188947258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24877290-G-T

http://identifiers.org/hco/3/GRCh38#188947301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#24877331-C-A

188947468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24877511-A-G

188947549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24877589-G-A

188947549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24877589-G-T

http://identifiers.org/hco/3/GRCh38#188947740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#24877780-C-A

http://identifiers.org/hco/3/GRCh38#188947742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#24877782-C-A

188948282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24878306-G-A

188948483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24878507-C-T

http://identifiers.org/hco/3/GRCh38#188948750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#24878713-C-A

188948878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24878795-C-T

188948975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24878896-T-C

188949101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24879008-A-G

188949403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24879234-T-G

188949440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24879269-T-G

188949781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24879563-A-G

188949867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24879702-T-C

188950767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24880364-A-G

188950767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24880364-A-T

http://identifiers.org/hco/3/GRCh38#188951003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#24880529-C-A

188951003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24880529-C-T

http://identifiers.org/hco/3/GRCh38#188951064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#24880587-C-A

188951099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24880621-T-A

188951303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24880832-T-G

188951366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24880895-G-A

188951366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24880895-G-C

188951611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24881210-G-A

188951616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24881215-A-G

188951859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24881419-G-A

188951990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24881569-C-T

188952571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24881793-G-A

188952577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24881799-T-C

188952826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24881996-G-A

188952846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882016-T-C

188952868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882029-T-C

188952947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882108-G-C

188953026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882195-C-T

188953135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882266-C-T

188953187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882319-A-G

188953237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882358-G-A

188953287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882407-G-A

188953287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882407-G-T

188953356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882478-G-A

188953472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882573-A-T

http://identifiers.org/hco/3/GRCh38#188953488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24882587-C-A

188953488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882587-C-T

188953489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882588-G-A

188953489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882588-G-T

188953572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882655-A-G

188953587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882670-T-A

188953656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24882735-A-G

http://identifiers.org/hco/3/GRCh38#188954334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24883042-A-C

188954666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24883377-G-A

188954672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24883383-A-G

188954732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24883435-G-A

188954784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24883489-G-C

188955296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24884563-A-G

188955333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24884602-T-C

188955581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24884901-G-A

188956279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24885909-A-G

188956442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24886037-G-T

188957117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24886607-C-T

188957148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24886638-T-G

188957200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24886833-A-G

188957212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24886845-G-A

188957242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24886874-T-C

188957310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24886936-T-C

188957333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24886959-G-A

188957333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24886959-G-T

188958172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24887050-T-A

188958433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24887275-T-A

188958698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24889032-G-A

188958698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24889032-G-T

188958835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24889094-G-T

188958889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24889122-A-G

188959292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24889471-G-T

http://identifiers.org/hco/3/GRCh38#188959435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24889593-A-C

188959504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24889657-T-C

188959748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24889891-T-A

188959859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24889995-T-C

188959896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24890059-A-G

188959898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24890061-G-A

188959998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24890275-T-C

188960323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24890550-T-G

188960471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24890712-T-C

188960494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24890734-G-C

http://identifiers.org/hco/3/GRCh38#188960541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24890759-C-A

188960541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24890759-C-T

188960542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24890760-G-A

188961740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24891808-C-T

188961743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24891811-C-T

188961744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24891812-C-T

188962156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24892829-T-G

188962169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24892842-A-T

188962421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24893075-G-T

188962422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24893076-C-T

188962579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24893222-A-G

188962593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24893236-C-T

188962892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24893538-T-A

188962892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24893538-T-C

188963178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24893915-G-T

188963468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24894208-C-T

188963699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24894408-T-G

188964090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24894757-A-T

188964303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24895181-T-G

188964373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24895230-C-T

188964438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24895281-C-G

188964468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24895310-G-T

188964850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24896470-A-G

188964930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24896539-C-G

188964930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24896539-C-T

188964996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24896605-T-G

188965242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24896837-C-T

188965319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 24896920-A-T

http://identifiers.org/hco/3/GRCh38#188965369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24896979-A-C

188965369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24896979-A-G

http://identifiers.org/hco/3/GRCh38#188965553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24897078-C-A

188969138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24897888-T-C

188969139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24897889-A-T

188972075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24899373-T-C

188972595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24899879-G-A

188972603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24899887-C-T

188972803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24900028-T-C

188972900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24900113-G-A

188972911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24900124-T-C

188973064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24900265-G-A

188973164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24900394-G-A

188973201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24900472-T-C

188973212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24900515-C-T

188973253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24900554-G-T

188973665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24900893-G-A

188973817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901045-A-G

188973855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901083-G-A

188973903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901116-G-A

188974124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901298-C-T

188974225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901394-T-C

188974250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901419-C-T

188974275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901440-A-G

188974309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901486-T-C

188974457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901628-C-T

188974489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901664-G-T

188974693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901852-G-A

http://identifiers.org/hco/3/GRCh38#188974758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24901916-C-A

188974758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24901916-C-T

188974918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24902286-A-G

188974999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24902364-A-G

188975316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24902647-C-T

188975684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24903010-A-G

188975799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24903121-C-T

188976091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24903402-T-G

188976224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24903546-T-C

188976381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24903703-G-A

188976466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24903800-T-A

188976593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 24903923-A-T

http://identifiers.org/hco/3/GRCh38#188976829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24904168-C-A

188976829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24904168-C-T

188976859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24904198-A-G

http://identifiers.org/hco/3/GRCh38#188976889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24904228-C-A

188976889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904228-C-T

188976892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904231-C-G

188976914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904266-A-G

188977053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904394-C-T

188977181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904467-C-T

http://identifiers.org/hco/3/GRCh38#188977458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24904925-A-C

