15111542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 5 prime UTR variant
orthologous variants: 114341899-G-A

15111593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114341947-T-C

15111793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114342478-C-G

15112186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114342824-G-A

http://identifiers.org/hco/11/GRCh38#15112372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114343019-C-A

http://identifiers.org/hco/11/GRCh38#15112482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114343128-C-A

15112482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, missense_variant
orthologous variants: 114343128-C-T

15112627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343538-T-C

15112627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343538-T-G

15112632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343543-G-A

15112632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343543-G-T

http://identifiers.org/hco/11/GRCh38#15112644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114343555-A-C

15112644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343555-A-G

15112644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343555-A-T

15112727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343640-G-A

15112727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343640-G-C

15112809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343722-T-C

http://identifiers.org/hco/11/GRCh38#15113486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114343929-C-A

15113526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343967-C-T

15113554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114343999-C-T

15113759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114344198-T-C

15113928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114344335-C-T

15114042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114344376-G-C

15114099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114344428-A-G

15114266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114344578-T-A

15114266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114344578-T-C

15114266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114344578-T-G

15114271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114344583-T-C

15114271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114344583-T-G

15114586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114344859-G-A

15114794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345055-G-A

http://identifiers.org/hco/11/GRCh38#15114799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114345060-C-A

15114799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345060-C-T

15114802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345063-G-A

15114802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345063-G-C

15114802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345063-G-T

15114807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345068-T-C

15114811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345075-G-T

15114837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345087-C-G

15114837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345087-C-T

http://identifiers.org/hco/11/GRCh38#15114852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114345095-C-A

15114852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345095-C-T

15114912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345139-G-A

http://identifiers.org/hco/11/GRCh38#15114983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114345220-C-A

15114983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114345220-C-T

15114991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114345227-T-C

15115041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345291-G-A

15115041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345291-G-T

15115055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345305-T-C

15115114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345347-A-G

15115317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345495-G-C

15115397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345558-G-A

15115431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345595-G-C

15115577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345759-C-G

15115688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114345837-G-C

15116023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114346088-G-A

15116546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114346258-G-A

15116618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114346338-T-A

15116627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114346347-C-G

15118180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114347263-G-A

15118777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114347821-G-A

15118985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114347992-G-A

15118986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114347993-T-A

15119532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114348513-G-A

15119666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114348646-C-T

15119898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114348871-G-T

15120004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114348971-C-G

15120047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114349014-G-A

15120089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114349040-T-C

15120293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114349214-G-A

15120353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114349269-A-G

15121116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114350130-G-A

15121140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114350153-A-G

15121208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114350351-G-C

15121484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114350734-C-T

15121706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114350939-G-A

15121706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114350939-G-T

15122160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114351375-C-G

http://identifiers.org/hco/11/GRCh38#15122862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114352033-C-A

15122862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352033-C-T

15122868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352039-T-A

15122868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352039-T-C

15122972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352123-T-A

15122972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352123-T-C

http://identifiers.org/hco/11/GRCh38#15123103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114352146-C-A

15123109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352152-C-T

15123358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352338-T-C

15123461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352448-T-C

15123461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352448-T-G

15123495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352482-G-A

15123686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352626-A-G

15124031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352938-T-C

15124036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352943-C-G

15124036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114352943-C-T

http://identifiers.org/hco/11/GRCh38#15124087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114353002-C-A

http://identifiers.org/hco/11/GRCh38#15124119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114353034-C-A

15124150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353066-C-T

15124241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353151-T-C

15124254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353163-G-A

15124264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353167-C-T

15124511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353353-G-T

15124657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353470-C-G

15124664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353477-T-C

http://identifiers.org/hco/11/GRCh38#15124764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114353571-C-A

15124764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353571-C-T

15124775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353582-T-A

15124847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353652-G-A

15124863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353668-C-G

15124870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353675-T-A

15124874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353679-T-C

15124981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353770-T-C

15125010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353802-G-A

15125031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114353822-A-G

15125273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114354043-G-A

15125273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114354043-G-C

15125379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114354125-T-C

15125415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114354157-A-G

15125424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114354166-A-G

http://identifiers.org/hco/11/GRCh38#15125431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114354173-A-C

http://identifiers.org/hco/11/GRCh38#15125477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114354224-A-C

15125477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114354224-A-G

15125877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114354722-G-A

http://identifiers.org/hco/11/GRCh38#15126006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114354844-A-C

