UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.77917603A= | CA1177620127 | NEXN | c.65A= (p.Tyr22=) c.28-357A= (n.28-357A=) | |
| 1 | g.77917603A>C | CA340885085 | NEXN | c.65A>C (p.Tyr22Ser) c.28-357A>C (n.28-357A>C) | |
| 1 | g.77917603A>G | CA16042401 | NEXN | c.65A>G (p.Tyr22Cys) c.28-357A>G (n.28-357A>G) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 1 | g.77917603A>T | CA340885086 | NEXN | c.65A>T (p.Tyr22Phe) c.28-357A>T (n.28-357A>T) | |
| 1 | g.77917604T>A | CA340885087 | NEXN | c.66T>A (p.Tyr22Ter) c.28-356T>A (n.28-356T>A) | |
| 1 | g.77917604T>C | CA918558 | NEXN | c.66T>C (p.Tyr22=) c.28-356T>C (n.28-356T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917604T>G | CA340885089 | NEXN | c.66T>G (p.Tyr22Ter) c.28-356T>G (n.28-356T>G) | |
| 1 | g.77917604T= | CA1149071512 | NEXN | c.66T= (p.Tyr22=) c.28-356T= (n.28-356T=) | |
| 1 | g.77917605G>A | CA24705157 | NEXN | c.67G>A (p.Val23Ile) c.28-355G>A (n.28-355G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917605G>C | CA340885098 | NEXN | c.67G>C (p.Val23Leu) c.28-355G>C (n.28-355G>C) | |
| 1 | g.77917605G= | CA1147623050 | NEXN | c.67G= (p.Val23=) c.28-355G= (n.28-355G=) | |
| 1 | g.77917605G>T | CA340885101 | NEXN | c.67G>T (p.Val23Leu) c.28-355G>T (n.28-355G>T) | |
| 1 | g.77917606T>A | CA340885105 | NEXN | c.68T>A (p.Val23Glu) c.28-354T>A (n.28-354T>A) | |
| 1 | g.77917606T>C | CA340885108 | NEXN | c.68T>C (p.Val23Ala) c.28-354T>C (n.28-354T>C) | COSMIC COSMIC |
| 1 | g.77917606T>G | CA340885111 | NEXN | c.68T>G (p.Val23Gly) c.28-354T>G (n.28-354T>G) | |
| 1 | g.77917607A>C | CA418571028 | NEXN | c.69A>C (p.Val23=) c.28-353A>C (n.28-353A>C) | |
| 1 | g.77917607A>G | CA418571030 | NEXN | c.69A>G (p.Val23=) c.28-353A>G (n.28-353A>G) | |
| 1 | g.77917607A>T | CA418571031 | NEXN | c.69A>T (p.Val23=) c.28-353A>T (n.28-353A>T) | |
| 1 | g.77917608C>A | CA340885119 | NEXN | c.70C>A (p.Pro24Thr) c.28-352C>A (n.28-352C>A) | |
| 1 | g.77917608C= | CA1177620128 | NEXN | c.70C= (p.Pro24=) c.28-352C= (n.28-352C=) | |
| 1 | g.77917608C>G | CA340885125 | NEXN | c.70C>G (p.Pro24Ala) c.28-352C>G (n.28-352C>G) | ClinVar dbSNP |
| 1 | g.77917608C>T | CA340885115 | NEXN | c.70C>T (p.Pro24Ser) c.28-352C>T (n.28-352C>T) | |
| 1 | g.77917609C>A | CA24705158 | NEXN | c.71C>A (p.Pro24Gln) c.28-351C>A (n.28-351C>A) | dbSNP |
| 1 | g.77917609C= | CA1177620129 | NEXN | c.71C= (p.Pro24=) c.28-351C= (n.28-351C=) | |
| 1 | g.77917609C>G | CA340885129 | NEXN | c.71C>G (p.Pro24Arg) c.28-351C>G (n.28-351C>G) | gnomAD v4 |
| 1 | g.77917609C>T | CA918559 | NEXN | c.71C>T (p.Pro24Leu) c.28-351C>T (n.28-351C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917610A>C | CA418571033 | NEXN | c.72A>C (p.Pro24=) c.28-350A>C (n.28-350A>C) | |
| 1 | g.77917610A>G | CA418571035 | NEXN | c.72A>G (p.Pro24=) c.28-350A>G (n.28-350A>G) | |
| 1 | g.77917610A>T | CA418571037 | NEXN | c.72A>T (p.Pro24=) c.28-350A>T (n.28-350A>T) | |
| 1 | g.77917611A>C | CA340885135 | NEXN | c.73A>C (p.Lys25Gln) c.28-349A>C (n.28-349A>C) | gnomAD v4 |
| 1 | g.77917611A>G | CA340885136 | NEXN | c.73A>G (p.Lys25Glu) c.28-349A>G (n.28-349A>G) | |
| 1 | g.77917611A>T | CA340885142 | NEXN | c.73A>T (p.Lys25Ter) c.28-349A>T (n.28-349A>T) | |
| 1 | g.77917612A>C | CA340885155 | NEXN | c.74A>C (p.Lys25Thr) c.28-348A>C (n.28-348A>C) | |
| 1 | g.77917612A>G | CA340885146 | NEXN | c.74A>G (p.Lys25Arg) c.28-348A>G (n.28-348A>G) | |
| 1 | g.77917612A>T | CA340885151 | NEXN | c.74A>T (p.Lys25Ile) c.28-348A>T (n.28-348A>T) | |
| 1 | g.77917613A>C | CA340885159 | NEXN | c.75A>C (p.Lys25Asn) c.28-347A>C (n.28-347A>C) | |
| 1 | g.77917613A>G | CA418571038 | NEXN | c.75A>G (p.Lys25=) c.28-347A>G (n.28-347A>G) | |
| 1 | g.77917613A>T | CA340885161 | NEXN | c.75A>T (p.Lys25Asn) c.28-347A>T (n.28-347A>T) | |
| 1 | g.77917614C>A | CA340885166 | NEXN | c.76C>A (p.Leu26Ile) c.28-346C>A (n.28-346C>A) | |
| 1 | g.77917614C= | CA1177620130 | NEXN | c.76C= (p.Leu26=) c.28-346C= (n.28-346C=) | |
| 1 | g.77917614C>G | CA340885172 | NEXN | c.76C>G (p.Leu26Val) c.28-346C>G (n.28-346C>G) | |
| 1 | g.77917614C>T | CA340885187 | NEXN | c.76C>T (p.Leu26Phe) c.28-346C>T (n.28-346C>T) | dbSNP |
| 1 | g.77917615T>A | CA340885191 | NEXN | c.77T>A (p.Leu26His) c.28-345T>A (n.28-345T>A) | |
| 1 | g.77917615T>C | CA340885205 | NEXN | c.77T>C (p.Leu26Pro) c.28-345T>C (n.28-345T>C) | |
