119294399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38533363-G-A

119294399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38533363-G-T

http://identifiers.org/hco/3/GRCh38#119294409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38533354-C-A

119294419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5 prime UTR variant
orthologous variants: 38533344-G-A

http://identifiers.org/hco/3/GRCh38#119294508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38533259-C-A

119294508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5 prime UTR variant
orthologous variants: 38533259-C-G

119294508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5 prime UTR variant
orthologous variants: 38533259-C-T

http://identifiers.org/hco/3/GRCh38#119294604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38533196-C-A

119294850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5 prime UTR variant
orthologous variants: 38533084-G-A

119294850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5 prime UTR variant
orthologous variants: 38533084-G-T

119295032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38532919-C-T

119295033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38532918-C-T

119295221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38532737-C-T

119295285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38532671-A-G

119295288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38532668-G-C

119295389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38532577-G-A

119295401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38532565-A-G

119295440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38532526-G-T

http://identifiers.org/hco/3/GRCh38#119295503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38532464-A-C

119295503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38532464-A-G

119295503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38532464-A-T

119296275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38531711-G-C

119296487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38531481-G-T

119296800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38531053-C-T

119296995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38530887-T-C

119297115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38530764-A-T

119297133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38530746-T-C

119297306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38530576-A-G

119297448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38530433-C-T

119297449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38530432-C-T

119297482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38530399-G-A

119297947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38529966-G-A

119298281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38529606-A-G

http://identifiers.org/hco/3/GRCh38#119298765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38529212-A-C

119298765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38529212-A-G

119298765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38529212-A-T

119298780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38529197-T-C

http://identifiers.org/hco/3/GRCh38#119298784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38529193-C-A

119298784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38529193-C-G

119298784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38529193-C-T

119298785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38529192-A-G

119298785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38529192-A-T

http://identifiers.org/hco/3/GRCh38#119298986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38529106-C-A

119298986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38529106-C-T

119299462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38528796-G-A

http://identifiers.org/hco/3/GRCh38#119299782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38528446-C-A

119299815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38528413-C-T

119300044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38528212-G-A

119300392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38527907-G-A

119300921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38527645-C-G

119300979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38527587-C-G

119300979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38527587-C-T

119301092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38527476-T-A

119301363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38527201-T-A

119301493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38527078-C-T

119301568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38527001-T-C

119301668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38526924-C-T

119301735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38526853-G-C

119302219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38526378-A-T

119302384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38526185-T-C

119302887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38525697-A-G

119302887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38525697-A-T

119303044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38525433-G-C

119303058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38525419-C-T

119303099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38525376-C-G

119303180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38525293-G-A

119303180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38525293-G-C

119303538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38525016-A-G

119303635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38524937-T-C

119303802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38524792-T-C

119304387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38524187-A-T

119304530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38524047-G-A

119305154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38522651-A-G

119305284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38522540-A-G

119306099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38521788-G-A

119306608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38521372-C-T

119307695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38520566-G-A

119307804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38520454-C-T

119308129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38520176-A-G

119308280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38520041-A-G

119308302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38520018-G-C

119308457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38519868-C-T

http://identifiers.org/hco/3/GRCh38#119308626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38519742-C-A

119309168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38519551-G-A

http://identifiers.org/hco/3/GRCh38#119310363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38516561-A-C

119310837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38516428-C-T

119311044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38516211-T-G

119311137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38516122-C-T

119311523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38515739-T-G

http://identifiers.org/hco/3/GRCh38#119311679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38515584-A-C

119311934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38515353-G-A

119311968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38515318-A-G

119311972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38515314-C-G

119311972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38515314-C-T

119312027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38515259-A-G

119312079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38515217-C-G

119312705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38513382-C-T

119312934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38513152-C-T

119313017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38512612-G-A

119313173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38512469-C-T

119313329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38512344-A-G

119313897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511796-C-T

119313901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511792-A-G

119314121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511605-C-G

119314122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511604-G-A

119314122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511604-G-C

119314167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511560-T-C

http://identifiers.org/hco/3/GRCh38#119314180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38511547-C-A

119314180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511547-C-T

119314183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511544-T-C

119314189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511539-G-T

119314253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511484-G-C

119314265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511472-G-A

119314265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511472-G-T

119314269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511468-G-T

119314282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38511455-G-T

http://identifiers.org/hco/3/GRCh38#119314288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38511448-C-A

119314373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511356-A-G

119314472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511258-T-C

119314510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511225-T-C

http://identifiers.org/hco/3/GRCh38#119314544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38511191-C-A

