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 |
|---|---|---|---|---|---|
| X | g.5892909T>A | CA412012426 | NLGN4X | c.2359A>T (p.Thr787Ser) c.2419A>T (p.Thr807Ser) n.277+10168A>T c.2362A>T (p.Thr788Ser) | |
| X | g.5892909T>C | CA412012427 | NLGN4X | c.2359A>G (p.Thr787Ala) c.2419A>G (p.Thr807Ala) n.277+10168A>G c.2362A>G (p.Thr788Ala) | |
| X | g.5892909T>G | CA412012428 | NLGN4X | c.2359A>C (p.Thr787Pro) c.2419A>C (p.Thr807Pro) n.277+10168A>C c.2362A>C (p.Thr788Pro) | |
| X | g.5892910C>A | CA515367930 | NLGN4X | c.2358G>T (p.Leu786=) c.2418G>T (p.Leu806=) n.277+10167G>T c.2361G>T (p.Leu787=) | dbSNP |
| X | g.5892910C>G | CA515367931 | NLGN4X | c.2358G>C (p.Leu786=) c.2418G>C (p.Leu806=) n.277+10167G>C c.2361G>C (p.Leu787=) | |
| X | g.5892910C>T | CA515367932 | NLGN4X | c.2358G>A (p.Leu786=) c.2418G>A (p.Leu806=) n.277+10167G>A c.2361G>A (p.Leu787=) | |
| X | g.5892911A= | CA2413689052 | NLGN4X | c.2357T= (p.Leu786=) c.2417T= (p.Leu806=) n.277+10166T= c.2360T= (p.Leu787=) | |
| X | g.5892911A>C | CA412012429 | NLGN4X | c.2357T>G (p.Leu786Arg) c.2417T>G (p.Leu806Arg) n.277+10166T>G c.2360T>G (p.Leu787Arg) | |
| X | g.5892911A>G | CA412012430 | NLGN4X | c.2357T>C (p.Leu786Pro) c.2417T>C (p.Leu806Pro) n.277+10166T>C c.2360T>C (p.Leu787Pro) | dbSNP |
| X | g.5892911A>T | CA412012431 | NLGN4X | c.2357T>A (p.Leu786Gln) c.2417T>A (p.Leu806Gln) n.277+10166T>A c.2360T>A (p.Leu787Gln) | |
| X | g.5892912G>A | CA515367933 | NLGN4X | c.2356C>T (p.Leu786=) c.2416C>T (p.Leu806=) n.277+10165C>T c.2359C>T (p.Leu787=) | |
| X | g.5892912G>C | CA412012432 | NLGN4X | c.2356C>G (p.Leu786Val) c.2416C>G (p.Leu806Val) n.277+10165C>G c.2359C>G (p.Leu787Val) | |
| X | g.5892912G>T | CA412012433 | NLGN4X | c.2356C>A (p.Leu786Met) c.2416C>A (p.Leu806Met) n.277+10165C>A c.2359C>A (p.Leu787Met) | |
| X | g.5892913T>A | CA515367934 | NLGN4X | c.2355A>T (p.Thr785=) c.2415A>T (p.Thr805=) n.277+10164A>T c.2358A>T (p.Thr786=) | |
| X | g.5892913T>C | CA515367935 | NLGN4X | c.2355A>G (p.Thr785=) c.2415A>G (p.Thr805=) n.277+10164A>G c.2358A>G (p.Thr786=) | |
| X | g.5892913T>G | CA515367936 | NLGN4X | c.2355A>C (p.Thr785=) c.2415A>C (p.Thr805=) n.277+10164A>C c.2358A>C (p.Thr786=) | COSMIC COSMIC |
| X | g.5892914G>A | CA412012434 | NLGN4X | c.2354C>T (p.Thr785Ile) c.2414C>T (p.Thr805Ile) n.277+10163C>T c.2357C>T (p.Thr786Ile) | |
| X | g.5892914G>C | CA412012435 | NLGN4X | c.2354C>G (p.Thr785Arg) c.2414C>G (p.Thr805Arg) n.277+10163C>G c.2357C>G (p.Thr786Arg) | |
| X | g.5892914G= | CA2413689053 | NLGN4X | c.2354C= (p.Thr785=) c.2414C= (p.Thr805=) n.277+10163C= c.2357C= (p.Thr786=) | |
| X | g.5892914G>T | CA10340891 | NLGN4X | c.2354C>A (p.Thr785Lys) c.2414C>A (p.Thr805Lys) n.277+10163C>A c.2357C>A (p.Thr786Lys) | dbSNP ExAC gnomAD v2 |
| X | g.5892915T>A | CA412012437 | NLGN4X | c.2353A>T (p.Thr785Ser) c.2413A>T (p.Thr805Ser) n.277+10162A>T c.2356A>T (p.Thr786Ser) | gnomAD v4 |
| X | g.5892915T>C | CA412012438 | NLGN4X | c.2353A>G (p.Thr785Ala) c.2413A>G (p.Thr805Ala) n.277+10162A>G c.2356A>G (p.Thr786Ala) | |
| X | g.5892915T>G | CA412012436 | NLGN4X | c.2353A>C (p.Thr785Pro) c.2413A>C (p.Thr805Pro) n.277+10162A>C c.2356A>C (p.Thr786Pro) | |
| X | g.5892916G>A | CA515367937 | NLGN4X | c.2352C>T (p.Asn784=) c.2412C>T (p.Asn804=) n.277+10161C>T c.2355C>T (p.Asn785=) | |
| X | g.5892916G>C | CA412012439 | NLGN4X | c.2352C>G (p.Asn784Lys) c.2412C>G (p.Asn804Lys) n.277+10161C>G c.2355C>G (p.Asn785Lys) | |
| X | g.5892916G>T | CA412012440 | NLGN4X | c.2352C>A (p.Asn784Lys) c.2412C>A (p.Asn804Lys) n.277+10161C>A c.2355C>A (p.Asn785Lys) | |
| X | g.5892917T>A | CA412012441 | NLGN4X | c.2351A>T (p.Asn784Ile) c.2411A>T (p.Asn804Ile) n.277+10160A>T c.2354A>T (p.Asn785Ile) | |
| X | g.5892917T>C | CA412012442 | NLGN4X | c.2351A>G (p.Asn784Ser) c.2411A>G (p.Asn804Ser) n.277+10160A>G c.2354A>G (p.Asn785Ser) | dbSNP |
| X | g.5892917T>G | CA412012443 | NLGN4X | c.2351A>C (p.Asn784Thr) c.2411A>C (p.Asn804Thr) n.277+10160A>C c.2354A>C (p.Asn785Thr) | |
| X | g.5892917T= | CA2413689054 | NLGN4X | c.2351A= (p.Asn784=) c.2411A= (p.Asn804=) n.277+10160A= c.2354A= (p.Asn785=) | |
| X | g.5892918T>A | CA412012444 | NLGN4X | c.2350A>T (p.Asn784Tyr) c.2410A>T (p.Asn804Tyr) n.277+10159A>T c.2353A>T (p.Asn785Tyr) | |
| X | g.5892918T>C | CA412012445 | NLGN4X | c.2350A>G (p.Asn784Asp) c.2410A>G (p.Asn804Asp) n.277+10159A>G c.2353A>G (p.Asn785Asp) | |
| X | g.5892918T>G | CA412012446 | NLGN4X | c.2350A>C (p.Asn784His) c.2410A>C (p.Asn804His) n.277+10159A>C c.2353A>C (p.Asn785His) | |
| X | g.5892919T>A | CA515367938 | NLGN4X | c.2349A>T (p.Pro783=) c.2409A>T (p.Pro803=) n.277+10158A>T c.2352A>T (p.Pro784=) | |
| X | g.5892919T>C | CA515367939 | NLGN4X | c.2349A>G (p.Pro783=) c.2409A>G (p.Pro803=) n.277+10158A>G c.2352A>G (p.Pro784=) | |
| X | g.5892919T>G | CA515367940 | NLGN4X | c.2349A>C (p.Pro783=) c.2409A>C (p.Pro803=) n.277+10158A>C c.2352A>C (p.Pro784=) | |
| X | g.5892920G>A | CA412012447 | NLGN4X | c.2348C>T (p.Pro783Leu) c.2408C>T (p.Pro803Leu) n.277+10157C>T c.2351C>T (p.Pro784Leu) | |
| X | g.5892920G>C | CA412012448 | NLGN4X | c.2348C>G (p.Pro783Arg) c.2408C>G (p.Pro803Arg) n.277+10157C>G c.2351C>G (p.Pro784Arg) | |
| X | g.5892920G>T | CA412012449 | NLGN4X | c.2348C>A (p.Pro783Gln) c.2408C>A (p.Pro803Gln) n.277+10157C>A c.2351C>A (p.Pro784Gln) | |
| X | g.5892921G>A | CA412012450 | NLGN4X | c.2347C>T (p.Pro783Ser) c.2407C>T (p.Pro803Ser) n.277+10156C>T c.2350C>T (p.Pro784Ser) | |
| X | g.5892921G>C | CA412012451 | NLGN4X | c.2347C>G (p.Pro783Ala) c.2407C>G (p.Pro803Ala) n.277+10156C>G c.2350C>G (p.Pro784Ala) | |
| X | g.5892921G>T | CA412012452 | NLGN4X | c.2347C>A (p.Pro783Thr) c.2407C>A (p.Pro803Thr) n.277+10156C>A c.2350C>A (p.Pro784Thr) | |
| X | g.5892922A>C | CA412012453 | NLGN4X | c.2346T>G (p.Ile782Met) c.2406T>G (p.Ile802Met) n.277+10155T>G c.2349T>G (p.Ile783Met) | |
| X | g.5892922A>G | CA515367941 | NLGN4X | c.2346T>C (p.Ile782=) c.2406T>C (p.Ile802=) n.277+10155T>C c.2349T>C (p.Ile783=) | |