188977458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904925-A-G

http://identifiers.org/hco/3/GRCh38#188977571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24905033-C-A

188977571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24905033-C-G

188978499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906223-T-A

188978862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906585-G-C

188979633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907347-T-G

http://identifiers.org/hco/3/GRCh38#188979712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24907431-A-C

188979766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907485-G-C

188979846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907565-G-A

http://identifiers.org/hco/3/GRCh38#188979889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24907609-C-A

188979889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907609-C-G

188979919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907639-G-A

188980125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907794-A-G

188980169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24907831-A-G

188980580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908270-G-A

188980580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908270-G-C

188980580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908270-G-T

188980680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908329-T-C

188980926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908573-G-C

188981051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908690-G-A

188981065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908704-T-C

188981241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908851-G-T

http://identifiers.org/hco/3/GRCh38#188981279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24908887-C-A

188981337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908938-A-G

188981478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909080-T-C

188981597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909191-A-G

188981688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909280-C-T

188981705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909295-C-T

188981720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909310-C-T

http://identifiers.org/hco/3/GRCh38#188982052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24909385-A-C

188982135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909470-G-C

188982398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909691-G-A

188982490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909778-G-A

188982493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909781-T-C

188982633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909904-T-C

http://identifiers.org/hco/3/GRCh38#188982685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24909946-C-A

188982893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910064-A-G

188982893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910064-A-T

188982900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910071-C-T

188983366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24910499-T-A

188990357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24920275-T-A

188990423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24920347-A-G

188990903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24920812-T-G

http://identifiers.org/hco/3/GRCh38#188990991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24920905-C-A

188991088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24921531-G-A

188991187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24921627-A-G

188991194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24921634-A-G

188991200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24921640-G-C

188991202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24921642-C-T

188992642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24922880-G-A

188993038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24923207-G-T

188993088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24923257-T-C

http://identifiers.org/hco/3/GRCh38#188993118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24923287-A-C

188994239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24924646-A-G

http://identifiers.org/hco/3/GRCh38#188994264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24924671-C-A

188994265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24924672-C-T

188994342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24924740-T-C

188994503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24924875-C-G

188994524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24924896-A-G

188994626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24925000-A-T

188995019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24925362-G-A

188995094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24925436-C-T

188995181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24925545-C-G

188995411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24925796-G-C

188995466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24925858-T-C

188995512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24925908-T-A

188995594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24925990-T-A

http://identifiers.org/hco/3/GRCh38#188995748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24926148-C-A

188995810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24926206-C-T

188995870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24926264-C-T

189003113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24940477-C-T

189003221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24940580-G-C

189003318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24940665-C-G

189005262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24943917-C-T

189005696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24944590-G-A

189005767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24944656-A-G

189005864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24945892-C-T

189005924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24945941-T-G

189005934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24945951-G-C

189005947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24945962-G-A

189006136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24946180-A-G

http://identifiers.org/hco/3/GRCh38#189006182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24946217-C-A

189006182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24946217-C-T

189006183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24946218-T-C

189006183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24946218-T-G

189006227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24946260-T-C

189008230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24947862-G-A

189008405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24948042-A-G

189008703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24948290-A-G

189008866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24948472-A-G

189025782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24951743-G-A

189025782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24951743-G-C

189026410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24952307-A-G

189026595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24952473-G-A

189026662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24952536-G-A

189026779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24952636-G-C

189026783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24952640-G-A

189026837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24952694-G-A

189027037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24952924-G-A

189027133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24953015-A-G

http://identifiers.org/hco/3/GRCh38#189027139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24953021-C-A

189027139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24953021-C-G

189027258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24953142-T-C

http://identifiers.org/hco/3/GRCh38#189027374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24953265-A-C

189027427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24953318-T-C

189027921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24953803-G-A

189027938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24953821-T-C

189028151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24953918-T-C

189028500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954092-G-A

189028703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954279-G-A

189028765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954333-T-C

189028775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954343-T-C

189028806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954372-T-C

189028853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954429-C-T

189029053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954625-T-A

189029053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954625-T-G

189029100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954669-G-T

189029114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954681-G-A

189029152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24954723-T-G

189029297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24958356-A-T

189030077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24958749-T-C

189030081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24958753-T-G

189030089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24958761-T-G

189030104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24958773-A-G

189030247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24958924-G-T

189030322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24958999-C-T

189030808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24963573-T-G

189030864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24963626-T-C

189031414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24963889-T-C

189031445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24963928-C-T

189031460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24963943-A-G

189031863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24964287-G-A

http://identifiers.org/hco/3/GRCh38#189031995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24964424-A-C

189032017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24964446-A-T

189032100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24964529-G-A

189032100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24964529-G-T

189034149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24966313-G-A

189034453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24966601-G-C

189034564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24966736-A-T

189041757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24971685-G-A

189041759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24971687-C-T

189041803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24971729-A-G

189041860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24971784-C-T

189042290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24972160-T-C

189042622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24972803-C-T

189043533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24976959-C-G

189043589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24977013-C-T

189043613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24977035-T-C

189043969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24977385-T-G

http://identifiers.org/hco/3/GRCh38#189043993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24977408-C-A

189044292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24977546-C-T

189044577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24977663-T-A

189044577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24977663-T-G

189044653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24977731-A-G

189044898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24977961-G-T

189044918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24978117-A-G

189044929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24978130-T-C

189044965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24978257-T-C

189045022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24978314-C-T

http://identifiers.org/hco/3/GRCh38#189045121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24978412-C-A

189045548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24978440-G-A

189045717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24978608-G-T

189045749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24978705-G-T

http://identifiers.org/hco/3/GRCh38#189045814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24978768-A-C