119314544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511191-C-T

119314547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511188-T-C

119314609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511130-C-G

119314614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511125-G-T

119314618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511121-G-A

119314618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511121-G-T

119314642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511098-T-C

119314654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511086-A-G

119314681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511062-G-A

119314681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38511062-G-T

119314845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38510659-G-T

119315215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38509804-A-T

119315923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38508803-A-G

119316078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38508649-C-G

119316348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38508382-A-G

119316358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38508372-C-G

119316358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38508372-C-T

119316526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38508197-C-G

119316596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38508127-A-G

119316936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38507811-C-T

119316947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38507801-C-T

119317139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38507630-G-A

119318267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38504466-C-T

119318401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38504390-G-A

http://identifiers.org/hco/3/GRCh38#119318522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38504271-C-A

http://identifiers.org/hco/3/GRCh38#119318955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38503772-C-A

119319040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38503693-C-T

119319209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38503526-T-G

119319453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38503292-G-A

119319556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38503186-C-T

119319629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38503143-T-C

119319667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38503106-G-A

119319710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38503066-C-G

119319710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38503066-C-T

119319914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38502777-G-T

119319940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38502729-G-A

119320043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38502564-A-G

119320184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38502427-A-G

119320214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38502395-T-G

119320305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38502322-C-T

119320319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38502309-T-C

http://identifiers.org/hco/3/GRCh38#119320363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38502264-A-C

119320363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38502264-A-G

119322060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38501251-T-A

119322367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500931-A-G

119322460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500853-G-A

119322475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500835-G-T

http://identifiers.org/hco/3/GRCh38#119322579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38500758-C-A

119322579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500758-C-T

119322589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500748-G-A

119322589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500748-G-T

http://identifiers.org/hco/3/GRCh38#119322593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38500744-C-A

119322593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500744-C-T

http://identifiers.org/hco/3/GRCh38#119322611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38500728-C-A

119322611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500728-C-G

119322611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500728-C-T

119322626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500721-G-A

119322626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500721-G-T

119322686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500667-G-A

119322688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500665-G-T

119322699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38500654-C-T

119323674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38500338-T-G

119323814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38500200-T-G

119323891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38500117-T-C

119324012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38500029-C-T

119324333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38499723-A-G

119324485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38499604-T-C

119324508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38499573-A-G

119324848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38497857-A-G

119324876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38497829-C-T

119324900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38497806-G-A

http://identifiers.org/hco/3/GRCh38#119325006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38497700-C-A

119325040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38497666-G-C

119325818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38496919-A-G

119325818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38496919-A-T

119326457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38496620-G-A

119326630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38496476-G-A

119327663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38496129-A-G

119327663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38496129-A-T

119327713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38496079-G-A

119328497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38495410-G-A

119329617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38494198-G-A

http://identifiers.org/hco/3/GRCh38#119329932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38493890-C-A

119329998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38493824-C-T

119330066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38493758-A-G

119330086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38493738-G-A

119330086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38493738-G-C

119330115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38493709-G-A

http://identifiers.org/hco/3/GRCh38#119330141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38493691-A-C

119330266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38493587-C-T

119330457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38493417-A-G

119330654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38493235-T-G

119330849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38493087-C-T

119331110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38492832-C-T

119331572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38492411-T-C

119332021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38492035-A-G

119332620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38491574-C-G

119332641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38491553-A-T

119332649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38491545-A-T

119332670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38491524-C-T

119333236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38491001-G-A

http://identifiers.org/hco/3/GRCh38#119333272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38490359-A-C

119333663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38489977-G-T

119333833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38489813-T-A

119334104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38489569-T-G

119334468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38489225-G-A

119334739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38488920-A-G

119335123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38487876-A-G

119335335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38487672-G-A

119335342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38487665-T-C

119335446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38487310-C-T

119335485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38487274-C-T

119335534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38487191-C-G

119335780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38486965-A-G

119335843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38486925-G-A

http://identifiers.org/hco/3/GRCh38#119338126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38485797-A-C

119338347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38485672-T-A

119338347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38485672-T-C

119338591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38485436-C-G

119338856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38484986-C-G

http://identifiers.org/hco/3/GRCh38#119339192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38484634-C-A

119339203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38484623-C-T

119339216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38484609-G-A

http://identifiers.org/hco/3/GRCh38#119339259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38484566-A-C