| X | g.5892922A>T | CA515367942 | NLGN4X | c.2346T>A (p.Ile782=) c.2406T>A (p.Ile802=) n.277+10155T>A c.2349T>A (p.Ile783=) | |
| X | g.5892923A>C | CA412012454 | NLGN4X | c.2345T>G (p.Ile782Ser) c.2405T>G (p.Ile802Ser) n.277+10154T>G c.2348T>G (p.Ile783Ser) | |
| X | g.5892923A>G | CA412012455 | NLGN4X | c.2345T>C (p.Ile782Thr) c.2405T>C (p.Ile802Thr) n.277+10154T>C c.2348T>C (p.Ile783Thr) | |
| X | g.5892923A>T | CA412012456 | NLGN4X | c.2345T>A (p.Ile782Asn) c.2405T>A (p.Ile802Asn) n.277+10154T>A c.2348T>A (p.Ile783Asn) | |
| X | g.5892924T>A | CA412012457 | NLGN4X | c.2344A>T (p.Ile782Phe) c.2404A>T (p.Ile802Phe) n.277+10153A>T c.2347A>T (p.Ile783Phe) | COSMIC COSMIC |
| X | g.5892924T>C | CA412012458 | NLGN4X | c.2344A>G (p.Ile782Val) c.2404A>G (p.Ile802Val) n.277+10153A>G c.2347A>G (p.Ile783Val) | |
| X | g.5892924T>G | CA412012459 | NLGN4X | c.2344A>C (p.Ile782Leu) c.2404A>C (p.Ile802Leu) n.277+10153A>C c.2347A>C (p.Ile783Leu) | |
| X | g.5892925C>A | CA412012460 | NLGN4X | c.2343G>T (p.Met781Ile) c.2403G>T (p.Met801Ile) n.277+10152G>T c.2346G>T (p.Met782Ile) | |
| X | g.5892925C>G | CA412012461 | NLGN4X | c.2343G>C (p.Met781Ile) c.2403G>C (p.Met801Ile) n.277+10152G>C c.2346G>C (p.Met782Ile) | |
| X | g.5892925C>T | CA412012462 | NLGN4X | c.2343G>A (p.Met781Ile) c.2403G>A (p.Met801Ile) n.277+10152G>A c.2346G>A (p.Met782Ile) | |
| X | g.5892926A= | CA2413689055 | NLGN4X | c.2342T= (p.Met781=) c.2402T= (p.Met801=) n.277+10151T= c.2345T= (p.Met782=) | |
| X | g.5892926A>C | CA412012463 | NLGN4X | c.2342T>G (p.Met781Arg) c.2402T>G (p.Met801Arg) n.277+10151T>G c.2345T>G (p.Met782Arg) | |
| X | g.5892926A>G | CA412012464 | NLGN4X | c.2342T>C (p.Met781Thr) c.2402T>C (p.Met801Thr) n.277+10151T>C c.2345T>C (p.Met782Thr) | dbSNP |
| X | g.5892926A>T | CA412012465 | NLGN4X | c.2342T>A (p.Met781Lys) c.2402T>A (p.Met801Lys) n.277+10151T>A c.2345T>A (p.Met782Lys) | |
| X | g.5892927T>A | CA412012467 | NLGN4X | c.2341A>T (p.Met781Leu) c.2401A>T (p.Met801Leu) n.277+10150A>T c.2344A>T (p.Met782Leu) | |
| X | g.5892927T>C | CA412012468 | NLGN4X | c.2341A>G (p.Met781Val) c.2401A>G (p.Met801Val) n.277+10150A>G c.2344A>G (p.Met782Val) | gnomAD v4 |
| X | g.5892927T>G | CA412012466 | NLGN4X | c.2341A>C (p.Met781Leu) c.2401A>C (p.Met801Leu) n.277+10150A>C c.2344A>C (p.Met782Leu) | |
| X | g.5892928G>A | CA10340892 | NLGN4X | c.2340C>T (p.Thr780=) c.2400C>T (p.Thr800=) n.277+10149C>T c.2343C>T (p.Thr781=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5892928G>C | CA515367943 | NLGN4X | c.2340C>G (p.Thr780=) c.2400C>G (p.Thr800=) n.277+10149C>G c.2343C>G (p.Thr781=) | |
| X | g.5892928G= | CA2413689056 | NLGN4X | c.2340C= (p.Thr780=) c.2400C= (p.Thr800=) n.277+10149C= c.2343C= (p.Thr781=) | |
| X | g.5892928G>T | CA515367944 | NLGN4X | c.2340C>A (p.Thr780=) c.2400C>A (p.Thr800=) n.277+10149C>A c.2343C>A (p.Thr781=) | |
| X | g.5892929G>A | CA412012469 | NLGN4X | c.2339C>T (p.Thr780Ile) c.2399C>T (p.Thr800Ile) n.277+10148C>T c.2342C>T (p.Thr781Ile) | |
| X | g.5892929G>C | CA412012470 | NLGN4X | c.2339C>G (p.Thr780Ser) c.2399C>G (p.Thr800Ser) n.277+10148C>G c.2342C>G (p.Thr781Ser) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.5892929G= | CA2413689057 | NLGN4X | c.2339C= (p.Thr780=) c.2399C= (p.Thr800=) n.277+10148C= c.2342C= (p.Thr781=) | |
| X | g.5892929G>T | CA412012471 | NLGN4X | c.2339C>A (p.Thr780Asn) c.2399C>A (p.Thr800Asn) n.277+10148C>A c.2342C>A (p.Thr781Asn) | |
| X | g.5892930T>A | CA10340893 | NLGN4X | c.2338A>T (p.Thr780Ser) c.2398A>T (p.Thr800Ser) n.277+10147A>T c.2341A>T (p.Thr781Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.5892930T>C | CA412012472 | NLGN4X | c.2338A>G (p.Thr780Ala) c.2398A>G (p.Thr800Ala) n.277+10147A>G c.2341A>G (p.Thr781Ala) | |
| X | g.5892930T>G | CA412012473 | NLGN4X | c.2338A>C (p.Thr780Pro) c.2398A>C (p.Thr800Pro) n.277+10147A>C c.2341A>C (p.Thr781Pro) | |
| X | g.5892930T= | CA2413689058 | NLGN4X | c.2338A= (p.Thr780=) c.2398A= (p.Thr800=) n.277+10147A= c.2341A= (p.Thr781=) | |
| X | g.5892931G>A | CA515367945 | NLGN4X | c.2337C>T (p.Ile779=) c.2397C>T (p.Ile799=) n.277+10146C>T c.2340C>T (p.Ile780=) | gnomAD v4 |
| X | g.5892931G>C | CA412012474 | NLGN4X | c.2337C>G (p.Ile779Met) c.2397C>G (p.Ile799Met) n.277+10146C>G c.2340C>G (p.Ile780Met) | |
| X | g.5892931G>T | CA515367946 | NLGN4X | c.2337C>A (p.Ile779=) c.2397C>A (p.Ile799=) n.277+10146C>A c.2340C>A (p.Ile780=) | |
| X | g.5892932A>C | CA412012475 | NLGN4X | c.2336T>G (p.Ile779Ser) c.2396T>G (p.Ile799Ser) n.277+10145T>G c.2339T>G (p.Ile780Ser) | |
| X | g.5892932A>G | CA412012476 | NLGN4X | c.2336T>C (p.Ile779Thr) c.2396T>C (p.Ile799Thr) n.277+10145T>C c.2339T>C (p.Ile780Thr) | |
| X | g.5892932A>T | CA412012477 | NLGN4X | c.2336T>A (p.Ile779Asn) c.2396T>A (p.Ile799Asn) n.277+10145T>A c.2339T>A (p.Ile780Asn) | |
| X | g.5892933T>A | CA412012478 | NLGN4X | c.2335A>T (p.Ile779Phe) c.2395A>T (p.Ile799Phe) n.277+10144A>T c.2338A>T (p.Ile780Phe) | |
| X | g.5892933T>C | CA412012479 | NLGN4X | c.2335A>G (p.Ile779Val) c.2395A>G (p.Ile799Val) n.277+10144A>G c.2338A>G (p.Ile780Val) | gnomAD v4 |
| X | g.5892933T>G | CA412012480 | NLGN4X | c.2335A>C (p.Ile779Leu) c.2395A>C (p.Ile799Leu) n.277+10144A>C c.2338A>C (p.Ile780Leu) | |
| X | g.5892934G>A | CA515367949 | NLGN4X | c.2334C>T (p.Thr778=) c.2394C>T (p.Thr798=) n.277+10143C>T c.2337C>T (p.Thr779=) | |
| X | g.5892934G>C | CA515367948 | NLGN4X | c.2334C>G (p.Thr778=) c.2394C>G (p.Thr798=) n.277+10143C>G c.2337C>G (p.Thr779=) | |
| X | g.5892934G>T | CA515367947 | NLGN4X | c.2334C>A (p.Thr778=) c.2394C>A (p.Thr798=) n.277+10143C>A c.2337C>A (p.Thr779=) | |
| X | g.5892935G>A | CA412012481 | NLGN4X | c.2333C>T (p.Thr778Ile) c.2393C>T (p.Thr798Ile) n.277+10142C>T c.2336C>T (p.Thr779Ile) | COSMIC COSMIC |
| X | g.5892935G>C | CA412012483 | NLGN4X | c.2333C>G (p.Thr778Ser) c.2393C>G (p.Thr798Ser) n.277+10142C>G c.2336C>G (p.Thr779Ser) | |
| X | g.5892935G>T | CA412012482 | NLGN4X | c.2333C>A (p.Thr778Asn) c.2393C>A (p.Thr798Asn) n.277+10142C>A c.2336C>A (p.Thr779Asn) | |