| 1 | g.77917615T>G | CA340885202 | NEXN | c.77T>G (p.Leu26Arg) c.28-345T>G (n.28-345T>G) | gnomAD v4 |
| 1 | g.77917616T>A | CA418571041 | NEXN | c.78T>A (p.Leu26=) c.28-344T>A (n.28-344T>A) | |
| 1 | g.77917616T>C | CA918560 | NEXN | c.78T>C (p.Leu26=) c.28-344T>C (n.28-344T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917616T>G | CA418571042 | NEXN | c.78T>G (p.Leu26=) c.28-344T>G (n.28-344T>G) | |
| 1 | g.77917616T= | CA1144132795 | NEXN | c.78T= (p.Leu26=) c.28-344T= (n.28-344T=) | |
| 1 | g.77917617G>A | CA340885212 | NEXN | c.79G>A (p.Gly27Ser) c.28-343G>A (n.28-343G>A) | gnomAD v4 |
| 1 | g.77917617G>C | CA340885213 | NEXN | c.79G>C (p.Gly27Arg) c.28-343G>C (n.28-343G>C) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77917617G= | CA1177620131 | NEXN | c.79G= (p.Gly27=) c.28-343G= (n.28-343G=) | |
| 1 | g.77917617G>T | CA340885218 | NEXN | c.79G>T (p.Gly27Cys) c.28-343G>T (n.28-343G>T) | |
| 1 | g.77917618G>A | CA340885220 | NEXN | c.80G>A (p.Gly27Asp) c.28-342G>A (n.28-342G>A) | |
| 1 | g.77917618G>C | CA340885230 | NEXN | c.80G>C (p.Gly27Ala) c.28-342G>C (n.28-342G>C) | |
| 1 | g.77917618G= | CA1177620132 | NEXN | c.80G= (p.Gly27=) c.28-342G= (n.28-342G=) | |
| 1 | g.77917618G>T | CA340885232 | NEXN | c.80G>T (p.Gly27Val) c.28-342G>T (n.28-342G>T) | ClinVar dbSNP |
| 1 | g.77917619C>A | CA418571044 | NEXN | c.81C>A (p.Gly27=) c.28-341C>A (n.28-341C>A) | |
| 1 | g.77917619C>G | CA418571046 | NEXN | c.81C>G (p.Gly27=) c.28-341C>G (n.28-341C>G) | |
| 1 | g.77917619C>T | CA418571045 | NEXN | c.81C>T (p.Gly27=) c.28-341C>T (n.28-341C>T) | |
| 1 | g.77917620A>C | CA340885234 | NEXN | c.82A>C (p.Lys28Gln) c.28-340A>C (n.28-340A>C) | |
| 1 | g.77917620A>G | CA340885235 | NEXN | c.82A>G (p.Lys28Glu) c.28-340A>G (n.28-340A>G) | |
| 1 | g.77917620A>T | CA340885236 | NEXN | c.82A>T (p.Lys28Ter) c.28-340A>T (n.28-340A>T) | |
| 1 | g.77917621A>C | CA340885237 | NEXN | c.83A>C (p.Lys28Thr) c.28-339A>C (n.28-339A>C) | |
| 1 | g.77917621A>G | CA340885238 | NEXN | c.83A>G (p.Lys28Arg) c.28-339A>G (n.28-339A>G) | |
| 1 | g.77917621A>T | CA340885239 | NEXN | c.83A>T (p.Lys28Met) c.28-339A>T (n.28-339A>T) | |
| 1 | g.77917622G>A | CA418571048 | NEXN | c.84G>A (p.Lys28=) c.28-338G>A (n.28-338G>A) | |
| 1 | g.77917622G>C | CA340885241 | NEXN | c.84G>C (p.Lys28Asn) c.28-338G>C (n.28-338G>C) | dbSNP gnomAD v2 |
| 1 | g.77917622G= | CA1177620133 | NEXN | c.84G= (p.Lys28=) c.28-338G= (n.28-338G=) | |
| 1 | g.77917622G>T | CA340885240 | NEXN | c.84G>T (p.Lys28Asn) c.28-338G>T (n.28-338G>T) | gnomAD v4 |
| 1 | g.77917623G>A | CA340885245 | NEXN | c.85G>A (p.Gly29Ser) c.28-337G>A (n.28-337G>A) | dbSNP gnomAD v4 |
| 1 | g.77917623G>C | CA340885260 | NEXN | c.85G>C (p.Gly29Arg) c.28-337G>C (n.28-337G>C) | |
| 1 | g.77917623G= | CA1148561786 | NEXN | c.85G= (p.Gly29=) c.28-337G= (n.28-337G=) | |
| 1 | g.77917623G>T | CA918561 | NEXN | c.85G>T (p.Gly29Cys) c.28-337G>T (n.28-337G>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77917624G>A | CA340885265 | NEXN | c.86G>A (p.Gly29Asp) c.28-336G>A (n.28-336G>A) | |
| 1 | g.77917624G>C | CA340885267 | NEXN | c.86G>C (p.Gly29Ala) c.28-336G>C (n.28-336G>C) | gnomAD v4 |
| 1 | g.77917624G= | CA1177620134 | NEXN | c.86G= (p.Gly29=) c.28-336G= (n.28-336G=) | |
| 1 | g.77917624G>T | CA10576434 | NEXN | c.86G>T (p.Gly29Val) c.28-336G>T (n.28-336G>T) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77917625T>A | CA418571049 | NEXN | c.87T>A (p.Gly29=) c.28-335T>A (n.28-335T>A) | |
| 1 | g.77917625T>C | CA418571051 | NEXN | c.87T>C (p.Gly29=) c.28-335T>C (n.28-335T>C) | dbSNP |
| 1 | g.77917625T>G | CA418571050 | NEXN | c.87T>G (p.Gly29=) c.28-335T>G (n.28-335T>G) | |
| 1 | g.77917625T= | CA1177620135 | NEXN | c.87T= (p.Gly29=) c.28-335T= (n.28-335T=) | |
| 1 | g.77917626G>A | CA340885271 | NEXN | c.88G>A (p.Asp30Asn) c.28-334G>A (n.28-334G>A) | |
| 1 | g.77917626G>C | CA340885273 | NEXN | c.88G>C (p.Asp30His) c.28-334G>C (n.28-334G>C) | gnomAD v4 |
| 1 | g.77917626G>T | CA340885278 | NEXN | c.88G>T (p.Asp30Tyr) c.28-334G>T (n.28-334G>T) | |
| 1 | g.77917627A>C | CA340885282 | NEXN | c.89A>C (p.Asp30Ala) c.28-333A>C (n.28-333A>C) | |
| 1 | g.77917627A>G | CA340885288 | NEXN | c.89A>G (p.Asp30Gly) c.28-333A>G (n.28-333A>G) | |
