OUTAGE/INTERRUPTION NOTICE:2024-06-14T21:00:00-0400 — 2024-06-17T08:00:00-0400
The first of two essential broad service outages will occur over the weekend.
The outage is expected to be shorter than the indicated time, but due to its scope and importance, a longer window is planned.
Affected ClinGen services include the UIs and APIs of the Allele Registry, ACI, Cspec, Erepo, LDH
The first of two essential broad service outages will occur over the weekend.
The outage is expected to be shorter than the indicated time, but due to its scope and importance, a longer window is planned.
Affected ClinGen services include the UIs and APIs of the Allele Registry, ACI, Cspec, Erepo, LDH
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28768123dup | CA2573053898 | FOXG1 | c.844dup (p.Ala282GlyfsTer?) | ClinVar dbSNP |
| 14 | g.28768123G>A | CA314626 | FOXG1 | c.844G>A (p.Ala282Thr) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768123G>C | CA389475984 | FOXG1 | c.844G>C (p.Ala282Pro) | |
| 14 | g.28768123G= | CA2126000291 | FOXG1 | c.844G= (p.Ala282=) | |
| 14 | g.28768123G>T | CA389475985 | FOXG1 | c.844G>T (p.Ala282Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768124C>A | CA389475986 | FOXG1 | c.845C>A (p.Ala282Asp) | |
| 14 | g.28768124C>G | CA389475987 | FOXG1 | c.845C>G (p.Ala282Gly) | |
| 14 | g.28768124C>T | CA389475988 | FOXG1 | c.845C>T (p.Ala282Val) | COSMIC |
| 14 | g.28768125C>A | CA486099070 | FOXG1 | c.846C>A (p.Ala282=) | gnomAD v4 |
| 14 | g.28768125C>G | CA486099071 | FOXG1 | c.846C>G (p.Ala282=) | |
| 14 | g.28768125C>T | CA486099069 | FOXG1 | c.846C>T (p.Ala282=) | |
| 14 | g.28768126A>C | CA389475989 | FOXG1 | c.847A>C (p.Lys283Gln) | |
| 14 | g.28768126A>G | CA389475990 | FOXG1 | c.847A>G (p.Lys283Glu) | |
| 14 | g.28768126A>T | CA389475991 | FOXG1 | c.847A>T (p.Lys283Ter) | ClinVar |
| 14 | g.28768126_28768127insGACC | CA961450741 | FOXG1 | c.847_848insGACC (p.Lys283ArgfsTer?) | gnomAD v3 gnomAD v4 |
| 14 | g.28768127A>C | CA389475993 | FOXG1 | c.848A>C (p.Lys283Thr) | |
| 14 | g.28768127A>G | CA389475994 | FOXG1 | c.848A>G (p.Lys283Arg) | COSMIC |
| 14 | g.28768127A>T | CA389475992 | FOXG1 | c.848A>T (p.Lys283Met) | |
| 14 | g.28768128G>A | CA486099072 | FOXG1 | c.849G>A (p.Lys283=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768128G>C | CA389475995 | FOXG1 | c.849G>C (p.Lys283Asn) | |
| 14 | g.28768128G= | CA2126000292 | FOXG1 | c.849G= (p.Lys283=) | |
| 14 | g.28768128G>T | CA389475996 | FOXG1 | c.849G>T (p.Lys283Asn) | |
| 14 | g.28768129C>A | CA389475997 | FOXG1 | c.850C>A (p.Leu284Met) | |
| 14 | g.28768129C= | CA2126000293 | FOXG1 | c.850C= (p.Leu284=) | |
| 14 | g.28768129C>G | CA389475998 | FOXG1 | c.850C>G (p.Leu284Val) | |
| 14 | g.28768129C>T | CA258396582 | FOXG1 | c.850C>T (p.Leu284=) | dbSNP gnomAD v4 |
| 14 | g.28768130T>A | CA389475999 | FOXG1 | c.851T>A (p.Leu284Gln) | |
| 14 | g.28768130T>C | CA389476000 | FOXG1 | c.851T>C (p.Leu284Pro) | |
| 14 | g.28768130T>G | CA389476001 | FOXG1 | c.851T>G (p.Leu284Arg) | |
| 14 | g.28768131G>A | CA7140635 | FOXG1 | c.852G>A (p.Leu284=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768131G>C | CA486099074 | FOXG1 | c.852G>C (p.Leu284=) | |
| 14 | g.28768131G= | CA2126000294 | FOXG1 | c.852G= (p.Leu284=) | |
| 14 | g.28768131G>T | CA486099073 | FOXG1 | c.852G>T (p.Leu284=) | gnomAD v4 |
| 14 | g.28768132G>A | CA389476002 | FOXG1 | c.853G>A (p.Ala285Thr) | dbSNP |
| 14 | g.28768132G>C | CA389476003 | FOXG1 | c.853G>C (p.Ala285Pro) | |
