217631512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186947336-G-A

217631613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186947223-T-C

217631693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186947147-T-C

217631838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186947021-T-G

217632341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186946679-G-A

217632360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186946657-A-T

217632446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186946576-C-T

217632448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186946574-A-G

217632456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186946566-T-C

217632468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186946554-A-G

http://identifiers.org/hco/1/GRCh38#217632513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186946509-A-C

217632520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186946502-C-T

http://identifiers.org/hco/1/GRCh38#217632533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186946491-C-A

217632533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186946491-C-T

http://identifiers.org/hco/1/GRCh38#217632850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186946152-C-A

217637555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186945810-G-A

217637577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186945788-A-T

217637591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186945775-T-C

217637710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186945675-T-C

217637722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186945665-T-C

http://identifiers.org/hco/1/GRCh38#217637855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186945497-A-C

217637874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186945482-T-A

217638327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186945012-A-G

217638436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186944924-T-C

http://identifiers.org/hco/1/GRCh38#217638448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186944912-A-C

217638448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186944912-A-G

217639965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186942342-T-C

217640161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186942168-A-T

217640343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186941714-T-G

http://identifiers.org/hco/1/GRCh38#217640349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186941708-A-C

217640349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186941708-A-G

217640352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186941705-C-T

217640475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186941606-T-G

217640858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186941057-A-G

217641115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186940849-G-A

http://identifiers.org/hco/1/GRCh38#217641169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186940795-C-A

217641617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186940368-G-A

217642117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186939515-C-T

217642272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186939359-A-G

217642433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186939218-A-T

217643007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186939081-C-T

217643015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186939060-C-T

217643105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186938976-A-G

217643356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186938676-G-A

217643605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186938480-C-T

217643669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186938426-A-G

217644225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186938273-T-A

217644443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186938074-C-T

217644606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186937914-A-G

217645331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186937210-C-T

217645484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186937048-G-A

217645680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186936883-A-G

217645680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186936883-A-T

217648355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186926717-C-T

217648916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 186926176-G-A

217648916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 186926176-G-T

217648922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 186926170-G-A

217648955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 186926137-G-A

217648978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 186926114-T-A

217648978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 186926114-T-G

217649016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186926079-A-G

217649036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186926058-T-C

217649193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186925895-T-C

http://identifiers.org/hco/1/GRCh38#217651057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186925251-C-A

http://identifiers.org/hco/1/GRCh38#217651063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186925245-A-C

217651063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186925245-A-G

http://identifiers.org/hco/1/GRCh38#217651165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186925147-A-C

217651165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 186925147-A-G

217651203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186925108-A-G

http://identifiers.org/hco/1/GRCh38#217654110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186922080-A-C

217654110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186922080-A-G

217659232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186921735-G-A

217659335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186921639-G-A

217659335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186921639-G-T

217659344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186921630-A-G

217662221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186921233-G-A

217662279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186921176-G-A

217662460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186921063-G-A

217662639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186920887-G-C

217663181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186920368-A-T

217663222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186920317-A-G

217663222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186920317-A-T

217663242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186920300-C-G

217663242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186920300-C-T

http://identifiers.org/hco/1/GRCh38#217663260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186920282-C-A

http://identifiers.org/hco/1/GRCh38#217664906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186919007-A-C

217665212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186918683-A-G

217665437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 186918486-C-T

http://identifiers.org/hco/1/GRCh38#217665505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186918429-C-A

217665505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186918429-C-G

217665505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186918429-C-T

217665574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186918361-T-C

217665930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186918019-A-G

217668090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186916978-G-T

217668166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186916892-T-C

217668237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186916294-T-C

217669037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 186915461-C-T

217669136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186915362-T-C

217669414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186915087-G-A

217672820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186914123-C-G

217672906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186914052-G-A

217673015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186913942-A-G

217676893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186913793-A-G

217677618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186913148-G-A

217677630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186913136-A-G

217677783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186913004-G-A

217678501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186912924-C-T

217678692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186912735-G-A

217679308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186912146-A-T

217679402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186912056-A-G

217679444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186912015-A-G

217679633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186911456-T-C

217679779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186911346-T-C

217679849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186911244-A-G

217679915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186911177-A-G

217679987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186911116-T-G

217680239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186910956-T-G

217680508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186910721-T-C

217682043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186909632-C-T

217682187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186909523-T-C

217682295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186909448-T-A

217682312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186909432-T-C

http://identifiers.org/hco/1/GRCh38#217682340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186909405-C-A

