140620887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83999455-C-T

140620914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83999428-A-T

140621224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83999117-G-A

140621280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83999090-G-A

140621373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998976-A-T

http://identifiers.org/hco/4/GRCh38#140621431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83998918-C-A

140621526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998845-G-T

140621733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998641-C-T

140621776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998606-T-G

http://identifiers.org/hco/4/GRCh38#140621779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83998603-C-A

http://identifiers.org/hco/4/GRCh38#140621926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83998483-C-A

140621926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998483-C-T

http://identifiers.org/hco/4/GRCh38#140621988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83998428-C-A

140621988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998428-C-G

140621988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998428-C-T

140622018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998398-A-T

http://identifiers.org/hco/4/GRCh38#140622082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83998336-C-A

140622082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998336-C-T

140622135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998275-G-A

140622135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 3 prime UTR variant
orthologous variants: 83998275-G-T

140622769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83997669-T-C

140622770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83997668-T-C

140622829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83997609-A-G

140622847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83997591-T-C

140622904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83997534-T-A

140622904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83997534-T-C

140622921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83997517-A-G

http://identifiers.org/hco/4/GRCh38#140622942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83997496-A-C

140622942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83997496-A-G

140623062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83997414-T-C

140623701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83996575-C-G

140623701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83996575-C-T

140623874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83996421-G-A

140623986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83996304-A-G

140623986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83996304-A-T

http://identifiers.org/hco/4/GRCh38#140624256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83995734-C-A

140624478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83995528-T-A

140624497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83995509-T-C

http://identifiers.org/hco/4/GRCh38#140624500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83995506-C-A

140624500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83995506-C-T

http://identifiers.org/hco/4/GRCh38#140624504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83995502-C-A

140624504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83995502-C-G

140624519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83995487-A-G

140624519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83995487-A-T

140624520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83995486-A-G

140625066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83994890-T-A

140625111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83994841-G-A

140625112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83994840-T-C

140625247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83994725-A-G

http://identifiers.org/hco/4/GRCh38#140625352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83994666-C-A

140627356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992879-C-T

140627371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992864-A-G

140627393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992844-G-A

140627393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992844-G-T

140627404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992833-A-G

140627415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992822-T-C

140627589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992670-T-A

140627658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992604-A-G

140627683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992584-T-C

140627696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992567-T-C

140627727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992536-C-T

140627731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992532-C-G

140627736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992527-A-G

140627737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992526-C-G

http://identifiers.org/hco/4/GRCh38#140627827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83992439-C-A

140627827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992439-C-T

140627916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83992375-G-T

140628191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83991669-T-A

140628191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83991669-T-C

140628307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: synonymous variant
orthologous variants: 83991532-G-A

140628496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83991332-G-A

140628496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83991332-G-T

http://identifiers.org/hco/4/GRCh38#140628498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83991330-C-A

140628498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83991330-C-T

140628500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83991328-T-C

140628853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83990991-T-C

140628926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83990910-A-G

140628926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83990910-A-T

140628936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83990900-T-A

140629058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83990785-A-G

140632836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83989690-A-T

140632846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83989680-A-G

140632933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83989631-T-C

140632995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83989579-T-C

http://identifiers.org/hco/4/GRCh38#140633247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83988997-C-A

140633277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83988967-T-C

140633409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83988848-T-C

140633435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83988792-G-A

140633571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83988634-A-T

140633812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83987947-T-C

http://identifiers.org/hco/4/GRCh38#140633888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83987847-C-A

140633888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83987847-C-T

http://identifiers.org/hco/4/GRCh38#140633925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83987809-A-C

140633933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83987801-G-A

http://identifiers.org/hco/4/GRCh38#140633935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83987799-A-C

140634007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83987727-T-C

http://identifiers.org/hco/4/GRCh38#140634016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83987718-C-A

140634016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83987718-C-T

140634124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83987610-C-T

140634793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83987466-T-C

140634845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83987416-T-G

140634883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83987381-A-G

140637925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83987300-A-G

140638054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83987221-A-T

140638110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, undefined
orthologous variants: 83987163-G-A

140638284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83986973-C-T

140638355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83986891-A-T

140638809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83986303-C-T

140638885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83986230-A-G

140639032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83986060-T-C

140639056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83986029-G-A

140639056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83986029-G-T

140639135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83985950-T-A

140639135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83985950-T-G

140639193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985907-A-G

140639196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985904-A-G

140639196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985904-A-T

140639204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985896-G-T

140639209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985891-G-T

140639257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985855-A-T

http://identifiers.org/hco/4/GRCh38#140639267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83985826-A-C