| 14 | g.28768132G= | CA2126000296 | FOXG1 | c.853G= (p.Ala285=) | |
| 14 | g.28768132G>T | CA389476004 | FOXG1 | c.853G>T (p.Ala285Ser) | |
| 14 | g.28768132_28768133delinsGC | CA2126000295 | FOXG1 | c.853_854delinsGC (p.Ala285=) | |
| 14 | g.28768133C>A | CA389476005 | FOXG1 | c.854C>A (p.Ala285Asp) | |
| 14 | g.28768133C>G | CA389476006 | FOXG1 | c.854C>G (p.Ala285Gly) | |
| 14 | g.28768133C>T | CA389476007 | FOXG1 | c.854C>T (p.Ala285Val) | |
| 14 | g.28768134del | CA658798197 | FOXG1 | c.855del (p.Phe286SerfsTer?) | ClinVar dbSNP |
| 14 | g.28768134C>A | CA486099075 | FOXG1 | c.855C>A (p.Ala285=) | gnomAD v4 |
| 14 | g.28768134C= | CA2126000297 | FOXG1 | c.855C= (p.Ala285=) | |
| 14 | g.28768134C>G | CA486099077 | FOXG1 | c.855C>G (p.Ala285=) | |
| 14 | g.28768134C>T | CA486099076 | FOXG1 | c.855C>T (p.Ala285=) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768135T>A | CA389476010 | FOXG1 | c.856T>A (p.Phe286Ile) | |
| 14 | g.28768135T>C | CA389476009 | FOXG1 | c.856T>C (p.Phe286Leu) | |
| 14 | g.28768135T>G | CA389476008 | FOXG1 | c.856T>G (p.Phe286Val) | |
| 14 | g.28768136del | CA2695219196 | FOXG1 | c.857del (p.Phe286SerfsTer?) | |
| 14 | g.28768136T>A | CA389476011 | FOXG1 | c.857T>A (p.Phe286Tyr) | gnomAD v4 |
| 14 | g.28768136T>C | CA389476013 | FOXG1 | c.857T>C (p.Phe286Ser) | |
| 14 | g.28768136T>G | CA389476012 | FOXG1 | c.857T>G (p.Phe286Cys) | |
| 14 | g.28768137C>A | CA7140636 | FOXG1 | c.858C>A (p.Phe286Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768137C= | CA2126000298 | FOXG1 | c.858C= (p.Phe286=) | |
| 14 | g.28768137C>G | CA389476014 | FOXG1 | c.858C>G (p.Phe286Leu) | |
| 14 | g.28768137C>T | CA486099078 | FOXG1 | c.858C>T (p.Phe286=) | |
| 14 | g.28768137dup | CA2695219197 | FOXG1 | c.858dup (p.Lys287GlnfsTer?) | |
| 14 | g.28768138A= | CA2126000299 | FOXG1 | c.859A= (p.Lys287=) | |
| 14 | g.28768138A>C | CA389476015 | FOXG1 | c.859A>C (p.Lys287Gln) | |
| 14 | g.28768138A>G | CA389476017 | FOXG1 | c.859A>G (p.Lys287Glu) | |
| 14 | g.28768138A>T | CA389476016 | FOXG1 | c.859A>T (p.Lys287Ter) | ClinVar dbSNP |
| 14 | g.28768139A>C | CA389476018 | FOXG1 | c.860A>C (p.Lys287Thr) | |
| 14 | g.28768139A>G | CA389476019 | FOXG1 | c.860A>G (p.Lys287Arg) | |
| 14 | g.28768139A>T | CA389476020 | FOXG1 | c.860A>T (p.Lys287Met) | |
| 14 | g.28768140G>A | CA486099079 | FOXG1 | c.861G>A (p.Lys287=) | COSMIC |
| 14 | g.28768140G>C | CA389476021 | FOXG1 | c.861G>C (p.Lys287Asn) | |
| 14 | g.28768140G>T | CA389476022 | FOXG1 | c.861G>T (p.Lys287Asn) | |
| 14 | g.28768141C>A | CA389476023 | FOXG1 | c.862C>A (p.Arg288Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768141C= | CA2126000300 | FOXG1 | c.862C= (p.Arg288=) | |
| 14 | g.28768141C>G | CA389476024 | FOXG1 | c.862C>G (p.Arg288Gly) | |
| 14 | g.28768141C>T | CA389476025 | FOXG1 | c.862C>T (p.Arg288Cys) | |
| 14 | g.28768142G>A | CA389476026 | FOXG1 | c.863G>A (p.Arg288His) | COSMIC |
| 14 | g.28768142G>C | CA389476027 | FOXG1 | c.863G>C (p.Arg288Pro) | |
| 14 | g.28768142G>T | CA389476028 | FOXG1 | c.863G>T (p.Arg288Leu) | |
| 14 | g.28768143C>A | CA486099080 | FOXG1 | c.864C>A (p.Arg288=) | ClinVar |
| 14 | g.28768143C= | CA2126000301 | FOXG1 | c.864C= (p.Arg288=) | |
| 14 | g.28768143C>G | CA486099081 | FOXG1 | c.864C>G (p.Arg288=) | ClinVar dbSNP |
| 14 | g.28768143C>T | CA486099082 | FOXG1 | c.864C>T (p.Arg288=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768144G>A | CA389476031 | FOXG1 | c.865G>A (p.Gly289Ser) | COSMIC |