| X | g.5892936T>A | CA412012484 | NLGN4X | c.2332A>T (p.Thr778Ser) c.2392A>T (p.Thr798Ser) n.277+10141A>T c.2335A>T (p.Thr779Ser) | |
| X | g.5892936T>C | CA412012485 | NLGN4X | c.2332A>G (p.Thr778Ala) c.2392A>G (p.Thr798Ala) n.277+10141A>G c.2335A>G (p.Thr779Ala) | |
| X | g.5892936T>G | CA412012486 | NLGN4X | c.2332A>C (p.Thr778Pro) c.2392A>C (p.Thr798Pro) n.277+10141A>C c.2335A>C (p.Thr779Pro) | |
| X | g.5892937G>A | CA515367950 | NLGN4X | c.2331C>T (p.Asn777=) c.2391C>T (p.Asn797=) n.277+10140C>T c.2334C>T (p.Asn778=) | |
| X | g.5892937G>C | CA412012487 | NLGN4X | c.2331C>G (p.Asn777Lys) c.2391C>G (p.Asn797Lys) n.277+10140C>G c.2334C>G (p.Asn778Lys) | |
| X | g.5892937G>T | CA412012488 | NLGN4X | c.2331C>A (p.Asn777Lys) c.2391C>A (p.Asn797Lys) n.277+10140C>A c.2334C>A (p.Asn778Lys) | |
| X | g.5892938T>A | CA412012489 | NLGN4X | c.2330A>T (p.Asn777Ile) c.2390A>T (p.Asn797Ile) n.277+10139A>T c.2333A>T (p.Asn778Ile) | COSMIC COSMIC |
| X | g.5892938T>C | CA412012490 | NLGN4X | c.2330A>G (p.Asn777Ser) c.2390A>G (p.Asn797Ser) n.277+10139A>G c.2333A>G (p.Asn778Ser) | ClinVar gnomAD v4 |
| X | g.5892938T>G | CA412012491 | NLGN4X | c.2330A>C (p.Asn777Thr) c.2390A>C (p.Asn797Thr) n.277+10139A>C c.2333A>C (p.Asn778Thr) | |
| X | g.5892939T>A | CA412012492 | NLGN4X | c.2329A>T (p.Asn777Tyr) c.2389A>T (p.Asn797Tyr) n.277+10138A>T c.2332A>T (p.Asn778Tyr) | |
| X | g.5892939T>C | CA412012493 | NLGN4X | c.2329A>G (p.Asn777Asp) c.2389A>G (p.Asn797Asp) n.277+10138A>G c.2332A>G (p.Asn778Asp) | dbSNP gnomAD v4 |
| X | g.5892939T>G | CA412012494 | NLGN4X | c.2329A>C (p.Asn777His) c.2389A>C (p.Asn797His) n.277+10138A>C c.2332A>C (p.Asn778His) | |
| X | g.5892939T= | CA2413689059 | NLGN4X | c.2329A= (p.Asn777=) c.2389A= (p.Asn797=) n.277+10138A= c.2332A= (p.Asn778=) | |
| X | g.5892940T>A | CA515367951 | NLGN4X | c.2328A>T (p.Pro776=) c.2388A>T (p.Pro796=) n.277+10137A>T c.2331A>T (p.Pro777=) | |
| X | g.5892940T>C | CA515367953 | NLGN4X | c.2328A>G (p.Pro776=) c.2388A>G (p.Pro796=) n.277+10137A>G c.2331A>G (p.Pro777=) | |
| X | g.5892940T>G | CA515367952 | NLGN4X | c.2328A>C (p.Pro776=) c.2388A>C (p.Pro796=) n.277+10137A>C c.2331A>C (p.Pro777=) | |
| X | g.5892941G>A | CA412012497 | NLGN4X | c.2327C>T (p.Pro776Leu) c.2387C>T (p.Pro796Leu) n.277+10136C>T c.2330C>T (p.Pro777Leu) | |
| X | g.5892941G>C | CA412012496 | NLGN4X | c.2327C>G (p.Pro776Arg) c.2387C>G (p.Pro796Arg) n.277+10136C>G c.2330C>G (p.Pro777Arg) | |
| X | g.5892941G= | CA2413689060 | NLGN4X | c.2327C= (p.Pro776=) c.2387C= (p.Pro796=) n.277+10136C= c.2330C= (p.Pro777=) | |
| X | g.5892941G>T | CA412012495 | NLGN4X | c.2327C>A (p.Pro776Gln) c.2387C>A (p.Pro796Gln) n.277+10136C>A c.2330C>A (p.Pro777Gln) | dbSNP gnomAD v4 |
| X | g.5892942G>A | CA412012498 | NLGN4X | c.2326C>T (p.Pro776Ser) c.2386C>T (p.Pro796Ser) n.277+10135C>T c.2329C>T (p.Pro777Ser) | |
| X | g.5892942G>C | CA412012500 | NLGN4X | c.2326C>G (p.Pro776Ala) c.2386C>G (p.Pro796Ala) n.277+10135C>G c.2329C>G (p.Pro777Ala) | |
| X | g.5892942G= | CA2413689061 | NLGN4X | c.2326C= (p.Pro776=) c.2386C= (p.Pro796=) n.277+10135C= c.2329C= (p.Pro777=) | |
| X | g.5892942G>T | CA412012499 | NLGN4X | c.2326C>A (p.Pro776Thr) c.2386C>A (p.Pro796Thr) n.277+10135C>A c.2329C>A (p.Pro777Thr) | dbSNP gnomAD v4 |
| X | g.5892943C>A | CA515367954 | NLGN4X | c.2325G>T (p.Thr775=) c.2385G>T (p.Thr795=) n.277+10134G>T c.2328G>T (p.Thr776=) | dbSNP COSMIC |
| X | g.5892943C= | CA2413689062 | NLGN4X | c.2325G= (p.Thr775=) c.2385G= (p.Thr795=) n.277+10134G= c.2328G= (p.Thr776=) | |
| X | g.5892943C>G | CA515367955 | NLGN4X | c.2325G>C (p.Thr775=) c.2385G>C (p.Thr795=) n.277+10134G>C c.2328G>C (p.Thr776=) | |
| X | g.5892943C>T | CA10340894 | NLGN4X | c.2325G>A (p.Thr775=) c.2385G>A (p.Thr795=) n.277+10134G>A c.2328G>A (p.Thr776=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.5892944G>A | CA10340895 | NLGN4X | c.2324C>T (p.Thr775Met) c.2384C>T (p.Thr795Met) n.277+10133C>T c.2327C>T (p.Thr776Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5892944G>C | CA412012501 | NLGN4X | c.2324C>G (p.Thr775Arg) c.2384C>G (p.Thr795Arg) n.277+10133C>G c.2327C>G (p.Thr776Arg) | |
| X | g.5892944G= | CA2413689063 | NLGN4X | c.2324C= (p.Thr775=) c.2384C= (p.Thr795=) n.277+10133C= c.2327C= (p.Thr776=) | |
| X | g.5892944G>T | CA412012502 | NLGN4X | c.2324C>A (p.Thr775Lys) c.2384C>A (p.Thr795Lys) n.277+10133C>A c.2327C>A (p.Thr776Lys) | |
| X | g.5892945T>A | CA412012503 | NLGN4X | c.2323A>T (p.Thr775Ser) c.2383A>T (p.Thr795Ser) n.277+10132A>T c.2326A>T (p.Thr776Ser) | |
| X | g.5892945T>C | CA412012504 | NLGN4X | c.2323A>G (p.Thr775Ala) c.2383A>G (p.Thr795Ala) n.277+10132A>G c.2326A>G (p.Thr776Ala) | |
| X | g.5892945T>G | CA412012505 | NLGN4X | c.2323A>C (p.Thr775Pro) c.2383A>C (p.Thr795Pro) n.277+10132A>C c.2326A>C (p.Thr776Pro) | |
| X | g.5892946C>A | CA412012506 | NLGN4X | c.2322G>T (p.Met774Ile) c.2382G>T (p.Met794Ile) n.277+10131G>T c.2325G>T (p.Met775Ile) | |
| X | g.5892946C>G | CA412012507 | NLGN4X | c.2322G>C (p.Met774Ile) c.2382G>C (p.Met794Ile) n.277+10131G>C c.2325G>C (p.Met775Ile) | |
| X | g.5892946C>T | CA412012508 | NLGN4X | c.2322G>A (p.Met774Ile) c.2382G>A (p.Met794Ile) n.277+10131G>A c.2325G>A (p.Met775Ile) | |
| X | g.5892947A= | CA2413689064 | NLGN4X | c.2321T= (p.Met774=) c.2381T= (p.Met794=) n.277+10130T= c.2324T= (p.Met775=) | |
| X | g.5892947A>C | CA412012509 | NLGN4X | c.2321T>G (p.Met774Arg) c.2381T>G (p.Met794Arg) n.277+10130T>G c.2324T>G (p.Met775Arg) | gnomAD v4 |
| X | g.5892947A>G | CA10340896 | NLGN4X | c.2321T>C (p.Met774Thr) c.2381T>C (p.Met794Thr) n.277+10130T>C c.2324T>C (p.Met775Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5892947A>T | CA412012510 | NLGN4X | c.2321T>A (p.Met774Lys) c.2381T>A (p.Met794Lys) n.277+10130T>A c.2324T>A (p.Met775Lys) | gnomAD v4 |
| X | g.5892948T>A | CA412012511 | NLGN4X | c.2320A>T (p.Met774Leu) c.2380A>T (p.Met794Leu) n.277+10129A>T c.2323A>T (p.Met775Leu) | |