15126121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114354953-G-A

15126348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114355156-A-G

15126349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114355157-G-T

15126387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114355206-C-T

15127165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114356334-A-G

15128936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114356543-T-C

http://identifiers.org/hco/11/GRCh38#15129400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114356949-C-A

15129673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114357226-C-T

15129781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114357349-A-G

15129985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114357543-G-A

15130076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114357586-A-G

15130355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114357833-G-T

15130560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114357989-C-T

15132938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114358595-T-C

15133008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114358661-T-C

15133101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114358708-C-G

15133152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114358758-C-T

http://identifiers.org/hco/11/GRCh38#15133351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114358891-A-C

15133610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114359157-C-T

15133623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114359170-T-C

15133826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114359365-T-C

15133975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114359913-A-G

15134010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114359949-C-G

15134382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114360295-T-C

15135429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -A-G

15135525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -G-C

15135594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -T-C

15135872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -T-G

15135881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -T-C

15135883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -T-A

15135883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -T-C

http://identifiers.org/hco/11/GRCh38#15135893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -C-A

15135893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -C-T

http://identifiers.org/hco/11/GRCh38#15135922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -C-A

15135922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: -C-T

15138623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114361436-G-A

15138623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114361436-G-C

15138663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114361466-T-C

http://identifiers.org/hco/11/GRCh38#15138980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114361743-A-C

15139225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114361980-C-T

15139802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114362490-G-A

15139822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114362510-G-A

15139828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114362516-C-T

15140172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114363286-C-T

15141035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114364256-T-C

15141275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114364478-G-C

15141307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114364510-T-C

15141308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114364511-G-A

15141327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114364530-T-C

15141501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114364633-C-T

15141689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114364821-A-T

15141848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114364968-A-G

15141951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365055-G-C

15141961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365065-C-T

15144143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365156-T-C

http://identifiers.org/hco/11/GRCh38#15144227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114365225-C-A

15144303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365281-C-G

15144387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365364-T-G

15144662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365592-G-A

15144790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365720-G-C

15144847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365777-G-A

15144853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365783-G-A

15144894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365814-A-G

15144919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114365835-T-C

http://identifiers.org/hco/11/GRCh38#15148144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114367394-C-A

15148161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114367411-G-A

15148218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114367470-T-A

15148218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114367470-T-C

15148821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114367871-C-G

15148821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114367871-C-T

15149026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114368072-A-G

15149026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114368072-A-T

15149080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114368124-G-A

15149080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114368124-G-C

15149080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114368124-G-T

15149090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114368134-T-C

http://identifiers.org/hco/11/GRCh38#15149135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114368172-C-A

15149135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 114368172-C-T

15149211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: missense variant
orthologous variants: 114368248-G-A

15149709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114368396-G-A

15149819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114368501-G-A

15150211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114370995-A-G

15150238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114371013-A-G

15152778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114372630-A-G

15152826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114372677-C-T

15152914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114372752-G-C

15153249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114373044-C-T

15153508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114373287-G-A

15153738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114373514-T-C

15153738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114373514-T-G

15154129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114373811-T-G

15154646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114374776-A-T

15154789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114374905-G-A

15154801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114374917-C-G

15155100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114375192-C-T

15155175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114375266-T-C

http://identifiers.org/hco/11/GRCh38#15155965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114376325-C-A

http://identifiers.org/hco/11/GRCh38#15156118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114376464-C-A

15156121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114376467-G-T

15156328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114376657-G-A

15156330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114376659-A-G

15156382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114376710-T-C

15156536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114376837-T-C

15156625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114376902-C-T

15156671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114376951-G-T

15156719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114376998-A-G

15156846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114377110-A-G

15156869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114377132-C-T

15156915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114377168-T-G

15156938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114377191-A-G

15157500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114377737-G-A

15157691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114377927-C-T

15157734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114377969-C-T

15157755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114377991-G-A

15157776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378012-T-A

15157776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378012-T-C

15157776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378012-T-G

15157864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378111-G-A

15157868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378116-T-C

15157890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378138-C-T

15157975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378227-C-T

15158345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378567-C-T

15158434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378643-G-A

15158499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378709-G-T

http://identifiers.org/hco/11/GRCh38#15158673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114378878-C-A

15158673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378878-C-T

15158675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378880-A-G

15158693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114378898-A-G

15158904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114379090-C-T

15159226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114379373-C-T

15159238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114379385-G-A

15159241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114379388-G-A

15159276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114379422-G-T

15159472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114379607-T-C

15159484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114379619-C-T

http://identifiers.org/hco/11/GRCh38#15159524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114379659-C-A