140639267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985826-A-G

140639306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985744-C-T

140639494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985555-A-G

http://identifiers.org/hco/4/GRCh38#140639516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83985537-C-A

140639542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985509-G-A

140639619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985462-C-T

140639666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83985416-C-T

140655648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83984636-G-A

140655648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83984636-G-C

http://identifiers.org/hco/4/GRCh38#140655746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83984537-A-C

140655750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83984533-A-G

140655920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83983259-C-T

140655924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83983255-A-T

140655938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83983249-C-G

140655940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83983247-A-G

140656025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83983189-G-A

140657098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 83982550-T-A

140657131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83982517-A-G

140657131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83982517-A-T

http://identifiers.org/hco/4/GRCh38#140657272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83982376-C-A

140657397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83981629-A-G

140657397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83981629-A-T

140657512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83981554-G-A

140657512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83981554-G-T

140657641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83981425-A-G

140657820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83981250-A-G

http://identifiers.org/hco/4/GRCh38#140657875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83981201-C-A

140659547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83980242-G-T

140659840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83978954-G-T

140659844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83978950-T-C

140660058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83978729-T-C

140660107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83978679-T-A

140660115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83978671-C-T

140660121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83978665-G-T

140660342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83978456-G-C

140660371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83978427-T-C

140660424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83978374-G-A

140660424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83978374-G-C

140660592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83978218-T-C

140660594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83978216-C-T

140660660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83978150-T-G

140661987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83976149-T-C

140662063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: synonymous variant
orthologous variants: 83976073-G-A

140662077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83976059-C-T

140662198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975943-T-A

140662240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975908-A-G

140662360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975799-A-G

140662360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975799-A-T

140662421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, undefined
orthologous variants: 83975742-T-C

140662446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975717-G-T

140662452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975711-G-C

140662456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975707-C-T

140662499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975680-T-A

140662517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975661-A-G

140662604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975577-C-T

140662619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975567-T-C

140662637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975549-T-C

140662703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975476-T-C

http://identifiers.org/hco/4/GRCh38#140662739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83975430-C-A

140662856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975313-G-T

140662887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83975278-A-G

140667230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83971139-C-T

140667753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83970598-G-A

http://identifiers.org/hco/4/GRCh38#140667905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83970455-A-C

140667990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83970365-A-G

140668049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83970302-A-G

140668134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83970224-G-A

140668250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83970136-A-G

140668324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969960-G-A

140668332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969952-C-T

140668384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969903-G-C

140668644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969568-T-C

140668665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969545-G-A

140668841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969416-G-T

http://identifiers.org/hco/4/GRCh38#140668861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83969391-C-A

140668861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969391-C-G

140668861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969391-C-T

140668872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969380-G-T

140668889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969363-G-A

http://identifiers.org/hco/4/GRCh38#140668934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83969282-A-C

140669076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969140-G-A

140669082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969134-G-A

140669116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969101-G-A

140669116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969101-G-C

140669116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969101-G-T

http://identifiers.org/hco/4/GRCh38#140669139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83969078-C-A

140669139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969078-C-G

http://identifiers.org/hco/4/GRCh38#140669150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83969069-C-A

140669150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969069-C-G

140669150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969069-C-T

140669184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83969036-T-A

140669275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968954-C-G

140669275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968954-C-T

140669493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968713-A-G

140669597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968372-A-G

140669800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83968169-T-C

140669818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968153-G-C

140669837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968137-G-A

140669844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968130-G-T

140669876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968108-T-C

140669879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968105-G-C

140669879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968105-G-T

http://identifiers.org/hco/4/GRCh38#140669893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83968092-A-C

140669893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968092-A-G

140669896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968089-T-C

http://identifiers.org/hco/4/GRCh38#140669897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83968088-C-A

140669897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968088-C-G

140669898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968087-A-G

140669899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968086-T-A

140669899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968086-T-C

140669899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83968086-T-G

http://identifiers.org/hco/4/GRCh38#140669951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83968011-A-C

140670214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83967492-T-C

140670225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83967481-A-G

140670225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83967481-A-T

140670270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83967447-T-G

140670315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83967402-T-C

140670317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83967400-G-A

http://identifiers.org/hco/4/GRCh38#140670457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83967301-C-A

http://identifiers.org/hco/4/GRCh38#140670463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83967295-C-A