| 1 | g.77917627A>T | CA340885290 | NEXN | c.89A>T (p.Asp30Val) c.28-333A>T (n.28-333A>T) | |
| 1 | g.77917628T>A | CA340885304 | NEXN | c.90T>A (p.Asp30Glu) c.28-332T>A (n.28-332T>A) | |
| 1 | g.77917628T>C | CA418571053 | NEXN | c.90T>C (p.Asp30=) c.28-332T>C (n.28-332T>C) | gnomAD v4 |
| 1 | g.77917628T>G | CA340885305 | NEXN | c.90T>G (p.Asp30Glu) c.28-332T>G (n.28-332T>G) | |
| 1 | g.77917629G>A | CA340885310 | NEXN | c.91G>A (p.Val31Ile) c.28-331G>A (n.28-331G>A) | |
| 1 | g.77917629G>C | CA340885309 | NEXN | c.91G>C (p.Val31Leu) c.28-331G>C (n.28-331G>C) | |
| 1 | g.77917629G>T | CA340885308 | NEXN | c.91G>T (p.Val31Leu) c.28-331G>T (n.28-331G>T) | |
| 1 | g.77917630T>A | CA340885311 | NEXN | c.92T>A (p.Val31Glu) c.28-330T>A (n.28-330T>A) | |
| 1 | g.77917630T>C | CA340885312 | NEXN | c.92T>C (p.Val31Ala) c.28-330T>C (n.28-330T>C) | |
| 1 | g.77917630T>G | CA340885313 | NEXN | c.92T>G (p.Val31Gly) c.28-330T>G (n.28-330T>G) | |
| 1 | g.77917631A>C | CA418571054 | NEXN | c.93A>C (p.Val31=) c.28-329A>C (n.28-329A>C) | |
| 1 | g.77917631A>G | CA418571055 | NEXN | c.93A>G (p.Val31=) c.28-329A>G (n.28-329A>G) | COSMIC COSMIC |
| 1 | g.77917631A>T | CA418571056 | NEXN | c.93A>T (p.Val31=) c.28-329A>T (n.28-329A>T) | |
| 1 | g.77917632A>C | CA340885315 | NEXN | c.94A>C (p.Lys32Gln) c.28-328A>C (n.28-328A>C) | |
| 1 | g.77917632A>G | CA340885319 | NEXN | c.94A>G (p.Lys32Glu) c.28-328A>G (n.28-328A>G) | |
| 1 | g.77917632A>T | CA340885329 | NEXN | c.94A>T (p.Lys32Ter) c.28-328A>T (n.28-328A>T) | |
| 1 | g.77917633A>C | CA340885332 | NEXN | c.95A>C (p.Lys32Thr) c.28-327A>C (n.28-327A>C) | |
| 1 | g.77917633A>G | CA340885333 | NEXN | c.95A>G (p.Lys32Arg) c.28-327A>G (n.28-327A>G) | |
| 1 | g.77917633A>T | CA340885334 | NEXN | c.95A>T (p.Lys32Met) c.28-327A>T (n.28-327A>T) | |
| 1 | g.77917634G>A | CA418571058 | NEXN | c.96G>A (p.Lys32=) c.28-326G>A (n.28-326G>A) | |
| 1 | g.77917634G>C | CA340885335 | NEXN | c.96G>C (p.Lys32Asn) c.28-326G>C (n.28-326G>C) | |
| 1 | g.77917634G>T | CA340885336 | NEXN | c.96G>T (p.Lys32Asn) c.28-326G>T (n.28-326G>T) | |
| 1 | g.77917635G>A | CA340885339 | NEXN | c.97G>A (p.Asp33Asn) c.28-325G>A (n.28-325G>A) | |
| 1 | g.77917635G>C | CA340885343 | NEXN | c.97G>C (p.Asp33His) c.28-325G>C (n.28-325G>C) | |
| 1 | g.77917635G>T | CA340885344 | NEXN | c.97G>T (p.Asp33Tyr) c.28-325G>T (n.28-325G>T) | |
| 1 | g.77917636A= | CA1177620136 | NEXN | c.98A= (p.Asp33=) c.28-324A= (n.28-324A=) | |
| 1 | g.77917636A>C | CA340885347 | NEXN | c.98A>C (p.Asp33Ala) c.28-324A>C (n.28-324A>C) | |
| 1 | g.77917636A>G | CA918562 | NEXN | c.98A>G (p.Asp33Gly) c.28-324A>G (n.28-324A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917636A>T | CA340885345 | NEXN | c.98A>T (p.Asp33Val) c.28-324A>T (n.28-324A>T) | |
| 1 | g.77917637T>A | CA340885363 | NEXN | c.99T>A (p.Asp33Glu) c.28-323T>A (n.28-323T>A) | |
| 1 | g.77917637T>C | CA418571060 | NEXN | c.99T>C (p.Asp33=) c.28-323T>C (n.28-323T>C) | |
| 1 | g.77917637T>G | CA340885365 | NEXN | c.99T>G (p.Asp33Glu) c.28-323T>G (n.28-323T>G) | |
| 1 | g.77917638A>C | CA340885368 | NEXN | c.100A>C (p.Lys34Gln) c.28-322A>C (n.28-322A>C) | |
| 1 | g.77917638A>G | CA340885369 | NEXN | c.100A>G (p.Lys34Glu) c.28-322A>G (n.28-322A>G) | |
| 1 | g.77917638A>T | CA340885370 | NEXN | c.100A>T (p.Lys34Ter) c.28-322A>T (n.28-322A>T) | |
| 1 | g.77917639A= | CA1177620137 | NEXN | c.101A= (p.Lys34=) c.28-321A= (n.28-321A=) | |
| 1 | g.77917639A>C | CA340885371 | NEXN | c.101A>C (p.Lys34Thr) c.28-321A>C (n.28-321A>C) | gnomAD v4 |
| 1 | g.77917639A>G | CA340885372 | NEXN | c.101A>G (p.Lys34Arg) c.28-321A>G (n.28-321A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77917639A>T | CA340885373 | NEXN | c.101A>T (p.Lys34Met) c.28-321A>T (n.28-321A>T) | |
| 1 | g.77917640G>A | CA418571062 | NEXN | c.102G>A (p.Lys34=) c.28-320G>A (n.28-320G>A) | gnomAD v4 |
| 1 | g.77917640G>C | CA340885375 | NEXN | c.102G>C (p.Lys34Asn) c.28-320G>C (n.28-320G>C) | |
| 1 | g.77917640G>T | CA340885377 | NEXN | c.102G>T (p.Lys34Asn) c.28-320G>T (n.28-320G>T) | |
| 1 | g.77917641T>A | CA340885380 | NEXN | c.103T>A (p.Phe35Ile) c.28-319T>A (n.28-319T>A) | |
| 1 | g.77917641T>C | CA340885388 | NEXN | c.103T>C (p.Phe35Leu) c.28-319T>C (n.28-319T>C) | |
| 1 | g.77917641T>G | CA340885391 | NEXN | c.103T>G (p.Phe35Val) c.28-319T>G (n.28-319T>G) | ClinVar |