189045846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24978799-G-T

189045983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24978922-G-A

189046137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24979005-G-T

189046173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24979690-G-T

189046178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24979695-A-G

189046279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24979779-G-T

189046368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24979873-A-G

189046382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24979887-C-G

189046452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24979944-A-G

189046543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24980035-G-A

189046556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24980048-T-G

189056488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24983525-A-G

189056563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24983586-C-T

189056617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24983633-A-T

189056694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24983704-T-A

189056766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24983779-C-T

189056834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24983854-A-G

189056841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24983861-A-G

189057463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24984453-C-T

http://identifiers.org/hco/3/GRCh38#189057517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24984500-C-A

189057517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24984500-C-T

189057520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24984503-A-T

189058305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24985195-A-G

189058524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24985964-T-A

189058572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24986010-G-A

http://identifiers.org/hco/3/GRCh38#189058574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#24986012-C-A

189058574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24986012-C-T

189058593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24986029-G-C

189059189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24986613-C-T

189070436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25002963-A-G

189070456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25003008-A-G

189070598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25003140-A-T

http://identifiers.org/hco/3/GRCh38#189070661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25003235-A-C

http://identifiers.org/hco/3/GRCh38#189070681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25003265-A-C

189070860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25003430-G-A

189070906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25003460-C-T

189071466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25003987-C-T

189071468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25003989-C-T

189071490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25004008-C-T

189071814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25004359-T-C

189071866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25004411-A-G

189072037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25004576-G-A

189075490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25007723-A-G

189075679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25007874-T-C

189075679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25007874-T-G

189075690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25007885-G-A

189075725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25007918-A-G

189075726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25007919-C-T

189075846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25008031-G-A

189075961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25008143-C-T

189076005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25008186-A-G

189076215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25008390-G-T

189076297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25008469-C-T

189076428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25009213-T-C

http://identifiers.org/hco/3/GRCh38#189076544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25009312-C-A

189076544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25009312-C-T

189076558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25009314-T-C

189076581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25009337-G-A

189076581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25009337-G-T

189076621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25009381-A-G

189076728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25009489-C-T

http://identifiers.org/hco/3/GRCh38#189080525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25018234-C-A

189080525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25018234-C-T

189080537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25018246-G-A

189080542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25018251-G-A

http://identifiers.org/hco/3/GRCh38#189082038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25018638-C-A

189082842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25019982-A-G

189082946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020075-C-G

189082979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020107-A-G

189083025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020168-G-C

189083036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020179-A-G

189083157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020281-C-T

189083183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020307-G-A

189083194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020317-G-T

189083229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020352-G-C

189083247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020370-C-T

189084304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020630-T-C

189084354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020677-A-G

189089105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25021746-T-A

http://identifiers.org/hco/3/GRCh38#189089263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25022019-A-C

189089374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25022058-A-G

189089467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25022162-A-G

189093527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25028756-G-A

http://identifiers.org/hco/3/GRCh38#189093570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25028798-A-C

189093980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25030611-G-T

189094028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25030659-T-C

189094084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25030709-G-T

189094089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25030714-A-G

189094220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25030800-C-T

189094297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25030874-C-T

189094512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25031041-C-T

189094586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25031112-C-T

189094758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25031277-G-A

189094830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25031329-G-A

189094973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25031464-G-A

189095256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25031741-A-G

189095264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25031749-C-T

189095343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25031793-A-G

189095505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25031943-A-G

189095577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25032011-G-C

189095754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25032155-G-A

189095776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25032778-T-C

189095868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25032851-C-T

189096122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25033072-A-G

189096236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25033155-T-A

189096334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25033257-C-T

189096388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25033319-C-G

189096388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25033319-C-T

189096398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25033329-G-A

189096487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25033414-A-G

189097825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25037896-T-C

189097882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25037953-T-G

189097899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25037970-G-A

189098341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25038343-A-G

http://identifiers.org/hco/3/GRCh38#189098506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25038497-C-A

189098518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25038703-G-C

189098648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25038897-G-C

http://identifiers.org/hco/3/GRCh38#189098760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25039010-C-A

189098760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25039010-C-T

189098847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25039091-T-C

189099006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25039255-C-T

189099396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25039651-G-T

189099444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25039706-G-A

189099526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25039793-C-T

189099593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25039859-G-A

189099637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25039901-T-C

189099675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25039937-C-T

189099676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25039938-G-A

189099677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25039939-C-T

189099678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25039940-C-T

189099719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25039981-G-A

189099832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25040105-C-T

189100041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25040273-A-G

189100058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25040290-A-G

http://identifiers.org/hco/3/GRCh38#189100111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25040348-C-A

189100111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25040348-C-T

http://identifiers.org/hco/3/GRCh38#189100112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25040349-C-A

189100184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25040435-G-T

http://identifiers.org/hco/3/GRCh38#189100197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25040448-C-A

189100197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25040448-C-T

189100222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25040454-T-A

189100222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25040454-T-C

189100265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25040477-C-T

189100348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25040554-A-T

189100377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25040589-A-G

189100758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25040954-C-T

http://identifiers.org/hco/3/GRCh38#189101027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25041531-A-C

189101093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25041590-C-T

http://identifiers.org/hco/3/GRCh38#189103552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25042517-C-A

189103648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25042615-C-T

189103857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25045322-C-T

189104161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25045477-G-T

189104435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25045741-C-T

189104460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25045766-G-A

189107434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25048941-C-T

189107530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049031-A-G

189107563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049051-T-A

189107573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049061-G-A

189107671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049143-C-T

189107935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049377-A-G

189107942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049384-G-C

189108031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049472-A-G

189108149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049610-A-G

189108299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049762-G-A

189108406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25049860-A-G

189108780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25050577-T-C

189108795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25050589-G-A

189108795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25050589-G-T

189109005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25050822-G-T

189109172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051118-G-A

189109172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051118-G-T

189109182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051208-A-G

189109309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051335-C-T

189109425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051422-G-A

189109628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051576-G-C

189109632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051580-T-C

http://identifiers.org/hco/3/GRCh38#189109874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25051924-C-A