217682348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186909397-T-A

217682499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186909267-T-C

217682573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186909201-T-C

http://identifiers.org/hco/1/GRCh38#217682731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186909068-A-C

217682731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186909068-A-G

217683124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186908114-A-G

217683165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186906779-T-A

http://identifiers.org/hco/1/GRCh38#217683173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186906771-C-A

217683173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186906771-C-G

217683184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186906760-T-G

217683201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186906746-T-C

http://identifiers.org/hco/1/GRCh38#217683210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186906737-A-C

217683210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186906737-A-T

217683374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186906561-A-G

217683747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186906384-T-C

217684051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186906118-C-G

217684126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186906045-A-G

217684152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186906019-A-G

217684251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186905931-A-G

217684275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186905907-C-G

217709192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186895327-A-G

217709231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186895285-A-G

217709337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186895175-A-T

217709470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186895061-C-G

217709481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186895050-G-T

217709494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186895037-T-C

217709669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186894872-T-A

217709875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186894676-G-A

217709875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186894676-G-T

217709902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186894649-A-T

217710463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186894123-A-T

217710596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186893987-A-G

217710596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186893987-A-T

217711455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186893070-T-C

217711508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186893016-A-G

217711519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186893005-C-T

217711832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186892713-C-G

217711835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186892710-A-T

217711840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186892705-T-C

217711867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186892678-A-G

217711883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186892662-T-C

217715643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186889623-T-A

217715648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186889618-T-A

217715710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186889558-T-A

217717668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186887506-A-G

217717668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186887506-A-T

217717688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186887486-C-G

217717718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186887456-A-G

217717754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186887420-G-T

217720715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186886647-G-A

217721759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186885841-T-C

217721869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186885788-C-T

217721910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186885747-G-A

217722064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186885612-C-G

217722064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186885612-C-T

217722528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186885271-C-T

217722614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186885193-G-A

217722614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186885193-G-T

217723304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186884479-G-A

217723304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186884479-G-T

217723378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186884441-C-T

217728524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186883933-T-G

217728548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186883906-C-T

217728687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186883742-C-T

217728873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186883565-C-T

217732507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186882016-G-C

217732521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186882002-T-C

217732662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186881872-G-A

217732727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186881814-C-G

217732727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186881814-C-T

217732864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186881691-A-G

217732864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186881691-A-T

217733012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186880729-G-A

http://identifiers.org/hco/1/GRCh38#217736042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186877204-A-C

217736103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186877146-A-G

217736492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186876715-G-C

217736582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186876516-A-G

217736706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186876327-T-C

217737067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186876002-A-G

217737217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186875848-A-G

217737701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186875428-G-T

217737706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186875423-T-C

http://identifiers.org/hco/1/GRCh38#217737725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186875401-C-A

http://identifiers.org/hco/1/GRCh38#217737743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186875383-C-A

http://identifiers.org/hco/1/GRCh38#217737752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186875374-C-A

217737764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186875364-T-C

217737764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 186875364-T-G

http://identifiers.org/hco/1/GRCh38#217737864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186875295-C-A

217737864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 186875295-C-T

217737921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 186875276-T-C

http://identifiers.org/hco/1/GRCh38#217738392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186875037-A-C

217738520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186874938-C-G

217739324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186874475-G-T

http://identifiers.org/hco/1/GRCh38#217739344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186874456-C-A

217740364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186874285-A-T

217740385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186874264-T-C

217741330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186873304-G-C

217741330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186873304-G-T

217741360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186873274-T-G

http://identifiers.org/hco/1/GRCh38#217741765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186872899-A-C

217741975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 186872691-G-A

http://identifiers.org/hco/1/GRCh38#217742035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186872631-A-C

