120787608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3 prime UTR variant
orthologous variants: 21771670-C-T

120787685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3 prime UTR variant
orthologous variants: 21771754-A-G

120787883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3 prime UTR variant
orthologous variants: 21771938-G-T

http://identifiers.org/hco/7/GRCh38#120788027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21772085-A-C

120788027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3 prime UTR variant
orthologous variants: 21772085-A-G

120788133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3 prime UTR variant
orthologous variants: 21772192-G-T

120788295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3 prime UTR variant
orthologous variants: 21772352-T-A

120788458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21772508-A-G

120788471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21772517-C-T

120788475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21772521-G-T

120788644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 21772682-T-C

120790265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21778414-T-C

120790339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21778454-G-A

120790388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21778498-G-A

120790452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21778547-A-G

120791463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21779388-C-G

120791634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21779566-G-T

120791966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21779886-C-G

120792023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21779923-T-C

120792033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21779933-C-T

http://identifiers.org/hco/7/GRCh38#120792052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21779952-C-A

120792052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21779952-C-G

120792052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21779952-C-T

120792110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21780010-A-T

120792132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21780028-C-T

120792293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21780166-G-C

http://identifiers.org/hco/7/GRCh38#120792484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21780357-C-A

120792673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21780561-T-A

120792673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21780561-T-C

120793258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21781839-C-T

http://identifiers.org/hco/7/GRCh38#120793374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21781946-C-A

120793563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21782126-C-T

http://identifiers.org/hco/7/GRCh38#120793711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21782406-C-A

120793876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21782605-C-T

120795118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21783801-C-T

http://identifiers.org/hco/7/GRCh38#120795600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21784293-A-C

120795628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21784325-T-C

120795929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21784630-C-T

120796216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21784874-G-A

120796219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21784877-C-T

120796329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21784971-G-A

120797457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21786469-G-C

120797553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21786556-C-T

120797558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21786561-G-A

120797736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21786741-A-G

120797825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21786827-T-C

120797966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787200-T-C

120798061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787296-A-G

120798203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787411-T-G

120798211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787419-C-T

120798252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787469-C-T

120798257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787474-C-T

http://identifiers.org/hco/7/GRCh38#120798259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21787476-A-C

120798458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787667-T-C

http://identifiers.org/hco/7/GRCh38#120798466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21787675-C-A

120798466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787675-C-G

120798485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787688-C-T

120798486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787689-G-A

120798591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787794-T-A

120798599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787802-C-T

120798679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787871-G-A

120798775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21787945-C-G

http://identifiers.org/hco/7/GRCh38#120799035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21788187-C-A

http://identifiers.org/hco/7/GRCh38#120799251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21788375-A-C

120800080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21788624-G-T

120800143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21788680-G-C

120800190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21788733-G-A

120800322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21788833-C-T

120800357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21788851-T-A

120801568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21790062-C-G

http://identifiers.org/hco/7/GRCh38#120801853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21790309-C-A

120802198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21790690-C-T

http://identifiers.org/hco/7/GRCh38#120802262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21790755-A-C

120802409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21790888-A-G

120802515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21790991-T-A

120802515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21790991-T-C

120802883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21791314-T-A

120802911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21791344-A-G

120803260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21791690-T-G

120803291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21791721-T-A

http://identifiers.org/hco/7/GRCh38#120803789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21792147-A-C

120803866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792215-G-A

120803866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792215-G-T

120803985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792332-C-T

120804010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792357-C-T

120804032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792376-A-G

120804033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792377-T-C

120804090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792422-T-C

http://identifiers.org/hco/7/GRCh38#120804433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21793213-C-A

120804444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793224-A-G

120804498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793275-C-T

http://identifiers.org/hco/7/GRCh38#120804866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21793637-C-A

120805844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21794934-G-A

120805950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795029-G-A

120806124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795182-T-C

120806277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795293-A-G

120806346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21795400-C-T

120806419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795462-A-T

120806425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795468-G-C

120806425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795468-G-T

120806435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795475-A-T

120806449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795488-T-G

120806479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795518-A-G

120806507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795535-G-T

120806512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795540-C-T

120806537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795565-A-G

120806538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795566-T-C

http://identifiers.org/hco/7/GRCh38#120806786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21795817-C-A

120806799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795830-T-G

http://identifiers.org/hco/7/GRCh38#120806802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21795833-C-A