189109917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25051981-C-T

http://identifiers.org/hco/3/GRCh38#189109955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25052023-A-C

189109989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052061-C-T

189110085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052157-C-T

189110133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052206-C-T

189110139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052212-G-A

189110139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052212-G-T

189110211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052283-G-A

189110211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052283-G-C

189110245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052314-T-C

189110514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052548-C-G

189110537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052573-T-C

189110540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052576-T-G

189110553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052578-A-G

189110571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052596-G-C

189110571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052596-G-T

http://identifiers.org/hco/3/GRCh38#189110645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25052649-A-C

189110701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052710-T-C

189110820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25052819-A-G

189111135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25053069-A-G

189111298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25053227-G-A

189111332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25053252-T-A

189111334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25053254-G-A

189117296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25053754-A-G

189117345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25053794-C-T

189117381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25053827-A-T

189120017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25053976-A-G

189120794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25055938-C-T

189120800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25055944-A-G

189120888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25056021-T-G

189121191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25056217-G-A

189121265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25056234-A-G

189121635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25056512-T-A

189121645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25056519-T-C

189121658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25056534-C-T

189121664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25056540-G-A

189121664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25056540-G-T

189121682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25056558-T-C

189121787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25056647-G-A

189121787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25056647-G-T

http://identifiers.org/hco/3/GRCh38#189121844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25056695-C-A

189121844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25056695-C-T

189122180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057155-C-T

189122253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057228-A-G

http://identifiers.org/hco/3/GRCh38#189122391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25057366-C-A

189122482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057455-A-G

189122525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057496-A-G

189122550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057512-G-A

189122725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057671-G-T

189122800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057742-G-A

189122836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25057778-G-T

189123087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25058044-C-T

http://identifiers.org/hco/3/GRCh38#189123370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25058333-A-C

http://identifiers.org/hco/3/GRCh38#189123461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25058424-C-A

189123807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25058770-G-T

189123999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25058891-G-A

189123999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25058891-G-C

189124037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25058925-G-A

189124037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25058925-G-C

189124138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059008-G-A

189124191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059060-G-T

189124388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059245-G-A

189124674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059462-G-A

189124885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059664-C-T

189124903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25059682-A-G

189125263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060055-C-T

189125354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060123-G-A

189125382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060149-A-G

189125433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060198-T-C

189125473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060238-G-A

189125504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060269-T-C

http://identifiers.org/hco/3/GRCh38#189125660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25060423-C-A

189125660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060423-C-T

189125880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060589-A-G

189125880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060589-A-T

189126311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25060992-T-A

189126739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25061390-G-T

http://identifiers.org/hco/3/GRCh38#189126897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25061509-C-A

http://identifiers.org/hco/3/GRCh38#189126995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25061615-C-A

http://identifiers.org/hco/3/GRCh38#189127005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25061625-C-A

189127116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25061703-A-T

189127235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25061795-G-A

189127235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25061795-G-T

http://identifiers.org/hco/3/GRCh38#189127241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25061801-C-A

189127472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25062031-T-A

189127472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25062031-T-C

189127858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25063249-G-A

189127914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25063284-T-C

189127914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25063284-T-G

http://identifiers.org/hco/3/GRCh38#189128054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25063396-C-A

189128054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25063396-C-T

189128218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25063558-T-C

189128443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25063780-A-G

189128462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25063799-T-C

189128613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25063937-T-C

189128962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064083-T-G

189129096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064241-A-G

189129096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064241-A-T

189129121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064266-A-G

189129230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064361-C-T

189129359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25064470-G-A

189129359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25064470-G-T

189129540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064624-T-C

http://identifiers.org/hco/3/GRCh38#189129600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25064702-C-A

189129600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064702-C-T

189129608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064710-C-T

189129618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25064720-A-G

http://identifiers.org/hco/3/GRCh38#189129864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25064952-A-C

189129894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25064982-G-T

189130316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25065329-C-T

189130387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25065399-A-G

189130505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25065499-G-T

189130666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25065708-A-G

189130860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25065932-G-C

189130860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25065932-G-T

189130864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25065936-G-A

189130903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25065983-A-G

189130940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25066020-T-C

189130979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25066077-T-C

189131074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25066168-C-G

189131105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25066200-T-G

189131257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25066385-T-A

189131387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25066603-A-G

189131405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25066627-A-G

189131406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25066628-A-G

189131542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25066761-C-T

189131682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25066891-C-G

189131933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067151-T-G

189132141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067327-C-G

http://identifiers.org/hco/3/GRCh38#189132177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25067358-C-A

189132200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067381-A-G

189132257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067438-G-A

189132310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067496-T-C

http://identifiers.org/hco/3/GRCh38#189132321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25067507-C-A

189132321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067507-C-G

189132321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067507-C-T

189132368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067554-G-C

189132368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067554-G-T

189132524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25067703-T-A

189132609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25067788-G-A

189132609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25067788-G-T

189132669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25067846-G-A

189132684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25067861-A-G

http://identifiers.org/hco/3/GRCh38#189132735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25067911-C-A