| X | g.5892948T>C | CA412012512 | NLGN4X | c.2320A>G (p.Met774Val) c.2380A>G (p.Met794Val) n.277+10129A>G c.2323A>G (p.Met775Val) | gnomAD v4 |
| X | g.5892948T>G | CA412012513 | NLGN4X | c.2320A>C (p.Met774Leu) c.2380A>C (p.Met794Leu) n.277+10129A>C c.2323A>C (p.Met775Leu) | |
| X | g.5892949A>C | CA515367957 | NLGN4X | c.2319T>G (p.Leu773=) c.2379T>G (p.Leu793=) n.277+10128T>G c.2322T>G (p.Leu774=) | |
| X | g.5892949A>G | CA515367958 | NLGN4X | c.2319T>C (p.Leu773=) c.2379T>C (p.Leu793=) n.277+10128T>C c.2322T>C (p.Leu774=) | gnomAD v4 |
| X | g.5892949A>T | CA515367956 | NLGN4X | c.2319T>A (p.Leu773=) c.2379T>A (p.Leu793=) n.277+10128T>A c.2322T>A (p.Leu774=) | |
| X | g.5892950A>C | CA412012514 | NLGN4X | c.2318T>G (p.Leu773Arg) c.2378T>G (p.Leu793Arg) n.277+10127T>G c.2321T>G (p.Leu774Arg) | COSMIC COSMIC |
| X | g.5892950A>G | CA412012516 | NLGN4X | c.2318T>C (p.Leu773Pro) c.2378T>C (p.Leu793Pro) n.277+10127T>C c.2321T>C (p.Leu774Pro) | |
| X | g.5892950A>T | CA412012515 | NLGN4X | c.2318T>A (p.Leu773His) c.2378T>A (p.Leu793His) n.277+10127T>A c.2321T>A (p.Leu774His) | |
| X | g.5892951G>A | CA326308989 | NLGN4X | c.2317C>T (p.Leu773Phe) c.2377C>T (p.Leu793Phe) n.277+10126C>T c.2320C>T (p.Leu774Phe) | ClinVar dbSNP |
| X | g.5892951G>C | CA412012517 | NLGN4X | c.2317C>G (p.Leu773Val) c.2377C>G (p.Leu793Val) n.277+10126C>G c.2320C>G (p.Leu774Val) | |
| X | g.5892951G= | CA2413689065 | NLGN4X | c.2317C= (p.Leu773=) c.2377C= (p.Leu793=) n.277+10126C= c.2320C= (p.Leu774=) | |
| X | g.5892951G>T | CA412012518 | NLGN4X | c.2317C>A (p.Leu773Ile) c.2377C>A (p.Leu793Ile) n.277+10126C>A c.2320C>A (p.Leu774Ile) | |
| X | g.5892952T>A | CA515367959 | NLGN4X | c.2316A>T (p.Pro772=) c.2376A>T (p.Pro792=) n.277+10125A>T c.2319A>T (p.Pro773=) | |
| X | g.5892952T>C | CA515367960 | NLGN4X | c.2316A>G (p.Pro772=) c.2376A>G (p.Pro792=) n.277+10125A>G c.2319A>G (p.Pro773=) | |
| X | g.5892952T>G | CA515367961 | NLGN4X | c.2316A>C (p.Pro772=) c.2376A>C (p.Pro792=) n.277+10125A>C c.2319A>C (p.Pro773=) | |
| X | g.5892953G>A | CA412012519 | NLGN4X | c.2315C>T (p.Pro772Leu) c.2375C>T (p.Pro792Leu) n.277+10124C>T c.2318C>T (p.Pro773Leu) | |
| X | g.5892953G>C | CA412012520 | NLGN4X | c.2315C>G (p.Pro772Arg) c.2375C>G (p.Pro792Arg) n.277+10124C>G c.2318C>G (p.Pro773Arg) | |
| X | g.5892953G>T | CA412012521 | NLGN4X | c.2315C>A (p.Pro772Gln) c.2375C>A (p.Pro792Gln) n.277+10124C>A c.2318C>A (p.Pro773Gln) | |
| X | g.5892954G>A | CA412012522 | NLGN4X | c.2314C>T (p.Pro772Ser) c.2374C>T (p.Pro792Ser) n.277+10123C>T c.2317C>T (p.Pro773Ser) | |
| X | g.5892954G>C | CA412012523 | NLGN4X | c.2314C>G (p.Pro772Ala) c.2374C>G (p.Pro792Ala) n.277+10123C>G c.2317C>G (p.Pro773Ala) | |
| X | g.5892954G>T | CA412012524 | NLGN4X | c.2314C>A (p.Pro772Thr) c.2374C>A (p.Pro792Thr) n.277+10123C>A c.2317C>A (p.Pro773Thr) | |
| X | g.5892955G>A | CA515367962 | NLGN4X | c.2313C>T (p.Ile771=) c.2373C>T (p.Ile791=) n.277+10122C>T c.2316C>T (p.Ile772=) | |
| X | g.5892955G>C | CA412012525 | NLGN4X | c.2313C>G (p.Ile771Met) c.2373C>G (p.Ile791Met) n.277+10122C>G c.2316C>G (p.Ile772Met) | |
| X | g.5892955G= | CA2413689066 | NLGN4X | c.2313C= (p.Ile771=) c.2373C= (p.Ile791=) n.277+10122C= c.2316C= (p.Ile772=) | |
| X | g.5892955G>T | CA515367963 | NLGN4X | c.2313C>A (p.Ile771=) c.2373C>A (p.Ile791=) n.277+10122C>A c.2316C>A (p.Ile772=) | dbSNP gnomAD v4 |
| X | g.5892956A>C | CA412012527 | NLGN4X | c.2312T>G (p.Ile771Ser) c.2372T>G (p.Ile791Ser) n.277+10121T>G c.2315T>G (p.Ile772Ser) | |
| X | g.5892956A>G | CA412012528 | NLGN4X | c.2312T>C (p.Ile771Thr) c.2372T>C (p.Ile791Thr) n.277+10121T>C c.2315T>C (p.Ile772Thr) | |
| X | g.5892956A>T | CA412012526 | NLGN4X | c.2312T>A (p.Ile771Asn) c.2372T>A (p.Ile791Asn) n.277+10121T>A c.2315T>A (p.Ile772Asn) | |
| X | g.5892957T>A | CA412012529 | NLGN4X | c.2311A>T (p.Ile771Phe) c.2371A>T (p.Ile791Phe) n.277+10120A>T c.2314A>T (p.Ile772Phe) | COSMIC COSMIC |
| X | g.5892957T>C | CA412012530 | NLGN4X | c.2311A>G (p.Ile771Val) c.2371A>G (p.Ile791Val) n.277+10120A>G c.2314A>G (p.Ile772Val) | |
| X | g.5892957T>G | CA412012531 | NLGN4X | c.2311A>C (p.Ile771Leu) c.2371A>C (p.Ile791Leu) n.277+10120A>C c.2314A>C (p.Ile772Leu) | |
| X | g.5892958G>A | CA10340897 | NLGN4X | c.2310C>T (p.Asp770=) c.2370C>T (p.Asp790=) n.277+10119C>T c.2313C>T (p.Asp771=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.5892958G>C | CA412012532 | NLGN4X | c.2310C>G (p.Asp770Glu) c.2370C>G (p.Asp790Glu) n.277+10119C>G c.2313C>G (p.Asp771Glu) | |
| X | g.5892958G= | CA2413689067 | NLGN4X | c.2310C= (p.Asp770=) c.2370C= (p.Asp790=) n.277+10119C= c.2313C= (p.Asp771=) | |
| X | g.5892958G>T | CA412012533 | NLGN4X | c.2310C>A (p.Asp770Glu) c.2370C>A (p.Asp790Glu) n.277+10119C>A c.2313C>A (p.Asp771Glu) | |
| X | g.5892959T>A | CA412012534 | NLGN4X | c.2309A>T (p.Asp770Val) c.2369A>T (p.Asp790Val) n.277+10118A>T c.2312A>T (p.Asp771Val) | |
| X | g.5892959T>C | CA10340898 | NLGN4X | c.2309A>G (p.Asp770Gly) c.2369A>G (p.Asp790Gly) n.277+10118A>G c.2312A>G (p.Asp771Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.5892959T>G | CA412012535 | NLGN4X | c.2309A>C (p.Asp770Ala) c.2369A>C (p.Asp790Ala) n.277+10118A>C c.2312A>C (p.Asp771Ala) | |
| X | g.5892959T= | CA2413689068 | NLGN4X | c.2309A= (p.Asp770=) c.2369A= (p.Asp790=) n.277+10118A= c.2312A= (p.Asp771=) | |
| X | g.5892960C>A | CA412012536 | NLGN4X | c.2308G>T (p.Asp770Tyr) c.2368G>T (p.Asp790Tyr) n.277+10117G>T c.2311G>T (p.Asp771Tyr) | |
| X | g.5892960C>G | CA412012537 | NLGN4X | c.2308G>C (p.Asp770His) c.2368G>C (p.Asp790His) n.277+10117G>C c.2311G>C (p.Asp771His) | |
| X | g.5892960C>T | CA412012538 | NLGN4X | c.2308G>A (p.Asp770Asn) c.2368G>A (p.Asp790Asn) n.277+10117G>A c.2311G>A (p.Asp771Asn) | |
| X | g.5892961A>C | CA412012540 | NLGN4X | c.2307T>G (p.Asp769Glu) c.2367T>G (p.Asp789Glu) n.277+10116T>G c.2310T>G (p.Asp770Glu) | |
| X | g.5892961A>G | CA515367964 | NLGN4X | c.2307T>C (p.Asp769=) c.2367T>C (p.Asp789=) n.277+10116T>C c.2310T>C (p.Asp770=) | |