217742035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 186872631-A-G

217742249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186872418-G-A

217742249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186872418-G-T

217742363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186872305-G-A

217742532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186872164-T-G

217745054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186871885-C-G

217745054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186871885-C-T

217745165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186871769-T-C

217745652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186871394-A-T

217745786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186871255-G-A

217746077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186871043-G-A

217746199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186870984-C-T

217746201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186870982-T-C

217746201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186870982-T-G

217746363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186870836-A-G

http://identifiers.org/hco/1/GRCh38#217746484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186870722-A-C

217746535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186870667-G-A

217747050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186870170-C-T

217747502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186869749-A-T

217747560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186869690-T-C

217747700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186869564-A-G

http://identifiers.org/hco/1/GRCh38#217749735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186868559-C-A

217749735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186868559-C-G

217749770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186868524-C-T

217749835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186867811-T-C

217750399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186867304-T-C

217750847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186866746-G-T

217750851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186866742-A-G

217751150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186866514-A-G

217751159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186866502-A-G

217751222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186866451-A-G

217751339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186866324-G-A

217751339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186866324-G-C

217751386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186866267-A-G

217751704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186865982-G-A

http://identifiers.org/hco/1/GRCh38#217751775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186865910-C-A

http://identifiers.org/hco/1/GRCh38#217751793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186865893-A-C

217751793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186865893-A-G

217752019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186865690-A-G

217752458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186865280-G-T

217756779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186859184-A-G

217756787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186859178-G-T

217756808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186859157-G-T

217756841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186859122-C-T

217757084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186858912-C-T

217757131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186858866-G-T

217757212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186858788-T-G

217757249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186858752-A-G

217757251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186858750-A-G

217757481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186858576-G-T

217757618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186858474-A-G

217757766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186858321-G-A

217757801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186858288-G-A

217767544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186857497-T-A

217767679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186857387-C-T

217767718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186857348-T-C

217767840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186857184-C-T

217767844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186857180-C-T

217767872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186857154-C-T

217767934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186856906-T-C

217768817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186856672-T-G

217768837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186856652-A-T

217768855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186856640-G-A

217769150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186856335-T-C

217769233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186856256-G-A

217769488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186855958-G-T

217769669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186855489-G-C

http://identifiers.org/hco/1/GRCh38#217770036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186855178-A-C

217770036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186855178-A-G

217770254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186854971-T-G

http://identifiers.org/hco/1/GRCh38#217770529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186854713-A-C

217771522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186853777-A-G

http://identifiers.org/hco/1/GRCh38#217771939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186853374-A-C

217772099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186853209-C-T

217772126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186853185-T-C

217772225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186853080-G-T

217772281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186853003-C-T

217772373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186852936-G-T

217772501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186852813-A-G

217772559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186852763-G-A

217772733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186852616-G-A

217772754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186852605-C-T

217772848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186852525-A-G

217772901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186852466-G-A

217773444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186851912-T-C

217773622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186851750-C-G

217773981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186850082-T-C

217773982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186850081-A-G

217774167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186849774-A-G

217774171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186849770-T-C

http://identifiers.org/hco/1/GRCh38#217774220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186849741-C-A

217774220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186849741-C-T

217774223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 186849738-T-C

http://identifiers.org/hco/1/GRCh38#217774389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186849609-A-C

217774423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 186849575-A-G

217774447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 186849548-C-T

217774448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 186849547-A-G

http://identifiers.org/hco/1/GRCh38#217774458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186849537-C-A

http://identifiers.org/hco/1/GRCh38#217774480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186849515-C-A

217774480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 186849515-C-G

217774480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 186849515-C-T

http://identifiers.org/hco/1/GRCh38#217774493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186849502-C-A

http://identifiers.org/hco/1/GRCh38#217774529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186849466-C-A

217774529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 186849466-C-T

217774581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186849413-T-C

217775971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186848718-G-C

217776017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186848668-T-C

217776031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186848654-A-G

217776064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186848620-G-C

217776380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186848327-A-G

217776495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186848277-A-G

217776507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186848265-G-C

217776897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186848081-A-G

217777202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186847843-C-T

217777268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186847786-A-G

http://identifiers.org/hco/1/GRCh38#217779647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186847514-C-A