189132737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067913-A-T

189132747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067923-G-T

189132758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25067934-G-T

189133083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068256-G-A

189133083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068256-G-C

189133192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068360-A-G

189133250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068407-G-T

189133273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068430-G-C

189133294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068449-G-A

189133294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068449-G-C

189134001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25068773-A-T

189135140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25070083-G-A

189135266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25070224-A-G

189135346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25070297-A-T

189135387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25070338-G-A

http://identifiers.org/hco/3/GRCh38#189135512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25070462-C-A

189135761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25070711-C-T

189135886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25070835-G-A

189136030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25071084-G-T

189136067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25071142-A-G

189136078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25071153-C-T

189136103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25071181-T-A

189136473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25071463-G-T

189136498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25071488-C-T

189136525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25071515-T-C

189136544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25071532-A-G

http://identifiers.org/hco/3/GRCh38#189136588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25071565-C-A

189136588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25071565-C-T

189136845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25072350-A-G

189136845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25072350-A-T

189137158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25072662-T-C

http://identifiers.org/hco/3/GRCh38#189137378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25072855-C-A

189137396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25072873-G-C

189138309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073133-T-C

189138359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073172-G-A

189138423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073234-A-T

189138517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073325-T-G

189138558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073362-C-G

189138558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073362-C-T

http://identifiers.org/hco/3/GRCh38#189138812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25073544-A-C

189138812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073544-A-G

189138844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073589-C-T

189139150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25073896-G-A

http://identifiers.org/hco/3/GRCh38#189139683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25074418-C-A

189139683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074418-C-T

189139718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074454-G-A

189139718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074454-G-T

189140238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25074962-G-A

189140332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075055-T-C

189140444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075165-G-A

189140444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075165-G-C

189140497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075210-C-T

189140580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075299-G-A

189140599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075318-G-T

http://identifiers.org/hco/3/GRCh38#189141195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25075782-C-A

http://identifiers.org/hco/3/GRCh38#189141208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25075809-C-A

189141324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25075951-G-T

189141404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25076016-T-G

189141446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25076039-C-G

189141500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25076089-T-C

189143032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25076897-A-G

189143357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077210-C-G

189143441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077295-A-G

189143818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077622-G-A

189143856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077663-G-A

189143989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077795-C-G

189144012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077824-C-G

189144165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077935-G-C

189144199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077969-A-G

189144208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25077978-A-G

189144411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25078181-A-G

189144505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25078262-G-A

189144904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25078638-C-T

http://identifiers.org/hco/3/GRCh38#189145285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25078950-C-A

189145285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25078950-C-T

189145570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079176-C-G

189145681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079278-A-G

189145765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079364-A-T

189145801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079399-T-C

189145801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079399-T-G

189145876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079473-A-G

189146047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079626-G-A

189146069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079647-C-T

189146211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079785-T-C

189146298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079842-C-T

189146370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079920-A-T

189146371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079921-A-G

189146410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079947-G-C

189146422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079959-T-C

189146451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25079988-G-A

189146498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080033-G-A

189146590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080133-C-T

189146871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080393-A-G

189147140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080637-C-T

189147165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080668-G-A

189147168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080671-G-A

189147186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080692-A-T

189147217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080721-C-G

189147232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25080736-A-G

189148311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25082793-C-T

189148335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25082817-C-G

189148345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25082827-T-C

189148618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083049-G-A

189148618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083049-G-C

189148618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083049-G-T

189148721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083152-G-T

189148746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083174-G-T

189148847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083244-G-T

189149013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083410-G-C

189149045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083440-A-G

189149105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083502-G-C

http://identifiers.org/hco/3/GRCh38#189149292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25083671-A-C

189149293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083672-G-A

189149363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083751-G-A

189149390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083765-A-G

189149391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083766-G-C

189149396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25083771-G-A

189149980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25084296-T-A

http://identifiers.org/hco/3/GRCh38#189150509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25084493-C-A

189150509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25084493-C-T

189150512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25084496-G-A

189150512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25084496-G-T

189150543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25084532-G-A

189150543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25084532-G-T

189150545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25084534-T-C

189150891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25084834-A-T

189150965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25084886-G-A

http://identifiers.org/hco/3/GRCh38#189151057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25085083-C-A

189151319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25085326-T-G

189151467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25085472-C-G

189151467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25085472-C-T

189151964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25085586-C-T

189152045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25085661-A-G

189152052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25085668-G-A

189152086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25085702-G-A

http://identifiers.org/hco/3/GRCh38#189152102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25085717-C-A

189152102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25085717-C-G

189152102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25085717-C-T

189153066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087070-A-G

189153147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087159-A-G

189153358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087351-A-G

189153491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087490-A-G

189153491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087490-A-T

189153588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087580-C-T

189153670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087645-T-C

189153833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087784-A-G

189153935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087874-G-A

189153935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087874-G-T

189153988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087930-G-A

189154050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25087989-T-C

189154120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25088054-G-A

189154230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25088165-C-T

189154860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25088593-A-G

http://identifiers.org/hco/3/GRCh38#189154988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25088647-A-C

189155027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25088675-A-G

189155123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25088763-G-C

189155434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25089065-G-A

189155639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25089185-G-A

189155746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25089299-A-G

189155882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25089431-C-T

189155909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25089459-G-A

189156260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25089780-C-G

189156299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25089815-T-G

189156568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25090071-G-A

189156568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25090071-G-T

189156606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25090105-C-T

189156699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25090197-C-T

http://identifiers.org/hco/3/GRCh38#189156712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25090221-C-A