| 1 | g.77917642T>A | CA340885406 | NEXN | c.104T>A (p.Phe35Tyr) c.28-318T>A (n.28-318T>A) | |
| 1 | g.77917642T>C | CA340885404 | NEXN | c.104T>C (p.Phe35Ser) c.28-318T>C (n.28-318T>C) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77917642T>G | CA340885394 | NEXN | c.104T>G (p.Phe35Cys) c.28-318T>G (n.28-318T>G) | |
| 1 | g.77917642T= | CA1177620138 | NEXN | c.104T= (p.Phe35=) c.28-318T= (n.28-318T=) | |
| 1 | g.77917643T>A | CA340885410 | NEXN | c.105T>A (p.Phe35Leu) c.28-317T>A (n.28-317T>A) | |
| 1 | g.77917643T>C | CA418571066 | NEXN | c.105T>C (p.Phe35=) c.28-317T>C (n.28-317T>C) | |
| 1 | g.77917643T>G | CA340885411 | NEXN | c.105T>G (p.Phe35Leu) c.28-317T>G (n.28-317T>G) | |
| 1 | g.77917644G>A | CA918563 | NEXN | c.106G>A (p.Glu36Lys) c.28-316G>A (n.28-316G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917644G>C | CA340885419 | NEXN | c.106G>C (p.Glu36Gln) c.28-316G>C (n.28-316G>C) | |
| 1 | g.77917644G= | CA1143411141 | NEXN | c.106G= (p.Glu36=) c.28-316G= (n.28-316G=) | |
| 1 | g.77917644G>T | CA340885421 | NEXN | c.106G>T (p.Glu36Ter) c.28-316G>T (n.28-316G>T) | |
| 1 | g.77917645A>C | CA340885425 | NEXN | c.107A>C (p.Glu36Ala) c.28-315A>C (n.28-315A>C) | gnomAD v4 |
| 1 | g.77917645A>G | CA340885428 | NEXN | c.107A>G (p.Glu36Gly) c.28-315A>G (n.28-315A>G) | |
| 1 | g.77917645A>T | CA340885430 | NEXN | c.107A>T (p.Glu36Val) c.28-315A>T (n.28-315A>T) | |
| 1 | g.77917646A>C | CA340885442 | NEXN | c.108A>C (p.Glu36Asp) c.28-314A>C (n.28-314A>C) | |
| 1 | g.77917646A>G | CA418571070 | NEXN | c.108A>G (p.Glu36=) c.28-314A>G (n.28-314A>G) | ClinVar |
| 1 | g.77917646A>T | CA340885445 | NEXN | c.108A>T (p.Glu36Asp) c.28-314A>T (n.28-314A>T) | |
| 1 | g.77917647G>A | CA340885447 | NEXN | c.109G>A (p.Ala37Thr) c.28-313G>A (n.28-313G>A) | |
| 1 | g.77917647G>C | CA340885448 | NEXN | c.109G>C (p.Ala37Pro) c.28-313G>C (n.28-313G>C) | |
| 1 | g.77917647G>T | CA340885455 | NEXN | c.109G>T (p.Ala37Ser) c.28-313G>T (n.28-313G>T) | |
| 1 | g.77917648C>A | CA340885459 | NEXN | c.110C>A (p.Ala37Asp) c.28-312C>A (n.28-312C>A) | |
| 1 | g.77917648C= | CA1148397320 | NEXN | c.110C= (p.Ala37=) c.28-312C= (n.28-312C=) | |
| 1 | g.77917648C>G | CA340885462 | NEXN | c.110C>G (p.Ala37Gly) c.28-312C>G (n.28-312C>G) | |
| 1 | g.77917648C>T | CA918564 | NEXN | c.110C>T (p.Ala37Val) c.28-312C>T (n.28-312C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 1 | g.77917649C>A | CA418571071 | NEXN | c.111C>A (p.Ala37=) c.28-311C>A (n.28-311C>A) | |
| 1 | g.77917649C>G | CA418571072 | NEXN | c.111C>G (p.Ala37=) c.28-311C>G (n.28-311C>G) | |
| 1 | g.77917649C>T | CA418571073 | NEXN | c.111C>T (p.Ala37=) c.28-311C>T (n.28-311C>T) | gnomAD v4 |
| 1 | g.77917650A= | CA1177620139 | NEXN | c.112A= (p.Met38=) c.28-310A= (n.28-310A=) | |
| 1 | g.77917650A>C | CA918565 | NEXN | c.112A>C (p.Met38Leu) c.28-310A>C (n.28-310A>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77917650A>G | CA340885474 | NEXN | c.112A>G (p.Met38Val) c.28-310A>G (n.28-310A>G) | gnomAD v4 |
| 1 | g.77917650A>T | CA340885466 | NEXN | c.112A>T (p.Met38Leu) c.28-310A>T (n.28-310A>T) | |
| 1 | g.77917651T>A | CA340885479 | NEXN | c.113T>A (p.Met38Lys) c.28-309T>A (n.28-309T>A) | |
| 1 | g.77917651T>C | CA340885489 | NEXN | c.113T>C (p.Met38Thr) c.28-309T>C (n.28-309T>C) | |
| 1 | g.77917651T>G | CA340885483 | NEXN | c.113T>G (p.Met38Arg) c.28-309T>G (n.28-309T>G) | |
| 1 | g.77917652G>A | CA340885492 | NEXN | c.114G>A (p.Met38Ile) c.28-308G>A (n.28-308G>A) | |
| 1 | g.77917652G>C | CA340885498 | NEXN | c.114G>C (p.Met38Ile) c.28-308G>C (n.28-308G>C) | |
| 1 | g.77917652G>T | CA340885503 | NEXN | c.114G>T (p.Met38Ile) c.28-308G>T (n.28-308G>T) | |
| 1 | g.77917653C>A | CA340885505 | NEXN | c.115C>A (p.Gln39Lys) c.28-307C>A (n.28-307C>A) | |
| 1 | g.77917653C>G | CA340885508 | NEXN | c.115C>G (p.Gln39Glu) c.28-307C>G (n.28-307C>G) | |
| 1 | g.77917653C>T | CA340885513 | NEXN | c.115C>T (p.Gln39Ter) c.28-307C>T (n.28-307C>T) | |
| 1 | g.77917654A= | CA1177620140 | NEXN | c.116A= (p.Gln39=) c.28-306A= (n.28-306A=) | |
| 1 | g.77917654A>C | CA340885516 | NEXN | c.116A>C (p.Gln39Pro) c.28-306A>C (n.28-306A>C) | |
| 1 | g.77917654A>G | CA340885518 | NEXN | c.116A>G (p.Gln39Arg) c.28-306A>G (n.28-306A>G) | dbSNP gnomAD v2 |
| 1 | g.77917654A>T | CA340885520 | NEXN | c.116A>T (p.Gln39Leu) c.28-306A>T (n.28-306A>T) | |