15159524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114379659-C-T

15159540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114379683-A-G

http://identifiers.org/hco/11/GRCh38#15159610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114379755-C-A

15159998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114380136-G-A

15159998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114380136-G-T

http://identifiers.org/hco/11/GRCh38#15160598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114381698-C-A

15160789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114381888-C-T

15161025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114382429-T-A

15161132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114382535-G-A

15161173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114382559-G-A

15161185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114382571-A-G

15161512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114382814-G-A

15161758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114383025-C-T

15161912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114383183-G-A

15162148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114383541-G-A

15162279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114383656-C-T

http://identifiers.org/hco/11/GRCh38#15162401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114383761-C-A

15162488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114383848-C-T

15162557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114383910-T-C

15162629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114383977-G-A

15162629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114383977-G-T

15163031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114384332-C-T

15169276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114385890-G-T

15169373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114385954-C-T

15169430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114386010-A-G

15170446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114387651-C-T

15170494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114387697-A-G

15170615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114387811-A-G

15170643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114387832-G-C

http://identifiers.org/hco/11/GRCh38#15171071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114388281-C-A

15171074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114388284-G-A

15174800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114389477-A-T

15175061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114389642-T-A

15175061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114389642-T-C

15175143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114389726-G-C

15175143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114389726-G-T

15175240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114389837-G-A

15175496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114389961-C-T

15175640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114390086-A-G

15175640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114390086-A-T

15175658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114390104-G-T

http://identifiers.org/hco/11/GRCh38#15175762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114390208-C-A

15175762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: synonymous variant
orthologous variants: 114390208-C-T

15175986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: missense variant
orthologous variants: 114390432-C-T

15176111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114390556-G-A

15176111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114390556-G-T

http://identifiers.org/hco/11/GRCh38#15176204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114390633-C-A

15176204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114390633-C-T

15176670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114391100-G-A

15176861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114391266-C-T

http://identifiers.org/hco/11/GRCh38#15176991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114391390-C-A

15176991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114391390-C-T

15177006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114391405-A-G

15177032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114391413-G-A

15177032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114391413-G-T

15177059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114391443-G-A

15177113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 114391483-T-G

15177211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114391577-G-A

15177354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114391872-G-C

15177637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114392127-C-T

15177638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114392128-A-T

15177669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114392159-T-C

http://identifiers.org/hco/11/GRCh38#15177804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114392298-A-C

http://identifiers.org/hco/11/GRCh38#15177826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114392318-C-A

15178000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114392881-C-T

15178268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393150-T-A

15178459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393340-C-T

15178507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393384-G-A

http://identifiers.org/hco/11/GRCh38#15178527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114393404-C-A

15178527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393404-C-G

15178527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393404-C-T

15178760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393575-T-C

15178765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393580-A-G

15178884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393599-T-C

15178953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393667-G-T

15179033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393736-G-T

15179154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393858-T-C

http://identifiers.org/hco/11/GRCh38#15179155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114393859-C-A

15179235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114393928-T-A

15179615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114394287-G-A

15179769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114394482-C-G

15182039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114396485-A-G

15185316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114397833-A-G

15185328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114397845-G-A

15185353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114397884-A-G

15185361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114397892-A-G

15185825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398352-G-A

15186002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398445-G-T

15186023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398466-G-T

15186224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398620-T-C

15186263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398659-G-T

15186277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398673-C-T

http://identifiers.org/hco/11/GRCh38#15186279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114398675-C-A

15186279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398675-C-G

15186287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398683-C-T

15186343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398725-C-T

15186397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398756-G-A

15186397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398756-G-T

15186531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398914-C-G

15186598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114398979-T-C

15186725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114399100-T-C

15186779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114399153-T-G

15187142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114399466-C-G

15187279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114399596-T-A

15187330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114399642-C-T

15187391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114399697-C-T

15187442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114399734-T-C

15187485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114399775-G-T

15187548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114399832-C-T

15187810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114400115-C-T

15187816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114400121-A-G

15187830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114400135-G-C

15187861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114400161-T-C

15187913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114400231-G-A

15187994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114400301-G-A

15188433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114401089-A-G

15188476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114401138-A-G

15189737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114402873-A-G

15190211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403275-G-A

15190211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403275-G-C

15190588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403595-G-A

15190600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403609-A-G

15190652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403665-G-A

15190652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403665-G-T

15190670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403684-A-G

http://identifiers.org/hco/11/GRCh38#15190678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114403693-C-A