189156850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25090347-T-G

189156918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25090417-G-A

189157101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25090567-C-T

189157177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25090639-T-C

189157303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25090757-A-G

189157592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091005-G-A

189157609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091022-A-G

189157704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091111-G-A

189157910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091304-G-A

189157914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091308-T-C

189157919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091313-A-G

189158034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091393-T-C

189158137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091497-G-T

189158188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091548-T-C

189158215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091575-T-C

189158708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091702-T-C

189158909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25091902-C-T

189159388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25092300-G-A

189159743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25092631-G-T

189159824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25092700-C-T

189159970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25092801-T-C

189160046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25092881-T-G

189160141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25092958-G-C

189160253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25093026-G-A

189160318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25093075-A-G

189160757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25093439-G-T

189160812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25093483-G-A

189160812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25093483-G-C

189160878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25093524-C-T

189161038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25093663-C-T

http://identifiers.org/hco/3/GRCh38#189161042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25093666-C-A

http://identifiers.org/hco/3/GRCh38#189161169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25093784-A-C

189162419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25097191-G-A

189162642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25097408-G-C

189162652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25097418-A-G

189163356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25097806-T-A

189163555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25097993-A-G

189163596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25098031-G-A

189163601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25098039-T-A

189163611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25098049-A-G

189163615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25098053-G-A

189163615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25098053-G-T

http://identifiers.org/hco/3/GRCh38#189163717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25098167-C-A

189163727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25098177-T-C

189164595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25098776-T-A

http://identifiers.org/hco/3/GRCh38#189164909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25099099-A-C

189164946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099133-G-T

189165046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099208-T-G

189165061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099212-A-T

189165078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099229-T-C

189165098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099249-G-C

189165132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099279-G-A

189165297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099428-C-T

189165348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099478-A-G

189165446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099716-A-G

189165451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099721-C-G

189165569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099834-C-T

189165600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099864-G-A

189165666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25099927-A-G

189166311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25100427-C-T

189166320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25100436-C-T

189166369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25100568-G-A

189166369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25100568-G-C

189166426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25100722-G-A

189166478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25100774-A-G

http://identifiers.org/hco/3/GRCh38#189166481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25100777-C-A

189166556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25100845-T-G

189166729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25101011-T-A

189167118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25101447-T-G

189167307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25101618-T-C

189167328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25101634-C-T

189167411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25101708-G-A

189167426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25101723-C-G

http://identifiers.org/hco/3/GRCh38#189168039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25102242-C-A

189168112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25102300-T-C

http://identifiers.org/hco/3/GRCh38#189168255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25102420-C-A

189168255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25102420-C-G

189168255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25102420-C-T

189168314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25102477-A-G

189168314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25102477-A-T

189168519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25102662-T-G

189168961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103073-G-C

189169144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103237-A-G

189169651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103481-A-G

189169658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103488-T-C

189169701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103517-G-A

189169752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103566-G-A

189169808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103605-C-G

189169811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103608-G-T

http://identifiers.org/hco/3/GRCh38#189170133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25103909-A-C

189170234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103981-G-A

189170237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25103984-C-G

189170394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104118-C-T

189170453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104178-A-G

189170681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104404-G-C

189170692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104422-C-T

189170736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104478-T-C

189170801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104543-A-G

189170924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104664-A-G

189171045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104775-C-T

189171074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104804-C-G

189171167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104895-C-T

189171246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25104968-C-G

189171408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105126-G-A

189171680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105347-G-A

189171680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105347-G-T

189171966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105608-T-C

189172015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25105656-G-A

189172015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25105656-G-T

189172099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25105735-A-G

189172100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25105736-G-T

189172118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25105754-A-G

189172149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105790-G-C

189172149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105790-G-T

189172172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105805-T-C

189172191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25105824-T-C

http://identifiers.org/hco/3/GRCh38#189172272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25105886-C-A

http://identifiers.org/hco/3/GRCh38#189172350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25105951-C-A

189172427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106038-C-T

189172433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106044-G-A

189172504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106115-A-G

189172603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106210-G-A

189172604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106211-T-C

189172615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106221-A-G

189172911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106675-C-T

189172927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106690-G-A

189172946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106708-G-A

http://identifiers.org/hco/3/GRCh38#189173010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25106743-C-A

189173084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106811-T-C

189173225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25106925-G-T

189173736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107126-C-G

189173828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107212-T-A

189173867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107249-C-T

http://identifiers.org/hco/3/GRCh38#189174473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25107791-C-A

189174473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107791-C-T

http://identifiers.org/hco/3/GRCh38#189174500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25107810-C-A

189174547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107856-C-T

189174588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107898-G-A

189174588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107898-G-T

189174639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25107956-C-G

189175315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25108628-G-A

189175369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25108682-G-A

189175376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25108689-C-T

189175386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25108699-A-G

189175780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25109065-A-G

189175971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25109253-T-C

189176239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25109457-G-A

189176260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25109478-T-A

189176261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25109479-G-A

189176464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25109678-A-G

189177115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110413-A-T

189177159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110460-G-A

189177205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110504-G-A

189177244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110542-A-G

189177276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110575-G-A

189177386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110671-T-A

189177399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110684-T-A

189177418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110703-G-A

189177426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110711-A-G

189177430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110715-A-G

http://identifiers.org/hco/3/GRCh38#189177474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25110759-A-C

189177508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110793-G-A

189177508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110793-G-C

http://identifiers.org/hco/3/GRCh38#189177520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25110805-C-A

189177545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25110838-G-T

189177768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111056-A-G

189177770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111058-G-C

189177778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111066-T-C

189177815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111103-A-G

189177815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111103-A-T

189177895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111182-C-T

189177898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111185-A-G

189177908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111194-G-A

189177965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111228-C-T

189178185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111419-G-A

189178816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111765-A-G

189178840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111785-C-G

189178938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25111883-G-A

189179220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25112124-A-G

189179264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25112168-C-T

189179284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25112193-T-C

189179284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25112193-T-G

189179302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25112225-C-G

189179315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25112238-C-G

189179324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25112247-C-G

189179324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25112247-C-T

189179375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25112300-C-T

189179540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25112427-A-G

189185833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25115900-A-G

189186056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25116251-C-G

189186177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25116375-C-T

189186266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25116461-G-A

189186314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25116490-C-T

http://identifiers.org/hco/3/GRCh38#189186435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25116582-A-C

