0006 | c0003 | t0002 | g0024 | AFR | ACB | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01891 | hp2 | a0004 | c0005 | t0018 | g0022 | AFR | ACB | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01928 | hp1 | a0008 | c0009 | t0005 | g0030 | AMR | PEL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01993 | hp1 | a0008 | c0009 | t0005 | g0027 | AMR | PEL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02165 | hp1 | a0002 | c0002 | t0012 | g0004 | EAS | CDX | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02165 | hp2 | a0001 | c0001 | t0006 | g0042 | EAS | CDX | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02258 | hp1 | a0003 | c0004 | t0002 | g0055 | AFR | ACB | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02258 | hp2 | a0009 | c0026 | t0016 | g0056 | AFR | ACB | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02602 | hp1 | a0001 | c0001 | t0020 | g0036 | SAS | PJL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02602 | hp2 | a0003 | c0006 | t0002 | g0057 | SAS | PJL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02886 | hp1 | a0006 | c0003 | t0002 | g0017 | AFR | GWD | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02886 | hp2 | a0006 | c0003 | t0007 | g0005 | AFR | GWD | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03017 | hp1 | a0010 | c0019 | t0024 | g0019 | SAS | PJL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03017 | hp2 | a0005 | c0021 | t0008 | g0002 | SAS | PJL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03041 | hp1 | a0002 | c0011 | t0022 | g0016 | AFR | GWD | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03041 | hp2 | a0004 | c0005 | t0017 | g0052 | AFR | GWD | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03139 | hp1 | a0002 | c0023 | t0003 | g0012 | AFR | ESN | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03139 | hp2 | a0001 | c0012 | t0009 | g0023 | AFR | ESN | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03225 | hp1 | a0004 | c0005 | t0004 | g0020 | AFR | MSL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03225 | hp2 | a0002 | c0002 | t0010 | g0038 | AFR | MSL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03453 | hp1 | a0004 | c0005 | t0004 | g0021 | AFR | MSL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03453 | hp2 | a0011 | c0024 | t0002 | g0053 | AFR | MSL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03492 | hp1 | a0001 | c0001 | t0014 | g0040 | SAS | PJL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG03492 | hp2 | a0005 | c0016 | t0025 | g0015 | SAS | PJL | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
NA18906 | hp1 | a0012 | c0025 | t0009 | g0046 | AFR | YRI | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
NA18906 | hp2 | a0003 | c0004 | t0002 | g0054 | AFR | YRI | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
NA18944 | hp1 | a0013 | c0010 | t0001 | g0026 | EAS | JPT | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
NA18944 | hp2 | a0005 | c0014 | t0011 | g0007 | EAS | JPT | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
NA18982 | hp1 | a0002 | c0002 | t0023 | g0011 | EAS | JPT | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
NA18982 | hp2 | a0001 | c0007 | t0013 | g0001 | EAS | JPT | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
NA18990 | hp1 | a0003 | c0006 | t0002 | g0058 | EAS | JPT | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
NA20805 | hp1 | a0014 | c0013 | t0015 | g0014 | EUR | TSI | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02559 | hp1 | a0001 | c0022 | t0006 | g0031 | AFR | ACB | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG02559 | hp2 | a0006 | c0003 | t0002 | g0018 | AFR | ACB | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG06807 | hp1 | a0002 | c0002 | t0010 | g0039 | AFR | USA | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
HG06807 | hp2 | a0001 | c0007 | t0021 | g0048 | AFR | USA | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
homoSapiens | grch38p0 | a0003 | c0004 | t0007 | g0006 | REF | REF | RASA4B_chr7_102474976_102522777 | RASA4B | chr7 | 102474976 | 102522777 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:102483656 | T | C | 3 | a0007 a0009 a0014 |
4 | HG00280.hp2 HG01258.hp1 HG02258.hp2 others(1): Show |
missense_variant | MODERATE | c.2348A>G | p.His783Arg | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2415/6095 | 2348/2412 | 783/803 | chr7 | 102483656 | |||
chr7:102485069 | C | T | 1 | a0008 | 2 | HG01928.hp1 HG01993.hp1 |
missense_variant | MODERATE | c.2195G>A | p.Arg732Gln | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/21 | 2262/6095 | 2195/2412 | 732/803 | chr7 | 102485069 | |||
chr7:102485096 | T | C | 4 | a0002 a0007 a0010 others(1): Show |
13 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(10): Show |
missense_variant | MODERATE | c.2168A>G | p.His723Arg | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/21 | 2235/6095 | 2168/2412 | 723/803 | chr7 | 102485096 | |||
chr7:102491039 | C | T | 1 | a0004 | 6 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(3): Show |
missense_variant | MODERATE | c.1915G>A | p.Val639Ile | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/21 | 1982/6095 | 1915/2412 | 639/803 | chr7 | 102491039 | |||
chr7:102491048 | C | T | 1 | a0006 | 4 | HG01891.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
missense_variant | MODERATE | c.1906G>A | p.Val636Ile | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/21 | 1973/6095 | 1906/2412 | 636/803 | chr7 | 102491048 | |||
chr7:102493273 | T | C | 1 | a0005 | 4 | HG01175.hp2 HG03017.hp2 HG03492.hp2 others(1): Show |
missense_variant | MODERATE | c.1673A>G | p.Gln558Arg | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/21 | 1740/6095 | 1673/2412 | 558/803 | chr7 | 102493273 | |||
chr7:102493887 | T | C | 11 | a0001 a0002 a0004 others(8): Show |
47 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(44): Show |
missense_variant | MODERATE | c.1598A>G | p.His533Arg | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 15/21 | 1665/6095 | 1598/2412 | 533/803 | chr7 | 102493887 | |||
chr7:102495324 | T | A | 1 | a0011 | 1 | HG03453.hp2 | stop_gained | HIGH | c.1138A>T | p.Lys380* | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 12/21 | 1205/6095 | 1138/2412 | 380/803 | chr7 | 102495324 | |||
chr7:102495359 | A | G | 1 | a0014 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1103T>C | p.Leu368Pro | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 12/21 | 1170/6095 | 1103/2412 | 368/803 | chr7 | 102495359 | |||
chr7:102496474 | C | A | 1 | a0012 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1001G>T | p.Arg334Leu | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 10/21 | 1068/6095 | 1001/2412 | 334/803 | chr7 | 102496474 | |||
chr7:102506701 | T | C | 3 | a0007 a0009 a0010 |
4 | HG00280.hp2 HG01258.hp1 HG02258.hp2 others(1): Show |
missense_variant | MODERATE | c.422A>G | p.Glu141Gly | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/21 | 489/6095 | 422/2412 | 141/803 | chr7 | 102506701 | |||
chr7:102510216 | C | T | 1 | a0013 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.199G>A | p.Ala67Thr | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 3/21 | 266/6095 | 199/2412 | 67/803 | chr7 | 102510216 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:102483664 | G | A | 2 | a0005c0021 a0009c0026 |
2 | HG02258.hp2 HG03017.hp2 |
synonymous_variant | LOW | c.2340C>T | p.Arg780Arg | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2407/6095 | 2340/2412 | 780/803 | chr7 | 102483664 | |||
chr7:102483664 | G | T | 3 | a0007c0017 a0007c0018 a0014c0013 |
3 | HG00280.hp2 HG01258.hp1 NA20805.hp1 |
synonymous_variant | LOW | c.2340C>A | p.Arg780Arg | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2407/6095 | 2340/2412 | 780/803 | chr7 | 102483664 | |||
chr7:102483712 | G | T | 1 | a0005c0014 | 1 | NA18944.hp2 | splice_region_variant&synonymous_variant | LOW | c.2292C>A | p.Val764Val | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2359/6095 | 2292/2412 | 764/803 | chr7 | 102483712 | |||
chr7:102483847 | C | T | 1 | a0001c0022 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.2268G>A | p.Thr756Thr | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 20/21 | 2335/6095 | 2268/2412 | 756/803 | chr7 | 102483847 | |||
chr7:102493281 | C | T | 3 | a0005c0014 a0005c0015 a0005c0021 |
3 | HG01175.hp2 HG03017.hp2 NA18944.hp2 |
synonymous_variant | LOW | c.1665G>A | p.Leu555Leu | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/21 | 1732/6095 | 1665/2412 | 555/803 | chr7 | 102493281 | |||
chr7:102494541 | G | A | 12 | a0001c0001 a0001c0022 a0002c0002 others(9): Show |
37 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(34): Show |
synonymous_variant | LOW | c.1512C>T | p.Ala504Ala | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 14/21 | 1579/6095 | 1512/2412 | 504/803 | chr7 | 102494541 | |||
chr7:102501153 | C | T | 1 | a0014c0013 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.585G>A | p.Ala195Ala | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 7/21 | 652/6095 | 585/2412 | 195/803 | chr7 | 102501153 | |||
chr7:102506784 | G | A | 9 | a0001c0012 a0001c0022 a0002c0023 others(6): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
synonymous_variant | LOW | c.339C>T | p.Asp113Asp | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/21 | 406/6095 | 339/2412 | 113/803 | chr7 | 102506784 | |||
chr7:102506799 | T | C | 24 | a0001c0001 a0001c0007 a0001c0012 others(21): Show |
51 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
synonymous_variant | LOW | c.324A>G | p.Thr108Thr | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/21 | 391/6095 | 324/2412 | 108/803 | chr7 | 102506799 | |||
chr7:102510214 | A | G | 2 | a0001c0012 a0002c0011 |
2 | HG03041.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.201T>C | p.Ala67Ala | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 3/21 | 268/6095 | 201/2412 | 67/803 | chr7 | 102510214 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:102480028 | C | G | 11 | a0001c0007t0021 a0002c0002t0003 a0002c0002t0010 others(8): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3564G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 3564 | chr7 | 102480028 | ||||||
chr7:102480077 | A | G | 27 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(24): Show |
43 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3515T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 3515 | chr7 | 102480077 | ||||||
chr7:102480101 | G | C | 1 | a0009c0026t0016 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3491C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 3491 | chr7 | 102480101 | ||||||
chr7:102480105 | G | A | 4 | a0004c0005t0004 a0004c0005t0017 a0004c0005t0018 others(1): Show |
6 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3487C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 3487 | chr7 | 102480105 | ||||||
chr7:102480215 | G | A | 2 | a0004c0005t0017 a0004c0005t0018 |
2 | HG01891.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3377C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 3377 | chr7 | 102480215 | ||||||
chr7:102480374 | T | G | 11 | a0001c0007t0021 a0002c0002t0003 a0002c0002t0010 others(8): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3218A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 3218 | chr7 | 102480374 | ||||||
chr7:102480387 | A | G | 5 | a0004c0005t0004 a0004c0005t0017 a0004c0005t0018 others(2): Show |
7 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3205T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 3205 | chr7 | 102480387 | ||||||
chr7:102480428 | G | T | 5 | a0004c0005t0004 a0004c0005t0017 a0004c0005t0018 others(2): Show |
7 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3164C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 3164 | chr7 | 102480428 | ||||||
chr7:102480677 | C | A | 13 | a0002c0002t0003 a0002c0002t0010 a0002c0002t0012 others(10): Show |
18 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2915G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2915 | chr7 | 102480677 | ||||||
chr7:102480822 | G | A | 5 | a0004c0005t0004 a0004c0005t0017 a0004c0005t0018 others(2): Show |
7 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2770C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2770 | chr7 | 102480822 | ||||||
chr7:102480828 | C | G | 4 | a0004c0005t0004 a0004c0005t0017 a0004c0005t0018 others(1): Show |
6 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2764G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2764 | chr7 | 102480828 | ||||||
chr7:102480945 | AC | A | 11 | a0001c0007t0021 a0002c0002t0003 a0002c0002t0010 others(8): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2646delG | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2646 | chr7 | 102480945 | ||||||
chr7:102480980 | T | C | 16 | a0001c0007t0021 a0002c0002t0003 a0002c0002t0010 others(13): Show |
21 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2612A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2612 | chr7 | 102480980 | ||||||