| X | g.5892961A>T | CA412012539 | NLGN4X | c.2307T>A (p.Asp769Glu) c.2367T>A (p.Asp789Glu) n.277+10116T>A c.2310T>A (p.Asp770Glu) | |
| X | g.5892962T>A | CA412012541 | NLGN4X | c.2306A>T (p.Asp769Val) c.2366A>T (p.Asp789Val) n.277+10115A>T c.2309A>T (p.Asp770Val) | |
| X | g.5892962T>C | CA412012542 | NLGN4X | c.2306A>G (p.Asp769Gly) c.2366A>G (p.Asp789Gly) n.277+10115A>G c.2309A>G (p.Asp770Gly) | gnomAD v4 |
| X | g.5892962T>G | CA412012543 | NLGN4X | c.2306A>C (p.Asp769Ala) c.2366A>C (p.Asp789Ala) n.277+10115A>C c.2309A>C (p.Asp770Ala) | |
| X | g.5892963C>A | CA412012544 | NLGN4X | c.2305G>T (p.Asp769Tyr) c.2365G>T (p.Asp789Tyr) n.277+10114G>T c.2308G>T (p.Asp770Tyr) | |
| X | g.5892963C= | CA2413689069 | NLGN4X | c.2305G= (p.Asp769=) c.2365G= (p.Asp789=) n.277+10114G= c.2308G= (p.Asp770=) | |
| X | g.5892963C>G | CA412012545 | NLGN4X | c.2305G>C (p.Asp769His) c.2365G>C (p.Asp789His) n.277+10114G>C c.2308G>C (p.Asp770His) | |
| X | g.5892963C>T | CA10340899 | NLGN4X | c.2305G>A (p.Asp769Asn) c.2365G>A (p.Asp789Asn) n.277+10114G>A c.2308G>A (p.Asp770Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.5892964T>A | CA515367965 | NLGN4X | c.2304A>T (p.Pro768=) c.2364A>T (p.Pro788=) n.277+10113A>T c.2307A>T (p.Pro769=) | |
| X | g.5892964T>C | CA515367966 | NLGN4X | c.2304A>G (p.Pro768=) c.2364A>G (p.Pro788=) n.277+10113A>G c.2307A>G (p.Pro769=) | dbSNP |
| X | g.5892964T>G | CA515367967 | NLGN4X | c.2304A>C (p.Pro768=) c.2364A>C (p.Pro788=) n.277+10113A>C c.2307A>C (p.Pro769=) | |
| X | g.5892964T= | CA2413689070 | NLGN4X | c.2304A= (p.Pro768=) c.2364A= (p.Pro788=) n.277+10113A= c.2307A= (p.Pro769=) | |
| X | g.5892965G>A | CA412012546 | NLGN4X | c.2303C>T (p.Pro768Leu) c.2363C>T (p.Pro788Leu) n.277+10112C>T c.2306C>T (p.Pro769Leu) | |
| X | g.5892965G>C | CA412012547 | NLGN4X | c.2303C>G (p.Pro768Arg) c.2363C>G (p.Pro788Arg) n.277+10112C>G c.2306C>G (p.Pro769Arg) | |
| X | g.5892965G>T | CA412012548 | NLGN4X | c.2303C>A (p.Pro768Gln) c.2363C>A (p.Pro788Gln) n.277+10112C>A c.2306C>A (p.Pro769Gln) | |
| X | g.5892966G>A | CA412012549 | NLGN4X | c.2302C>T (p.Pro768Ser) c.2362C>T (p.Pro788Ser) n.277+10111C>T c.2305C>T (p.Pro769Ser) | |
| X | g.5892966G>C | CA412012550 | NLGN4X | c.2302C>G (p.Pro768Ala) c.2362C>G (p.Pro788Ala) n.277+10111C>G c.2305C>G (p.Pro769Ala) | |
| X | g.5892966G>T | CA412012551 | NLGN4X | c.2302C>A (p.Pro768Thr) c.2362C>A (p.Pro788Thr) n.277+10111C>A c.2305C>A (p.Pro769Thr) | |
| X | g.5892967C>A | CA515367968 | NLGN4X | c.2301G>T (p.Ser767=) c.2361G>T (p.Ser787=) n.277+10110G>T c.2304G>T (p.Ser768=) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.5892967C= | CA2413689071 | NLGN4X | c.2301G= (p.Ser767=) c.2361G= (p.Ser787=) n.277+10110G= c.2304G= (p.Ser768=) | |
| X | g.5892967C>G | CA515367969 | NLGN4X | c.2301G>C (p.Ser767=) c.2361G>C (p.Ser787=) n.277+10110G>C c.2304G>C (p.Ser768=) | |
| X | g.5892967C>T | CA10340900 | NLGN4X | c.2301G>A (p.Ser767=) c.2361G>A (p.Ser787=) n.277+10110G>A c.2304G>A (p.Ser768=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| X | g.5892968G>A | CA10340901 | NLGN4X | c.2300C>T (p.Ser767Leu) c.2360C>T (p.Ser787Leu) n.277+10109C>T c.2303C>T (p.Ser768Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| X | g.5892968G>C | CA412012553 | NLGN4X | c.2300C>G (p.Ser767Trp) c.2360C>G (p.Ser787Trp) n.277+10109C>G c.2303C>G (p.Ser768Trp) | |
| X | g.5892968G= | CA2413689072 | NLGN4X | c.2300C= (p.Ser767=) c.2360C= (p.Ser787=) n.277+10109C= c.2303C= (p.Ser768=) | |
| X | g.5892968G>T | CA412012552 | NLGN4X | c.2300C>A (p.Ser767Ter) c.2360C>A (p.Ser787Ter) n.277+10109C>A c.2303C>A (p.Ser768Ter) | |
| X | g.5892969A>C | CA412012554 | NLGN4X | c.2299T>G (p.Ser767Ala) c.2359T>G (p.Ser787Ala) n.277+10108T>G c.2302T>G (p.Ser768Ala) | |
| X | g.5892969A>G | CA412012556 | NLGN4X | c.2299T>C (p.Ser767Pro) c.2359T>C (p.Ser787Pro) n.277+10108T>C c.2302T>C (p.Ser768Pro) | |
| X | g.5892969A>T | CA412012555 | NLGN4X | c.2299T>A (p.Ser767Thr) c.2359T>A (p.Ser787Thr) n.277+10108T>A c.2302T>A (p.Ser768Thr) | |
| X | g.5892970C>A | CA515367971 | NLGN4X | c.2298G>T (p.Arg766=) c.2358G>T (p.Arg786=) n.277+10107G>T c.2301G>T (p.Arg767=) | |
| X | g.5892970C>G | CA515367972 | NLGN4X | c.2298G>C (p.Arg766=) c.2358G>C (p.Arg786=) n.277+10107G>C c.2301G>C (p.Arg767=) | |
| X | g.5892970C>T | CA515367970 | NLGN4X | c.2298G>A (p.Arg766=) c.2358G>A (p.Arg786=) n.277+10107G>A c.2301G>A (p.Arg767=) | |
| X | g.5892971C>A | CA412012557 | NLGN4X | c.2297G>T (p.Arg766Leu) c.2357G>T (p.Arg786Leu) n.277+10106G>T c.2300G>T (p.Arg767Leu) | |
| X | g.5892971C= | CA2413689073 | NLGN4X | c.2297G= (p.Arg766=) c.2357G= (p.Arg786=) n.277+10106G= c.2300G= (p.Arg767=) | |
| X | g.5892971C>G | CA412012558 | NLGN4X | c.2297G>C (p.Arg766Pro) c.2357G>C (p.Arg786Pro) n.277+10106G>C c.2300G>C (p.Arg767Pro) | |
| X | g.5892971C>T | CA412012559 | NLGN4X | c.2297G>A (p.Arg766Gln) c.2357G>A (p.Arg786Gln) n.277+10106G>A c.2300G>A (p.Arg767Gln) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| X | g.5892972G>A | CA412012560 | NLGN4X | c.2296C>T (p.Arg766Trp) c.2356C>T (p.Arg786Trp) n.277+10105C>T c.2299C>T (p.Arg767Trp) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.5892972G>C | CA412012561 | NLGN4X | c.2296C>G (p.Arg766Gly) c.2356C>G (p.Arg786Gly) n.277+10105C>G c.2299C>G (p.Arg767Gly) | |
| X | g.5892972G>T | CA515367973 | NLGN4X | c.2296C>A (p.Arg766=) c.2356C>A (p.Arg786=) n.277+10105C>A c.2299C>A (p.Arg767=) | |
| X | g.5892973G>A | CA515367974 | NLGN4X | c.2295C>T (p.Arg765=) c.2355C>T (p.Arg785=) n.277+10104C>T c.2298C>T (p.Arg766=) | |
| X | g.5892973G>C | CA10340902 | NLGN4X | c.2295C>G (p.Arg765=) c.2355C>G (p.Arg785=) n.277+10104C>G c.2298C>G (p.Arg766=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5892973G= | CA2413689074 | NLGN4X | c.2295C= (p.Arg765=) c.2355C= (p.Arg785=) n.277+10104C= c.2298C= (p.Arg766=) | |
| X | g.5892973G>T | CA515367975 | NLGN4X | c.2295C>A (p.Arg765=) c.2355C>A (p.Arg785=) n.277+10104C>A c.2298C>A (p.Arg766=) | |