140670463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83967295-C-T

140670549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83966862-A-G

140670675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83966702-A-G

140670711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83966673-C-T

140670805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83966579-C-T

140670835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83966549-T-C

140670835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83966549-T-G

140670978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83966412-G-A

140671219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83966235-T-G

140671294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83966173-G-A

140671423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83966075-T-C

140671442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83966056-C-T

140671789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83965231-C-T

http://identifiers.org/hco/4/GRCh38#140677027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83963213-C-A

http://identifiers.org/hco/4/GRCh38#140677050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83963190-C-A

140677050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83963190-C-T

140677063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83963177-G-A

140677063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83963177-G-T

140677129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83963107-A-G

http://identifiers.org/hco/4/GRCh38#140677207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83963042-C-A

http://identifiers.org/hco/4/GRCh38#140677258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83962995-C-A

140678234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83961601-A-T

140678238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83961597-T-C

140678382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83961455-C-T

http://identifiers.org/hco/4/GRCh38#140678386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83961451-C-A

140678501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83961349-A-T

http://identifiers.org/hco/4/GRCh38#140678828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83961100-C-A

http://identifiers.org/hco/4/GRCh38#140678830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83961098-C-A

140678830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83961098-C-T

140678837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83961091-G-C

http://identifiers.org/hco/4/GRCh38#140679277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83960675-C-A

140679277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960675-C-T

http://identifiers.org/hco/4/GRCh38#140679278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83960674-C-A

140679278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960674-C-T

http://identifiers.org/hco/4/GRCh38#140679291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83960662-C-A

140679291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960662-C-T

http://identifiers.org/hco/4/GRCh38#140679338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83960622-C-A

140679478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960464-T-C

140679575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960374-G-T

140679683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83960267-G-A

140679683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83960267-G-C

140679847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83960103-A-G

140679869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960089-C-T

140679884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960077-T-C

140679896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960065-T-A

140679896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960065-T-C

http://identifiers.org/hco/4/GRCh38#140679900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83960061-C-A

140679900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960061-C-T

140679912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960054-G-A

140679912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960054-G-T

140679923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960039-T-C

140679952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960015-G-A

140679952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83960015-G-T

140679969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83959998-A-G

140679983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83959871-A-G

http://identifiers.org/hco/4/GRCh38#140679984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83959870-A-C

140679984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83959870-A-G

140680195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83959690-C-T

http://identifiers.org/hco/4/GRCh38#140680252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83959582-C-A

140680282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83959552-C-T

140680360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83959514-G-A

140680547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83958788-G-A

140680549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83958786-T-A

http://identifiers.org/hco/4/GRCh38#140680603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83958731-C-A

140680603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83958731-C-G

140680603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83958731-C-T

140680604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83958730-G-A

140680806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83958548-G-T

140680868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83958477-A-T

140681222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83954649-T-C

140681431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83954460-T-C

140681431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83954460-T-G

140681470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83954420-T-C

140681501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83954397-A-T

http://identifiers.org/hco/4/GRCh38#140681688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83954224-C-A

140682034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83953920-T-A

140682045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83953904-T-G

140682332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83953646-C-T

140682333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83953645-A-T

140682344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83953634-T-A

140682344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83953634-T-C

http://identifiers.org/hco/4/GRCh38#140682432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83953556-C-A

140683175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83952819-G-A

http://identifiers.org/hco/4/GRCh38#140683830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83952257-C-A

140684331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83951913-T-A

140684446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83951798-A-G

140684605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83951651-A-G

140685423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83949174-A-G

140685624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83948988-T-C

http://identifiers.org/hco/4/GRCh38#140686128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83948405-A-C

140686426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: stop gained
orthologous variants: 83948101-C-T

140686464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: splice acceptor variant
orthologous variants: 83948063-T-C

http://identifiers.org/hco/4/GRCh38#140686505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83948017-A-C

140686505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83948017-A-G

140686507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83948015-G-A

140686507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83948015-G-C

140686507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83948015-G-T

140686565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83947957-T-A

140686565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83947957-T-C

140686587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83947935-A-G

http://identifiers.org/hco/4/GRCh38#140686619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83947915-C-A

140686705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83947852-G-A

140686853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83947696-T-C

http://identifiers.org/hco/4/GRCh38#140687156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83947422-A-C