| 14 | g.28768144G>C | CA389476030 | FOXG1 | c.865G>C (p.Gly289Arg) | |
| 14 | g.28768144G>T | CA389476029 | FOXG1 | c.865G>T (p.Gly289Cys) | gnomAD v4 |
| 14 | g.28768145G>A | CA389476032 | FOXG1 | c.866G>A (p.Gly289Asp) | |
| 14 | g.28768145G>C | CA389476033 | FOXG1 | c.866G>C (p.Gly289Ala) | |
| 14 | g.28768145G>T | CA389476034 | FOXG1 | c.866G>T (p.Gly289Val) | |
| 14 | g.28768146T>A | CA486099083 | FOXG1 | c.867T>A (p.Gly289=) | gnomAD v4 |
| 14 | g.28768146T>C | CA486099084 | FOXG1 | c.867T>C (p.Gly289=) | |
| 14 | g.28768146T>G | CA486099085 | FOXG1 | c.867T>G (p.Gly289=) | gnomAD v4 |
| 14 | g.28768147G>A | CA389476035 | FOXG1 | c.868G>A (p.Ala290Thr) | COSMIC |
| 14 | g.28768147G>C | CA389476036 | FOXG1 | c.868G>C (p.Ala290Pro) | |
| 14 | g.28768147G>T | CA389476037 | FOXG1 | c.868G>T (p.Ala290Ser) | gnomAD v4 |
| 14 | g.28768148C>A | CA389476038 | FOXG1 | c.869C>A (p.Ala290Glu) | |
| 14 | g.28768148C>G | CA389476039 | FOXG1 | c.869C>G (p.Ala290Gly) | |
| 14 | g.28768148C>T | CA389476040 | FOXG1 | c.869C>T (p.Ala290Val) | ClinVar |
| 14 | g.28768149G>A | CA486099086 | FOXG1 | c.870G>A (p.Ala290=) | |
| 14 | g.28768149G>C | CA486099088 | FOXG1 | c.870G>C (p.Ala290=) | COSMIC |
| 14 | g.28768149G>T | CA486099087 | FOXG1 | c.870G>T (p.Ala290=) | gnomAD v4 |
| 14 | g.28768150C>A | CA389476041 | FOXG1 | c.871C>A (p.Arg291Ser) | |
| 14 | g.28768150C>G | CA389476042 | FOXG1 | c.871C>G (p.Arg291Gly) | |
| 14 | g.28768150C>T | CA389476043 | FOXG1 | c.871C>T (p.Arg291Cys) | |
| 14 | g.28768151G>A | CA389476046 | FOXG1 | c.872G>A (p.Arg291His) | |
| 14 | g.28768151G>C | CA389476045 | FOXG1 | c.872G>C (p.Arg291Pro) | |
| 14 | g.28768151G>T | CA389476044 | FOXG1 | c.872G>T (p.Arg291Leu) | gnomAD v4 |
| 14 | g.28768160_28768174del | CA2624399950 | FOXG1 | c.881_895del (p.Ser294_Thr298del) | gnomAD v4 |
| 14 | g.28768152C>A | CA486099089 | FOXG1 | c.873C>A (p.Arg291=) | |
| 14 | g.28768152C>G | CA486099090 | FOXG1 | c.873C>G (p.Arg291=) | |
| 14 | g.28768152C>T | CA486099091 | FOXG1 | c.873C>T (p.Arg291=) | |
| 14 | g.28768153C>A | CA389476047 | FOXG1 | c.874C>A (p.Leu292Ile) | |
| 14 | g.28768153C>G | CA389476048 | FOXG1 | c.874C>G (p.Leu292Val) | gnomAD v4 |
| 14 | g.28768153C>T | CA389476049 | FOXG1 | c.874C>T (p.Leu292Phe) | |
| 14 | g.28768154T>A | CA389476050 | FOXG1 | c.875T>A (p.Leu292His) | COSMIC |
| 14 | g.28768154T>C | CA389476051 | FOXG1 | c.875T>C (p.Leu292Pro) | |
| 14 | g.28768154T>G | CA389476052 | FOXG1 | c.875T>G (p.Leu292Arg) | |
| 14 | g.28768155C>A | CA486098208 | FOXG1 | c.876C>A (p.Leu292=) | |
| 14 | g.28768155C= | CA2126000302 | FOXG1 | c.876C= (p.Leu292=) | |
| 14 | g.28768155C>G | CA486098210 | FOXG1 | c.876C>G (p.Leu292=) | ClinVar |
| 14 | g.28768155C>T | CA486098209 | FOXG1 | c.876C>T (p.Leu292=) | dbSNP gnomAD v2 |
| 14 | g.28768156A= | CA2126000303 | FOXG1 | c.877A= (p.Thr293=) | |
| 14 | g.28768156A>C | CA258396583 | FOXG1 | c.877A>C (p.Thr293Pro) | dbSNP |
| 14 | g.28768156A>G | CA389476053 | FOXG1 | c.877A>G (p.Thr293Ala) | gnomAD v4 |
| 14 | g.28768156A>T | CA389476054 | FOXG1 | c.877A>T (p.Thr293Ser) | |
| 14 | g.28768157C>A | CA389476055 | FOXG1 | c.878C>A (p.Thr293Asn) | |
| 14 | g.28768157C>G | CA389476056 | FOXG1 | c.878C>G (p.Thr293Ser) | |
| 14 | g.28768157C>T | CA389476057 | FOXG1 | c.878C>T (p.Thr293Ile) | |
| 14 | g.28768158C>A | CA486098214 | FOXG1 | c.879C>A (p.Thr293=) | gnomAD v4 |
| 14 | g.28768158C= | CA2126000304 | FOXG1 | c.879C= (p.Thr293=) | |