| X | g.5892974C>A | CA412012562 | NLGN4X | c.2294G>T (p.Arg765Leu) c.2354G>T (p.Arg785Leu) n.277+10103G>T c.2297G>T (p.Arg766Leu) | |
| X | g.5892974C= | CA2413689075 | NLGN4X | c.2294G= (p.Arg765=) c.2354G= (p.Arg785=) n.277+10103G= c.2297G= (p.Arg766=) | |
| X | g.5892974C>G | CA412012563 | NLGN4X | c.2294G>C (p.Arg765Pro) c.2354G>C (p.Arg785Pro) n.277+10103G>C c.2297G>C (p.Arg766Pro) | |
| X | g.5892974C>T | CA412012564 | NLGN4X | c.2294G>A (p.Arg765His) c.2354G>A (p.Arg785His) n.277+10103G>A c.2297G>A (p.Arg766His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| X | g.5892975G>A | CA10340903 | NLGN4X | c.2293C>T (p.Arg765Cys) c.2353C>T (p.Arg785Cys) n.277+10102C>T c.2296C>T (p.Arg766Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| X | g.5892975G>C | CA412012565 | NLGN4X | c.2293C>G (p.Arg765Gly) c.2353C>G (p.Arg785Gly) n.277+10102C>G c.2296C>G (p.Arg766Gly) | |
| X | g.5892975G= | CA2413689076 | NLGN4X | c.2293C= (p.Arg765=) c.2353C= (p.Arg785=) n.277+10102C= c.2296C= (p.Arg766=) | |
| X | g.5892975G>T | CA412012566 | NLGN4X | c.2293C>A (p.Arg765Ser) c.2353C>A (p.Arg785Ser) n.277+10102C>A c.2296C>A (p.Arg766Ser) | |
| X | g.5892976C>A | CA515367976 | NLGN4X | c.2292G>T (p.Leu764=) c.2352G>T (p.Leu784=) n.277+10101G>T c.2295G>T (p.Leu765=) | dbSNP gnomAD v2 |
| X | g.5892976C= | CA2413689077 | NLGN4X | c.2292G= (p.Leu764=) c.2352G= (p.Leu784=) n.277+10101G= c.2295G= (p.Leu765=) | |
| X | g.5892976C>G | CA515367977 | NLGN4X | c.2292G>C (p.Leu764=) c.2352G>C (p.Leu784=) n.277+10101G>C c.2295G>C (p.Leu765=) | |
| X | g.5892976C>T | CA515367978 | NLGN4X | c.2292G>A (p.Leu764=) c.2352G>A (p.Leu784=) n.277+10101G>A c.2295G>A (p.Leu765=) | |
| X | g.5892977A>C | CA412012567 | NLGN4X | c.2291T>G (p.Leu764Arg) c.2351T>G (p.Leu784Arg) n.277+10100T>G c.2294T>G (p.Leu765Arg) | |
| X | g.5892977A>G | CA412012569 | NLGN4X | c.2291T>C (p.Leu764Pro) c.2351T>C (p.Leu784Pro) n.277+10100T>C c.2294T>C (p.Leu765Pro) | |
| X | g.5892977A>T | CA412012568 | NLGN4X | c.2291T>A (p.Leu764Gln) c.2351T>A (p.Leu784Gln) n.277+10100T>A c.2294T>A (p.Leu765Gln) | |
| X | g.5892978G>A | CA515367979 | NLGN4X | c.2290C>T (p.Leu764=) c.2350C>T (p.Leu784=) n.277+10099C>T c.2293C>T (p.Leu765=) | |
| X | g.5892978G>C | CA412012570 | NLGN4X | c.2290C>G (p.Leu764Val) c.2350C>G (p.Leu784Val) n.277+10099C>G c.2293C>G (p.Leu765Val) | |
| X | g.5892978G>T | CA412012571 | NLGN4X | c.2290C>A (p.Leu764Met) c.2350C>A (p.Leu784Met) n.277+10099C>A c.2293C>A (p.Leu765Met) | gnomAD v4 |
| X | g.5892979C>A | CA515367980 | NLGN4X | c.2289G>T (p.Thr763=) c.2349G>T (p.Thr783=) n.277+10098G>T c.2292G>T (p.Thr764=) | |
| X | g.5892979C= | CA2413689078 | NLGN4X | c.2289G= (p.Thr763=) c.2349G= (p.Thr783=) n.277+10098G= c.2292G= (p.Thr764=) | |
| X | g.5892979C>G | CA515367981 | NLGN4X | c.2289G>C (p.Thr763=) c.2349G>C (p.Thr783=) n.277+10098G>C c.2292G>C (p.Thr764=) | |
| X | g.5892979C>T | CA326308990 | NLGN4X | c.2289G>A (p.Thr763=) c.2349G>A (p.Thr783=) n.277+10098G>A c.2292G>A (p.Thr764=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5892980G>A | CA10340904 | NLGN4X | c.2288C>T (p.Thr763Met) c.2348C>T (p.Thr783Met) n.277+10097C>T c.2291C>T (p.Thr764Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| X | g.5892980G>C | CA412012572 | NLGN4X | c.2288C>G (p.Thr763Arg) c.2348C>G (p.Thr783Arg) n.277+10097C>G c.2291C>G (p.Thr764Arg) | dbSNP COSMIC |
| X | g.5892980G= | CA2413689079 | NLGN4X | c.2288C= (p.Thr763=) c.2348C= (p.Thr783=) n.277+10097C= c.2291C= (p.Thr764=) | |
| X | g.5892980G>T | CA412012573 | NLGN4X | c.2288C>A (p.Thr763Lys) c.2348C>A (p.Thr783Lys) n.277+10097C>A c.2291C>A (p.Thr764Lys) | |
| X | g.5892981T>A | CA412012574 | NLGN4X | c.2287A>T (p.Thr763Ser) c.2347A>T (p.Thr783Ser) n.277+10096A>T c.2290A>T (p.Thr764Ser) | |
| X | g.5892981T>C | CA412012575 | NLGN4X | c.2287A>G (p.Thr763Ala) c.2347A>G (p.Thr783Ala) n.277+10096A>G c.2290A>G (p.Thr764Ala) | |
| X | g.5892981T>G | CA412012576 | NLGN4X | c.2287A>C (p.Thr763Pro) c.2347A>C (p.Thr783Pro) n.277+10096A>C c.2290A>C (p.Thr764Pro) | |
| X | g.5892982G>A | CA515367982 | NLGN4X | c.2286C>T (p.Leu762=) c.2346C>T (p.Leu782=) n.277+10095C>T c.2289C>T (p.Leu763=) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.5892982G>C | CA515367983 | NLGN4X | c.2286C>G (p.Leu762=) c.2346C>G (p.Leu782=) n.277+10095C>G c.2289C>G (p.Leu763=) | |
| X | g.5892982G= | CA2413689080 | NLGN4X | c.2286C= (p.Leu762=) c.2346C= (p.Leu782=) n.277+10095C= c.2289C= (p.Leu763=) | |
| X | g.5892982G>T | CA515367984 | NLGN4X | c.2286C>A (p.Leu762=) c.2346C>A (p.Leu782=) n.277+10095C>A c.2289C>A (p.Leu763=) | |
| X | g.5892983A>C | CA412012578 | NLGN4X | c.2285T>G (p.Leu762Arg) c.2345T>G (p.Leu782Arg) n.277+10094T>G c.2288T>G (p.Leu763Arg) | |
| X | g.5892983A>G | CA412012579 | NLGN4X | c.2285T>C (p.Leu762Pro) c.2345T>C (p.Leu782Pro) n.277+10094T>C c.2288T>C (p.Leu763Pro) | |
| X | g.5892983A>T | CA412012577 | NLGN4X | c.2285T>A (p.Leu762His) c.2345T>A (p.Leu782His) n.277+10094T>A c.2288T>A (p.Leu763His) | |
| X | g.5892984G>A | CA412012580 | NLGN4X | c.2284C>T (p.Leu762Phe) c.2344C>T (p.Leu782Phe) n.277+10093C>T c.2287C>T (p.Leu763Phe) | |
| X | g.5892984G>C | CA10340905 | NLGN4X | c.2284C>G (p.Leu762Val) c.2344C>G (p.Leu782Val) n.277+10093C>G c.2287C>G (p.Leu763Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5892984G= | CA2413689081 | NLGN4X | c.2284C= (p.Leu762=) c.2344C= (p.Leu782=) n.277+10093C= c.2287C= (p.Leu763=) | |
| X | g.5892984G>T | CA412012581 | NLGN4X | c.2284C>A (p.Leu762Ile) c.2344C>A (p.Leu782Ile) n.277+10093C>A c.2287C>A (p.Leu763Ile) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.5892985G>A | CA515367985 | NLGN4X | c.2283C>T (p.Thr761=) c.2343C>T (p.Thr781=) n.277+10092C>T c.2286C>T (p.Thr762=) | |
| X | g.5892985G>C | CA515367986 | NLGN4X | c.2283C>G (p.Thr761=) c.2343C>G (p.Thr781=) n.277+10092C>G c.2286C>G (p.Thr762=) | |
| X | g.5892985G>T | CA515367987 | NLGN4X | c.2283C>A (p.Thr761=) c.2343C>A (p.Thr781=) n.277+10092C>A c.2286C>A (p.Thr762=) | |