217779647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186847514-C-T

217779706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186847472-G-A

217779706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186847472-G-C

217779706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186847472-G-T

217779761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186847425-C-G

http://identifiers.org/hco/1/GRCh38#217780930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186846445-C-A

217780949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186846430-T-A

217781248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 186846142-T-G

217781539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186845885-C-T

217781846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186845280-T-C

217781849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186845277-T-C

217781864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186845263-T-C

217782070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186844919-T-G

217782137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 186844857-T-C

http://identifiers.org/hco/1/GRCh38#217782147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186844848-A-C

217782213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 186844782-T-C

217782213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 186844782-T-G

217782369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186844647-T-C

217782385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186844630-T-C

217782385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186844630-T-G

217782404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186844611-A-G

217782781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186844079-T-C

217783039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186843815-A-G

217783132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186843710-T-C

217783708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186843007-A-T

217783922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186842798-G-A

http://identifiers.org/hco/1/GRCh38#217783965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186842754-A-C

217783965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186842754-A-T

217783980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186842739-G-A

217783980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186842739-G-T

217784016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186842705-T-A

217784290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186842437-T-C

217788883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186836183-C-T

217790825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186835478-A-T

217791201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186835085-G-C

217799024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186832610-T-G

217799230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186832425-A-G

217799334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186832349-C-G

217799411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186832280-G-A

217799597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186832092-T-C

217799647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186832063-A-G

http://identifiers.org/hco/1/GRCh38#217799651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186832059-A-C

217799724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186832001-G-A

217799810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186831910-T-C

217799810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186831910-T-G

217800270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186831565-C-T

217800449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186831332-C-G

217800467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186831302-T-G

http://identifiers.org/hco/1/GRCh38#217800516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186831219-A-C

217800516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186831219-A-G

217800524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186831211-T-C

217800526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186831180-A-G

217800687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186831009-T-C

217800730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830960-C-G

217801115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830697-T-C

217801119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830693-T-C

217801199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830609-C-T

217801278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830495-A-G

217801341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830428-G-A

http://identifiers.org/hco/1/GRCh38#217801529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186830233-A-C

217801529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830233-A-G

217801578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830188-G-A

217801578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830188-G-T

217801610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830178-A-T

217801675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830149-T-C

217801685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186830139-A-G

217802024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186829762-C-T

217809965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186827337-G-T

http://identifiers.org/hco/1/GRCh38#217809985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186827317-C-A

217810027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186827276-T-G

217810270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186827053-A-G

217811744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186826827-A-G

217811756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186826816-T-G

http://identifiers.org/hco/1/GRCh38#217812072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186826321-A-C

217812514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186825626-C-T

217812550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186825589-T-A

http://identifiers.org/hco/1/GRCh38#217812576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186825564-C-A

217812616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186825525-T-C

217812806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186825359-T-C

217812956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186825290-A-G

217813015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186825233-C-G

217813139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186825113-C-T

217813155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186825098-G-A

217813743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186824501-C-T

217813947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186824333-G-T

217813996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186824282-T-A

http://identifiers.org/hco/1/GRCh38#217814097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186824204-C-A

http://identifiers.org/hco/1/GRCh38#217814282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186824022-A-C

217814282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186824022-A-G

http://identifiers.org/hco/1/GRCh38#217814327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186823975-C-A

217814401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186823901-T-A

217815005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186823624-C-G

217815005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186823624-C-T

217815106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186823518-C-T

217815129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186823495-A-G

217815129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186823495-A-T

217818193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186823009-C-G

217818828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186822494-C-T

http://identifiers.org/hco/1/GRCh38#217818862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186822452-A-C

217818862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186822452-A-T

217818897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186822407-T-C

217818903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186822401-T-C

217818903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186822401-T-G

217818937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186822355-G-T

217819000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186822291-G-T

217819717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186821722-T-C

217819861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186821557-G-C

217820010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186821346-G-T

217820020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186821336-A-T

217820121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186821011-G-A

217831120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186818598-G-A

http://identifiers.org/hco/1/GRCh38#217831138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186818580-A-C