| 14 | g.28768158C>G | CA486098215 | FOXG1 | c.879C>G (p.Thr293=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768158C>T | CA486098216 | FOXG1 | c.879C>T (p.Thr293=) | gnomAD v4 |
| 14 | g.28768159T>A | CA389476059 | FOXG1 | c.880T>A (p.Ser294Thr) | |
| 14 | g.28768159T>C | CA314628 | FOXG1 | c.880T>C (p.Ser294Pro) | ClinVar dbSNP |
| 14 | g.28768159T>G | CA389476058 | FOXG1 | c.880T>G (p.Ser294Ala) | |
| 14 | g.28768159T= | CA2126000305 | FOXG1 | c.880T= (p.Ser294=) | |
| 14 | g.28768160C>A | CA389476060 | FOXG1 | c.881C>A (p.Ser294Tyr) | COSMIC |
| 14 | g.28768160C>G | CA389476061 | FOXG1 | c.881C>G (p.Ser294Cys) | |
| 14 | g.28768160C>T | CA389476062 | FOXG1 | c.881C>T (p.Ser294Phe) | |
| 14 | g.28768161C>A | CA486098221 | FOXG1 | c.882C>A (p.Ser294=) | |
| 14 | g.28768161C>G | CA486098222 | FOXG1 | c.882C>G (p.Ser294=) | |
| 14 | g.28768161C>T | CA486098223 | FOXG1 | c.882C>T (p.Ser294=) | gnomAD v4 |
| 14 | g.28768162A= | CA2126000306 | FOXG1 | c.883A= (p.Thr295=) | |
| 14 | g.28768162A>C | CA389476063 | FOXG1 | c.883A>C (p.Thr295Pro) | |
| 14 | g.28768162A>G | CA389476064 | FOXG1 | c.883A>G (p.Thr295Ala) | |
| 14 | g.28768162A>T | CA389476065 | FOXG1 | c.883A>T (p.Thr295Ser) | |
| 14 | g.28768163C>A | CA389476066 | FOXG1 | c.884C>A (p.Thr295Asn) | |
| 14 | g.28768163C>G | CA389476067 | FOXG1 | c.884C>G (p.Thr295Ser) | |
| 14 | g.28768163C>T | CA389476068 | FOXG1 | c.884C>T (p.Thr295Ile) | |
| 14 | g.28768164dup | CA16043741 | FOXG1 | c.885dup (p.Gly296ArgfsTer?) | ClinVar dbSNP |
| 14 | g.28768164C>A | CA486098226 | FOXG1 | c.885C>A (p.Thr295=) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768164C= | CA2126000307 | FOXG1 | c.885C= (p.Thr295=) | |
| 14 | g.28768164C>G | CA486098225 | FOXG1 | c.885C>G (p.Thr295=) | gnomAD v4 |
| 14 | g.28768164C>T | CA7140637 | FOXG1 | c.885C>T (p.Thr295=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768165G>A | CA389476069 | FOXG1 | c.886G>A (p.Gly296Ser) | ClinVar gnomAD v4 |
| 14 | g.28768165G>C | CA389476070 | FOXG1 | c.886G>C (p.Gly296Arg) | |
| 14 | g.28768165G>T | CA389476071 | FOXG1 | c.886G>T (p.Gly296Cys) | |
| 14 | g.28768166G>A | CA389476074 | FOXG1 | c.887G>A (p.Gly296Asp) | |
| 14 | g.28768166G>C | CA389476073 | FOXG1 | c.887G>C (p.Gly296Ala) | |
| 14 | g.28768166G= | CA2126000308 | FOXG1 | c.887G= (p.Gly296=) | |
| 14 | g.28768166G>T | CA389476072 | FOXG1 | c.887G>T (p.Gly296Val) | ClinVar dbSNP |
| 14 | g.28768167C>A | CA486098231 | FOXG1 | c.888C>A (p.Gly296=) | |
| 14 | g.28768167C>G | CA486098232 | FOXG1 | c.888C>G (p.Gly296=) | |
| 14 | g.28768167C>T | CA486098233 | FOXG1 | c.888C>T (p.Gly296=) | |
| 14 | g.28768168C>A | CA389476076 | FOXG1 | c.889C>A (p.Leu297Ile) | COSMIC |
| 14 | g.28768168C>G | CA389476075 | FOXG1 | c.889C>G (p.Leu297Val) | |
| 14 | g.28768168C>T | CA389476077 | FOXG1 | c.889C>T (p.Leu297Phe) | gnomAD v4 |
| 14 | g.28768169T>A | CA389476078 | FOXG1 | c.890T>A (p.Leu297His) | COSMIC |
| 14 | g.28768169T>C | CA389476079 | FOXG1 | c.890T>C (p.Leu297Pro) | |
| 14 | g.28768169T>G | CA389476080 | FOXG1 | c.890T>G (p.Leu297Arg) | |
| 14 | g.28768170C>A | CA486098236 | FOXG1 | c.891C>A (p.Leu297=) | |
| 14 | g.28768170C= | CA2126000309 | FOXG1 | c.891C= (p.Leu297=) | |
| 14 | g.28768170C>G | CA486098234 | FOXG1 | c.891C>G (p.Leu297=) | COSMIC |
| 14 | g.28768170C>T | CA486098238 | FOXG1 | c.891C>T (p.Leu297=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768171A>C | CA389476081 | FOXG1 | c.892A>C (p.Thr298Pro) | |