chr7:102481047 | T | TTGCTGTA others(7): Show |
16 | a0001c0007t0021 a0002c0002t0003 a0002c0002t0010 others(13): Show |
21 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2544_*2545insGGTG others(10): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2544 | chr7 | 102481047 | ||||||
chr7:102481098 | A | G | 5 | a0004c0005t0004 a0004c0005t0017 a0004c0005t0018 others(2): Show |
7 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2494T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2494 | chr7 | 102481098 | ||||||
chr7:102481214 | C | CT | 7 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(4): Show |
17 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2377dupA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2377 | chr7 | 102481214 | ||||||
chr7:102481214 | C | CTT | 6 | a0001c0001t0020 a0004c0005t0004 a0004c0005t0017 others(3): Show |
8 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2376_*2377dupAA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2377 | chr7 | 102481214 | ||||||
chr7:102481214 | C | CTTTTTT | 9 | a0002c0002t0003 a0002c0002t0010 a0002c0002t0012 others(6): Show |
12 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2372_*2377dupAAAA others(2): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2377 | chr7 | 102481214 | ||||||
chr7:102481214 | C | T | 1 | a0001c0007t0021 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2378G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2378 | chr7 | 102481214 | ||||||
chr7:102481345 | C | T | 5 | a0004c0005t0004 a0004c0005t0017 a0004c0005t0018 others(2): Show |
7 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2247G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2247 | chr7 | 102481345 | ||||||
chr7:102481462 | C | T | 10 | a0002c0002t0003 a0002c0002t0010 a0002c0002t0012 others(7): Show |
13 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2130G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2130 | chr7 | 102481462 | ||||||
chr7:102481494 | G | A | 1 | a0002c0002t0010 | 2 | HG03225.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2098C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 2098 | chr7 | 102481494 | ||||||
chr7:102481665 | C | CA | 10 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(7): Show |
20 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1926dupT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1926 | chr7 | 102481665 | ||||||
chr7:102481665 | C | CAA | 11 | a0001c0001t0006 a0001c0007t0021 a0001c0022t0006 others(8): Show |
15 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1925_*1926dupTT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1926 | chr7 | 102481665 | ||||||
chr7:102481686 | T | C | 27 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(24): Show |
43 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1906A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1906 | chr7 | 102481686 | ||||||
chr7:102481780 | C | T | 1 | a0001c0007t0021 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1812G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1812 | chr7 | 102481780 | ||||||
chr7:102481841 | TAGAGATA others(2): Show |
T | 2 | a0001c0012t0009 a0012c0025t0009 |
2 | HG03139.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1742_*1750delGTTA others(5): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1742 | chr7 | 102481841 | ||||||
chr7:102481940 | A | G | 32 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(29): Show |
48 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1652T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1652 | chr7 | 102481940 | ||||||
chr7:102481955 | T | C | 32 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(29): Show |
48 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1637A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1637 | chr7 | 102481955 | ||||||
chr7:102482166 | G | A | 2 | a0001c0007t0021 a0009c0026t0016 |
2 | HG02258.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1426C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1426 | chr7 | 102482166 | ||||||
chr7:102482173 | G | C | 10 | a0002c0002t0003 a0002c0002t0010 a0002c0002t0012 others(7): Show |
13 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1419C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1419 | chr7 | 102482173 | ||||||
chr7:102482188 | G | A | 1 | a0001c0007t0021 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1404C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1404 | chr7 | 102482188 | ||||||
chr7:102482288 | G | A | 2 | a0001c0012t0009 a0012c0025t0009 |
2 | HG03139.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1304C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1304 | chr7 | 102482288 | ||||||
chr7:102482296 | C | T | 1 | a0005c0016t0025 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1296G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1296 | chr7 | 102482296 | ||||||
chr7:102482353 | G | A | 1 | a0014c0013t0015 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1239C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1239 | chr7 | 102482353 | ||||||
chr7:102482499 | G | A | 11 | a0002c0002t0003 a0002c0002t0010 a0002c0002t0012 others(8): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1093C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1093 | chr7 | 102482499 | ||||||
chr7:102482558 | G | A | 4 | a0004c0005t0004 a0004c0005t0017 a0004c0005t0018 others(1): Show |
6 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1034C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 1034 | chr7 | 102482558 | ||||||
chr7:102482659 | A | G | 1 | a0002c0002t0012 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*933T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 933 | chr7 | 102482659 | ||||||
chr7:102483004 | T | G | 2 | a0009c0026t0016 a0014c0013t0015 |
2 | HG02258.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*588A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 588 | chr7 | 102483004 | ||||||
chr7:102483087 | G | A | 7 | a0003c0020t0011 a0005c0014t0011 a0005c0015t0008 others(4): Show |
7 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*505C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 505 | chr7 | 102483087 | ||||||
chr7:102483283 | C | T | 4 | a0004c0005t0004 a0004c0005t0017 a0004c0005t0018 others(1): Show |
6 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*309G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 309 | chr7 | 102483283 | ||||||
chr7:102483390 | C | A | 1 | a0009c0026t0016 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 202 | chr7 | 102483390 | ||||||
chr7:102483462 | C | G | 2 | a0009c0026t0016 a0014c0013t0015 |
2 | HG02258.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*130G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 130 | chr7 | 102483462 | ||||||
chr7:102483547 | C | T | 1 | a0001c0001t0014 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*45G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 21/21 | 45 | chr7 | 102483547 | ||||||
chr7:102517719 | G | C | 33 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(30): Show |
53 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(50): Show |
5_prime_UTR_variant | MODIFIER | c.-9C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/21 | 9 | chr7 | 102517719 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:102484093 | C | T | 1 | a0001c0022t0006g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2226-204G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/20 | chr7 | 102484093 | |||||||
chr7:102484131 | C | T | 1 | a0001c0007t0021g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2226-242G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/20 | chr7 | 102484131 | |||||||
chr7:102484448 | T | C | 14 | a0001c0007t0021g0048 a0002c0002t0003g0008 a0002c0002t0003g0013 others(11): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.2226-559A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/20 | chr7 | 102484448 | |||||||
chr7:102484699 | C | T | 26 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(23): Show |
26 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.2225+340G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/20 | chr7 | 102484699 | |||||||
chr7:102484707 | C | T | 41 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(38): Show |
41 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.2225+332G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/20 | chr7 | 102484707 | |||||||
chr7:102484770 | T | C | 15 | a0001c0007t0021g0048 a0002c0002t0003g0008 a0002c0002t0003g0013 others(12): Show |
15 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.2225+269A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/20 | chr7 | 102484770 | |||||||
chr7:102484806 | G | A | 2 | a0001c0007t0021g0048 a0002c0002t0010g0038 |
2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2225+233C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/20 | chr7 | 102484806 | |||||||
chr7:102484869 | T | C | 4 | a0001c0007t0021g0048 a0001c0012t0009g0023 a0002c0002t0010g0038 others(1): Show |
4 | HG03139.hp2 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2225+170A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/20 | chr7 | 102484869 | |||||||
chr7:102484881 | C | A | 2 | a0003c0004t0002g0054 a0003c0004t0019g0051 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2225+158G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/20 | chr7 | 102484881 | |||||||
chr7:102484950 | A | C | 12 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(9): Show |
12 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.2225+89T>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 19/20 | chr7 | 102484950 | |||||||
chr7:102485322 | C | A | 13 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(10): Show |
13 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.2105-163G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485322 | |||||||
chr7:102485351 | G | T | 8 | a0003c0004t0002g0054 a0003c0004t0019g0051 a0003c0006t0002g0057 others(5): Show |
8 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2105-192C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485351 | |||||||
chr7:102485396 | G | A | 12 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(9): Show |
12 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.2105-237C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485396 | |||||||
chr7:102485408 | C | T | 14 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(11): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.2105-249G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485408 | |||||||
chr7:102485432 | C | T | 12 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(9): Show |
12 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.2105-273G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485432 | |||||||
chr7:102485433 | G | T | 1 | a0002c0002t0023g0011 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2105-274C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485433 | |||||||
chr7:102485643 | T | C | 40 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(37): Show |
40 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.2105-484A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485643 | |||||||
chr7:102485654 | A | G | 6 | a0001c0001t0001g0047 a0003c0020t0011g0059 a0005c0014t0011g0007 others(3): Show |
6 | HG01175.hp2 HG01243.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.2105-495T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485654 | |||||||
chr7:102485684 | T | C | 14 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(11): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.2105-525A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485684 | |||||||
chr7:102485685 | T | C | 14 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(11): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.2105-526A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485685 | |||||||
chr7:102485686 | G | A | 14 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(11): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.2105-527C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485686 | |||||||
chr7:102485690 | G | A | 22 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(19): Show |
22 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.2105-531C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485690 | |||||||
chr7:102485732 | C | T | 18 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(15): Show |
18 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.2105-573G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485732 | |||||||
chr7:102485783 | G | T | 19 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.2105-624C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485783 | |||||||
chr7:102485819 | G | A | 2 | a0003c0020t0011g0059 a0005c0016t0025g0015 |