119339259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38484566-A-G

119339873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38483590-T-A

119339921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38483542-C-G

119340457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38482955-C-T

119341135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38482341-A-G

119341135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38482341-A-T

119341377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38481503-A-G

119341441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38481441-G-A

119341479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38481406-G-A

119341496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38481389-A-G

119341496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38481389-A-T

119342068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38480596-G-A

119342068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38480596-G-T

119342606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38480074-G-A

119342659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38480005-A-G

119342804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38479816-C-T

119342826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38479796-G-A

119342826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38479796-G-C

119343382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38479288-A-G

119343689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38478944-A-G

119343690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38478943-T-C

119343722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38478911-C-T

119343794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38478842-A-G

119343879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38478621-G-A

119344156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38478351-T-C

119344185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38478322-G-A

119344307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38478216-G-A

119344416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38478113-A-G

119344461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38478074-G-T

119345524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38475532-A-T

119345604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38475458-T-G

http://identifiers.org/hco/3/GRCh38#119345711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38475361-C-A

119345711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38475361-C-T

119345741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38475332-A-G

119345970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38475123-T-C

119346164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38474943-C-G

http://identifiers.org/hco/3/GRCh38#119346254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38474854-C-A

119346254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38474854-C-T

119346762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38474371-G-A

http://identifiers.org/hco/3/GRCh38#119346783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38474350-A-C

119346783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38474350-A-G

119346783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38474350-A-T

119349182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38473896-G-A

119349230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38473860-C-G

119349252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38473842-A-G

119349462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38473635-T-C

http://identifiers.org/hco/3/GRCh38#119349465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38473632-A-C

119349992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38473068-T-G

119350306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38472450-T-C

119350741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38472013-T-C

119350926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38471848-C-T

119351232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38471610-G-A

119351979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: -G-A

119352716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38470261-A-T

119352746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38470239-T-A

119352818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38470168-A-G

119352956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38470034-C-T

119352959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38470031-T-C

119353294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38469735-T-C

119353348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38469671-T-C

119354113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38469420-C-G

119354113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38469420-C-T

119354301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38469230-T-A

119355046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38468752-G-T

119355049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38468749-C-G

119355183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38468628-G-A

119355279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38468533-G-A

119360791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38463752-A-G

119360791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38463752-A-T

119361095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38463440-G-A

119361218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38463360-T-C

119363132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38462610-G-A

119363132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38462610-G-T

119363215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38462528-G-A

119363217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38462526-G-T

http://identifiers.org/hco/3/GRCh38#119363371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38462361-C-A

119363565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38462125-A-G

119363606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38462085-T-G

119363608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38462083-G-C

119363652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38462038-G-A

119363852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38461621-C-T

119363971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38461521-C-T

119364089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38461424-G-C

119364106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38461406-G-T

119364221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38461307-T-C

119364221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38461307-T-G

119365186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38460824-C-T

119365244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38460774-A-T

119365456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38460567-G-T

http://identifiers.org/hco/3/GRCh38#119365535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38460508-C-A

119365535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38460508-C-T

119365568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38460492-C-T

http://identifiers.org/hco/3/GRCh38#119365593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38460467-A-C

119366073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38459860-G-A

119366073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38459860-G-T

119366257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38459504-T-A

119366790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38458991-T-C

119366795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38458989-T-A

119366851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38458913-C-T

119367214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38458602-A-G

119367251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38458568-G-A

119367307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38458518-C-T

119367927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38457860-A-T

119368120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38457646-C-T

119368322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38457451-T-C

119368354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38457419-C-T

119368358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38457415-C-T

119368415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38457358-G-C

119368446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38457327-C-G

119368446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38457327-C-T

http://identifiers.org/hco/3/GRCh38#119368603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38457170-C-A

119368603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38457170-C-T

119368606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38457167-T-A

119368656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38457122-T-C

119368942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38456814-G-A

119368948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38456808-G-T

119374958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38452965-T-C

119375327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38452438-A-G

119375482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38452337-A-T

119375483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38452336-G-C

119375587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38452216-A-T

119377278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38450462-A-G

119377584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38450167-G-A

119378016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38449568-C-T

119378258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38449338-T-C

119378488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38448991-C-T

119378591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38448837-T-C

119378833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38448636-G-A

119378908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38448567-G-A

119378908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38448567-G-T

119378920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38448555-G-A

119379036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38448451-G-C

119380187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38446456-A-G

119380601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38446280-C-G

119380725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38446167-A-G

119380753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38446141-T-C

119381076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38445843-G-A

http://identifiers.org/hco/3/GRCh38#119381103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38445826-C-A

119381150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38445779-T-C

119381396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38445556-C-G

119381553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38445437-C-T

119381592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38445397-A-G

http://identifiers.org/hco/3/GRCh38#119382152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38445162-C-A

119382152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38445162-C-G

119382256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38445062-A-T

119382430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38444896-C-G

119382431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38444895-C-G

119382431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38444895-C-T

http://identifiers.org/hco/3/GRCh38#119382495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38444844-A-C