| 14 | g.28768171A>G | CA389476082 | FOXG1 | c.892A>G (p.Thr298Ala) | |
| 14 | g.28768171A>T | CA389476083 | FOXG1 | c.892A>T (p.Thr298Ser) | |
| 14 | g.28768172C>A | CA389476084 | FOXG1 | c.893C>A (p.Thr298Asn) | |
| 14 | g.28768172C>G | CA389476085 | FOXG1 | c.893C>G (p.Thr298Ser) | ClinVar dbSNP |
| 14 | g.28768172C>T | CA389476086 | FOXG1 | c.893C>T (p.Thr298Ile) | |
| 14 | g.28768173C>A | CA486098240 | FOXG1 | c.894C>A (p.Thr298=) | |
| 14 | g.28768173C= | CA2126000310 | FOXG1 | c.894C= (p.Thr298=) | |
| 14 | g.28768173C>G | CA486098241 | FOXG1 | c.894C>G (p.Thr298=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768173C>T | CA486098242 | FOXG1 | c.894C>T (p.Thr298=) | gnomAD v4 |
| 14 | g.28768174T>A | CA389476087 | FOXG1 | c.895T>A (p.Phe299Ile) | |
| 14 | g.28768174T>C | CA389476088 | FOXG1 | c.895T>C (p.Phe299Leu) | |
| 14 | g.28768174T>G | CA389476089 | FOXG1 | c.895T>G (p.Phe299Val) | |
| 14 | g.28768175T>A | CA389476092 | FOXG1 | c.896T>A (p.Phe299Tyr) | |
| 14 | g.28768175T>C | CA389476090 | FOXG1 | c.896T>C (p.Phe299Ser) | |
| 14 | g.28768175T>G | CA389476091 | FOXG1 | c.896T>G (p.Phe299Cys) | |
| 14 | g.28768176C>A | CA389476093 | FOXG1 | c.897C>A (p.Phe299Leu) | |
| 14 | g.28768176C= | CA2126000311 | FOXG1 | c.897C= (p.Phe299=) | |
| 14 | g.28768176C>G | CA389476094 | FOXG1 | c.897C>G (p.Phe299Leu) | |
| 14 | g.28768176C>T | CA486098247 | FOXG1 | c.897C>T (p.Phe299=) | dbSNP gnomAD v2 COSMIC |
| 14 | g.28768177A>C | CA389476095 | FOXG1 | c.898A>C (p.Met300Leu) | |
| 14 | g.28768177A>G | CA389476096 | FOXG1 | c.898A>G (p.Met300Val) | gnomAD v4 |
| 14 | g.28768177A>T | CA389476097 | FOXG1 | c.898A>T (p.Met300Leu) | |
| 14 | g.28768178T>A | CA389476098 | FOXG1 | c.899T>A (p.Met300Lys) | gnomAD v3 gnomAD v4 |
| 14 | g.28768178T>C | CA389476099 | FOXG1 | c.899T>C (p.Met300Thr) | |
| 14 | g.28768178T>G | CA389476100 | FOXG1 | c.899T>G (p.Met300Arg) | |
| 14 | g.28768179G>A | CA258396584 | FOXG1 | c.900G>A (p.Met300Ile) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768179G>C | CA389476101 | FOXG1 | c.900G>C (p.Met300Ile) | |
| 14 | g.28768179G= | CA2126000312 | FOXG1 | c.900G= (p.Met300=) | |
| 14 | g.28768179G>T | CA389476102 | FOXG1 | c.900G>T (p.Met300Ile) | |
| 14 | g.28768180G>A | CA389476104 | FOXG1 | c.901G>A (p.Asp301Asn) | |
| 14 | g.28768180G>C | CA389476105 | FOXG1 | c.901G>C (p.Asp301His) | |
| 14 | g.28768180G>T | CA389476103 | FOXG1 | c.901G>T (p.Asp301Tyr) | gnomAD v4 |
| 14 | g.28768181A>C | CA389476106 | FOXG1 | c.902A>C (p.Asp301Ala) | |
| 14 | g.28768181A>G | CA389476107 | FOXG1 | c.902A>G (p.Asp301Gly) | |
| 14 | g.28768181A>T | CA389476108 | FOXG1 | c.902A>T (p.Asp301Val) | |
| 14 | g.28768182C>A | CA389476109 | FOXG1 | c.903C>A (p.Asp301Glu) | COSMIC |
| 14 | g.28768182C= | CA2126000313 | FOXG1 | c.903C= (p.Asp301=) | |
| 14 | g.28768182C>G | CA389476110 | FOXG1 | c.903C>G (p.Asp301Glu) | |
| 14 | g.28768182C>T | CA258396585 | FOXG1 | c.903C>T (p.Asp301=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768183C>A | CA389476113 | FOXG1 | c.904C>A (p.Arg302Ser) | |
| 14 | g.28768183C>G | CA389476112 | FOXG1 | c.904C>G (p.Arg302Gly) | |
| 14 | g.28768183C>T | CA389476111 | FOXG1 | c.904C>T (p.Arg302Cys) | |
| 14 | g.28768184G>A | CA389476114 | FOXG1 | c.905G>A (p.Arg302His) | gnomAD v4 COSMIC |
| 14 | g.28768184G>C | CA389476115 | FOXG1 | c.905G>C (p.Arg302Pro) | |
| 14 | g.28768184G>T | CA389476116 | FOXG1 | c.905G>T (p.Arg302Leu) | gnomAD v4 |
| 14 | g.28768185C>A | CA486098264 | FOXG1 | c.906C>A (p.Arg302=) | |