2 | HG01243.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2105-660C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485819 | |||||||
chr7:102485896 | T | C | 5 | a0003c0020t0011g0059 a0005c0014t0011g0007 a0005c0015t0008g0003 others(2): Show |
5 | HG01175.hp2 HG01243.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.2105-737A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485896 | |||||||
chr7:102485959 | T | G | 18 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(15): Show |
18 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.2105-800A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102485959 | |||||||
chr7:102486408 | C | T | 1 | a0014c0013t0015g0014 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2105-1249G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486408 | |||||||
chr7:102486470 | G | A | 2 | a0001c0012t0009g0023 a0012c0025t0009g0046 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2105-1311C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486470 | |||||||
chr7:102486477 | A | G | 13 | a0001c0012t0009g0023 a0003c0020t0011g0059 a0004c0005t0004g0020 others(10): Show |
13 | HG01175.hp1 HG01175.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2105-1318T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486477 | |||||||
chr7:102486541 | A | G | 1 | a0012c0025t0009g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2105-1382T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486541 | |||||||
chr7:102486640 | G | T | 1 | a0004c0005t0018g0022 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2105-1481C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486640 | |||||||
chr7:102486659 | T | C | 1 | a0004c0005t0018g0022 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2105-1500A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486659 | |||||||
chr7:102486662 | T | G | 6 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(3): Show |
6 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.2105-1503A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486662 | |||||||
chr7:102486669 | T | G | 12 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(9): Show |
12 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.2105-1510A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486669 | |||||||
chr7:102486669 | TG | T | 5 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(2): Show |
5 | HG01175.hp1 HG01891.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2105-1511delC | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486669 | |||||||
chr7:102486671 | T | G | 1 | a0002c0002t0023g0011 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2105-1512A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486671 | |||||||
chr7:102486678 | G | T | 7 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(4): Show |
7 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2105-1519C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486678 | |||||||
chr7:102486686 | T | G | 2 | a0001c0012t0009g0023 a0012c0025t0009g0046 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2105-1527A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486686 | |||||||
chr7:102486752 | G | A | 54 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(51): Show |
54 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.2105-1593C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486752 | |||||||
chr7:102486864 | AT | A | 9 | a0002c0002t0003g0013 a0002c0002t0010g0038 a0002c0002t0010g0039 others(6): Show |
9 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2104+1598delA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102486864 | |||||||
chr7:102487026 | C | T | 5 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(2): Show |
5 | HG01175.hp1 HG01891.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2104+1437G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102487026 | |||||||
chr7:102487244 | TCGTGC | T | 43 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.2104+1214_2104+121 others(9): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102487244 | |||||||
chr7:102487292 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0006g0042 a0001c0001t0006g0044 others(1): Show |
4 | HG00438.hp1 HG00438.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.2104+1171A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102487292 | |||||||
chr7:102487904 | T | C | 2 | a0002c0002t0010g0038 a0002c0002t0010g0039 |
2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2104+559A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102487904 | |||||||
chr7:102487923 | AAAC | A | 20 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.2104+537_2104+539d others(5): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102487923 | |||||||
chr7:102487929 | C | A | 1 | a0009c0026t0016g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2104+534G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102487929 | |||||||
chr7:102487966 | G | C | 5 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(2): Show |
5 | HG01175.hp1 HG01891.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2104+497C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102487966 | |||||||
chr7:102488130 | C | A | 1 | a0011c0024t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2104+333G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102488130 | |||||||
chr7:102488167 | G | GA | 6 | a0003c0004t0002g0054 a0003c0004t0002g0055 a0003c0004t0019g0051 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.2104+295dupT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102488167 | |||||||
chr7:102488167 | GA | G | 43 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.2104+295delT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102488167 | |||||||
chr7:102488184 | AG | A | 2 | a0001c0012t0009g0023 a0012c0025t0009g0046 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2104+278delC | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102488184 | |||||||
chr7:102488307 | C | T | 6 | a0002c0002t0003g0008 a0002c0002t0003g0025 a0002c0002t0010g0038 others(3): Show |
6 | HG00280.hp1 HG01167.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2104+156G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102488307 | |||||||
chr7:102488396 | G | A | 1 | a0001c0022t0006g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2104+67C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102488396 | |||||||
chr7:102488440 | G | A | 2 | a0001c0012t0009g0023 a0012c0025t0009g0046 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2104+23C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 18/20 | chr7 | 102488440 | |||||||
chr7:102488756 | A | G | 15 | a0001c0012t0009g0023 a0002c0002t0003g0008 a0002c0002t0003g0013 others(12): Show |
15 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.1969-158T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102488756 | |||||||
chr7:102488863 | T | C | 1 | a0012c0025t0009g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1969-265A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102488863 | |||||||
chr7:102488873 | A | G | 1 | a0009c0026t0016g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1969-275T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102488873 | |||||||
chr7:102489132 | G | C | 1 | a0009c0026t0016g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1969-534C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489132 | |||||||
chr7:102489329 | C | T | 1 | a0012c0025t0009g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1969-731G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489329 | |||||||
chr7:102489477 | T | C | 12 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(9): Show |
12 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1969-879A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489477 | |||||||
chr7:102489488 | C | CTAAT | 8 | a0001c0001t0006g0044 a0001c0007t0013g0001 a0003c0020t0011g0059 others(5): Show |
8 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1969-894_1969-891d others(6): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489488 | |||||||
chr7:102489498 | T | A | 6 | a0001c0001t0001g0047 a0001c0012t0009g0023 a0003c0006t0002g0057 others(3): Show |
6 | HG02258.hp2 HG02300.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1969-900A>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489498 | |||||||
chr7:102489520 | G | A | 1 | a0002c0023t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1969-922C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489520 | |||||||
chr7:102489556 | G | C | 3 | a0003c0004t0002g0054 a0003c0004t0002g0055 a0003c0004t0019g0051 |
3 | HG01243.hp2 HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1969-958C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489556 | |||||||
chr7:102489595 | C | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0047 others(8): Show |
11 | HG00423.hp2 HG00544.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1969-997G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489595 | |||||||
chr7:102489612 | C | T | 9 | a0001c0001t0001g0043 a0001c0001t0006g0044 a0002c0002t0003g0008 others(6): Show |
9 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(6): Show |
intron_variant | MODIFIER | c.1969-1014G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489612 | |||||||
chr7:102489640 | C | G | 55 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(52): Show |
55 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1969-1042G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489640 | |||||||
chr7:102489642 | A | G | 55 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(52): Show |
55 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1969-1044T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489642 | |||||||
chr7:102489650 | A | G | 54 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(51): Show |
54 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1969-1052T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489650 | |||||||
chr7:102489654 | G | A | 23 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
23 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.1969-1056C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489654 | |||||||
chr7:102489664 | T | C | 1 | a0009c0026t0016g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1969-1066A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489664 | |||||||
chr7:102489704 | C | T | 1 | a0001c0007t0013g0001 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1969-1106G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489704 | |||||||
chr7:102489705 | T | G | 1 | a0001c0007t0013g0001 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1969-1107A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489705 | |||||||
chr7:102489706 | G | C | 1 | a0001c0007t0013g0001 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1969-1108C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489706 | |||||||
chr7:102489780 | C | CTTTTT | 10 | a0002c0002t0003g0013 a0002c0002t0010g0038 a0002c0002t0010g0039 others(7): Show |
10 | HG00280.hp2 HG00544.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1969-1187_1969-118 others(9): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489780 | |||||||
chr7:102489780 | C | CTTTTTT | 4 | a0002c0002t0003g0008 a0002c0002t0003g0025 a0002c0002t0023g0011 others(1): Show |
4 | HG00280.hp1 HG01167.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1969-1188_1969-118 others(10): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489780 | |||||||
chr7:102489780 | C | CTTTTTTT others(298): Show |
1 | a0014c0013t0015g0014 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1969-1183_1969-118 others(309): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489780 | |||||||
chr7:102489780 | CT | C | 19 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0047 others(16): Show |
19 | HG00423.hp2 HG00544.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1969-1183delA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489780 | |||||||
chr7:102489780 | CTTTTTTT | C | 13 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
13 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(10): Show |
intron_variant | MODIFIER | c.1969-1189_1969-118 others(11): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489780 | |||||||
chr7:102489792 | T | G | 15 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0047 others(12): Show |
15 | HG00423.hp2 HG00544.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1968+1194A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489792 | |||||||
chr7:102489793 | T | C | 15 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0047 others(12): Show |
15 | HG00423.hp2 HG00544.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1968+1193A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489793 | |||||||
chr7:102489793 | T | G | 1 | a0013c0010t0001g0026 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1968+1193A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489793 | |||||||