15190678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403693-C-G

15190817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403830-G-A

15195449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114404144-C-T

15195644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114404274-C-T

15195808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114404422-A-G

http://identifiers.org/hco/11/GRCh38#15195947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114404542-C-A

15196024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114404605-T-C

15196192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114404757-A-G

15196638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114405172-C-G

15196638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114405172-C-T

http://identifiers.org/hco/11/GRCh38#15196690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114405268-A-C

15197133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114406213-G-A

15197482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114406454-C-T

http://identifiers.org/hco/11/GRCh38#15197712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114406660-C-A

15197971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114406895-C-T

15198073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114406995-C-T

http://identifiers.org/hco/11/GRCh38#15198091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114407014-C-A

15198091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114407014-C-T

15198104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114407027-C-T

15198142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114407065-T-C

15198142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114407065-T-G

http://identifiers.org/hco/11/GRCh38#15198293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114407207-C-A

15198417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114407325-G-A

15198513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114408868-G-A

15198523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114408878-G-T

15198526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114408881-C-T

15198630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114408966-A-G

15198651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114408987-C-G

15198836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409147-A-T

15199020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409321-G-C

15199242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409494-T-C

15199361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409607-T-C

15199418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409664-G-A

15199418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409664-G-C

15199418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409664-G-T

15199483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409720-C-T

15199700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409933-C-T

15199871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410095-G-C

http://identifiers.org/hco/11/GRCh38#15200195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114410361-A-C

15200195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410361-A-T

15200364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410512-G-A

15200364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410512-G-T

15200371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410516-T-C

15200572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410668-G-A

15200617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410701-G-A

http://identifiers.org/hco/11/GRCh38#15200685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114410734-A-C

15200685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410734-A-T

15200725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410743-C-G

15200725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410743-C-T

15200739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410757-G-T

15200771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410789-G-T

15200877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114410891-C-G

15200892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114410906-G-A

15200892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114410906-G-T

http://identifiers.org/hco/11/GRCh38#15201011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114411001-C-A

15201011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114411001-C-T

15201024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114411013-A-G

http://identifiers.org/hco/11/GRCh38#15201061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114411050-C-A

15201093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114411083-T-A

15201093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114411083-T-C

15201095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114411085-G-A

15201200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114411890-G-A

15201443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412132-T-C

15201448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412165-G-T

15201837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412683-G-A

15201839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412685-G-A

15201905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412725-A-G

http://identifiers.org/hco/11/GRCh38#15201906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114412726-A-C

15201981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412796-T-C

15202300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413076-T-G

15202686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413409-G-A

15202703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413426-G-A

15202854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413563-C-T

15202857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413566-A-G

15203116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413807-G-A

15203232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413913-G-A

15203291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413954-C-T

15205979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114414565-C-T

http://identifiers.org/hco/11/GRCh38#15206930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114415333-A-C

15206953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114415357-C-T

15206960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114415364-T-C

15206982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114415386-G-T

http://identifiers.org/hco/11/GRCh38#15207232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114415602-A-C

15207499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114415862-C-T

15207691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114415993-G-A

15207913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114416173-G-A

15207923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114416181-C-T

15208074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114416370-C-T

15208205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114416476-G-A

15208324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114416573-G-A

15208668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114416851-C-T

15208714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114416898-C-T

15208715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114416899-A-G

15208894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114417050-T-A

15210089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114417959-C-T

15210290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418122-C-T

15210307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418139-A-G

15210414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418244-G-T

15210429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418246-G-T

15210484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418295-T-C

15210686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418466-G-A

15210709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418483-G-A

15210709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418483-G-T

15210843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418629-G-A

15211051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418764-A-T

15211084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114418789-A-G

http://identifiers.org/hco/11/GRCh38#15211185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114418893-C-A

15211355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114419066-T-G

http://identifiers.org/hco/11/GRCh38#15211584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114419308-C-A

15211584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114419308-C-T

http://identifiers.org/hco/11/GRCh38#15212665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114420199-A-C

15212721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420244-C-T

15212737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420260-A-G

15212763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420283-C-T

15212954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420482-A-G

15212954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420482-A-T

15213051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420528-G-A

15213081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420559-A-G

15213355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420831-T-C

15213355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420831-T-G

15213477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420960-T-A

15213914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114421364-T-A

15213971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114421425-G-A

http://identifiers.org/hco/11/GRCh38#15214002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114421451-C-A

15214002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114421451-C-T

http://identifiers.org/hco/11/GRCh38#15214285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114421800-C-A