| 14 | g.28768185C>G | CA486098263 | FOXG1 | c.906C>G (p.Arg302=) | |
| 14 | g.28768185C>T | CA486098262 | FOXG1 | c.906C>T (p.Arg302=) | COSMIC |
| 14 | g.28768186G>A | CA16606850 | FOXG1 | c.907G>A (p.Ala303Thr) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768186G>C | CA389476117 | FOXG1 | c.907G>C (p.Ala303Pro) | |
| 14 | g.28768186G= | CA2126000314 | FOXG1 | c.907G= (p.Ala303=) | |
| 14 | g.28768186G>T | CA7140638 | FOXG1 | c.907G>T (p.Ala303Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768187C>A | CA389476118 | FOXG1 | c.908C>A (p.Ala303Asp) | |
| 14 | g.28768187C>G | CA389476120 | FOXG1 | c.908C>G (p.Ala303Gly) | |
| 14 | g.28768187C>T | CA389476119 | FOXG1 | c.908C>T (p.Ala303Val) | COSMIC |
| 14 | g.28768188C>A | CA486098268 | FOXG1 | c.909C>A (p.Ala303=) | |
| 14 | g.28768188C= | CA2126000315 | FOXG1 | c.909C= (p.Ala303=) | |
| 14 | g.28768188C>G | CA486098269 | FOXG1 | c.909C>G (p.Ala303=) | |
| 14 | g.28768188C>T | CA486098272 | FOXG1 | c.909C>T (p.Ala303=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768189G>A | CA389476121 | FOXG1 | c.910G>A (p.Gly304Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768189G>C | CA389476122 | FOXG1 | c.910G>C (p.Gly304Arg) | |
| 14 | g.28768189G= | CA2126000316 | FOXG1 | c.910G= (p.Gly304=) | |
| 14 | g.28768189G>T | CA389476123 | FOXG1 | c.910G>T (p.Gly304Cys) | gnomAD v4 |
| 14 | g.28768190G>A | CA389476124 | FOXG1 | c.911G>A (p.Gly304Asp) | gnomAD v4 |
| 14 | g.28768190G>C | CA389476125 | FOXG1 | c.911G>C (p.Gly304Ala) | |
| 14 | g.28768190G>T | CA389476126 | FOXG1 | c.911G>T (p.Gly304Val) | |
| 14 | g.28768191C>A | CA486098276 | FOXG1 | c.912C>A (p.Gly304=) | |
| 14 | g.28768191C>G | CA486098278 | FOXG1 | c.912C>G (p.Gly304=) | |
| 14 | g.28768191C>T | CA486098280 | FOXG1 | c.912C>T (p.Gly304=) | |
| 14 | g.28768192T>A | CA389476127 | FOXG1 | c.913T>A (p.Ser305Thr) | |
| 14 | g.28768192T>C | CA389476128 | FOXG1 | c.913T>C (p.Ser305Pro) | |
| 14 | g.28768192T>G | CA389476129 | FOXG1 | c.913T>G (p.Ser305Ala) | |
| 14 | g.28768193C>A | CA389476130 | FOXG1 | c.914C>A (p.Ser305Tyr) | |
| 14 | g.28768193C>G | CA389476131 | FOXG1 | c.914C>G (p.Ser305Cys) | |
| 14 | g.28768193C>T | CA389476132 | FOXG1 | c.914C>T (p.Ser305Phe) | |
| 14 | g.28768194C>A | CA486098282 | FOXG1 | c.915C>A (p.Ser305=) | |
| 14 | g.28768194C= | CA2126000317 | FOXG1 | c.915C= (p.Ser305=) | |
| 14 | g.28768194C>G | CA486098283 | FOXG1 | c.915C>G (p.Ser305=) | gnomAD v4 |
| 14 | g.28768194C>T | CA7140639 | FOXG1 | c.915C>T (p.Ser305=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.28768195C>A | CA389476133 | FOXG1 | c.916C>A (p.Leu306Ile) | |
| 14 | g.28768195C= | CA2126000318 | FOXG1 | c.916C= (p.Leu306=) | |
| 14 | g.28768195C>G | CA389476134 | FOXG1 | c.916C>G (p.Leu306Val) | |
| 14 | g.28768195C>T | CA258396586 | FOXG1 | c.916C>T (p.Leu306Phe) | dbSNP gnomAD v4 |
| 14 | g.28768196T>A | CA389476135 | FOXG1 | c.917T>A (p.Leu306His) | |
| 14 | g.28768196T>C | CA389476137 | FOXG1 | c.917T>C (p.Leu306Pro) | |
| 14 | g.28768196T>G | CA389476136 | FOXG1 | c.917T>G (p.Leu306Arg) | |
| 14 | g.28768197C>A | CA486098287 | FOXG1 | c.918C>A (p.Leu306=) | COSMIC |
| 14 | g.28768197C= | CA2126000319 | FOXG1 | c.918C= (p.Leu306=) | |
| 14 | g.28768197C>G | CA486098288 | FOXG1 | c.918C>G (p.Leu306=) | gnomAD v4 |
| 14 | g.28768197C>T | CA486098289 | FOXG1 | c.918C>T (p.Leu306=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768198T>A | CA389476138 | FOXG1 | c.919T>A (p.Tyr307Asn) | |