chr7:102489794 | T | C | 1 | a0013c0010t0001g0026 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1968+1192A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489794 | |||||||
chr7:102489959 | C | T | 13 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(10): Show |
13 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.1968+1027G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102489959 | |||||||
chr7:102490070 | C | T | 1 | a0009c0026t0016g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1968+916G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490070 | |||||||
chr7:102490084 | T | C | 14 | a0001c0007t0021g0048 a0002c0002t0003g0008 a0002c0002t0003g0013 others(11): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.1968+902A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490084 | |||||||
chr7:102490208 | T | TTTTTAAA others(3): Show |
1 | a0002c0002t0010g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1968+768_1968+777d others(12): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490208 | |||||||
chr7:102490225 | G | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0047 others(3): Show |
6 | HG00423.hp2 HG00544.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1968+761C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490225 | |||||||
chr7:102490398 | C | A | 6 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(3): Show |
6 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1968+588G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490398 | |||||||
chr7:102490421 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0006g0042 |
2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1968+565G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490421 | |||||||
chr7:102490495 | G | A | 13 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(10): Show |
13 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.1968+491C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490495 | |||||||
chr7:102490624 | C | T | 1 | a0001c0007t0021g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1968+362G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490624 | |||||||
chr7:102490645 | G | A | 4 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1968+341C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490645 | |||||||
chr7:102490716 | C | CTCCCACA others(53): Show |
13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(10): Show |
13 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(10): Show |
intron_variant | MODIFIER | c.1968+269_1968+270i others(62): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490716 | |||||||
chr7:102490727 | G | C | 31 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(28): Show |
31 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1968+259C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490727 | |||||||
chr7:102490742 | C | G | 2 | a0001c0012t0009g0023 a0012c0025t0009g0046 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1968+244G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490742 | |||||||
chr7:102490773 | CCATTCCC others(13): Show |
C | 24 | a0001c0007t0021g0048 a0001c0012t0009g0023 a0002c0002t0003g0008 others(21): Show |
24 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1968+193_1968+212d others(22): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490773 | |||||||
chr7:102490787 | CCCAGGGC others(13): Show |
C | 5 | a0001c0007t0013g0001 a0005c0014t0011g0007 a0005c0015t0008g0003 others(2): Show |
5 | HG01175.hp2 HG03017.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1968+179_1968+198d others(22): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490787 | |||||||
chr7:102490814 | C | T | 13 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(10): Show |
13 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.1968+172G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490814 | |||||||
chr7:102490980 | C | T | 4 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1968+6G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 17/20 | chr7 | 102490980 | |||||||
chr7:102491380 | T | G | 3 | a0001c0007t0013g0001 a0003c0004t0002g0054 a0003c0004t0019g0051 |
3 | HG01243.hp2 NA18906.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1831-257A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491380 | |||||||
chr7:102491402 | C | T | 5 | a0005c0014t0011g0007 a0005c0015t0008g0003 a0005c0016t0025g0015 others(2): Show |
5 | HG01175.hp2 HG03017.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1831-279G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491402 | |||||||
chr7:102491493 | C | T | 18 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(15): Show |
18 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.1831-370G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491493 | |||||||
chr7:102491587 | G | A | 2 | a0008c0009t0005g0027 a0008c0009t0005g0030 |
2 | HG01928.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1831-464C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491587 | |||||||
chr7:102491590 | G | A | 49 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(46): Show |
49 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1831-467C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491590 | |||||||
chr7:102491596 | C | T | 5 | a0005c0014t0011g0007 a0005c0015t0008g0003 a0005c0016t0025g0015 others(2): Show |
5 | HG01175.hp2 HG03017.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1831-473G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491596 | |||||||
chr7:102491660 | G | C | 5 | a0005c0014t0011g0007 a0005c0015t0008g0003 a0005c0016t0025g0015 others(2): Show |
5 | HG01175.hp2 HG03017.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1831-537C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491660 | |||||||
chr7:102491708 | G | C | 7 | a0001c0007t0013g0001 a0001c0007t0021g0048 a0003c0006t0002g0057 others(4): Show |
7 | HG01258.hp2 HG01928.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1831-585C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491708 | |||||||
chr7:102491721 | C | T | 6 | a0002c0002t0003g0008 a0002c0002t0003g0025 a0002c0002t0010g0038 others(3): Show |
6 | HG00280.hp1 HG01167.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1831-598G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491721 | |||||||
chr7:102491738 | G | A | 11 | a0002c0002t0003g0008 a0002c0002t0003g0013 a0002c0002t0003g0025 others(8): Show |
11 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1831-615C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491738 | |||||||
chr7:102491767 | C | CA | 7 | a0002c0002t0003g0025 a0002c0002t0010g0038 a0002c0002t0010g0039 others(4): Show |
7 | HG00280.hp1 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1831-645dupT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491767 | |||||||
chr7:102491767 | CA | C | 13 | a0001c0001t0001g0041 a0001c0001t0005g0032 a0001c0001t0020g0036 others(10): Show |
13 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1831-645delT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491767 | |||||||
chr7:102491767 | CAA | C | 18 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(15): Show |
18 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.1831-646_1831-645d others(4): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491767 | |||||||
chr7:102491767 | CAAA | C | 16 | a0001c0007t0021g0048 a0001c0012t0009g0023 a0002c0002t0003g0013 others(13): Show |
16 | HG00280.hp2 HG00544.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1831-647_1831-645d others(5): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491767 | |||||||
chr7:102491834 | T | G | 4 | a0002c0002t0010g0038 a0002c0002t0010g0039 a0003c0006t0002g0057 others(1): Show |
4 | HG02602.hp2 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1831-711A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491834 | |||||||
chr7:102491880 | G | C | 3 | a0002c0002t0012g0004 a0002c0023t0003g0012 a0010c0019t0024g0019 |
3 | HG02165.hp1 HG03017.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1831-757C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491880 | |||||||
chr7:102491881 | G | T | 2 | a0002c0002t0012g0004 a0010c0019t0024g0019 |
2 | HG02165.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1831-758C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491881 | |||||||
chr7:102491937 | A | AC | 41 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(38): Show |
41 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1831-815dupG | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491937 | |||||||
chr7:102491957 | A | C | 7 | a0001c0012t0009g0023 a0002c0002t0003g0013 a0002c0002t0012g0004 others(4): Show |
7 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1831-834T>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102491957 | |||||||
chr7:102492153 | G | T | 1 | a0002c0011t0022g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1830+963C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492153 | |||||||
chr7:102492241 | C | T | 1 | a0009c0026t0016g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1830+875G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492241 | |||||||
chr7:102492278 | G | A | 6 | a0002c0002t0003g0013 a0002c0023t0003g0012 a0007c0017t0003g0010 others(3): Show |
6 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1830+838C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492278 | |||||||
chr7:102492408 | G | C | 8 | a0001c0001t0001g0035 a0001c0001t0001g0045 a0001c0007t0013g0001 others(5): Show |
8 | HG00423.hp1 HG01175.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1830+708C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492408 | |||||||
chr7:102492536 | A | T | 36 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(33): Show |
36 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1830+580T>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492536 | |||||||
chr7:102492667 | A | AT | 4 | a0002c0002t0003g0008 a0002c0002t0003g0025 a0003c0006t0002g0058 others(1): Show |
4 | HG00280.hp1 HG01167.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1830+448dupA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492667 | |||||||
chr7:102492667 | AT | A | 11 | a0001c0001t0001g0035 a0001c0007t0013g0001 a0001c0007t0021g0048 others(8): Show |
11 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1830+448delA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492667 | |||||||
chr7:102492687 | C | T | 7 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(4): Show |
7 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1830+429G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492687 | |||||||
chr7:102492710 | G | C | 1 | a0013c0010t0001g0026 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1830+406C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492710 | |||||||
chr7:102492747 | C | T | 49 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(46): Show |
49 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1830+369G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492747 | |||||||
chr7:102492750 | C | T | 49 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(46): Show |
49 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1830+366G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492750 | |||||||
chr7:102492867 | C | T | 42 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(39): Show |
42 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1830+249G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102492867 | |||||||
chr7:102493053 | G | A | 1 | a0001c0022t0006g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1830+63C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102493053 | |||||||
chr7:102493065 | C | T | 23 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(20): Show |
23 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.1830+51G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 16/20 | chr7 | 102493065 | |||||||
chr7:102493575 | G | A | 36 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(33): Show |
36 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1660+250C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 15/20 | chr7 | 102493575 | |||||||
chr7:102493610 | C | G | 47 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(44): Show |
47 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1660+215G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 15/20 | chr7 | 102493610 | |||||||
chr7:102493685 | A | G | 47 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(44): Show |
47 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1660+140T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 15/20 | chr7 | 102493685 | |||||||
chr7:102494036 | A | AC | 9 | a0001c0001t0001g0033 a0001c0007t0013g0001 a0001c0012t0009g0023 others(6): Show |
9 | HG00423.hp2 HG01167.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1516-68dupG | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 14/20 | chr7 | 102494036 | |||||||