140687404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83947326-A-G

140688705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83946612-T-C

http://identifiers.org/hco/4/GRCh38#140688711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83946606-A-C

140688752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83946565-G-C

http://identifiers.org/hco/4/GRCh38#140688852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83946472-A-C

140688961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83946295-G-A

140689020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83946239-T-C

140689184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83946068-T-C

140691741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83943644-C-G

140691741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83943644-C-T

140691754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83943631-T-G

140691785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83943607-T-C

140691973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83943413-T-C

140692005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83943381-T-G

140692195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83943243-C-T

140692454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83942997-T-G

140692556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83942727-C-T

140692698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83942600-C-G

140692698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83942600-C-T

140693388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83942351-A-T

140693573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83942200-C-T

140693705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83942053-T-C

140693769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83941991-T-A

140694705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83941218-T-G

140694727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83941184-A-G

140694826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83941074-G-A

140694874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83941027-A-T

140694879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83941022-C-T

140694882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83941019-G-A

140695069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83940499-C-T

140695074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83940494-G-A

140695074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83940494-G-C

140695205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83940362-A-G

140695328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83940247-C-T

140695415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83940160-A-T

140695424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83940151-C-G

140695438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83940136-G-A

140697525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83939171-A-G

140697617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83939063-G-A

140697617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83939063-G-T

140697885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83938847-G-A

140698050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83938696-C-T

140698073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83938676-T-G

140700979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83937635-C-T

140701049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83937562-T-C

140701388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83937268-A-G

140701404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83937251-G-T

140701475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83937187-C-G

140701475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83937187-C-T

140701678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83936989-G-C

140701678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83936989-G-T

http://identifiers.org/hco/4/GRCh38#140701689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83936978-C-A

140701691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83936976-T-C

140702010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83936457-G-C

140702019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83936450-G-A

140703189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83935606-T-C

140703483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83935339-C-T

140703496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83935328-G-A

140703654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83935170-C-T

http://identifiers.org/hco/4/GRCh38#140703696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83935128-A-C

140703707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83935117-A-G

140703882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83934943-T-A

140704487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83934611-A-G

http://identifiers.org/hco/4/GRCh38#140704498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83934591-A-C

140704574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83934539-T-A

140704614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83934496-C-T

140704899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83934317-G-A

140704899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83934317-G-T

http://identifiers.org/hco/4/GRCh38#140704963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83934235-A-C

140705278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933759-G-A

http://identifiers.org/hco/4/GRCh38#140705297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83933707-C-A

140705315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933653-T-A

140705324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933644-C-T

140705354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933613-A-T

140705393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933580-G-A

140705408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933565-G-A

140705411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933562-G-A

140705472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933497-C-T

140705586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933428-T-C

140705588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933426-T-G

140705610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83933407-C-T

140706014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83932591-T-C

140706119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83932487-C-G

140706940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83931652-T-C

140707787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83930826-A-G

140707831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83930698-C-T

140707872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83930526-C-G

140707948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83930402-A-G

140707980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83930370-A-G

140708068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83930305-A-G

140708616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929728-C-T

140708630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929714-G-A

140708673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929669-G-A

140708673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929669-G-T

140708689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929653-G-A

140708739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929625-T-C

140708744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929620-T-C

140708810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929548-C-T

http://identifiers.org/hco/4/GRCh38#140709065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83929308-A-C

140709065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929308-A-G

http://identifiers.org/hco/4/GRCh38#140709102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83929307-C-A

140709244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929229-T-A

140709268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929208-A-T

140709274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929202-A-T

140709276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929200-A-T

http://identifiers.org/hco/4/GRCh38#140709292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83929184-C-A

http://identifiers.org/hco/4/GRCh38#140709297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83929179-C-A

140709297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929179-C-T

140709299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929177-T-A

140709299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929177-T-C

140709379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83929095-T-C

140710112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83927828-C-G

140710112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83927828-C-T

140710145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83927791-T-C

http://identifiers.org/hco/4/GRCh38#140710151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83927785-C-A

140710467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83927504-G-C

140710778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83927194-T-C

140710795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83927177-C-T

140710807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83927165-G-A

140710807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83927165-G-T

140711245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, undefined
orthologous variants: 83926395-A-G

140711376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83926311-T-C

http://identifiers.org/hco/4/GRCh38#140715433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83922850-C-A