120806802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795833-C-G

120806802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795833-C-T

120807177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796226-G-A

120807361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796395-C-T

120807580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796620-C-T

120807791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796848-A-G

120807832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796879-A-G

120807874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796919-T-C

120807919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796945-C-T

120807927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796953-A-G

120807995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797018-T-C

120807997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797020-T-A

120807997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797020-T-C

120808131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797168-T-C

120808321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797343-A-G

120808557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797817-G-C

120808607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797865-T-C

120808607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797865-T-G

120808657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797908-A-G

120808684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797934-G-A

120808725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797974-T-C

http://identifiers.org/hco/7/GRCh38#120808816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21798055-C-A

120808897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21798134-T-C

120808944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21798180-G-T

120809022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21798272-G-A

120809027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21798277-G-A

120809037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21798354-C-T

120809038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21798355-G-A

120809667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21798986-A-G

http://identifiers.org/hco/7/GRCh38#120809713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21799029-C-A

120809761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799057-C-G

120809761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799057-C-T

120809923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799209-T-A

120810025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799295-G-A

http://identifiers.org/hco/7/GRCh38#120810109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21799373-A-C

120810350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799765-A-G

120810350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799765-A-T

120810367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799782-G-A

120810367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799782-G-T

120810401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799815-C-T

120810416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799830-T-G

120810420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799834-C-T

120810584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799999-G-A

120810584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21799999-G-T

http://identifiers.org/hco/7/GRCh38#120810589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21800004-A-C

120810589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21800004-A-T

http://identifiers.org/hco/7/GRCh38#120810609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21800015-C-A

120810609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21800015-C-T

120810643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21800071-C-T

http://identifiers.org/hco/7/GRCh38#120810646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21800074-A-C

120810667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21800095-T-A

120810667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21800095-T-C

120810667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21800095-T-G

120812635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21803456-C-T

120813791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21804774-C-T

120813857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21804836-A-G

120813864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21804843-G-T

http://identifiers.org/hco/7/GRCh38#120813933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21804921-C-A

http://identifiers.org/hco/7/GRCh38#120814067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21805047-C-A

120814067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21805047-C-T

http://identifiers.org/hco/7/GRCh38#120814081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21805064-C-A

120814081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21805064-C-T

120814093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21805076-A-G

120814094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21805077-G-C

120814094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21805077-G-T

http://identifiers.org/hco/7/GRCh38#120814115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21805098-C-A

120814140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21805120-A-T

120814144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21805124-T-C

http://identifiers.org/hco/7/GRCh38#120814195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21805172-C-A

120814249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant
orthologous variants: 21805226-T-C

120814435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21805349-T-C

120814459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21805369-G-A

120814896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21805776-C-T

120815126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21805972-G-T

120815185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21806030-G-A

http://identifiers.org/hco/7/GRCh38#120815744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#21806253-A-C

120815744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21806253-A-G

120815759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21806268-A-G

120815792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21806301-A-G

http://identifiers.org/hco/7/GRCh38#120815808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21806317-A-C

120815808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 21806317-A-G

120815860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21806353-A-G

120815891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21806383-A-G

120816220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21806696-G-A

120816288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21806767-T-C

120816389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21806840-T-A

120816389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21806840-T-G

120816476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21806895-G-A

120816498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21806914-T-C

120816622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21807013-G-A

120816622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21807013-G-C

120816748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21807140-A-G

120816828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21807213-G-A

120817068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21807445-T-G

120817173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21807483-A-G

120817174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21807484-G-C

120817443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21807504-C-G

120817588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21807646-T-C

120818078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21808110-T-C

120818172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21808190-T-C

120818217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21808227-C-T

120818399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21808389-G-C

120818591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809247-A-T

http://identifiers.org/hco/7/GRCh38#120818629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21809285-C-A

120818733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809382-G-A

120818779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809436-T-A

120818900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809556-G-T

http://identifiers.org/hco/7/GRCh38#120818912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21809568-C-A

120818912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809568-C-G

120818912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809568-C-T

120818924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809580-T-C

http://identifiers.org/hco/7/GRCh38#120819065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21809711-C-A

120819070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809716-G-C

120819143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809768-T-C

120819143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809768-T-G

120819202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21809826-T-C

http://identifiers.org/hco/7/GRCh38#120819263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21809894-C-A

120819775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21816546-C-T

120820041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21816803-G-C

120820559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21817005-C-G

120820722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21817159-G-T

120820729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21817166-C-T

120820831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21817280-T-G

120820988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21817437-G-A

120821128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21817585-T-C

120821557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21817820-T-C

120821640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21817895-G-A

120821967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21818180-T-C

120821985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21818197-G-A

120822097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21818307-T-G

120822190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21818435-C-T

120822204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21818449-G-A

120822615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21818837-G-A

120822618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21818840-G-A

120823053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21819186-A-G

120823458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21819522-A-G

120823557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21819621-T-C

120823662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21819713-C-G

120823692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21819749-T-C

120823926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21819979-T-C

120824038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21820129-C-G

120824694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21821977-C-T

120824966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21822215-C-T

120825024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21822269-C-T

http://identifiers.org/hco/7/GRCh38#120825352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21822600-A-C