189186439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25116586-A-G

189186546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25116691-C-T

189186581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25116726-G-A

189186691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25116832-G-C

189186801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25116931-A-G

http://identifiers.org/hco/3/GRCh38#189186874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25117008-C-A

189186883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25117019-T-C

189186896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25117036-G-A

189187759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25117273-C-T

189187976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25117490-G-C

189187982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25117496-A-G

189188335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25118413-A-T

189188524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25118578-C-T

189188576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25118630-T-C

189188601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25118658-T-C

189188779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25118835-G-C

189189303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25119377-G-T

189189367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25119440-A-G

189189493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25119530-C-T

189189801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25119846-A-G

189189806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25119851-A-G

189189881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25119925-A-G

189190762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25120065-A-G

189190858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25120144-C-T

http://identifiers.org/hco/3/GRCh38#189190971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25120257-A-C

189190990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25120276-G-C

189191037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25120323-T-C

http://identifiers.org/hco/3/GRCh38#189191121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25120406-C-A

189191149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25120433-T-A

189191149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25120433-T-G

189191152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25120436-G-A

http://identifiers.org/hco/3/GRCh38#189191751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25121281-C-A

189191974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25121501-G-A

189192119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25121646-T-A

189192119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25121646-T-C

189192213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25121738-G-A

189192386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25122050-G-C

189196926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25125822-G-A

189196938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25125834-C-G

189197045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25125906-T-A

189197052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25125913-A-G

189197108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25125969-A-G

189197140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25126001-A-G

189197230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25126090-C-T

189197323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25126172-G-A

http://identifiers.org/hco/3/GRCh38#189197357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25126205-C-A

189197357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25126205-C-T

189197480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25126317-T-C

189197505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25126335-G-C

189197621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25126447-A-G

189198244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127027-G-A

189198361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127128-A-T

189198577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127288-C-G

189198664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127356-A-G

189198664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127356-A-T

http://identifiers.org/hco/3/GRCh38#189198711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25127403-A-C

189198733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127425-A-G

189198820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127492-A-G

189198871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127544-A-G

189199132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127774-T-G

189199133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127775-T-C

189199143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127785-A-G

189199203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127845-G-A

189199251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25127897-G-T

189200091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25128276-C-T

189200207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25128390-C-T

189200709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25128880-T-C

189200787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25128966-G-A

189200798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25128977-C-T

189201155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25129258-T-C

189201201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25129304-G-T

189202095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25129771-A-G

189202097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25129773-T-C

189202204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25129878-G-T

http://identifiers.org/hco/3/GRCh38#189202598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25130434-C-A

189202745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25130588-G-C

189202842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25130669-C-T

http://identifiers.org/hco/3/GRCh38#189202849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25130676-C-A

189203205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25131282-G-T

189203428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25131546-A-G

189203761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25131929-G-A

189204141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25132388-G-A

189204447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25132705-C-T

http://identifiers.org/hco/3/GRCh38#189204469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25132727-A-C

189204474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25132732-G-A

189204991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25133295-C-T

189205173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25133447-G-A

189205173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25133447-G-T

189205244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25133520-G-T

189205358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25133614-C-T

189205706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134385-T-C

189206152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134774-T-G

189206348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25134952-T-C

189207074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25135700-C-T

189207077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25135703-G-A

189207168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25135817-C-T

189207247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25135878-T-G

189207265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25135895-G-A

189207294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25135922-C-T

http://identifiers.org/hco/3/GRCh38#189207312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25135940-C-A

189207312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25135940-C-T

189207336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25135961-G-T

189207601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25136239-T-G

http://identifiers.org/hco/3/GRCh38#189207643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25136273-C-A

189207643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25136273-C-T

189207702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25136332-T-G

http://identifiers.org/hco/3/GRCh38#189207718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25136348-C-A

189207718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25136348-C-T

189208945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25137915-A-G

189209006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25137961-T-C

189209233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25138169-C-T

189209326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25138255-T-G

189209845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25138904-G-A

189210160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25140468-A-G

http://identifiers.org/hco/3/GRCh38#189210331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25140624-C-A

http://identifiers.org/hco/3/GRCh38#189210491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25140782-A-C

189210968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25141187-C-T

189210973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25141192-G-C

189211003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25141225-T-C

189211115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25141333-C-T

189211450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25141649-C-G

189211767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25141913-A-G

189212779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25142920-C-T

189212935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143083-G-T

189213080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143222-G-A

189213295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143427-A-G

189213516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143643-C-T

189213532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143659-A-G

189213547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143674-C-T

189213682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143803-T-C

189213924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25143996-T-G

189214001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144069-A-G

189214122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144186-A-G

189214158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144222-C-T

189214300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144361-G-A

189214416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144475-A-G

189214523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144588-C-G

189214532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25144597-C-T

189214757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146358-C-G

189214870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146502-G-A

189215156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146880-A-T

http://identifiers.org/hco/3/GRCh38#189215167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25146889-C-A

189215167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25146889-C-T

http://identifiers.org/hco/3/GRCh38#189215198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25146911-C-A

189215280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147002-C-T

http://identifiers.org/hco/3/GRCh38#189215474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25147178-A-C

189215474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147178-A-G

189215498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147202-A-G

189215600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147293-T-A

189215786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25147461-A-G

189216683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25148275-T-C

http://identifiers.org/hco/3/GRCh38#189219460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25149747-C-A