chr7:102494221 | C | T | 10 | a0001c0012t0009g0023 a0002c0002t0003g0013 a0002c0002t0012g0004 others(7): Show |
10 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1516-252G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 14/20 | chr7 | 102494221 | |||||||
chr7:102494344 | G | A | 6 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(3): Show |
6 | HG00544.hp2 HG01258.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.1515+194C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 14/20 | chr7 | 102494344 | |||||||
chr7:102494346 | C | T | 6 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(3): Show |
6 | HG00544.hp2 HG01258.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.1515+192G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 14/20 | chr7 | 102494346 | |||||||
chr7:102494768 | G | C | 2 | a0001c0007t0013g0001 a0005c0016t0025g0015 |
2 | HG03492.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1378-93C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 13/20 | chr7 | 102494768 | |||||||
chr7:102495250 | C | CA | 5 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0037 others(2): Show |
5 | HG00423.hp2 HG00544.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+27dupT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 12/20 | chr7 | 102495250 | |||||||
chr7:102495712 | TG | T | 8 | a0001c0007t0013g0001 a0003c0006t0002g0057 a0006c0003t0002g0017 others(5): Show |
8 | HG01891.hp1 HG02559.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1072-323delC | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 11/20 | chr7 | 102495712 | |||||||
chr7:102495712 | TGGGGG | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(35): Show |
38 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.1072-327_1072-323d others(7): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 11/20 | chr7 | 102495712 | |||||||
chr7:102495716 | G | C | 1 | a0005c0015t0008g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1072-326C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 11/20 | chr7 | 102495716 | |||||||
chr7:102495719 | G | C | 1 | a0007c0017t0003g0010 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1072-329C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 11/20 | chr7 | 102495719 | |||||||
chr7:102495745 | G | C | 4 | a0005c0014t0011g0007 a0005c0015t0008g0003 a0005c0016t0025g0015 others(1): Show |
4 | HG01175.hp2 HG03017.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1072-355C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 11/20 | chr7 | 102495745 | |||||||
chr7:102495873 | A | T | 1 | a0002c0002t0023g0011 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1071+267T>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 11/20 | chr7 | 102495873 | |||||||
chr7:102496103 | G | A | 42 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(39): Show |
42 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1071+37C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 11/20 | chr7 | 102496103 | |||||||
chr7:102496129 | T | C | 19 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(16): Show |
19 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.1071+11A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 11/20 | chr7 | 102496129 | |||||||
chr7:102496693 | G | T | 27 | a0001c0007t0021g0048 a0001c0012t0009g0023 a0002c0002t0003g0008 others(24): Show |
27 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.856-74C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 9/20 | chr7 | 102496693 | |||||||
chr7:102496797 | G | A | 1 | a0004c0008t0004g0049 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.855+50C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 9/20 | chr7 | 102496797 | |||||||
chr7:102497030 | T | C | 12 | a0001c0007t0013g0001 a0001c0012t0009g0023 a0001c0022t0006g0031 others(9): Show |
12 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.738-66A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102497030 | |||||||
chr7:102497057 | G | A | 31 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(28): Show |
31 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.738-93C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102497057 | |||||||
chr7:102497088 | T | C | 43 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.738-124A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102497088 | |||||||
chr7:102497186 | A | C | 1 | a0001c0007t0013g0001 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.738-222T>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102497186 | |||||||
chr7:102497499 | T | C | 2 | a0001c0007t0013g0001 a0003c0004t0002g0055 |
2 | HG02258.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.738-535A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102497499 | |||||||
chr7:102497912 | G | A | 30 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(27): Show |
30 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.738-948C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102497912 | |||||||
chr7:102497980 | A | G | 10 | a0001c0007t0021g0048 a0002c0002t0003g0013 a0002c0002t0012g0004 others(7): Show |
10 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.738-1016T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102497980 | |||||||
chr7:102498260 | A | AT | 6 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(3): Show |
6 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.738-1297dupA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102498260 | |||||||
chr7:102498264 | A | T | 5 | a0001c0007t0021g0048 a0002c0023t0003g0012 a0004c0008t0004g0050 others(2): Show |
5 | HG01258.hp2 HG02258.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-1300T>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102498264 | |||||||
chr7:102498268 | T | A | 30 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(27): Show |
30 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.738-1304A>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102498268 | |||||||
chr7:102498324 | C | T | 1 | a0001c0007t0013g0001 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.738-1360G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102498324 | |||||||
chr7:102498519 | C | CA | 39 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(36): Show |
39 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.738-1556dupT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102498519 | |||||||
chr7:102498640 | C | T | 1 | a0009c0026t0016g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.738-1676G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102498640 | |||||||
chr7:102498666 | C | CAGCCTCC others(2): Show |
7 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(4): Show |
7 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.738-1703_738-1702i others(11): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102498666 | |||||||
chr7:102498757 | G | T | 7 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(4): Show |
7 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.738-1793C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102498757 | |||||||
chr7:102498977 | A | G | 7 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(4): Show |
7 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.737+1722T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102498977 | |||||||
chr7:102499184 | C | CA | 5 | a0001c0007t0013g0001 a0001c0012t0009g0023 a0005c0021t0008g0002 others(2): Show |
5 | HG02258.hp2 HG03017.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.737+1514dupT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499184 | |||||||
chr7:102499191 | AAAAT | A | 6 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(3): Show |
6 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+1504_737+1507d others(6): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499191 | |||||||
chr7:102499193 | A | AATAT | 23 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(20): Show |
23 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.737+1502_737+1505d others(6): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499193 | |||||||
chr7:102499195 | T | A | 6 | a0001c0007t0013g0001 a0003c0004t0019g0051 a0003c0006t0002g0057 others(3): Show |
6 | HG01243.hp2 HG02602.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.737+1504A>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499195 | |||||||
chr7:102499197 | T | A | 1 | a0005c0021t0008g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.737+1502A>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499197 | |||||||
chr7:102499197 | T | G | 6 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(3): Show |
6 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+1502A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499197 | |||||||
chr7:102499248 | C | CT | 6 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(3): Show |
6 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+1450dupA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499248 | |||||||
chr7:102499271 | C | G | 29 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(26): Show |
29 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.737+1428G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499271 | |||||||
chr7:102499304 | G | C | 1 | a0003c0020t0011g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.737+1395C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499304 | |||||||
chr7:102499466 | A | T | 5 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(2): Show |
5 | HG01175.hp1 HG01891.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.737+1233T>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499466 | |||||||
chr7:102499965 | TA | T | 2 | a0001c0001t0001g0035 a0002c0002t0023g0011 |
2 | NA18982.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.737+733delT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499965 | |||||||
chr7:102499991 | G | A | 1 | a0007c0017t0003g0010 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.737+708C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102499991 | |||||||
chr7:102500199 | G | A | 24 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(21): Show |
24 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.737+500C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102500199 | |||||||
chr7:102500201 | G | A | 1 | a0007c0017t0003g0010 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.737+498C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102500201 | |||||||
chr7:102500334 | C | T | 30 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(27): Show |
30 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.737+365G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102500334 | |||||||
chr7:102500341 | G | A | 30 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(27): Show |
30 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.737+358C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102500341 | |||||||
chr7:102500389 | G | A | 31 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(28): Show |
31 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.737+310C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102500389 | |||||||
chr7:102500471 | AAAAT | A | 37 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(34): Show |
37 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.737+224_737+227del others(4): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102500471 | |||||||
chr7:102500516 | G | C | 25 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(22): Show |
25 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.737+183C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102500516 | |||||||
chr7:102500693 | A | T | 27 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(24): Show |
27 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
splice_region_variant&intron_variant | LOW | c.737+6T>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 8/20 | chr7 | 102500693 | |||||||
chr7:102501069 | G | GC | 5 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(2): Show |
5 | HG00544.hp2 HG01258.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+26_642+27insG | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 7/20 | chr7 | 102501069 | |||||||
chr7:102501070 | A | G | 8 | a0001c0012t0009g0023 a0002c0002t0003g0013 a0002c0002t0012g0004 others(5): Show |
8 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.642+26T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 7/20 | chr7 | 102501070 | |||||||
chr7:102501073 | G | C | 1 | a0011c0024t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.642+23C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 7/20 | chr7 | 102501073 | |||||||
chr7:102501078 | C | G | 1 | a0005c0015t0008g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.642+18G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 7/20 | chr7 | 102501078 | |||||||
chr7:102501362 | AG | A | 2 | a0003c0006t0002g0057 a0003c0006t0002g0058 |