| 14 | g.28768198T>C | CA389476140 | FOXG1 | c.919T>C (p.Tyr307His) | |
| 14 | g.28768198T>G | CA389476139 | FOXG1 | c.919T>G (p.Tyr307Asp) | |
| 14 | g.28768198T= | CA2126000320 | FOXG1 | c.919T= (p.Tyr307=) | |
| 14 | g.28768199A>C | CA389476141 | FOXG1 | c.920A>C (p.Tyr307Ser) | |
| 14 | g.28768199A>G | CA389476142 | FOXG1 | c.920A>G (p.Tyr307Cys) | |
| 14 | g.28768199A>T | CA389476143 | FOXG1 | c.920A>T (p.Tyr307Phe) | |
| 14 | g.28768199dup | CA1139663427 | FOXG1 | c.920dup (p.Tyr307Ter) | ClinVar dbSNP |
| 14 | g.28768200C>A | CA389476144 | FOXG1 | c.921C>A (p.Tyr307Ter) | |
| 14 | g.28768200C>G | CA389476145 | FOXG1 | c.921C>G (p.Tyr307Ter) | ClinVar dbSNP |
| 14 | g.28768200C>T | CA486098293 | FOXG1 | c.921C>T (p.Tyr307=) | ClinVar dbSNP |
| 14 | g.28768201T>A | CA389476146 | FOXG1 | c.922T>A (p.Trp308Arg) | |
| 14 | g.28768201T>C | CA389476147 | FOXG1 | c.922T>C (p.Trp308Arg) | |
| 14 | g.28768201T>G | CA389476148 | FOXG1 | c.922T>G (p.Trp308Gly) | |
| 14 | g.28768202G>A | CA389476149 | FOXG1 | c.923G>A (p.Trp308Ter) | ClinVar dbSNP |
| 14 | g.28768202G>C | CA389476150 | FOXG1 | c.923G>C (p.Trp308Ser) | |
| 14 | g.28768202G>T | CA389476151 | FOXG1 | c.923G>T (p.Trp308Leu) | |
| 14 | g.28768203G>A | CA123555 | FOXG1 | c.924G>A (p.Trp308Ter) | ClinVar dbSNP |
| 14 | g.28768203G>C | CA389476153 | FOXG1 | c.924G>C (p.Trp308Cys) | COSMIC |
| 14 | g.28768203G= | CA2126000321 | FOXG1 | c.924G= (p.Trp308=) | |
| 14 | g.28768203G>T | CA389476152 | FOXG1 | c.924G>T (p.Trp308Cys) | |
| 14 | g.28768204C>A | CA389476154 | FOXG1 | c.925C>A (p.Pro309Thr) | |
| 14 | g.28768204C= | CA2126000322 | FOXG1 | c.925C= (p.Pro309=) | |
| 14 | g.28768204C>G | CA389476155 | FOXG1 | c.925C>G (p.Pro309Ala) | |
| 14 | g.28768204C>T | CA389476156 | FOXG1 | c.925C>T (p.Pro309Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768205C>A | CA389476157 | FOXG1 | c.926C>A (p.Pro309His) | |
| 14 | g.28768205C= | CA2126000323 | FOXG1 | c.926C= (p.Pro309=) | |
| 14 | g.28768205C>G | CA258396587 | FOXG1 | c.926C>G (p.Pro309Arg) | dbSNP |
| 14 | g.28768205C>T | CA389476158 | FOXG1 | c.926C>T (p.Pro309Leu) | |
| 14 | g.28768206C>A | CA486098300 | FOXG1 | c.927C>A (p.Pro309=) | gnomAD v4 |
| 14 | g.28768206C= | CA2126000324 | FOXG1 | c.927C= (p.Pro309=) | |
| 14 | g.28768206C>G | CA486098299 | FOXG1 | c.927C>G (p.Pro309=) | |
| 14 | g.28768206C>T | CA486098298 | FOXG1 | c.927C>T (p.Pro309=) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768207A>C | CA389476159 | FOXG1 | c.928A>C (p.Met310Leu) | gnomAD v4 |
| 14 | g.28768207A>G | CA389476160 | FOXG1 | c.928A>G (p.Met310Val) | |
| 14 | g.28768207A>T | CA389476161 | FOXG1 | c.928A>T (p.Met310Leu) | |
| 14 | g.28768208T>A | CA389476163 | FOXG1 | c.929T>A (p.Met310Lys) | |
| 14 | g.28768208T>C | CA389476164 | FOXG1 | c.929T>C (p.Met310Thr) | |
| 14 | g.28768208T>G | CA389476162 | FOXG1 | c.929T>G (p.Met310Arg) | |
| 14 | g.28768209G>A | CA389476165 | FOXG1 | c.930G>A (p.Met310Ile) | |
| 14 | g.28768209G>C | CA389476166 | FOXG1 | c.930G>C (p.Met310Ile) | |
| 14 | g.28768209G>T | CA389476167 | FOXG1 | c.930G>T (p.Met310Ile) | |
| 14 | g.28768210T>A | CA389476168 | FOXG1 | c.931T>A (p.Ser311Thr) | |
| 14 | g.28768210T>C | CA389476169 | FOXG1 | c.931T>C (p.Ser311Pro) | |
| 14 | g.28768210T>G | CA389476170 | FOXG1 | c.931T>G (p.Ser311Ala) | |
| 14 | g.28768211C>A | CA389476171 | FOXG1 | c.932C>A (p.Ser311Ter) | dbSNP |
| 14 | g.28768211C>G | CA389476172 | FOXG1 | c.932C>G (p.Ser311Trp) | |