189219540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25149812-T-C

189219567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 25149839-G-A

189219632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25149901-G-A

http://identifiers.org/hco/3/GRCh38#189219732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25149998-C-A

189219833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25150075-T-A

189219833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25150075-T-C

189219855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25150096-T-A

189219855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25150096-T-C

189220191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25150537-T-A

189220291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25150609-T-G

189220378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25150694-C-T

189220994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25150842-A-G

189221451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25151656-G-C

189221451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25151656-G-T

189221627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25151822-T-C

189221716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25152251-T-C

189221716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25152251-T-G

189221739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25152275-G-A

189221823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25152354-G-A

189221854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25152385-T-A

189222112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25152631-A-T

189222476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25153003-G-A

189222492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25153015-C-T

189222859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25153558-C-G

189222859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25153558-C-T

189222862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25153599-C-T

189222904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25153650-G-A

189223192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25154004-G-C

189223332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25154113-C-T

189223805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25154585-T-C

189225281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25155334-G-T

189225369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25155395-A-G

189225516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25155546-G-A

http://identifiers.org/hco/3/GRCh38#189225667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25155693-C-A

189225667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25155693-C-T

189225747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25155821-G-A

189225747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25155821-G-T

189225939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25156066-T-A

189225939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25156066-T-G

http://identifiers.org/hco/3/GRCh38#189225940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25156067-C-A

189225978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25156104-C-G

189226157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25156262-T-C

189226395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25156451-G-A

189226668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25156635-T-A

189226689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25156661-T-A

189226690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25156662-G-A

189226727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25156669-A-T

http://identifiers.org/hco/3/GRCh38#189226741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25156683-C-A

http://identifiers.org/hco/3/GRCh38#189226784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25156726-C-A

189229535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25162833-A-T

189229627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25162941-A-G

189229710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25163079-G-A

189229726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25163095-G-T

189229841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25163209-G-A

189229869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25163237-T-C

189229937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25163309-T-G

189230221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25163589-G-A

189230308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25163675-G-C

http://identifiers.org/hco/3/GRCh38#189230438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25163805-A-C

189230470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25163832-G-T

http://identifiers.org/hco/3/GRCh38#189230582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25164134-A-C

189230611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25164159-C-T

189230671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25164204-G-A

189230671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25164204-G-T

189230817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25164346-T-C

189230838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25164367-C-T

http://identifiers.org/hco/3/GRCh38#189231571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25164827-C-A

189231597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25164853-G-A

189231612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25164877-A-G

http://identifiers.org/hco/3/GRCh38#189231670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25164934-A-C

189231702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25164967-A-G

189232376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25167437-G-A

189232420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25167480-G-A

189232420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25167480-G-T

189232479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25167545-G-A

189232523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25167588-C-T

189233382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 25168514-G-A

189233475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 25168602-C-G

189233475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 25168602-C-T

189233511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 25168635-T-C

189233529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 25168653-T-C

189234519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25171343-G-T

189234562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25171378-C-T

http://identifiers.org/hco/3/GRCh38#189234747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25171455-A-C

http://identifiers.org/hco/3/GRCh38#189235236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25171938-C-A

189235236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25171938-C-T

http://identifiers.org/hco/3/GRCh38#189235461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25172265-C-A

189235463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25172267-T-C

189235564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25172362-G-C

189235781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25172541-C-T

189235807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25172569-G-A

189235953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25172701-G-A

189236037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25172792-T-C

189236085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25172840-A-T

189236358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25173148-G-A

189236376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25173161-C-G

189236551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 25173308-A-G

189236571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, undefined
orthologous variants: 25173328-C-T

http://identifiers.org/hco/3/GRCh38#189236587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25173358-A-C

189236635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25173405-T-C

189236837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25173593-A-G

http://identifiers.org/hco/3/GRCh38#189236919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25173670-A-C

http://identifiers.org/hco/3/GRCh38#189236929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25173681-A-C

189236981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25173725-A-G

189237000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25173744-T-C

189237068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25173806-A-G

189237069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25173807-G-T

189237223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25173942-G-C

189237223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25173942-G-T

189237752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25174580-A-G

189237752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25174580-A-T

189237764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25174593-G-A

189237764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25174593-G-C

189237916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25174799-G-A

189237941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25174845-T-G

189237997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25175052-T-C

189238059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25175113-T-C

189238304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25175302-G-C

189238333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25175332-C-T

189238467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25175447-C-T

189238632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25175610-G-T

http://identifiers.org/hco/3/GRCh38#189238639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25175625-C-A

189238639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron variant
orthologous variants: 25175625-C-T

189238757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25175715-G-A

http://identifiers.org/hco/3/GRCh38#189238805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/16/GRCm39#25175763-C-A

189238805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 25175763-C-G

189238805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25175763-C-T

189238862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25175820-T-C

http://identifiers.org/hco/3/GRCh38#189238863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25175821-C-A

189238863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25175821-C-T

189238889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25175847-C-G

189238889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25175847-C-T

189238952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25175914-T-C

http://identifiers.org/hco/3/GRCh38#189238961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25175921-A-C

189238961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25175921-A-G

http://identifiers.org/hco/3/GRCh38#189238974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25175931-C-A

189238974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25175931-C-T

189238981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25175940-T-A

http://identifiers.org/hco/3/GRCh38#189239029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#25175986-C-A

189239043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25175999-T-C

189239058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25176020-T-A

189239079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25176041-A-G

189239644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25176262-G-A

189239711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25176337-C-T

189239814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25176406-G-C

189239889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25176478-G-T

189239932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25176530-C-T

189240164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24759
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25176731-C-T