2 | HG02602.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.511-136delC | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102501362 | |||||||
chr7:102501609 | G | A | 1 | a0011c0024t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.511-382C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102501609 | |||||||
chr7:102501686 | G | C | 1 | a0003c0004t0019g0051 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511-459C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102501686 | |||||||
chr7:102501824 | G | A | 1 | a0001c0012t0009g0023 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.511-597C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102501824 | |||||||
chr7:102502013 | A | G | 8 | a0001c0007t0021g0048 a0002c0002t0003g0008 a0002c0002t0003g0025 others(5): Show |
8 | HG00280.hp1 HG01167.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.511-786T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502013 | |||||||
chr7:102502086 | C | T | 6 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0002c0023t0003g0012 others(3): Show |
6 | HG00280.hp2 HG00544.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-859G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502086 | |||||||
chr7:102502095 | A | G | 13 | a0001c0007t0013g0001 a0001c0022t0006g0031 a0002c0002t0003g0013 others(10): Show |
13 | HG00280.hp2 HG00544.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.511-868T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502095 | |||||||
chr7:102502157 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.511-930C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502157 | |||||||
chr7:102502170 | A | C | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.511-943T>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502170 | |||||||
chr7:102502172 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.511-945A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502172 | |||||||
chr7:102502174 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.511-947A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502174 | |||||||
chr7:102502175 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.511-948T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502175 | |||||||
chr7:102502176 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.511-949C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502176 | |||||||
chr7:102502182 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.511-955G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502182 | |||||||
chr7:102502184 | G | T | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.511-957C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502184 | |||||||
chr7:102502185 | G | T | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.511-958C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502185 | |||||||
chr7:102502296 | C | T | 44 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(41): Show |
44 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.510+867G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502296 | |||||||
chr7:102502429 | A | G | 7 | a0001c0007t0013g0001 a0004c0008t0004g0049 a0005c0014t0011g0007 others(4): Show |
7 | HG01175.hp1 HG01175.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+734T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502429 | |||||||
chr7:102502496 | T | G | 3 | a0001c0007t0013g0001 a0004c0008t0004g0049 a0014c0013t0015g0014 |
3 | HG01175.hp1 NA18982.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.510+667A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502496 | |||||||
chr7:102502554 | T | C | 4 | a0001c0007t0021g0048 a0002c0002t0003g0008 a0002c0002t0003g0025 others(1): Show |
4 | HG00280.hp1 HG01167.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+609A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502554 | |||||||
chr7:102502679 | C | G | 24 | a0001c0007t0013g0001 a0001c0007t0021g0048 a0001c0012t0009g0023 others(21): Show |
24 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.510+484G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502679 | |||||||
chr7:102502803 | A | C | 1 | a0002c0002t0023g0011 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.510+360T>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502803 | |||||||
chr7:102502854 | C | T | 4 | a0004c0005t0004g0020 a0004c0005t0017g0052 a0004c0005t0018g0022 others(1): Show |
4 | HG01175.hp1 HG01891.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+309G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502854 | |||||||
chr7:102502856 | A | G | 3 | a0004c0005t0004g0020 a0004c0005t0017g0052 a0004c0005t0018g0022 |
3 | HG01891.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.510+307T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102502856 | |||||||
chr7:102503070 | C | T | 1 | a0002c0023t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.510+93G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 6/20 | chr7 | 102503070 | |||||||
chr7:102503356 | G | A | 1 | a0002c0002t0003g0013 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.429-112C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102503356 | |||||||
chr7:102503560 | C | T | 5 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(2): Show |
5 | HG01175.hp1 HG01891.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.429-316G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102503560 | |||||||
chr7:102503601 | A | C | 19 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(16): Show |
19 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.429-357T>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102503601 | |||||||
chr7:102503663 | G | A | 1 | a0014c0013t0015g0014 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.429-419C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102503663 | |||||||
chr7:102503803 | CT | C | 19 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0034 others(16): Show |
19 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.429-560delA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102503803 | |||||||
chr7:102503803 | CTT | C | 28 | a0001c0007t0013g0001 a0001c0007t0021g0048 a0002c0002t0003g0008 others(25): Show |
28 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.429-561_429-560del others(2): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102503803 | |||||||
chr7:102503809 | T | C | 3 | a0002c0002t0003g0013 a0007c0017t0003g0010 a0010c0019t0024g0019 |
3 | HG00280.hp2 HG00544.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.429-565A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102503809 | |||||||
chr7:102503937 | G | T | 5 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(2): Show |
5 | HG01175.hp1 HG01891.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.429-693C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102503937 | |||||||
chr7:102504082 | G | A | 2 | a0007c0018t0003g0009 a0010c0019t0024g0019 |
2 | HG01258.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.429-838C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504082 | |||||||
chr7:102504093 | C | T | 5 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(2): Show |
5 | HG01175.hp1 HG01891.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.429-849G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504093 | |||||||
chr7:102504115 | C | CT | 20 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(17): Show |
20 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.429-872dupA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504115 | |||||||
chr7:102504132 | A | G | 1 | a0001c0012t0009g0023 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.429-888T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504132 | |||||||
chr7:102504142 | T | C | 1 | a0005c0016t0025g0015 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.429-898A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504142 | |||||||
chr7:102504181 | C | T | 36 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.429-937G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504181 | |||||||
chr7:102504469 | G | T | 51 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(48): Show |
51 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.429-1225C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504469 | |||||||
chr7:102504518 | G | C | 49 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(46): Show |
49 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.429-1274C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504518 | |||||||
chr7:102504543 | G | A | 1 | a0002c0011t0022g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429-1299C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504543 | |||||||
chr7:102504592 | G | A | 49 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(46): Show |
49 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.429-1348C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504592 | |||||||
chr7:102504679 | C | CA | 9 | a0001c0012t0009g0023 a0003c0020t0011g0059 a0004c0005t0004g0020 others(6): Show |
9 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-1436dupT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504679 | |||||||
chr7:102504679 | C | CAAAA | 15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(12): Show |
15 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.429-1439_429-1436d others(6): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504679 | |||||||
chr7:102504679 | C | CAAAAA | 6 | a0001c0001t0001g0043 a0001c0001t0006g0042 a0001c0001t0006g0044 others(3): Show |
6 | HG00438.hp1 HG00438.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.429-1440_429-1436d others(7): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504679 | |||||||
chr7:102504696 | C | A | 22 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(19): Show |
22 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.429-1452G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504696 | |||||||
chr7:102504701 | C | CA | 4 | a0001c0012t0009g0023 a0003c0020t0011g0059 a0009c0026t0016g0056 others(1): Show |
4 | HG01243.hp1 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-1458dupT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504701 | |||||||
chr7:102504701 | CA | C | 41 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(38): Show |
41 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.429-1458delT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504701 | |||||||
chr7:102504714 | A | C | 1 | a0001c0007t0021g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.429-1470T>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504714 | |||||||
chr7:102504788 | G | T | 26 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(23): Show |
26 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.429-1544C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102504788 | |||||||
chr7:102505174 | G | A | 2 | a0001c0001t0005g0032 a0001c0001t0020g0036 |
2 | HG01167.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.428+1521C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102505174 | |||||||
chr7:102505343 | T | C | 55 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(52): Show |
55 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.428+1352A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102505343 | |||||||
chr7:102505469 | G | A | 2 | a0002c0002t0010g0038 a0002c0002t0010g0039 |
2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.428+1226C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102505469 | |||||||
chr7:102505601 | C | T | 1 | a0010c0019t0024g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.428+1094G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102505601 | |||||||
chr7:102505663 | C | A | 2 | a0003c0004t0002g0054 a0003c0004t0019g0051 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.428+1032G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102505663 | |||||||
chr7:102505843 | A | G | 1 | a0003c0006t0002g0058 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.428+852T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102505843 | |||||||
chr7:102505970 | G | C | 45 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(42): Show |
45 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.428+725C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102505970 | |||||||
chr7:102506111 | C | A | 2 | a0001c0001t0001g0041 a0001c0001t0020g0036 |
2 | HG02602.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.428+584G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102506111 | |||||||
chr7:102506207 | G | A | 3 | a0002c0002t0003g0013 a0002c0002t0012g0004 a0014c0013t0015g0014 |
3 | HG00544.hp2 HG02165.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.428+488C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102506207 | |||||||
chr7:102506237 | C | T | 1 | a0002c0011t0022g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.428+458G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102506237 | |||||||