15214285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114421800-C-T

15214358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114421902-G-A

15214368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114421912-G-A

15214521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114422059-T-G

15215082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114422220-G-A

15215082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114422220-G-T

15215413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114422514-G-A

15215811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114422870-C-G

15215815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114422874-G-A

15215948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114422978-T-G

15216017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114423048-G-A

15216305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114423326-G-A

15216483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114423416-T-C

15216792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114423784-G-T

15217904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114424828-G-A

15217960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114424882-G-A

15217960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114424882-G-T

15218004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114424921-C-G

15218174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114425081-T-C

15218184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114425091-A-G

http://identifiers.org/hco/11/GRCh38#15218353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114425255-C-A

15218512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114425404-C-T

15218518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114425410-G-A

15218599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114425618-G-T

15218626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114425657-G-T

15218656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114425687-G-T

15218807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114425828-C-G

http://identifiers.org/hco/11/GRCh38#15218943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114425934-C-A

15218959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114425950-A-G

15219090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114426064-T-C

15219090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114426064-T-G

15219199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114426160-A-G

15219237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114426192-T-G

15219252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114426207-G-A

15219428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114426372-G-A

15219812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114426733-C-T

15219991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114426901-A-G

15220355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114427252-A-G

http://identifiers.org/hco/11/GRCh38#15220856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114427695-A-C

15220856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114427695-A-G

15221166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428002-C-T

15221345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428156-G-T

15221351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428161-G-T

15221389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428177-G-A

15221389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428177-G-T

15221407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428195-G-C

http://identifiers.org/hco/11/GRCh38#15221537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114428329-C-A

15221537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114428329-C-G

15221537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114428329-C-T

15221668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428462-G-A

15221679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428473-G-A

15221679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428473-G-C

15221687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428481-G-A

15221687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428481-G-T

15221788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428571-T-G

15221822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428604-G-A

15221901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428674-T-A

15222133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428872-C-T

15222205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428943-G-A

15222205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428943-G-C

15222446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429096-A-G

15222565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429218-C-T

15222568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429221-C-T

15222678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429331-C-T

15222711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429365-A-G

15222872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429522-G-A

15222889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429539-C-T

15223146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429758-T-C

15223202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114431787-T-C

15223536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114432116-G-A

15223598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114432178-G-A

15224287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114432766-G-C

15224643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433045-C-T

15224800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433169-T-C

15225441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433783-G-A

15225463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433806-T-C

15225536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433880-G-A

15225536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433880-G-C

15225536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433880-G-T

15225551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433895-T-C

15225571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433915-G-A

15225571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433915-G-C

http://identifiers.org/hco/11/GRCh38#15225584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114433928-C-A

15225584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433928-C-G

http://identifiers.org/hco/11/GRCh38#15225588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114433932-A-C

15225588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433932-A-G

15225589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433933-T-G

15225634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433972-T-C

15225685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114434023-C-T

http://identifiers.org/hco/11/GRCh38#15225762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114434100-C-A

15225836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114434174-G-A

15225836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114434174-G-C

15225836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114434174-G-T

15227640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114434250-A-G

15227687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114434304-G-T

15227729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114434340-A-G

15227888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114434545-C-T

15228054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114434687-G-C

15228180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114434777-C-T

15228258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114434853-C-T

15228288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114434879-T-C

15228375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114434972-G-A

15228448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114435038-C-T

15229053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114435715-G-A

15229382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114435993-T-C

15229382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114435993-T-G

15229472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114436079-G-C

15229590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114436181-G-T

15229648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114436240-A-G

15229742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114436330-T-A

15232051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114437332-C-G

15232051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114437332-C-T

15232598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114438106-T-G

15233307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114439270-C-T

15233421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114439385-C-T

15233422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114439386-T-G

http://identifiers.org/hco/11/GRCh38#15233939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114439865-C-A

15233939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114439865-C-G

15233939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114439865-C-T

15234191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114440046-G-A

15234232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114440090-G-A

15234552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114440369-G-A

15234785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114440600-C-T

15234887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114440718-G-A

15234947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114440778-C-T

http://identifiers.org/hco/11/GRCh38#15234960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114440791-C-A

15234996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114440834-G-A

http://identifiers.org/hco/11/GRCh38#15235012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114440854-C-A

http://identifiers.org/hco/11/GRCh38#15235118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114440914-C-A

15235118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114440914-C-T

15235156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114440942-G-T

15235194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114440980-A-G

http://identifiers.org/hco/11/GRCh38#15235298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114441066-C-A