120825372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21822620-T-C

120826566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21823839-G-T

120826570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21823843-G-A

120826650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21823919-A-T

http://identifiers.org/hco/7/GRCh38#120827324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21824333-A-C

120827329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21824338-G-T

120827356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21824365-T-C

http://identifiers.org/hco/7/GRCh38#120827399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21824410-C-A

120827399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21824410-C-T

120827719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21825915-A-G

http://identifiers.org/hco/7/GRCh38#120827940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21826224-A-C

120827979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21826262-T-C

120828023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21826306-T-A

120828023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21826306-T-C

120828023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21826306-T-G

http://identifiers.org/hco/7/GRCh38#120828206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21826416-A-C

120828286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21826500-A-G

120828286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21826500-A-T

120828556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827069-C-T

120828635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827151-T-C

120828640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827156-G-T

120828751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827233-A-T

120828801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827284-C-G

120828808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827291-C-G

120828888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827372-A-T

120829179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827638-T-C

http://identifiers.org/hco/7/GRCh38#120829211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21827674-A-C

120829219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827682-T-C

120829415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827828-C-G

120829415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21827828-C-T

120829595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828018-A-G

120829702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828109-T-A

120829702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828109-T-C

120829708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828115-G-A

120829708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828115-G-T

120829712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828119-G-C

120829712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828119-G-T

120829715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828122-A-G

120829751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828160-A-T

120829752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828161-G-A

120829757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828166-C-T

120829796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828184-T-C

120829954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828358-C-T

http://identifiers.org/hco/7/GRCh38#120830038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21828444-A-C

http://identifiers.org/hco/7/GRCh38#120832287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21828594-C-A

120832289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828596-A-G

120832494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828811-C-G

120832494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21828811-C-T

120832782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21829067-G-C

120832868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21829134-A-G

120832874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21829140-C-T

120832931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21829186-G-A

120833287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21829538-C-T

120833343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21829585-T-C

120833380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21829631-C-T

120833582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830002-A-G

http://identifiers.org/hco/7/GRCh38#120833766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21830175-C-A

120833767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830176-A-G

120834011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830419-T-C

120834103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830758-G-T

120834137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830801-C-T

120834327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21831057-G-A

120834481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21831230-G-T

120834534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21831285-T-C

http://identifiers.org/hco/7/GRCh38#120834687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21831450-A-C

120834794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21831559-A-T

120834921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21831677-G-A

120835082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21831901-C-T

120835148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21831954-G-C

120835239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21832007-G-A

120835498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21832286-A-G

120835809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21832551-G-A

120835833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21832575-T-C

120836001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21832741-A-G

120836113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21832933-G-A

120836113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21832933-G-C

120836547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21833364-C-T

http://identifiers.org/hco/7/GRCh38#120836608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21833428-A-C

120836749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21833609-T-C

120836754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21833614-T-G

120836972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21833792-A-G

120837033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21833853-G-A

120837060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21833890-A-G

120837152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21833979-G-A

120837609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21834301-G-A

120837651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21834347-A-G

120837771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21834463-T-C

120837860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21834553-T-C

120837875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21834568-A-G

120837883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21834576-T-A

120837883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21834576-T-C

120838047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21834703-C-T

120838106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21834766-T-C

http://identifiers.org/hco/7/GRCh38#120838148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21834799-A-C

http://identifiers.org/hco/7/GRCh38#120838255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21834902-A-C

http://identifiers.org/hco/7/GRCh38#120838296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#21834960-C-A

120838391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21835057-C-T

120838556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21835163-G-A

120838587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21835192-A-G

120838644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21835253-G-T

120838922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21835532-G-T

120838976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21835603-G-A

http://identifiers.org/hco/7/GRCh38#120839059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21835683-A-C

120839059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21835683-A-T

120839073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21835690-T-C

120839095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21835713-C-T

120839229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21835803-G-A

http://identifiers.org/hco/7/GRCh38#120839853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21836220-C-A

http://identifiers.org/hco/7/GRCh38#120839877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21836244-C-A

120839946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836315-G-A

120839946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836315-G-T

120839965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836334-G-A

120839965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836334-G-T

http://identifiers.org/hco/7/GRCh38#120839966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21836335-C-A