119382516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38444830-T-C

119382568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38444783-A-T

119382686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38444665-T-C

119382849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38444498-G-C

119383011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38444384-C-T

119383074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38444323-C-T

119383077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38444320-A-G

119383197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38444201-A-G

119383250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38444143-C-T

119383327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443954-T-C

119383330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443951-G-A

119383330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443951-G-C

119383343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443941-G-A

119383343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443941-G-T

119383611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443671-G-A

119383668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443619-G-A

119383728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443559-G-C

119383749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443538-C-T

119383900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443313-A-G

119383908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443305-T-C

119383917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38443292-A-G

119390428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38441792-C-G

119391007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38441242-T-A

119391087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38441156-G-A

119391087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38441156-G-C

119391087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38441156-G-T

http://identifiers.org/hco/3/GRCh38#119391120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38441123-C-A

119391120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38441123-C-T

119391185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38441074-C-T

119391314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38440981-T-G

119391329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38440967-T-G

119391382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38440931-T-C

119392597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38439630-G-A

119392613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38439615-A-G

119392657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38439569-C-G

119392755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38439463-C-T

119392778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38439440-A-G

119392824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38439419-C-T

http://identifiers.org/hco/3/GRCh38#119393327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38438857-C-A

119393327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38438857-C-G

119393329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38438855-T-C

119393329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38438855-T-G

http://identifiers.org/hco/3/GRCh38#119393410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38438774-A-C

119393413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38438771-T-C

http://identifiers.org/hco/3/GRCh38#119393441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38438727-A-C

119393615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38438479-T-C

119393725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38438386-T-A

http://identifiers.org/hco/3/GRCh38#119393767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38438348-A-C

119394148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38437977-G-A

119394194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38437934-C-T

119394518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38437611-T-A

119394916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38437383-G-A

http://identifiers.org/hco/3/GRCh38#119394950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38437350-A-C

119395001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38437296-G-A

119395188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38437124-C-T

119395567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38436815-C-T

119395635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38436784-T-C

119395697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38436749-C-T

119395776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38436680-T-C

119395866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38436591-C-T

http://identifiers.org/hco/3/GRCh38#119396198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38436264-C-A

119396258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38436201-A-G

119396932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38434006-T-C

119397573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38433272-G-T

119397693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38433151-G-A

119397693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38433151-G-C

119397703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38433141-G-A

119398340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38432520-C-T

119398347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38432513-G-T

http://identifiers.org/hco/3/GRCh38#119398627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38431947-A-C

119398850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38431732-A-T

119398918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38431441-T-G

119399058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38431319-G-C

119399058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38431319-G-T

http://identifiers.org/hco/3/GRCh38#119401766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38429865-C-A

119401766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38429865-C-T

119401821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, splice_acceptor_variant, undefined
orthologous variants: 38429812-G-A

119401821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, splice_acceptor_variant, undefined
orthologous variants: 38429812-G-T

119402086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense_variant, undefined
orthologous variants: 38429574-A-G

http://identifiers.org/hco/3/GRCh38#119402462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38429200-A-C

119402462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38429200-A-G

119402499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38429163-G-A

119402499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38429163-G-T

119402515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38429147-T-C

119402686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38428998-A-G

119402981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38428374-C-G

http://identifiers.org/hco/3/GRCh38#119409265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38427554-C-A

119409265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38427554-C-T

119409352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38427501-A-G

http://identifiers.org/hco/3/GRCh38#119409391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38427463-C-A

119409398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38427456-T-C

119409441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron_variant, undefined
orthologous variants: 38427339-G-A

119409523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense_variant, undefined
orthologous variants: 38427212-A-G

119409555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38427180-A-G

119409555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38427180-A-T

119409641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: synonymous variant
orthologous variants: 38427097-A-G

119409750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38426988-G-C

119409750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38426988-G-T

http://identifiers.org/hco/3/GRCh38#119409768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38426970-C-A

119409768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38426970-C-T

http://identifiers.org/hco/3/GRCh38#119409781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38426957-A-C

119409781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38426957-A-G

119409781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38426957-A-T

119410049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38426177-A-T

http://identifiers.org/hco/3/GRCh38#119410488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38425819-A-C

119410804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38425529-C-T

119410887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38425454-T-C

119413814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38424217-A-G

119413837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: intron variant
orthologous variants: 38424194-G-C

119413973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38424058-A-G

119413974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38424057-T-C

http://identifiers.org/hco/3/GRCh38#119414070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38423988-C-A