chr7:102506249 | T | C | 8 | a0001c0012t0009g0023 a0002c0002t0010g0038 a0002c0011t0022g0016 others(5): Show |
8 | HG01891.hp2 HG03041.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.428+446A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102506249 | |||||||
chr7:102506275 | A | G | 6 | a0002c0002t0003g0013 a0003c0004t0002g0054 a0003c0004t0019g0051 others(3): Show |
6 | HG00280.hp2 HG00544.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.428+420T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102506275 | |||||||
chr7:102506500 | G | A | 3 | a0001c0022t0006g0031 a0002c0002t0012g0004 a0005c0021t0008g0002 |
3 | HG02165.hp1 HG02559.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.428+195C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102506500 | |||||||
chr7:102506536 | G | C | 51 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(48): Show |
51 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.428+159C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102506536 | |||||||
chr7:102506537 | G | A | 6 | a0002c0002t0003g0008 a0002c0002t0003g0025 a0004c0005t0004g0020 others(3): Show |
6 | HG00280.hp1 HG01167.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.428+158C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102506537 | |||||||
chr7:102506615 | C | G | 5 | a0001c0001t0001g0041 a0007c0017t0003g0010 a0007c0018t0003g0009 others(2): Show |
5 | HG00280.hp2 HG01258.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+80G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 5/20 | chr7 | 102506615 | |||||||
chr7:102506837 | C | T | 11 | a0002c0002t0023g0011 a0002c0011t0022g0016 a0002c0023t0003g0012 others(8): Show |
11 | HG01175.hp1 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-13G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102506837 | |||||||
chr7:102506890 | A | G | 3 | a0003c0020t0011g0059 a0011c0024t0002g0053 a0012c0025t0009g0046 |
3 | HG01243.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.299-66T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102506890 | |||||||
chr7:102506985 | T | C | 51 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(48): Show |
51 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.299-161A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102506985 | |||||||
chr7:102507038 | AC | A | 2 | a0011c0024t0002g0053 a0012c0025t0009g0046 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.299-215delG | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507038 | |||||||
chr7:102507077 | G | A | 2 | a0011c0024t0002g0053 a0012c0025t0009g0046 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.299-253C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507077 | |||||||
chr7:102507232 | C | CAAAAA | 4 | a0002c0002t0003g0008 a0002c0002t0003g0025 a0002c0002t0010g0038 others(1): Show |
4 | HG00280.hp1 HG01167.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-413_299-409dup others(5): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507232 | |||||||
chr7:102507232 | C | CAAAAAA | 4 | a0001c0001t0001g0047 a0001c0007t0021g0048 a0002c0002t0010g0039 others(1): Show |
4 | HG02300.hp1 HG03041.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-414_299-409dup others(6): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507232 | |||||||
chr7:102507232 | CAAAAAAA others(4): Show |
C | 5 | a0001c0012t0009g0023 a0004c0005t0004g0020 a0004c0005t0004g0021 others(2): Show |
5 | HG01891.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-419_299-409del others(11): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507232 | |||||||
chr7:102507232 | CAAAAAAA others(5): Show |
C | 8 | a0002c0002t0023g0011 a0002c0023t0003g0012 a0003c0006t0002g0057 others(5): Show |
8 | HG01175.hp1 HG01258.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-420_299-409del others(12): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507232 | |||||||
chr7:102507244 | A | AAT | 17 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(14): Show |
17 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-421_299-420ins others(2): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507244 | |||||||
chr7:102507252 | A | T | 18 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(15): Show |
18 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.299-428T>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507252 | |||||||
chr7:102507313 | A | C | 18 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(15): Show |
18 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.299-489T>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507313 | |||||||
chr7:102507362 | G | A | 1 | a0012c0025t0009g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.299-538C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507362 | |||||||
chr7:102507369 | C | T | 1 | a0010c0019t0024g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.299-545G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507369 | |||||||
chr7:102507437 | T | G | 3 | a0006c0003t0002g0017 a0006c0003t0002g0018 a0006c0003t0002g0024 |
3 | HG01891.hp1 HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.299-613A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507437 | |||||||
chr7:102507510 | CA | C | 20 | a0001c0001t0001g0047 a0001c0007t0013g0001 a0001c0012t0009g0023 others(17): Show |
20 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-687delT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507510 | |||||||
chr7:102507510 | CAA | C | 17 | a0001c0007t0021g0048 a0002c0002t0023g0011 a0002c0023t0003g0012 others(14): Show |
17 | HG00280.hp2 HG01175.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-688_299-687del others(2): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507510 | |||||||
chr7:102507510 | CAAAA | C | 17 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(14): Show |
17 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-690_299-687del others(4): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507510 | |||||||
chr7:102507511 | A | AAAAAAAA others(259): Show |
1 | a0003c0020t0011g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.299-688_299-687ins others(266): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507511 | |||||||
chr7:102507553 | G | A | 1 | a0001c0012t0009g0023 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.299-729C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507553 | |||||||
chr7:102507619 | G | A | 19 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(16): Show |
19 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.299-795C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507619 | |||||||
chr7:102507763 | A | G | 1 | a0001c0012t0009g0023 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.299-939T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102507763 | |||||||
chr7:102508050 | T | C | 6 | a0001c0007t0021g0048 a0002c0002t0023g0011 a0003c0006t0002g0057 others(3): Show |
6 | HG01175.hp1 HG01258.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1226A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102508050 | |||||||
chr7:102508184 | A | AT | 5 | a0001c0001t0001g0028 a0001c0001t0006g0042 a0001c0012t0009g0023 others(2): Show |
5 | HG01993.hp1 HG02165.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1361dupA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102508184 | |||||||
chr7:102508184 | AT | A | 20 | a0001c0001t0001g0037 a0001c0007t0013g0001 a0002c0002t0003g0013 others(17): Show |
20 | HG00544.hp1 HG00544.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-1361delA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102508184 | |||||||
chr7:102508184 | ATT | A | 12 | a0001c0007t0021g0048 a0002c0002t0023g0011 a0003c0006t0002g0057 others(9): Show |
12 | HG00280.hp2 HG01243.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-1362_299-1361d others(4): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102508184 | |||||||
chr7:102508261 | C | G | 4 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+1338G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102508261 | |||||||
chr7:102508481 | T | C | 1 | a0002c0002t0010g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.298+1118A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102508481 | |||||||
chr7:102508663 | GT | G | 2 | a0007c0017t0003g0010 a0007c0018t0003g0009 |
2 | HG00280.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.298+935delA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102508663 | |||||||
chr7:102508806 | T | C | 4 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+793A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102508806 | |||||||
chr7:102508844 | C | T | 40 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(37): Show |
40 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.298+755G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102508844 | |||||||
chr7:102509036 | T | C | 3 | a0001c0007t0013g0001 a0002c0002t0003g0013 a0014c0013t0015g0014 |
3 | HG00544.hp2 NA18982.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.298+563A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102509036 | |||||||
chr7:102509074 | TGGGATTA others(2): Show |
T | 6 | a0001c0007t0013g0001 a0001c0012t0009g0023 a0002c0002t0012g0004 others(3): Show |
6 | HG01175.hp2 HG02165.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+516_298+524del others(9): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102509074 | |||||||
chr7:102509097 | G | A | 1 | a0004c0008t0004g0050 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.298+502C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102509097 | |||||||
chr7:102509114 | T | TTAA | 14 | a0001c0001t0001g0047 a0001c0007t0021g0048 a0001c0012t0009g0023 others(11): Show |
14 | HG00280.hp1 HG01167.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.298+484_298+485ins others(3): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102509114 | |||||||
chr7:102509114 | T | TTAAA | 6 | a0002c0002t0010g0038 a0002c0002t0010g0039 a0003c0004t0002g0054 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+484_298+485ins others(4): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102509114 | |||||||
chr7:102509114 | T | TTTA | 12 | a0001c0007t0013g0001 a0002c0002t0003g0013 a0002c0002t0012g0004 others(9): Show |
12 | HG00544.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+484_298+485ins others(3): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102509114 | |||||||
chr7:102509115 | A | T | 5 | a0005c0014t0011g0007 a0005c0016t0025g0015 a0007c0017t0003g0010 others(2): Show |
5 | HG00280.hp2 HG01258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+484T>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102509115 | |||||||
chr7:102509157 | C | G | 17 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(14): Show |
17 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+442G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 4/20 | chr7 | 102509157 | |||||||
chr7:102509675 | C | T | 3 | a0002c0002t0003g0013 a0007c0017t0003g0010 a0007c0018t0003g0009 |
3 | HG00280.hp2 HG00544.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.237-15G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 3/20 | chr7 | 102509675 | |||||||
chr7:102509990 | T | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(8): Show |
11 | HG00423.hp1 HG00544.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.236+189A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 3/20 | chr7 | 102509990 | |||||||
chr7:102510119 | T | C | 4 | a0004c0005t0004g0020 a0004c0005t0004g0021 a0004c0005t0017g0052 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+60A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 3/20 | chr7 | 102510119 | |||||||
chr7:102510527 | C | T | 2 | a0002c0002t0003g0013 a0014c0013t0015g0014 |
2 | HG00544.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.123-235G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 2/20 | chr7 | 102510527 | |||||||
chr7:102510674 | T | G | 1 | a0009c0026t0016g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123-382A>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 2/20 | chr7 | 102510674 | |||||||
chr7:102510705 | C | G | 17 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(14): Show |
17 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.123-413G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 2/20 | chr7 | 102510705 | |||||||
chr7:102510772 | T | C | 3 | a0001c0007t0013g0001 a0002c0011t0022g0016 a0010c0019t0024g0019 |
3 | HG03017.hp1 HG03041.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.123-480A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 2/20 | chr7 | 102510772 | |||||||
chr7:102510961 | G | C | 1 | a0001c0001t0001g0041 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.123-669C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 2/20 | chr7 | 102510961 | |||||||
chr7:102511034 | C | T | 1 | a0003c0020t0011g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123-742G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 2/20 | chr7 | 102511034 | |||||||