140715456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83922827-C-T

140715566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83922722-T-C

140716127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83922211-G-C

140716127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83922211-G-T

http://identifiers.org/hco/4/GRCh38#140716129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83922209-C-A

http://identifiers.org/hco/4/GRCh38#140716889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83921462-C-A

140716908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83921443-G-A

140716908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83921443-G-T

140716912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83921439-T-A

140716912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83921439-T-C

140716912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83921439-T-G

140716914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83921437-G-A

140716914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83921437-G-T

140717134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83921269-G-A

140717296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83921014-A-G

140717302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83921008-G-C

140717322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83920988-T-C

140717333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83920977-A-G

140717725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83920453-T-G

http://identifiers.org/hco/4/GRCh38#140717838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83920341-C-A

140718243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83920001-T-A

140718243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83920001-T-C

http://identifiers.org/hco/4/GRCh38#140718246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83919998-A-C

140718246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83919998-A-T

140718350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83919929-C-G

140718610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83919675-T-C

140718610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83919675-T-G

140718668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83919617-G-A

140718676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83919609-A-G

140719709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83918367-G-A

140721887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83917420-A-G

140721938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83917373-C-T

140722324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83917040-T-C

140722569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83916821-C-G

http://identifiers.org/hco/4/GRCh38#140722934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83916532-C-A

140722934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83916532-C-G

140723067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83916410-T-C

140724153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83915988-G-A

140724176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83915966-C-G

140724176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83915966-C-T

140724211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83915935-A-G

140727200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83914582-A-G

140727206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83914576-T-C

http://identifiers.org/hco/4/GRCh38#140727480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83914328-C-A

140727480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83914328-C-T

140727631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83914180-G-A

140727761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83914086-G-C

140727897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83913972-C-T

140728330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83913147-G-C

140728342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83913135-G-A

140728360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83913114-G-T

140728364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83913110-T-G

140728369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83913107-G-A

140728369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83913107-G-T

140728420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83913065-A-T

http://identifiers.org/hco/4/GRCh38#140728439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83913046-C-A

140728439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83913046-C-T

140729093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83912286-T-A

140729137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83912243-C-T

140729207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83912173-T-C

140729527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83912052-C-T

140731026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83910404-T-A

140731026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83910404-T-C

140731102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83910340-G-A

140731599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83910209-G-A

140731604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83910204-G-A

140731742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83910080-G-A

140731933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83909716-A-G

140731933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83909716-A-T

140732400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83909305-T-C

140732408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83909297-T-C

140732412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83909293-T-A

140732924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83909020-G-A

140732994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83908981-A-G

140733021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83908958-A-G

140733047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83908940-C-T

http://identifiers.org/hco/4/GRCh38#140733605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83908418-C-A

140733618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83908407-C-T

140733650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83908377-G-A

140733651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83908376-T-C

140733814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83908233-T-C

140734043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83908060-T-C

http://identifiers.org/hco/4/GRCh38#140735240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83907799-C-A

140735866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83907262-C-T

140735941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83907183-A-G

140738955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83906677-G-A

140738955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83906677-G-T

140743295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83903417-T-C

140743935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83902067-T-G

140744024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83901978-G-A

140753526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83894864-C-T

140753939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83894433-C-T

http://identifiers.org/hco/4/GRCh38#140753969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83894403-A-C

140753969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83894403-A-G

140754987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83893660-G-T

140755060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83893596-T-C

140755210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83893461-C-G

140755475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83893226-C-T

http://identifiers.org/hco/4/GRCh38#140755736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83892997-A-C

http://identifiers.org/hco/4/GRCh38#140755801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83892923-C-A

140755801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83892923-C-T

140755814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83892906-C-T

http://identifiers.org/hco/4/GRCh38#140755837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83892884-C-A

140755837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83892884-C-T

http://identifiers.org/hco/4/GRCh38#140755851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83892870-C-A

140755851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83892870-C-T

140755912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: intron variant
orthologous variants: 83892835-T-C

140755933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83892814-C-T

140755948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83892799-G-A

140755948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: missense variant
orthologous variants: 83892799-G-T

140756252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 5 prime UTR variant
orthologous variants: 83892528-A-G

http://identifiers.org/hco/4/GRCh38#140756256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#83892524-C-A

140756256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 5 prime UTR variant
orthologous variants: 83892524-C-G

140756343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21710
most severe consequence: 5 prime UTR variant
orthologous variants: 83892461-C-T