| 1 | g.77917655G>A | CA418571079 | NEXN | c.117G>A (p.Gln39=) c.28-305G>A (n.28-305G>A) | |
| 1 | g.77917655G>C | CA340885522 | NEXN | c.117G>C (p.Gln39His) c.28-305G>C (n.28-305G>C) | |
| 1 | g.77917655G>T | CA340885525 | NEXN | c.117G>T (p.Gln39His) c.28-305G>T (n.28-305G>T) | |
| 1 | g.77917656A>C | CA418571080 | NEXN | c.118A>C (p.Arg40=) c.28-304A>C (n.28-304A>C) | |
| 1 | g.77917656A>G | CA340885532 | NEXN | c.118A>G (p.Arg40Gly) c.28-304A>G (n.28-304A>G) | |
| 1 | g.77917656A>T | CA340885531 | NEXN | c.118A>T (p.Arg40Ter) c.28-304A>T (n.28-304A>T) | |
| 1 | g.77917657G>A | CA340885533 | NEXN | c.119G>A (p.Arg40Lys) c.28-303G>A (n.28-303G>A) | |
| 1 | g.77917657G>C | CA340885534 | NEXN | c.119G>C (p.Arg40Thr) c.28-303G>C (n.28-303G>C) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77917657G= | CA1177620141 | NEXN | c.119G= (p.Arg40=) c.28-303G= (n.28-303G=) | |
| 1 | g.77917657G>T | CA340885535 | NEXN | c.119G>T (p.Arg40Ile) c.28-303G>T (n.28-303G>T) | |
| 1 | g.77917658A>C | CA340885536 | NEXN | c.120A>C (p.Arg40Ser) c.28-302A>C (n.28-302A>C) | |
| 1 | g.77917658A>G | CA418571082 | NEXN | c.120A>G (p.Arg40=) c.28-302A>G (n.28-302A>G) | |
| 1 | g.77917658A>T | CA340885540 | NEXN | c.120A>T (p.Arg40Ser) c.28-302A>T (n.28-302A>T) | |
| 1 | g.77917659G>A | CA340885543 | NEXN | c.121G>A (p.Ala41Thr) c.28-301G>A (n.28-301G>A) | |
| 1 | g.77917659G>C | CA340885544 | NEXN | c.121G>C (p.Ala41Pro) c.28-301G>C (n.28-301G>C) | |
| 1 | g.77917659G>T | CA340885546 | NEXN | c.121G>T (p.Ala41Ser) c.28-301G>T (n.28-301G>T) | |
| 1 | g.77917660C>A | CA340885552 | NEXN | c.122C>A (p.Ala41Asp) c.28-300C>A (n.28-300C>A) | |
| 1 | g.77917660C>G | CA340885554 | NEXN | c.122C>G (p.Ala41Gly) c.28-300C>G (n.28-300C>G) | |
| 1 | g.77917660C>T | CA340885557 | NEXN | c.122C>T (p.Ala41Val) c.28-300C>T (n.28-300C>T) | |
| 1 | g.77917661C>A | CA418571087 | NEXN | c.123C>A (p.Ala41=) c.28-299C>A (n.28-299C>A) | |
| 1 | g.77917661C= | CA1177620142 | NEXN | c.123C= (p.Ala41=) c.28-299C= (n.28-299C=) | |
| 1 | g.77917661C>G | CA418571088 | NEXN | c.123C>G (p.Ala41=) c.28-299C>G (n.28-299C>G) | |
| 1 | g.77917661C>T | CA418571086 | NEXN | c.123C>T (p.Ala41=) c.28-299C>T (n.28-299C>T) | dbSNP gnomAD v2 |
| 1 | g.77917662A>C | CA418571089 | NEXN | c.124A>C (p.Arg42=) c.28-298A>C (n.28-298A>C) | |
| 1 | g.77917662A>G | CA340885561 | NEXN | c.124A>G (p.Arg42Gly) c.28-298A>G (n.28-298A>G) | |
| 1 | g.77917662A>T | CA340885559 | NEXN | c.124A>T (p.Arg42Trp) c.28-298A>T (n.28-298A>T) | |
| 1 | g.77917663G>A | CA918566 | NEXN | c.125G>A (p.Arg42Lys) c.28-297G>A (n.28-297G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917663G>C | CA340885571 | NEXN | c.125G>C (p.Arg42Thr) c.28-297G>C (n.28-297G>C) | gnomAD v4 |
| 1 | g.77917663G= | CA1177620143 | NEXN | c.125G= (p.Arg42=) c.28-297G= (n.28-297G=) | |
| 1 | g.77917663G>T | CA340885573 | NEXN | c.125G>T (p.Arg42Met) c.28-297G>T (n.28-297G>T) | COSMIC |
| 1 | g.77917665dup | CA2646301195 | NEXN | c.127dup (p.Glu43GlyfsTer9) c.28-295dup (n.28-295dup) | gnomAD v4 |
| 1 | g.77917664G>A | CA418571090 | NEXN | c.126G>A (p.Arg42=) c.28-296G>A (n.28-296G>A) | gnomAD v4 |
| 1 | g.77917664G>C | CA340885577 | NEXN | c.126G>C (p.Arg42Ser) c.28-296G>C (n.28-296G>C) | |
| 1 | g.77917664G>T | CA340885582 | NEXN | c.126G>T (p.Arg42Ser) c.28-296G>T (n.28-296G>T) | |
| 1 | g.77917665G>A | CA340885585 | NEXN | c.127G>A (p.Glu43Lys) c.28-295G>A (n.28-295G>A) | dbSNP |
| 1 | g.77917665G>C | CA340885588 | NEXN | c.127G>C (p.Glu43Gln) c.28-295G>C (n.28-295G>C) | |
| 1 | g.77917665G>T | CA340885589 | NEXN | c.127G>T (p.Glu43Ter) c.28-295G>T (n.28-295G>T) | |
| 1 | g.77917666A>C | CA340885599 | NEXN | c.128A>C (p.Glu43Ala) c.28-294A>C (n.28-294A>C) | |
| 1 | g.77917666A>G | CA340885600 | NEXN | c.128A>G (p.Glu43Gly) c.28-294A>G (n.28-294A>G) | |
| 1 | g.77917666A>T | CA340885601 | NEXN | c.128A>T (p.Glu43Val) c.28-294A>T (n.28-294A>T) | gnomAD v4 |
| 1 | g.77917667A>C | CA340885602 | NEXN | c.129A>C (p.Glu43Asp) c.28-293A>C (n.28-293A>C) | |
| 1 | g.77917667A>G | CA418571091 | NEXN | c.129A>G (p.Glu43=) c.28-293A>G (n.28-293A>G) | gnomAD v4 |
| 1 | g.77917667A>T | CA340885603 | NEXN | c.129A>T (p.Glu43Asp) c.28-293A>T (n.28-293A>T) | |
| 1 | g.77917668G>A | CA340885610 | NEXN | c.130G>A (p.Glu44Lys) c.28-292G>A (n.28-292G>A) | |