| 14 | g.28768211C>T | CA389476173 | FOXG1 | c.932C>T (p.Ser311Leu) | |
| 14 | g.28768212G>A | CA486098302 | FOXG1 | c.933G>A (p.Ser311=) | ClinVar |
| 14 | g.28768212G>C | CA486098304 | FOXG1 | c.933G>C (p.Ser311=) | gnomAD v4 |
| 14 | g.28768212G= | CA2126000325 | FOXG1 | c.933G= (p.Ser311=) | |
| 14 | g.28768212G>T | CA486098303 | FOXG1 | c.933G>T (p.Ser311=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768213C>A | CA389476174 | FOXG1 | c.934C>A (p.Pro312Thr) | |
| 14 | g.28768213C>G | CA389476175 | FOXG1 | c.934C>G (p.Pro312Ala) | |
| 14 | g.28768213C>T | CA389476176 | FOXG1 | c.934C>T (p.Pro312Ser) | gnomAD v4 |
| 14 | g.28768214C>A | CA389476179 | FOXG1 | c.935C>A (p.Pro312His) | |
| 14 | g.28768214C>G | CA389476177 | FOXG1 | c.935C>G (p.Pro312Arg) | |
| 14 | g.28768214C>T | CA389476178 | FOXG1 | c.935C>T (p.Pro312Leu) | |
| 14 | g.28768215C>A | CA486098308 | FOXG1 | c.936C>A (p.Pro312=) | |
| 14 | g.28768215C= | CA2126000326 | FOXG1 | c.936C= (p.Pro312=) | |
| 14 | g.28768215C>G | CA486098309 | FOXG1 | c.936C>G (p.Pro312=) | gnomAD v4 |
| 14 | g.28768215C>T | CA486098310 | FOXG1 | c.936C>T (p.Pro312=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768216T>A | CA389476180 | FOXG1 | c.937T>A (p.Phe313Ile) | |
| 14 | g.28768216T>C | CA389476181 | FOXG1 | c.937T>C (p.Phe313Leu) | gnomAD v4 |
| 14 | g.28768216T>G | CA389476182 | FOXG1 | c.937T>G (p.Phe313Val) | |
| 14 | g.28768217T>A | CA389476183 | FOXG1 | c.938T>A (p.Phe313Tyr) | |
| 14 | g.28768217T>C | CA389476184 | FOXG1 | c.938T>C (p.Phe313Ser) | |
| 14 | g.28768217T>G | CA389476185 | FOXG1 | c.938T>G (p.Phe313Cys) | |
| 14 | g.28768218C>A | CA389476186 | FOXG1 | c.939C>A (p.Phe313Leu) | gnomAD v4 |
| 14 | g.28768218C>G | CA389476187 | FOXG1 | c.939C>G (p.Phe313Leu) | |
| 14 | g.28768218C>T | CA486098314 | FOXG1 | c.939C>T (p.Phe313=) | gnomAD v4 |
| 14 | g.28768219C>A | CA389476188 | FOXG1 | c.940C>A (p.Leu314Met) | |
| 14 | g.28768219C= | CA2126000327 | FOXG1 | c.940C= (p.Leu314=) | |
| 14 | g.28768219C>G | CA389476189 | FOXG1 | c.940C>G (p.Leu314Val) | |
| 14 | g.28768219C>T | CA486098315 | FOXG1 | c.940C>T (p.Leu314=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768220T>A | CA389476190 | FOXG1 | c.941T>A (p.Leu314Gln) | |
| 14 | g.28768220T>C | CA389476191 | FOXG1 | c.941T>C (p.Leu314Pro) | |
| 14 | g.28768220T>G | CA389476192 | FOXG1 | c.941T>G (p.Leu314Arg) | |
| 14 | g.28768221G>A | CA486098316 | FOXG1 | c.942G>A (p.Leu314=) | gnomAD v4 |
| 14 | g.28768221G>C | CA486098317 | FOXG1 | c.942G>C (p.Leu314=) | ClinVar dbSNP |
| 14 | g.28768221G>T | CA486098318 | FOXG1 | c.942G>T (p.Leu314=) | gnomAD v4 |
| 14 | g.28768222T>A | CA389476194 | FOXG1 | c.943T>A (p.Ser315Thr) | |
| 14 | g.28768222T>C | CA389476195 | FOXG1 | c.943T>C (p.Ser315Pro) | gnomAD v4 COSMIC |
| 14 | g.28768222T>G | CA389476193 | FOXG1 | c.943T>G (p.Ser315Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768222T= | CA2126000328 | FOXG1 | c.943T= (p.Ser315=) | |
| 14 | g.28768222_28768223delinsTC | CA2126000329 | FOXG1 | c.943_944delinsTC (p.Ser315=) | |
| 14 | g.28768222_28768228dup | CA2499222616 | FOXG1 | c.943_949dup (p.His317LeufsTer?) | ClinVar dbSNP |
| 14 | g.28768223C>A | CA389476196 | FOXG1 | c.944C>A (p.Ser315Tyr) | |
| 14 | g.28768223C>G | CA389476197 | FOXG1 | c.944C>G (p.Ser315Cys) | gnomAD v4 |
| 14 | g.28768223C>T | CA389476198 | FOXG1 | c.944C>T (p.Ser315Phe) | |
| 14 | g.28768225del | CA658798198 | FOXG1 | c.946del (p.Leu316CysfsTer10) | ClinVar dbSNP |