15235298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114441066-C-T

15235480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114441241-G-A

15235480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114441241-G-T

15235607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114441363-G-T

15235672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114441428-T-C

15235729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114441467-T-C

http://identifiers.org/hco/11/GRCh38#15235747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114441486-C-A

15235798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114441524-G-A

15235798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114441524-G-T

15236043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114441567-G-A

15236300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114441763-G-A

15236743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114442105-G-A

15236761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114442123-G-A

15237004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114442352-G-A

15237024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114442372-G-A

15237481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114442831-C-G

15237575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114442904-G-A

15237610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114442938-T-C

15237743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443071-C-T

15237766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443089-G-A

15237791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443104-T-C

15237933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443385-A-T

http://identifiers.org/hco/11/GRCh38#15238002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114443457-C-A

15238067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443502-G-C

15238132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443558-A-T

15238174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443617-G-A

15238174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443617-G-C

15238177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443620-C-T

15238182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443625-A-G

15238516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443863-T-G

15238687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444016-A-T

http://identifiers.org/hco/11/GRCh38#15238803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114444137-C-A

15238803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444137-C-T

15239017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114444350-A-G

15239064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114444397-G-A

15239116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444445-T-G

http://identifiers.org/hco/11/GRCh38#15239164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114444489-A-C

15239164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444489-A-G

15239165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444490-G-A

15239165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444490-G-T

15239179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444504-T-C

http://identifiers.org/hco/11/GRCh38#15239189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114444514-C-A

15239189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444514-C-T

15239202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444528-G-A

15239202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444528-G-C

15239202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444528-G-T

15239336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444640-C-T

15239399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444707-A-G

15239405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444713-C-T

15239572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444843-A-G

15240188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445319-C-T

15240189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445321-A-G

http://identifiers.org/hco/11/GRCh38#15240228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114445374-C-A

15240363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445582-G-A

15240363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445582-G-C

15240363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445582-G-T

15240369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445588-A-G

15240380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445622-A-G

15240422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445665-G-T

15240430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445670-C-T

15240553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445793-C-G

15240553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445793-C-T

15240565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445806-G-A

15240565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445806-G-T

15240583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445822-C-T

15240643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445879-G-T

15240762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445969-C-T

15240774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445981-A-T

15241010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446222-A-G

15241148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446346-G-A

15241150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446348-T-G

15241184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446380-G-T

15241408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446590-C-T

15241460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446640-G-A

15241460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446640-G-T

15241482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446661-G-A

15241539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446714-T-C

15241643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114446805-A-G

15241686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114446847-C-T

15241727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114446891-A-G

15241973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114447175-G-A

15242089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114447351-G-T

15242402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114447690-C-T

15242495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114447779-G-A

15243000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114448216-G-C

15243390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114448282-G-A

15245504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114448636-G-T

15245542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114448675-T-C

15245562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114448699-T-C

http://identifiers.org/hco/11/GRCh38#15245836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114448974-C-A

15245836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114448974-C-T

http://identifiers.org/hco/11/GRCh38#15245856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114448994-C-A

15245856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114448994-C-T

http://identifiers.org/hco/11/GRCh38#15245862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114449002-C-A

15245871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449011-G-A

15245876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449016-G-A

15245927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114449066-T-C

15245941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114449080-C-T

15245944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114449083-T-A

15245944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114449083-T-C

15246007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114449146-A-G

15246007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114449146-A-T

15246045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449184-T-C

15246046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449185-G-A

15246046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449185-G-T

15246221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449307-G-T

15246240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449316-T-C

15246266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449338-G-C

15246266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449338-G-T

15246267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449339-T-C

15246269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449341-G-A

15246269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449341-G-T

15246272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449344-G-T

15246302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114449374-A-G

15246344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114449416-C-G

http://identifiers.org/hco/11/GRCh38#15247256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114450298-C-A

15247300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114450335-G-A

15247336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114450371-A-G

15247339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114450374-A-T

15247355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114450390-A-G

15247488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114450489-T-C

15247706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114450760-T-A

15248110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114451343-G-A

http://identifiers.org/hco/11/GRCh38#15248168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#114451405-A-C

15248337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114451569-A-G

15248396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114451632-G-T

15248483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114451716-A-G

15248577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114451811-C-T

15248910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114452085-C-T

15249176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114452315-G-C

15249210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33116
most severe consequence: intron variant
orthologous variants: 114452349-G-A