| 1 | g.77917668G>C | CA340885604 | NEXN | c.130G>C (p.Glu44Gln) c.28-292G>C (n.28-292G>C) | |
| 1 | g.77917668G>T | CA340885608 | NEXN | c.130G>T (p.Glu44Ter) c.28-292G>T (n.28-292G>T) | |
| 1 | g.77917669A>C | CA340885612 | NEXN | c.131A>C (p.Glu44Ala) c.28-291A>C (n.28-291A>C) | |
| 1 | g.77917669A>G | CA340885615 | NEXN | c.131A>G (p.Glu44Gly) c.28-291A>G (n.28-291A>G) | |
| 1 | g.77917669A>T | CA340885617 | NEXN | c.131A>T (p.Glu44Val) c.28-291A>T (n.28-291A>T) | |
| 1 | g.77917670A>C | CA340885619 | NEXN | c.132A>C (p.Glu44Asp) c.28-290A>C (n.28-290A>C) | |
| 1 | g.77917670A>G | CA418571092 | NEXN | c.132A>G (p.Glu44=) c.28-290A>G (n.28-290A>G) | |
| 1 | g.77917670A>T | CA340885622 | NEXN | c.132A>T (p.Glu44Asp) c.28-290A>T (n.28-290A>T) | |
| 1 | g.77917671A>C | CA418571093 | NEXN | c.133A>C (p.Arg45=) c.28-289A>C (n.28-289A>C) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77917671A>G | CA340885623 | NEXN | c.133A>G (p.Arg45Gly) c.28-289A>G (n.28-289A>G) | |
| 1 | g.77917671A>T | CA340885624 | NEXN | c.133A>T (p.Arg45Ter) c.28-289A>T (n.28-289A>T) | |
| 1 | g.77917672G>A | CA340885633 | NEXN | c.134G>A (p.Arg45Lys) c.28-288G>A (n.28-288G>A) | |
| 1 | g.77917672G>C | CA24705189 | NEXN | c.134G>C (p.Arg45Thr) c.28-288G>C (n.28-288G>C) | dbSNP |
| 1 | g.77917672G= | CA1177620144 | NEXN | c.134G= (p.Arg45=) c.28-288G= (n.28-288G=) | |
| 1 | g.77917672G>T | CA340885637 | NEXN | c.134G>T (p.Arg45Ile) c.28-288G>T (n.28-288G>T) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77917673A= | CA1177620145 | NEXN | c.135A= (p.Arg45=) c.28-287A= (n.28-287A=) | |
| 1 | g.77917673A>C | CA340885638 | NEXN | c.135A>C (p.Arg45Ser) c.28-287A>C (n.28-287A>C) | |
| 1 | g.77917673A>G | CA418571094 | NEXN | c.135A>G (p.Arg45=) c.28-287A>G (n.28-287A>G) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77917673A>T | CA340885639 | NEXN | c.135A>T (p.Arg45Ser) c.28-287A>T (n.28-287A>T) | |
| 1 | g.77917675del | CA2573132567 | NEXN | c.137del (p.Asn46IlefsTer?) c.28-285del (n.28-285del) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77917674A>C | CA340885641 | NEXN | c.136A>C (p.Asn46His) c.28-286A>C (n.28-286A>C) | |
| 1 | g.77917674A>G | CA340885645 | NEXN | c.136A>G (p.Asn46Asp) c.28-286A>G (n.28-286A>G) | |
| 1 | g.77917674A>T | CA340885640 | NEXN | c.136A>T (p.Asn46Tyr) c.28-286A>T (n.28-286A>T) | |
| 1 | g.77917675A>C | CA340885647 | NEXN | c.137A>C (p.Asn46Thr) c.28-285A>C (n.28-285A>C) | |
| 1 | g.77917675A>G | CA340885649 | NEXN | c.137A>G (p.Asn46Ser) c.28-285A>G (n.28-285A>G) | |
| 1 | g.77917675A>T | CA340885651 | NEXN | c.137A>T (p.Asn46Ile) c.28-285A>T (n.28-285A>T) | |
| 1 | g.77917676T>A | CA340885652 | NEXN | c.138T>A (p.Asn46Lys) c.28-284T>A (n.28-284T>A) | |
| 1 | g.77917676T>C | CA418571095 | NEXN | c.138T>C (p.Asn46=) c.28-284T>C (n.28-284T>C) | dbSNP |
| 1 | g.77917676T>G | CA340885653 | NEXN | c.138T>G (p.Asn46Lys) c.28-284T>G (n.28-284T>G) | |
| 1 | g.77917676T= | CA1177620146 | NEXN | c.138T= (p.Asn46=) c.28-284T= (n.28-284T=) | |
| 1 | g.77917677C>A | CA340885659 | NEXN | c.139C>A (p.Gln47Lys) c.28-283C>A (n.28-283C>A) | |
| 1 | g.77917677C>G | CA340885658 | NEXN | c.139C>G (p.Gln47Glu) c.28-283C>G (n.28-283C>G) | |
| 1 | g.77917677C>T | CA340885656 | NEXN | c.139C>T (p.Gln47Ter) c.28-283C>T (n.28-283C>T) | |
| 1 | g.77917678A>C | CA340885661 | NEXN | c.140A>C (p.Gln47Pro) c.28-282A>C (n.28-282A>C) | |
| 1 | g.77917678A>G | CA340885663 | NEXN | c.140A>G (p.Gln47Arg) c.28-282A>G (n.28-282A>G) | |
| 1 | g.77917678A>T | CA340885664 | NEXN | c.140A>T (p.Gln47Leu) c.28-282A>T (n.28-282A>T) | |
| 1 | g.77917680del | CA2580063254 | NEXN | c.142del (p.Arg48GlyfsTer?) c.28-280del (n.28-280del) | ClinVar |
| 1 | g.77917679A= | CA1177620147 | NEXN | c.141A= (p.Gln47=) c.28-281A= (n.28-281A=) | |
| 1 | g.77917679A>C | CA340885665 | NEXN | c.141A>C (p.Gln47His) c.28-281A>C (n.28-281A>C) | |
| 1 | g.77917679A>G | CA418571096 | NEXN | c.141A>G (p.Gln47=) c.28-281A>G (n.28-281A>G) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77917679A>T | CA340885666 | NEXN | c.141A>T (p.Gln47His) c.28-281A>T (n.28-281A>T) | |
| 1 | g.77917680A>C | CA418571097 | NEXN | c.142A>C (p.Arg48=) c.28-280A>C (n.28-280A>C) | |
| 1 | g.77917680A>G | CA340885667 | NEXN | c.142A>G (p.Arg48Gly) c.28-280A>G (n.28-280A>G) | |