217831401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186818409-C-T

217831453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186818366-A-G

217831644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186818081-T-G

217831764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186817974-T-C

http://identifiers.org/hco/1/GRCh38#217831769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186817969-C-A

217832210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186817299-C-T

217832414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186817134-C-T

217832432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186817130-T-G

217832458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186817104-G-C

http://identifiers.org/hco/1/GRCh38#217832549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186817021-A-C

217832549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186817021-A-G

217832587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186816983-C-T

217832876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186816905-C-G

217833061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186816818-T-G

217833102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186816790-A-G

217833219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186816671-T-C

http://identifiers.org/hco/1/GRCh38#217833624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186815790-C-A

217833624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186815790-C-T

217833627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186815784-A-G

217833628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186815783-G-A

217833726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186815659-A-G

217833812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186815524-A-G

217836648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186814347-G-C

217836648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186814347-G-T

http://identifiers.org/hco/1/GRCh38#217836964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186814058-A-C

217836993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186814050-A-G

217837004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186814039-G-C

217837377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186813731-T-C

217837394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186813714-G-A

217837652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186813462-C-G

217837652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186813462-C-T

217837698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186813418-G-T

217837757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186813364-A-G

217837876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186813252-C-G

217837898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186813230-G-A

217838142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186810835-T-C

http://identifiers.org/hco/1/GRCh38#217838201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186810777-C-A

217838366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186810630-A-G

http://identifiers.org/hco/1/GRCh38#217838407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186810593-C-A

217838407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186810593-C-T

217838525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186810480-A-G

217838525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186810480-A-T

217838562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186810442-A-T

217838689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186810324-C-T

http://identifiers.org/hco/1/GRCh38#217838777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186810237-C-A

217838889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186810125-G-A

217839125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186809914-G-A

217839501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186809547-T-A

217839501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186809547-T-C

217839526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186809522-G-A

217839738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186809320-A-G

217842436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186808656-G-T

217842573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186808485-C-T

217842609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186808430-C-T

217842623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186808417-G-T

217842655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186808385-A-G

217842742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186808307-T-G

http://identifiers.org/hco/1/GRCh38#217842871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186808185-A-C

217842897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186808159-C-T

217843204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186807900-T-A

217843228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186807875-A-G

217843264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186807843-G-T

217843301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186807807-T-C

http://identifiers.org/hco/1/GRCh38#217843322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186807786-A-C

217843495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186807751-A-G

217843802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186807471-G-C

217843826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186807447-A-G

217844165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186807249-C-G

217844377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186807061-G-A

217844422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186807010-G-A

217844555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186806881-T-C

217844747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186806735-T-C

217844758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186806724-T-C

217845178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186806231-C-T

217845318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186806102-C-T

217846325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186804934-A-T

217846465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186804705-A-G

217846465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186804705-A-T

217846517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186804665-A-G

217846594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186804573-T-C

217846762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186804411-A-G

217846804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186804372-A-G

217846922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186804235-A-T

http://identifiers.org/hco/1/GRCh38#217847067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186803850-C-A

217847079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186803845-G-C

217847079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186803845-G-T

217847138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186803790-A-G

217847198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186803724-T-G

217847214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186803708-G-A

217847400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186803503-T-C

http://identifiers.org/hco/1/GRCh38#217848133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186803019-C-A

217848133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186803019-C-T

217850812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186792036-C-G

217851225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186791640-G-A

217851771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186791097-G-A

217851973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186790895-G-C

217852050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186790818-G-A

217852050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186790818-G-T

217852111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186790769-G-A

217852111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186790769-G-T

217852312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186790142-T-G

http://identifiers.org/hco/1/GRCh38#217852480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186789985-A-C

217852500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186789965-C-G

217852502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186789963-G-A

217852539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186789925-C-T

217852590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186789876-C-G

217852590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186789876-C-T

217852591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186789875-G-A

217852656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186789820-T-A

217853077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186789485-A-G

217853247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186789342-C-T

217853311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186789279-T-C

217853423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186788863-T-C

217853442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186788844-T-C

217853615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186788671-A-G

217854816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186787719-A-T

217855146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186787435-T-C

217855169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186787412-G-A

http://identifiers.org/hco/1/GRCh38#217855588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186787044-C-A