| X | g.5892986G>A | CA412012582 | NLGN4X | c.2282C>T (p.Thr761Ile) c.2342C>T (p.Thr781Ile) n.277+10091C>T c.2285C>T (p.Thr762Ile) | gnomAD v4 |
| X | g.5892986G>C | CA412012583 | NLGN4X | c.2282C>G (p.Thr761Ser) c.2342C>G (p.Thr781Ser) n.277+10091C>G c.2285C>G (p.Thr762Ser) | |
| X | g.5892986G= | CA2413689082 | NLGN4X | c.2282C= (p.Thr761=) c.2342C= (p.Thr781=) n.277+10091C= c.2285C= (p.Thr762=) | |
| X | g.5892986G>T | CA10340906 | NLGN4X | c.2282C>A (p.Thr761Asn) c.2342C>A (p.Thr781Asn) n.277+10091C>A c.2285C>A (p.Thr762Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5892987T>A | CA10340907 | NLGN4X | c.2281A>T (p.Thr761Ser) c.2341A>T (p.Thr781Ser) n.277+10090A>T c.2284A>T (p.Thr762Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.5892987T>C | CA412012584 | NLGN4X | c.2281A>G (p.Thr761Ala) c.2341A>G (p.Thr781Ala) n.277+10090A>G c.2284A>G (p.Thr762Ala) | |
| X | g.5892987T>G | CA412012585 | NLGN4X | c.2281A>C (p.Thr761Pro) c.2341A>C (p.Thr781Pro) n.277+10090A>C c.2284A>C (p.Thr762Pro) | |
| X | g.5892987T= | CA2413689083 | NLGN4X | c.2281A= (p.Thr761=) c.2341A= (p.Thr781=) n.277+10090A= c.2284A= (p.Thr762=) | |
| X | g.5892988G>A | CA149108 | NLGN4X | c.2280C>T (p.Tyr760=) c.2340C>T (p.Tyr780=) n.277+10089C>T c.2283C>T (p.Tyr761=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5892988G>C | CA412012586 | NLGN4X | c.2280C>G (p.Tyr760Ter) c.2340C>G (p.Tyr780Ter) n.277+10089C>G c.2283C>G (p.Tyr761Ter) | |
| X | g.5892988G= | CA2413689084 | NLGN4X | c.2280C= (p.Tyr760=) c.2340C= (p.Tyr780=) n.277+10089C= c.2283C= (p.Tyr761=) | |
| X | g.5892988G>T | CA412012587 | NLGN4X | c.2280C>A (p.Tyr760Ter) c.2340C>A (p.Tyr780Ter) n.277+10089C>A c.2283C>A (p.Tyr761Ter) | |
| X | g.5892989T>A | CA412012589 | NLGN4X | c.2279A>T (p.Tyr760Phe) c.2339A>T (p.Tyr780Phe) n.277+10088A>T c.2282A>T (p.Tyr761Phe) | |
| X | g.5892989T>C | CA412012590 | NLGN4X | c.2279A>G (p.Tyr760Cys) c.2339A>G (p.Tyr780Cys) n.277+10088A>G c.2282A>G (p.Tyr761Cys) | |
| X | g.5892989T>G | CA412012588 | NLGN4X | c.2279A>C (p.Tyr760Ser) c.2339A>C (p.Tyr780Ser) n.277+10088A>C c.2282A>C (p.Tyr761Ser) | |
| X | g.5892990A>C | CA412012591 | NLGN4X | c.2278T>G (p.Tyr760Asp) c.2338T>G (p.Tyr780Asp) n.277+10087T>G c.2281T>G (p.Tyr761Asp) | |
| X | g.5892990A>G | CA412012592 | NLGN4X | c.2278T>C (p.Tyr760His) c.2338T>C (p.Tyr780His) n.277+10087T>C c.2281T>C (p.Tyr761His) | |
| X | g.5892990A>T | CA412012593 | NLGN4X | c.2278T>A (p.Tyr760Asn) c.2338T>A (p.Tyr780Asn) n.277+10087T>A c.2281T>A (p.Tyr761Asn) | |
| X | g.5892991G>A | CA515367988 | NLGN4X | c.2277C>T (p.Asp759=) c.2337C>T (p.Asp779=) n.277+10086C>T c.2280C>T (p.Asp760=) | gnomAD v4 |
| X | g.5892991G>C | CA412012594 | NLGN4X | c.2277C>G (p.Asp759Glu) c.2337C>G (p.Asp779Glu) n.277+10086C>G c.2280C>G (p.Asp760Glu) | gnomAD v4 |
| X | g.5892991G>T | CA412012595 | NLGN4X | c.2277C>A (p.Asp759Glu) c.2337C>A (p.Asp779Glu) n.277+10086C>A c.2280C>A (p.Asp760Glu) | |
| X | g.5892992T>A | CA412012598 | NLGN4X | c.2276A>T (p.Asp759Val) c.2336A>T (p.Asp779Val) n.277+10085A>T c.2279A>T (p.Asp760Val) | |
| X | g.5892992T>C | CA412012596 | NLGN4X | c.2276A>G (p.Asp759Gly) c.2336A>G (p.Asp779Gly) n.277+10085A>G c.2279A>G (p.Asp760Gly) | |
| X | g.5892992T>G | CA412012597 | NLGN4X | c.2276A>C (p.Asp759Ala) c.2336A>C (p.Asp779Ala) n.277+10085A>C c.2279A>C (p.Asp760Ala) | |
| X | g.5892993C>A | CA412012599 | NLGN4X | c.2275G>T (p.Asp759Tyr) c.2335G>T (p.Asp779Tyr) n.277+10084G>T c.2278G>T (p.Asp760Tyr) | |
| X | g.5892993C= | CA2413689085 | NLGN4X | c.2275G= (p.Asp759=) c.2335G= (p.Asp779=) n.277+10084G= c.2278G= (p.Asp760=) | |
| X | g.5892993C>G | CA412012600 | NLGN4X | c.2275G>C (p.Asp759His) c.2335G>C (p.Asp779His) n.277+10084G>C c.2278G>C (p.Asp760His) | |
| X | g.5892993C>T | CA412012601 | NLGN4X | c.2275G>A (p.Asp759Asn) c.2335G>A (p.Asp779Asn) n.277+10084G>A c.2278G>A (p.Asp760Asn) | dbSNP |
| X | g.5892994T>A | CA515367989 | NLGN4X | c.2274A>T (p.Pro758=) c.2334A>T (p.Pro778=) n.277+10083A>T c.2277A>T (p.Pro759=) | |
| X | g.5892994T>C | CA515367990 | NLGN4X | c.2274A>G (p.Pro758=) c.2334A>G (p.Pro778=) n.277+10083A>G c.2277A>G (p.Pro759=) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.5892994T>G | CA515367991 | NLGN4X | c.2274A>C (p.Pro758=) c.2334A>C (p.Pro778=) n.277+10083A>C c.2277A>C (p.Pro759=) | |
| X | g.5892994T= | CA2413689086 | NLGN4X | c.2274A= (p.Pro758=) c.2334A= (p.Pro778=) n.277+10083A= c.2277A= (p.Pro759=) | |
| X | g.5892995G>A | CA412012602 | NLGN4X | c.2273C>T (p.Pro758Leu) c.2333C>T (p.Pro778Leu) n.277+10082C>T c.2276C>T (p.Pro759Leu) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.5892995G>C | CA412012603 | NLGN4X | c.2273C>G (p.Pro758Arg) c.2333C>G (p.Pro778Arg) n.277+10082C>G c.2276C>G (p.Pro759Arg) | |
| X | g.5892995G= | CA2413689087 | NLGN4X | c.2273C= (p.Pro758=) c.2333C= (p.Pro778=) n.277+10082C= c.2276C= (p.Pro759=) | |
| X | g.5892995G>T | CA412012604 | NLGN4X | c.2273C>A (p.Pro758Gln) c.2333C>A (p.Pro778Gln) n.277+10082C>A c.2276C>A (p.Pro759Gln) | |
| X | g.5892996G>A | CA412012606 | NLGN4X | c.2272C>T (p.Pro758Ser) c.2332C>T (p.Pro778Ser) n.277+10081C>T c.2275C>T (p.Pro759Ser) | |
| X | g.5892996G>C | CA412012607 | NLGN4X | c.2272C>G (p.Pro758Ala) c.2332C>G (p.Pro778Ala) n.277+10081C>G c.2275C>G (p.Pro759Ala) | |
| X | g.5892996G>T | CA412012605 | NLGN4X | c.2272C>A (p.Pro758Thr) c.2332C>A (p.Pro778Thr) n.277+10081C>A c.2275C>A (p.Pro759Thr) | |
| X | g.5892997C>A | CA515367992 | NLGN4X | c.2271G>T (p.Pro757=) c.2331G>T (p.Pro777=) n.277+10080G>T c.2274G>T (p.Pro758=) | dbSNP gnomAD v4 |
| X | g.5892997C= | CA2413689088 | NLGN4X | c.2271G= (p.Pro757=) c.2331G= (p.Pro777=) n.277+10080G= c.2274G= (p.Pro758=) | |
| X | g.5892997C>G | CA515367993 | NLGN4X | c.2271G>C (p.Pro757=) c.2331G>C (p.Pro777=) n.277+10080G>C c.2274G>C (p.Pro758=) | gnomAD v4 |