chr7:102511374 | A | G | 27 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(24): Show |
27 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.122+551T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 2/20 | chr7 | 102511374 | |||||||
chr7:102511390 | G | C | 2 | a0001c0007t0013g0001 a0005c0015t0008g0003 |
2 | HG01175.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.122+535C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 2/20 | chr7 | 102511390 | |||||||
chr7:102511477 | GT | G | 46 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(43): Show |
46 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.122+447delA | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 2/20 | chr7 | 102511477 | |||||||
chr7:102512390 | G | C | 34 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(31): Show |
34 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.66-409C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512390 | |||||||
chr7:102512496 | A | C | 14 | a0001c0001t0001g0047 a0001c0007t0013g0001 a0001c0007t0021g0048 others(11): Show |
14 | HG00280.hp2 HG01175.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.66-515T>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512496 | |||||||
chr7:102512574 | G | A | 2 | a0002c0002t0003g0013 a0014c0013t0015g0014 |
2 | HG00544.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.66-593C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512574 | |||||||
chr7:102512593 | GGGAGGGG others(18): Show |
G | 28 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0006g0042 others(25): Show |
28 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.66-637_66-613delTA others(23): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512593 | |||||||
chr7:102512612 | G | A | 2 | a0002c0002t0003g0013 a0014c0013t0015g0014 |
2 | HG00544.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.66-631C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512612 | |||||||
chr7:102512614 | GAGTAGGA others(17): Show |
G | 1 | a0003c0006t0002g0058 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.66-657_66-634delTC others(22): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512614 | |||||||
chr7:102512618 | A | AAGAG | 2 | a0002c0002t0003g0013 a0014c0013t0015g0014 |
2 | HG00544.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.66-638_66-637insCT others(2): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512618 | |||||||
chr7:102512618 | A | AGGAGGGG others(148): Show |
1 | a0001c0001t0001g0045 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.66-638_66-637insCT others(153): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512618 | |||||||
chr7:102512625 | GGAGAGAG others(20): Show |
G | 20 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(17): Show |
20 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.66-671_66-645delTC others(25): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512625 | |||||||
chr7:102512637 | G | A | 2 | a0002c0002t0003g0013 a0014c0013t0015g0014 |
2 | HG00544.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.66-656C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512637 | |||||||
chr7:102512643 | A | AAGAG | 2 | a0002c0002t0003g0013 a0014c0013t0015g0014 |
2 | HG00544.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.66-663_66-662insCT others(2): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512643 | |||||||
chr7:102512704 | G | C | 2 | a0001c0001t0001g0045 a0001c0007t0013g0001 |
2 | HG00423.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.66-723C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512704 | |||||||
chr7:102512713 | GA | G | 2 | a0003c0004t0002g0054 a0003c0004t0019g0051 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.66-733delT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512713 | |||||||
chr7:102512787 | T | TGAGGGGG others(67): Show |
1 | a0010c0019t0024g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.66-880_66-807dupCC others(72): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512787 | |||||||
chr7:102512823 | G | A | 1 | a0003c0004t0019g0051 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.66-842C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512823 | |||||||
chr7:102512883 | G | A | 43 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(40): Show |
43 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.66-902C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512883 | |||||||
chr7:102512960 | C | T | 1 | a0003c0004t0002g0055 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.66-979G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512960 | |||||||
chr7:102512998 | A | G | 3 | a0002c0002t0003g0008 a0002c0002t0003g0025 a0006c0003t0002g0024 |
3 | HG00280.hp1 HG01167.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.66-1017T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102512998 | |||||||
chr7:102513000 | C | T | 1 | a0003c0006t0002g0057 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.66-1019G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513000 | |||||||
chr7:102513129 | T | C | 43 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.66-1148A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513129 | |||||||
chr7:102513130 | G | C | 2 | a0005c0015t0008g0003 a0005c0021t0008g0002 |
2 | HG01175.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.66-1149C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513130 | |||||||
chr7:102513135 | T | C | 11 | a0001c0001t0001g0047 a0001c0007t0021g0048 a0001c0012t0009g0023 others(8): Show |
11 | HG00280.hp2 HG01175.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.66-1154A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513135 | |||||||
chr7:102513184 | G | C | 43 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.66-1203C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513184 | |||||||
chr7:102513188 | C | CCAGGA | 10 | a0001c0001t0001g0047 a0001c0007t0021g0048 a0001c0012t0009g0023 others(7): Show |
10 | HG00280.hp2 HG01175.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.66-1212_66-1208dup others(5): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513188 | |||||||
chr7:102513202 | G | A | 1 | a0004c0005t0017g0052 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.66-1221C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513202 | |||||||
chr7:102513320 | G | T | 1 | a0006c0003t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.66-1339C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513320 | |||||||
chr7:102513484 | T | C | 1 | a0009c0026t0016g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.66-1503A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513484 | |||||||
chr7:102513553 | A | AGTGAGGG others(10): Show |
1 | a0001c0012t0009g0023 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.66-1589_66-1573dup others(17): Show |
RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513553 | |||||||
chr7:102513638 | A | T | 1 | a0003c0004t0002g0054 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.66-1657T>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513638 | |||||||
chr7:102513686 | T | A | 1 | a0003c0004t0019g0051 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.66-1705A>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513686 | |||||||
chr7:102513753 | A | G | 3 | a0002c0023t0003g0012 a0004c0005t0017g0052 a0009c0026t0016g0056 |
3 | HG02258.hp2 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.66-1772T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513753 | |||||||
chr7:102513778 | C | A | 1 | a0002c0023t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.66-1797G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513778 | |||||||
chr7:102513902 | G | A | 1 | a0011c0024t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.66-1921C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102513902 | |||||||
chr7:102514101 | G | A | 1 | a0002c0023t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.66-2120C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102514101 | |||||||
chr7:102514111 | T | C | 3 | a0002c0023t0003g0012 a0004c0005t0017g0052 a0009c0026t0016g0056 |
3 | HG02258.hp2 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.66-2130A>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102514111 | |||||||
chr7:102514219 | G | GC | 33 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(30): Show |
33 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.66-2239dupG | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102514219 | |||||||
chr7:102514224 | C | A | 1 | a0004c0005t0017g0052 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.66-2243G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102514224 | |||||||
chr7:102514326 | G | A | 5 | a0001c0007t0013g0001 a0002c0002t0012g0004 a0005c0015t0008g0003 others(2): Show |
5 | HG01175.hp2 HG02165.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.66-2345C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102514326 | |||||||
chr7:102514332 | G | C | 4 | a0001c0007t0013g0001 a0002c0002t0012g0004 a0005c0015t0008g0003 others(1): Show |
4 | HG01175.hp2 HG02165.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.66-2351C>G | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102514332 | |||||||
chr7:102514774 | C | T | 43 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.66-2793G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102514774 | |||||||
chr7:102514788 | A | G | 33 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(30): Show |
33 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.66-2807T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102514788 | |||||||
chr7:102514900 | G | T | 2 | a0003c0006t0002g0057 a0003c0006t0002g0058 |
2 | HG02602.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.65+2746C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102514900 | |||||||
chr7:102515080 | C | T | 18 | a0001c0007t0013g0001 a0002c0002t0012g0004 a0002c0023t0003g0012 others(15): Show |
18 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.65+2566G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102515080 | |||||||
chr7:102515332 | A | G | 1 | a0002c0011t0022g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.65+2314T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102515332 | |||||||
chr7:102515462 | C | A | 2 | a0003c0004t0002g0054 a0003c0004t0002g0055 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.65+2184G>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102515462 | |||||||
chr7:102515755 | C | T | 2 | a0005c0014t0011g0007 a0005c0016t0025g0015 |
2 | HG03492.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.65+1891G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102515755 | |||||||
chr7:102515920 | A | T | 1 | a0005c0021t0008g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.65+1726T>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102515920 | |||||||
chr7:102516172 | G | A | 1 | a0009c0026t0016g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.65+1474C>T | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102516172 | |||||||
chr7:102516418 | C | T | 1 | a0002c0023t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.65+1228G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102516418 | |||||||
chr7:102516503 | C | T | 1 | a0006c0003t0007g0005 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.65+1143G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102516503 | |||||||
chr7:102516573 | AG | A | 3 | a0002c0002t0012g0004 a0005c0015t0008g0003 a0005c0021t0008g0002 |
3 | HG01175.hp2 HG02165.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.65+1072delC | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102516573 | |||||||
chr7:102516886 | A | G | 4 | a0001c0007t0013g0001 a0002c0002t0012g0004 a0005c0015t0008g0003 others(1): Show |
4 | HG01175.hp2 HG02165.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.65+760T>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102516886 | |||||||
chr7:102516900 | G | T | 10 | a0001c0007t0013g0001 a0002c0002t0003g0013 a0002c0002t0012g0004 others(7): Show |
10 | HG00544.hp2 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.65+746C>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102516900 | |||||||
chr7:102517275 | C | CA | 3 | a0003c0006t0002g0057 a0003c0006t0002g0058 a0003c0020t0011g0059 |
3 | HG01243.hp1 HG02602.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.65+370dupT | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102517275 | |||||||
chr7:102517356 | C | G | 4 | a0002c0002t0003g0008 a0002c0002t0023g0011 a0007c0017t0003g0010 others(1): Show |
4 | HG00280.hp2 HG01167.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.65+290G>C | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102517356 | |||||||
chr7:102517522 | C | T | 1 | a0005c0014t0011g0007 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.65+124G>A | RASA4B | ENSG00000170667.16 | transcript | ENST00000465829.6 | protein_coding | 1/20 | chr7 | 102517522 |