119414071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: synonymous variant
orthologous variants: 38423987-T-C

http://identifiers.org/hco/3/GRCh38#119414167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38423864-C-A

119414167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423864-C-G

119414167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: synonymous variant
orthologous variants: 38423864-C-T

119414174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423857-C-T

119414181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423850-G-A

119414181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423850-G-T

119414186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423845-G-C

http://identifiers.org/hco/3/GRCh38#119414204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38423827-C-A

119414204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423827-C-G

http://identifiers.org/hco/3/GRCh38#119414294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38423737-A-C

119414294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423737-A-G

119414335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: synonymous variant
orthologous variants: 38423696-C-T

http://identifiers.org/hco/3/GRCh38#119414340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38423691-C-A

119414340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423691-C-G

119414340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423691-C-T

119414462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423569-G-T

http://identifiers.org/hco/3/GRCh38#119414522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38423509-A-C

119414612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423419-A-G

119414672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423359-A-G

119414744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: synonymous variant
orthologous variants: 38423287-T-C

119414744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38423287-T-G

119415041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38422990-A-T

119415056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38422975-G-A

119415248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38422783-C-T

119415263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38422768-G-A

http://identifiers.org/hco/3/GRCh38#119415272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38422759-A-C

119415272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38422759-A-G

119415272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38422759-A-T

119415314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38422717-T-G

119415355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: synonymous variant
orthologous variants: 38422676-C-T

http://identifiers.org/hco/3/GRCh38#119415412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38422625-C-A

http://identifiers.org/hco/3/GRCh38#119415737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38422300-A-C

119415856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: synonymous variant
orthologous variants: 38422181-G-A

119415872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38422165-G-A

119415872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38422165-G-C

http://identifiers.org/hco/3/GRCh38#119416181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38421868-C-A

119416181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: missense variant
orthologous variants: 38421868-C-G

119416271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421778-T-G

119416297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421752-C-T

119416379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421671-T-C

http://identifiers.org/hco/3/GRCh38#119416405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38421622-C-A

119416500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421531-A-G

119416556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421476-A-G

119416557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421475-G-C

119416557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421475-G-T

119416654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421391-T-C

119416703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421350-C-T

119416764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421288-G-T

119416816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421226-C-T

119416893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421158-G-T

119417006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421047-C-T

119417060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421000-G-A

119417060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38421000-G-T

119417180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420908-G-T

119417219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420887-G-T

119417227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420879-T-A

119417227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420879-T-C

119417250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420857-T-A

119417296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420814-A-G

http://identifiers.org/hco/3/GRCh38#119417299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38420811-C-A

119417409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420751-G-A

119417409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420751-G-T

119417452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420708-G-T

119417462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420698-G-A

119417462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420698-G-T

119417662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420645-T-C

119417695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420609-T-C

http://identifiers.org/hco/3/GRCh38#119418009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38420366-C-A

119418009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420366-C-T

119418010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420365-A-G

119418197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420180-G-T

119418216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420167-G-A

119418292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420094-T-C

119418292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38420094-T-G

http://identifiers.org/hco/3/GRCh38#119418423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38419961-C-A

119418423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38419961-C-T

119418425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38419959-C-T

http://identifiers.org/hco/3/GRCh38#119418436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#38419953-C-A

119418436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38419953-C-T

http://identifiers.org/hco/3/GRCh38#119418613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38419816-C-A

119418694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419749-C-T

119419041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419453-T-A

119419041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419453-T-C

119419055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419439-T-C

http://identifiers.org/hco/3/GRCh38#119419064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38419430-C-A

119419106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419391-T-C

119419106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419391-T-G

119419168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419337-G-C

119419171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419334-G-A

119419171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419334-G-T

119419220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419298-G-A

119419220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419298-G-T

119419280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419244-T-C

119419280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419244-T-G

119419336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38419167-A-G

119419501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418950-G-C

119419501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418950-G-T

119419541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418908-A-G

119419634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418824-G-A

http://identifiers.org/hco/3/GRCh38#119419965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38418524-C-A

http://identifiers.org/hco/3/GRCh38#119419983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38418506-C-A

119420218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418289-G-A

119420218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418289-G-T

119420221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418286-A-G

119420233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418274-G-A

119420236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418271-C-T

119420268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418243-T-A

119420268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38418243-T-C

http://identifiers.org/hco/3/GRCh38#119420321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38418023-A-C

119420346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38417998-G-A

119420346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38417998-G-T

119420391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38417953-G-A

119420391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38417953-G-T

http://identifiers.org/hco/3/GRCh38#119420537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#38417846-C-A

119420712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29216
most severe consequence: 3 prime UTR variant
orthologous variants: 38417675-G-T