120839966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836335-C-G

120839982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836359-T-C

120840150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836536-G-A

120840150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836536-G-T

120840204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836594-A-G

120840224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836615-G-A

120840224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836615-G-T

120840497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836867-A-G

120840676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21836986-T-C

120840874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21837201-T-C

120841077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21837380-C-G

120841117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21837419-G-A

120841122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21837426-T-C

http://identifiers.org/hco/7/GRCh38#120841383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21837786-A-C

120841516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21837923-G-A

120841596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21837991-T-C

120841666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21838069-T-C

120841810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21838164-T-A

120841826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21838180-G-A

120841968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21838484-C-T

120842151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21838638-G-A

120842288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21838760-C-G

120846627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21839247-G-A

120846642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21839254-C-T

120846750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21839357-G-A

120846762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21839369-T-C

120847192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21839782-T-A

http://identifiers.org/hco/7/GRCh38#120847276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21839835-C-A

120847276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21839835-C-T

120847308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21839867-C-T

120847407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21839953-A-G

120847442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21839975-T-C

120847472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21840001-T-A

120847659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21840197-G-A

120847659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21840197-G-T

120848126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21840613-T-C

http://identifiers.org/hco/7/GRCh38#120848150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21840637-C-A

120848401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21840836-A-G

120848506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21840913-T-A

120848506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21840913-T-G

120848580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21840975-A-G

120848584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21840979-T-G

120848689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21841084-C-T

120848721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21841116-T-C

120848732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21841127-C-T

120848914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21841249-C-T

120849235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21845685-A-G

120849340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21845795-G-A

120849978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21846237-G-A

120850170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21846417-T-C

120850188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21846435-A-G

120850329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21846560-G-C

120850366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21846589-C-T

120850488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21846686-T-G

120850498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21846696-C-T

120851302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21847149-A-G

120851495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21847274-C-T

120851698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21847448-T-C

120851709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21847459-G-C

120852270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21847990-C-G

http://identifiers.org/hco/7/GRCh38#120852366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#21848080-C-A

120852442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21848148-C-T

120852557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21848345-T-C

120852562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21848353-C-G

120852562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21848353-C-T

120852619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21848425-C-T

120852667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21848472-G-A

120852671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21848476-A-G

120853108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21848886-A-T

120853113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21848891-G-A

120853113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21848891-G-T

120854991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21849386-T-A

120855383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21849742-T-C

120855387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21849746-A-G

120855405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21849764-G-A

120855668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21850010-T-G

120855743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21850083-T-C

120856421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21850739-A-G

120856438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21850756-T-C

120856622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21850938-T-C

120856638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21850954-G-A

120856656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21850971-A-G

120856674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21850989-G-C

120856674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron variant
orthologous variants: 21850989-G-T

120856827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 21851138-C-T

120856842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron_variant, undefined
orthologous variants: 21851153-G-T

120856855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron_variant, undefined
orthologous variants: 21851167-G-A

120856855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron_variant, undefined
orthologous variants: 21851167-G-C

120856855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron_variant, undefined
orthologous variants: 21851167-G-T

120856893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron_variant, undefined
orthologous variants: 21851186-G-A

120856893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron_variant, undefined
orthologous variants: 21851186-G-T

120856979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron_variant, undefined
orthologous variants: 21851265-T-C

120857068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21851354-G-A

120857068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21851354-G-C

http://identifiers.org/hco/7/GRCh38#120857074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#21851360-A-C

http://identifiers.org/hco/7/GRCh38#120857096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#21851376-C-A

120857096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21851376-C-T

http://identifiers.org/hco/7/GRCh38#120857135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#21851404-A-C

120857135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21851404-A-G

http://identifiers.org/hco/7/GRCh38#120857177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#21851428-C-A

http://identifiers.org/hco/7/GRCh38#120857233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#21851481-C-A

120857233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 21851481-C-G

120857233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 21851481-C-T

http://identifiers.org/hco/7/GRCh38#120857256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#21851507-C-A

120857256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21851507-C-T

120857265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21851516-C-T

120857660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron_variant, undefined
orthologous variants: 21851903-C-T

120857869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21852048-C-T

120857892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21852071-C-T

120857999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21852202-G-A

120857999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21852202-G-C

120857999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21852202-G-T

120858017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21852220-T-A

120858017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21852220-T-C

120858017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21852220-T-G

http://identifiers.org/hco/7/GRCh38#120858044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#21852247-C-A

http://identifiers.org/hco/7/GRCh38#120858155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#21852357-C-A

120858253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21852454-G-T

120858354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21641
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 21852553-G-T