217857174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186785146-G-A

217857186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186785129-C-G

217857186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186785129-C-T

217857329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784989-T-C

217857407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784914-C-T

217857499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784822-T-C

217857552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784768-C-T

217857558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784763-C-T

217857576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784747-A-G

217857577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784746-C-T

217857651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784663-G-T

217857668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784646-T-C

217857918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784437-G-T

217857943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784419-A-T

217857944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186784418-G-A

217860173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186783231-G-C

217860235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186783174-A-G

http://identifiers.org/hco/1/GRCh38#217860686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186782673-C-A

217860686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186782673-C-G

217860737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186782619-A-G

217860835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186782564-T-C

217861033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186782334-G-A

217861098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186782289-T-C

217861241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186782162-A-G

217861253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186782155-A-G

217861703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186781803-A-G

217861752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186781756-T-C

217861815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186781709-A-T

217862308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186781304-C-T

217862312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186781300-A-G

217862365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186781256-T-C

217862380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186781241-T-C

217862539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186781089-G-A

http://identifiers.org/hco/1/GRCh38#217862594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186781017-A-C

217862621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780837-T-G

http://identifiers.org/hco/1/GRCh38#217862625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186780833-C-A

217862625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780833-C-T

217862632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780826-T-G

217862633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780825-T-C

217862633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780825-T-G

217862635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780822-T-C

217862637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780820-T-G

217862653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780804-G-A

217862653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780804-G-T

217862714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780738-A-G

http://identifiers.org/hco/1/GRCh38#217862732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186780721-C-A

217862735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780720-G-A

217862735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780720-G-T

217862739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780716-A-T

217862742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780713-T-C

http://identifiers.org/hco/1/GRCh38#217862769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186780689-C-A

217862792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 186780666-C-T

217862799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 186780659-T-A

http://identifiers.org/hco/1/GRCh38#217862888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186780565-A-C

217862888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780565-A-G

217862958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780501-A-G

http://identifiers.org/hco/1/GRCh38#217863110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186780364-A-C

217863110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186780364-A-T

217863609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186779984-G-C

217863882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186779703-C-T

217863910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186779677-G-A

217863964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186779623-G-A

217864175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186779402-A-G

217864265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186779322-T-C

217865707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186777908-G-A

217865742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186777884-T-A

217865743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186777883-A-G

217865810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186777816-G-A

http://identifiers.org/hco/1/GRCh38#217865842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186777786-C-A

217865842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186777786-C-T

217866048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186777594-C-T

217866274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186777370-G-A

http://identifiers.org/hco/1/GRCh38#217866491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186777324-C-A

217866491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 186777324-C-T

http://identifiers.org/hco/1/GRCh38#217866492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186777323-A-C

217866492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 186777323-A-G

217866540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 186777284-A-G

http://identifiers.org/hco/1/GRCh38#217866545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186777279-C-A

217866545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 186777279-C-T

217866750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 186777181-C-T

217867076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186776783-A-G

http://identifiers.org/hco/1/GRCh38#217867148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186776686-C-A

217867238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186776541-T-C

217867268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186776511-G-A

217867268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186776511-G-T

217867350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186776416-G-T

http://identifiers.org/hco/1/GRCh38#217867351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186776415-C-A

217867351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186776415-C-G

217867353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186776413-G-T

217867354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186776412-G-A

217867354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186776412-G-T

217867521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186775756-A-G

217867551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186775727-A-G

217867562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 186775716-C-G

217867607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3 prime UTR variant
orthologous variants: 186775669-G-A

217867607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3 prime UTR variant
orthologous variants: 186775669-G-T

http://identifiers.org/hco/1/GRCh38#217867608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186775668-A-C

http://identifiers.org/hco/1/GRCh38#217867623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186775650-C-A

http://identifiers.org/hco/1/GRCh38#217867780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#186775511-C-A

217867789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25184
most severe consequence: 3 prime UTR variant
orthologous variants: 186775501-T-C