| 1 | g.77917680A>T | CA340885668 | NEXN | c.142A>T (p.Arg48Trp) c.28-280A>T (n.28-280A>T) | |
| 1 | g.77917681G>A | CA340885670 | NEXN | c.143G>A (p.Arg48Lys) c.28-279G>A (n.28-279G>A) | |
| 1 | g.77917681G>C | CA340885673 | NEXN | c.143G>C (p.Arg48Thr) c.28-279G>C (n.28-279G>C) | |
| 1 | g.77917681G>T | CA340885672 | NEXN | c.143G>T (p.Arg48Met) c.28-279G>T (n.28-279G>T) | |
| 1 | g.77917682G>A | CA418571098 | NEXN | c.144G>A (p.Arg48=) c.28-278G>A (n.28-278G>A) | gnomAD v4 |
| 1 | g.77917682G>C | CA340885675 | NEXN | c.144G>C (p.Arg48Ser) c.28-278G>C (n.28-278G>C) | |
| 1 | g.77917682G>T | CA340885676 | NEXN | c.144G>T (p.Arg48Ser) c.28-278G>T (n.28-278G>T) | |
| 1 | g.77917683A>C | CA418571099 | NEXN | c.145A>C (p.Arg49=) c.28-277A>C (n.28-277A>C) | |
| 1 | g.77917683A>G | CA340885677 | NEXN | c.145A>G (p.Arg49Gly) c.28-277A>G (n.28-277A>G) | |
| 1 | g.77917683A>T | CA340885678 | NEXN | c.145A>T (p.Arg49Ter) c.28-277A>T (n.28-277A>T) | |
| 1 | g.77917684G>A | CA340885679 | NEXN | c.146G>A (p.Arg49Lys) c.28-276G>A (n.28-276G>A) | |
| 1 | g.77917684G>C | CA340885680 | NEXN | c.146G>C (p.Arg49Thr) c.28-276G>C (n.28-276G>C) | gnomAD v4 |
| 1 | g.77917684G>T | CA340885681 | NEXN | c.146G>T (p.Arg49Ile) c.28-276G>T (n.28-276G>T) | |
| 1 | g.77917685A= | CA1177620148 | NEXN | c.147A= (p.Arg49=) c.28-275A= (n.28-275A=) | |
| 1 | g.77917685A>C | CA340885682 | NEXN | c.147A>C (p.Arg49Ser) c.28-275A>C (n.28-275A>C) | dbSNP |
| 1 | g.77917685A>G | CA418571100 | NEXN | c.147A>G (p.Arg49=) c.28-275A>G (n.28-275A>G) | |
| 1 | g.77917685A>T | CA340885685 | NEXN | c.147A>T (p.Arg49Ser) c.28-275A>T (n.28-275A>T) | gnomAD v4 |
| 1 | g.77917686T>A | CA340885687 | NEXN | c.148T>A (p.Ser50Thr) c.28-274T>A (n.28-274T>A) | |
| 1 | g.77917686T>C | CA340885688 | NEXN | c.148T>C (p.Ser50Pro) c.28-274T>C (n.28-274T>C) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77917686T>G | CA340885690 | NEXN | c.148T>G (p.Ser50Ala) c.28-274T>G (n.28-274T>G) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77917686T= | CA1177620149 | NEXN | c.148T= (p.Ser50=) c.28-274T= (n.28-274T=) | |
| 1 | g.77917687C>A | CA340885691 | NEXN | c.149C>A (p.Ser50Tyr) c.28-273C>A (n.28-273C>A) | |
| 1 | g.77917687C>G | CA340885694 | NEXN | c.149C>G (p.Ser50Cys) c.28-273C>G (n.28-273C>G) | |
| 1 | g.77917687C>T | CA340885693 | NEXN | c.149C>T (p.Ser50Phe) c.28-273C>T (n.28-273C>T) | |
| 1 | g.77917688T>A | CA418571101 | NEXN | c.150T>A (p.Ser50=) c.28-272T>A (n.28-272T>A) | |
| 1 | g.77917688T>C | CA918567 | NEXN | c.150T>C (p.Ser50=) c.28-272T>C (n.28-272T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77917688T>G | CA418571102 | NEXN | c.150T>G (p.Ser50=) c.28-272T>G (n.28-272T>G) | |
| 1 | g.77917688T= | CA1177620150 | NEXN | c.150T= (p.Ser50=) c.28-272T= (n.28-272T=) | |
| 1 | g.77917689A= | CA1177620151 | NEXN | c.151A= (p.Arg51=) c.28-271A= (n.28-271A=) | |
| 1 | g.77917689A>C | CA418571103 | NEXN | c.151A>C (p.Arg51=) c.28-271A>C (n.28-271A>C) | ClinVar |
| 1 | g.77917689A>G | CA918568 | NEXN | c.151A>G (p.Arg51Gly) c.28-271A>G (n.28-271A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 1 | g.77917689A>T | CA340885695 | NEXN | c.151A>T (p.Arg51Ter) c.28-271A>T (n.28-271A>T) | |
| 1 | g.77917690G>A | CA340885696 | NEXN | c.152G>A (p.Arg51Lys) c.28-270G>A (n.28-270G>A) | |
| 1 | g.77917690G>C | CA340885697 | NEXN | c.152G>C (p.Arg51Thr) c.28-270G>C (n.28-270G>C) | |
| 1 | g.77917690G>T | CA340885698 | NEXN | c.152G>T (p.Arg51Ile) c.28-270G>T (n.28-270G>T) | |
| 1 | g.77917691A>C | CA340885700 | NEXN | c.153A>C (p.Arg51Ser) c.28-269A>C (n.28-269A>C) | |
| 1 | g.77917691A>G | CA418571104 | NEXN | c.153A>G (p.Arg51=) c.28-269A>G (n.28-269A>G) | |
| 1 | g.77917691A>T | CA340885699 | NEXN | c.153A>T (p.Arg51Ser) c.28-269A>T (n.28-269A>T) | |
| 1 | g.77917692G>A | CA340885702 | NEXN | c.154G>A (p.Asp52Asn) c.28-268G>A (n.28-268G>A) | dbSNP gnomAD v4 |
| 1 | g.77917692G>C | CA340885703 | NEXN | c.154G>C (p.Asp52His) c.28-268G>C (n.28-268G>C) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77917692G= | CA1177620152 | NEXN | c.154G= (p.Asp52=) c.28-268G= (n.28-268G=) | |
| 1 | g.77917692G>T | CA340885704 | NEXN | c.154G>T (p.Asp52Tyr) c.28-268G>T (n.28-268G>T) | |
| 1 | g.77917693A>C | CA340885706 | NEXN | c.155A>C (p.Asp52Ala) c.28-267A>C (n.28-267A>C) | |