| X | g.5892997C>T | CA149105 | NLGN4X | c.2271G>A (p.Pro757=) c.2331G>A (p.Pro777=) n.277+10080G>A c.2274G>A (p.Pro758=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5892998G>A | CA10340908 | NLGN4X | c.2270C>T (p.Pro757Leu) c.2330C>T (p.Pro777Leu) n.277+10079C>T c.2273C>T (p.Pro758Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.5892998G>C | CA412012609 | NLGN4X | c.2270C>G (p.Pro757Arg) c.2330C>G (p.Pro777Arg) n.277+10079C>G c.2273C>G (p.Pro758Arg) | |
| X | g.5892998G= | CA2413689089 | NLGN4X | c.2270C= (p.Pro757=) c.2330C= (p.Pro777=) n.277+10079C= c.2273C= (p.Pro758=) | |
| X | g.5892998G>T | CA412012608 | NLGN4X | c.2270C>A (p.Pro757Gln) c.2330C>A (p.Pro777Gln) n.277+10079C>A c.2273C>A (p.Pro758Gln) | COSMIC COSMIC |
| X | g.5892999G>A | CA412012610 | NLGN4X | c.2269C>T (p.Pro757Ser) c.2329C>T (p.Pro777Ser) n.277+10078C>T c.2272C>T (p.Pro758Ser) | |
| X | g.5892999G>C | CA412012611 | NLGN4X | c.2269C>G (p.Pro757Ala) c.2329C>G (p.Pro777Ala) n.277+10078C>G c.2272C>G (p.Pro758Ala) | |
| X | g.5892999G>T | CA412012612 | NLGN4X | c.2269C>A (p.Pro757Thr) c.2329C>A (p.Pro777Thr) n.277+10078C>A c.2272C>A (p.Pro758Thr) | COSMIC COSMIC |
| X | g.5893000G>A | CA515367994 | NLGN4X | c.2268C>T (p.Cys756=) c.2328C>T (p.Cys776=) n.277+10077C>T c.2271C>T (p.Cys757=) | gnomAD v4 |
| X | g.5893000G>C | CA412012613 | NLGN4X | c.2268C>G (p.Cys756Trp) c.2328C>G (p.Cys776Trp) n.277+10077C>G c.2271C>G (p.Cys757Trp) | |
| X | g.5893000G>T | CA412012614 | NLGN4X | c.2268C>A (p.Cys756Ter) c.2328C>A (p.Cys776Ter) n.277+10077C>A c.2271C>A (p.Cys757Ter) | |
| X | g.5893001C>A | CA412012615 | NLGN4X | c.2267G>T (p.Cys756Phe) c.2327G>T (p.Cys776Phe) n.277+10076G>T c.2270G>T (p.Cys757Phe) | |
| X | g.5893001C>G | CA412012616 | NLGN4X | c.2267G>C (p.Cys756Ser) c.2327G>C (p.Cys776Ser) n.277+10076G>C c.2270G>C (p.Cys757Ser) | |
| X | g.5893001C>T | CA412012617 | NLGN4X | c.2267G>A (p.Cys756Tyr) c.2327G>A (p.Cys776Tyr) n.277+10076G>A c.2270G>A (p.Cys757Tyr) | |
| X | g.5893002A= | CA2413689090 | NLGN4X | c.2266T= (p.Cys756=) c.2326T= (p.Cys776=) n.277+10075T= c.2269T= (p.Cys757=) | |
| X | g.5893002A>C | CA412012618 | NLGN4X | c.2266T>G (p.Cys756Gly) c.2326T>G (p.Cys776Gly) n.277+10075T>G c.2269T>G (p.Cys757Gly) | |
| X | g.5893002A>G | CA412012619 | NLGN4X | c.2266T>C (p.Cys756Arg) c.2326T>C (p.Cys776Arg) n.277+10075T>C c.2269T>C (p.Cys757Arg) | |
| X | g.5893002A>T | CA412012620 | NLGN4X | c.2266T>A (p.Cys756Ser) c.2326T>A (p.Cys776Ser) n.277+10075T>A c.2269T>A (p.Cys757Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5893003G>A | CA515367995 | NLGN4X | c.2265C>T (p.Thr755=) c.2325C>T (p.Thr775=) n.277+10074C>T c.2268C>T (p.Thr756=) | |
| X | g.5893003G>C | CA515367996 | NLGN4X | c.2265C>G (p.Thr755=) c.2325C>G (p.Thr775=) n.277+10074C>G c.2268C>G (p.Thr756=) | |
| X | g.5893003G>T | CA515367997 | NLGN4X | c.2265C>A (p.Thr755=) c.2325C>A (p.Thr775=) n.277+10074C>A c.2268C>A (p.Thr756=) | COSMIC COSMIC |
| X | g.5893004G>A | CA412012622 | NLGN4X | c.2264C>T (p.Thr755Ile) c.2324C>T (p.Thr775Ile) n.277+10073C>T c.2267C>T (p.Thr756Ile) | |
| X | g.5893004G>C | CA412012621 | NLGN4X | c.2264C>G (p.Thr755Ser) c.2324C>G (p.Thr775Ser) n.277+10073C>G c.2267C>G (p.Thr756Ser) | |
| X | g.5893004G= | CA2413689091 | NLGN4X | c.2264C= (p.Thr755=) c.2324C= (p.Thr775=) n.277+10073C= c.2267C= (p.Thr756=) | |
| X | g.5893004G>T | CA10340909 | NLGN4X | c.2264C>A (p.Thr755Asn) c.2324C>A (p.Thr775Asn) n.277+10073C>A c.2267C>A (p.Thr756Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.5893005T>A | CA412012623 | NLGN4X | c.2263A>T (p.Thr755Ser) c.2323A>T (p.Thr775Ser) n.277+10072A>T c.2266A>T (p.Thr756Ser) | |
| X | g.5893005T>C | CA412012624 | NLGN4X | c.2263A>G (p.Thr755Ala) c.2323A>G (p.Thr775Ala) n.277+10072A>G c.2266A>G (p.Thr756Ala) | |
| X | g.5893005T>G | CA412012625 | NLGN4X | c.2263A>C (p.Thr755Pro) c.2323A>C (p.Thr775Pro) n.277+10072A>C c.2266A>C (p.Thr756Pro) | |
| X | g.5893006G>A | CA515367998 | NLGN4X | c.2262C>T (p.Leu754=) c.2322C>T (p.Leu774=) n.277+10071C>T c.2265C>T (p.Leu755=) | gnomAD v4 |
| X | g.5893006G>C | CA326308991 | NLGN4X | c.2262C>G (p.Leu754=) c.2322C>G (p.Leu774=) n.277+10071C>G c.2265C>G (p.Leu755=) | dbSNP |
| X | g.5893006G= | CA2413689092 | NLGN4X | c.2262C= (p.Leu754=) c.2322C= (p.Leu774=) n.277+10071C= c.2265C= (p.Leu755=) | |
| X | g.5893006G>T | CA515367999 | NLGN4X | c.2262C>A (p.Leu754=) c.2322C>A (p.Leu774=) n.277+10071C>A c.2265C>A (p.Leu755=) | |
| X | g.5893007A= | CA2413689093 | NLGN4X | c.2261T= (p.Leu754=) c.2321T= (p.Leu774=) n.277+10070T= c.2264T= (p.Leu755=) | |
| X | g.5893007A>C | CA412012626 | NLGN4X | c.2261T>G (p.Leu754Arg) c.2321T>G (p.Leu774Arg) n.277+10070T>G c.2264T>G (p.Leu755Arg) | |
| X | g.5893007A>G | CA412012627 | NLGN4X | c.2261T>C (p.Leu754Pro) c.2321T>C (p.Leu774Pro) n.277+10070T>C c.2264T>C (p.Leu755Pro) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.5893007A>T | CA412012628 | NLGN4X | c.2261T>A (p.Leu754His) c.2321T>A (p.Leu774His) n.277+10070T>A c.2264T>A (p.Leu755His) | |
| X | g.5893008G>A | CA412012629 | NLGN4X | c.2260C>T (p.Leu754Phe) c.2320C>T (p.Leu774Phe) n.277+10069C>T c.2263C>T (p.Leu755Phe) | |
| X | g.5893008G>C | CA412012630 | NLGN4X | c.2260C>G (p.Leu754Val) c.2320C>G (p.Leu774Val) n.277+10069C>G c.2263C>G (p.Leu755Val) | dbSNP |
| X | g.5893008G= | CA2413689094 | NLGN4X | c.2260C= (p.Leu754=) c.2320C= (p.Leu774=) n.277+10069C= c.2263C= (p.Leu755=) | |
| X | g.5893008G>T | CA412012631 | NLGN4X | c.2260C>A (p.Leu754Ile) c.2320C>A (p.Leu774Ile) n.277+10069C>A c.2263C>A (p.Leu755Ile) | |
| X | g.5893009C>A | CA412012632 | NLGN4X | c.2259G>T (p.Arg753Ser) c.2319G>T (p.Arg773Ser) n.277+10068G>T c.2262G>T (p.Arg754Ser) | ClinVar dbSNP |
| X | g.5893009C= | CA2413689095 | NLGN4X | c.2259G= (p.Arg753=) c.2319G= (p.Arg773=) n.277+10068G= c.2262G= (p.Arg754=) | |
| X | g.5893009C>G | CA10604882 | NLGN4X | c.2259G>C (p.Arg753Ser) c.2319G>C (p.Arg773Ser) n.277+10068G>C c.2262G>C (p.Arg754Ser) | ClinVar dbSNP gnomAD v4 |
| X | g.5893009C>T | CA515368000 | NLGN4X | c.2259G>A (p.Arg753=) c.2319G>A (p.Arg773=) n.277+10068G>A c.2262G>A (p.Arg754=) | dbSNP gnomAD v4 |