| 1 | g.77917693A>G | CA340885714 | NEXN | c.155A>G (p.Asp52Gly) c.28-267A>G (n.28-267A>G) | |
| 1 | g.77917693A>T | CA340885716 | NEXN | c.155A>T (p.Asp52Val) c.28-267A>T (n.28-267A>T) | |
| 1 | g.77917694C>A | CA340885717 | NEXN | c.156C>A (p.Asp52Glu) c.28-266C>A (n.28-266C>A) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77917694C= | CA1143794913 | NEXN | c.156C= (p.Asp52=) c.28-266C= (n.28-266C=) | |
| 1 | g.77917694C>G | CA340885720 | NEXN | c.156C>G (p.Asp52Glu) c.28-266C>G (n.28-266C>G) | |
| 1 | g.77917694C>T | CA918569 | NEXN | c.156C>T (p.Asp52=) c.28-266C>T (n.28-266C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917695G>A | CA918570 | NEXN | c.157G>A (p.Glu53Lys) c.28-265G>A (n.28-265G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917695G>C | CA340885721 | NEXN | c.157G>C (p.Glu53Gln) c.28-265G>C (n.28-265G>C) | |
| 1 | g.77917695G= | CA1143951072 | NEXN | c.157G= (p.Glu53=) c.28-265G= (n.28-265G=) | |
| 1 | g.77917695G>T | CA340885722 | NEXN | c.157G>T (p.Glu53Ter) c.28-265G>T (n.28-265G>T) | |
| 1 | g.77917696A>C | CA340885723 | NEXN | c.158A>C (p.Glu53Ala) c.28-264A>C (n.28-264A>C) | |
| 1 | g.77917696A>G | CA340885724 | NEXN | c.158A>G (p.Glu53Gly) c.28-264A>G (n.28-264A>G) | |
| 1 | g.77917696A>T | CA340885730 | NEXN | c.158A>T (p.Glu53Val) c.28-264A>T (n.28-264A>T) | |
| 1 | g.77917700del | CA2744231266 | NEXN | c.162del (p.Lys54AsnfsTer?) c.28-260del (n.28-260del) | |
| 1 | g.77917697A>C | CA340885732 | NEXN | c.159A>C (p.Glu53Asp) c.28-263A>C (n.28-263A>C) | |
| 1 | g.77917697A>G | CA418708615 | NEXN | c.159A>G (p.Glu53=) c.28-263A>G (n.28-263A>G) | |
| 1 | g.77917697A>T | CA340885733 | NEXN | c.159A>T (p.Glu53Asp) c.28-263A>T (n.28-263A>T) | |
| 1 | g.77917698A>C | CA340885735 | NEXN | c.160A>C (p.Lys54Gln) c.28-262A>C (n.28-262A>C) | |
| 1 | g.77917698A>G | CA340885736 | NEXN | c.160A>G (p.Lys54Glu) c.28-262A>G (n.28-262A>G) | |
| 1 | g.77917698A>T | CA340885737 | NEXN | c.160A>T (p.Lys54Ter) c.28-262A>T (n.28-262A>T) | |
| 1 | g.77917699A>C | CA340885739 | NEXN | c.161A>C (p.Lys54Thr) c.28-261A>C (n.28-261A>C) | |
| 1 | g.77917699A>G | CA340885742 | NEXN | c.161A>G (p.Lys54Arg) c.28-261A>G (n.28-261A>G) | |
| 1 | g.77917699A>T | CA340885740 | NEXN | c.161A>T (p.Lys54Ile) c.28-261A>T (n.28-261A>T) | |
| 1 | g.77917700A>C | CA340885745 | NEXN | c.162A>C (p.Lys54Asn) c.28-260A>C (n.28-260A>C) | |
| 1 | g.77917700A>G | CA418708622 | NEXN | c.162A>G (p.Lys54=) c.28-260A>G (n.28-260A>G) | |
| 1 | g.77917700A>T | CA340885746 | NEXN | c.162A>T (p.Lys54Asn) c.28-260A>T (n.28-260A>T) | |
| 1 | g.77917701C>A | CA340885747 | NEXN | c.163C>A (p.Gln55Lys) c.28-259C>A (n.28-259C>A) | gnomAD v4 |
| 1 | g.77917701C>G | CA340885752 | NEXN | c.163C>G (p.Gln55Glu) c.28-259C>G (n.28-259C>G) | gnomAD v2 |
| 1 | g.77917701C>T | CA340885750 | NEXN | c.163C>T (p.Gln55Ter) c.28-259C>T (n.28-259C>T) | |
| 1 | g.77917701_77917705delinsCAAAG | CA1177620153 | NEXN | c.163_167delinsCAAAG (p.Gln55=) c.28-259_28-255delinsCAAAG (n.28-259_28-255delinsCAAAG) | |
| 1 | g.77917702A= | CA1177620154 | NEXN | c.164A= (p.Gln55=) c.28-258A= (n.28-258A=) | |
| 1 | g.77917702A>C | CA340885756 | NEXN | c.164A>C (p.Gln55Pro) c.28-258A>C (n.28-258A>C) | |
| 1 | g.77917702A>G | CA918572 | NEXN | c.164A>G (p.Gln55Arg) c.28-258A>G (n.28-258A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77917702A>T | CA340885770 | NEXN | c.164A>T (p.Gln55Leu) c.28-258A>T (n.28-258A>T) | |
| 1 | g.77917702_77917705delinsAAAG | CA1177620155 | NEXN | c.164_167delinsAAAG (p.Gln55=) c.28-258_28-255delinsAAAG (n.28-258_28-255delinsAAAG) | |
| 1 | g.77917704_77917707del | CA918571 | NEXN | c.166_169del (p.Arg56GlufsTer?) c.28-256_28-253del (n.28-256_28-253del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77917702_77917703insT | CA524230650 | NEXN | c.164_165insT (p.Gln55HisfsTer9) c.28-258_28-257insT (n.28-258_28-257insT) | gnomAD v2 |
| 1 | g.77917703A>C | CA340885772 | NEXN | c.165A>C (p.Gln55His) c.28-257A>C (n.28-257A>C) | |
| 1 | g.77917703A>G | CA418708629 | NEXN | c.165A>G (p.Gln55=) c.28-257A>G (n.28-257A>G) | |
| 1 | g.77917703A>T | CA340885778 | NEXN | c.165A>T (p.Gln55His) c.28-257A>T (n.28-257A>T) | |
| 1 | g.77917708_77917710del | CA739076541 | NEXN | c.170_172del (p.Arg57del) c.28-252_28-250del (n.28-252_28-250del) | ClinVar dbSNP gnomAD v3 gnomAD v4 |