24415225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135222357-G-A

24415225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135222357-G-T

24415448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135222153-G-A

24415552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135222070-C-T

24415731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135221911-G-A

24416004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135221664-C-T

http://identifiers.org/hco/1/GRCh38#24416136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135221520-A-C

http://identifiers.org/hco/1/GRCh38#24416203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135221481-C-A

24416223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135221464-G-T

24416232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 135221455-G-A

24416232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 135221455-G-T

http://identifiers.org/hco/1/GRCh38#24416259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135221438-C-A

24416291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221407-C-T

24416456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221284-G-A

24416524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221183-G-C

24416525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221182-G-C

24416525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221182-G-T

http://identifiers.org/hco/1/GRCh38#24416565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135221138-C-A

24416565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221138-C-T

24416672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221046-A-G

24416826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135220908-G-A

http://identifiers.org/hco/1/GRCh38#24416836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135220898-C-A

24416836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135220898-C-G

24416836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135220898-C-T

24416931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135220808-A-G

24416952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135220785-T-C

24416952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135220785-T-G

24417000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135220767-G-T

24417470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135220422-C-T

http://identifiers.org/hco/1/GRCh38#24417535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135220329-A-C

24417535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135220329-A-G

24417816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135220124-C-T

24418090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135219816-C-T

24418645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135219263-G-A

24418784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135219141-A-G

24418785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135219140-G-C

24418797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135219129-C-T

24419083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135218739-A-G

24419192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135218676-G-A

24419192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135218676-G-C

24419192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135218676-G-T

24419234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135218639-G-A

24419234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135218639-G-T

http://identifiers.org/hco/1/GRCh38#24419235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135218638-C-A

24419456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 135218434-A-G

24419485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135218408-G-A

24419485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135218408-G-T

24419507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135218386-C-G

24419507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135218386-C-T

http://identifiers.org/hco/1/GRCh38#24419535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135218359-C-A

24419535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135218359-C-G

24419535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135218359-C-T

24419617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135218265-A-G

24419689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135218194-G-A

http://identifiers.org/hco/1/GRCh38#24419711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135218173-C-A

http://identifiers.org/hco/1/GRCh38#24419776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135218108-C-A

24419776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135218108-C-G

24419779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135218105-G-T

24419809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135218075-G-T

24419979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135217926-A-G

24420036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135217872-G-A

24420036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135217872-G-T

24420088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135217818-A-G

24420099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135217761-A-G

http://identifiers.org/hco/1/GRCh38#24420109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135217751-C-A

24420109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135217751-C-T

24420141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135217694-G-T

24420166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135217670-A-G

24420174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135217662-G-T

24420176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135217660-A-G

24420196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135217640-A-G

24420474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135217465-T-C

http://identifiers.org/hco/1/GRCh38#24420636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135217362-A-C

24420705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135217293-A-G

24420737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135217251-C-T

24420969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135217055-A-G

24421004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135217031-T-G

24421569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135216257-T-C

24421648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135216180-C-G

24421659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135216170-A-G

24421660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135216169-G-T

24421723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135216097-T-A

24421724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135216096-T-A

24421727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135216093-T-C

http://identifiers.org/hco/1/GRCh38#24421754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135216067-C-A

24421775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135216046-G-T

http://identifiers.org/hco/1/GRCh38#24421793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135216028-C-A

24421849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135215973-G-T

24421857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135215964-T-C

24422125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135215737-T-C

24422252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135215609-A-G

24422289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135215563-G-A

24422291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135215561-G-C

24425706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135214459-G-A

http://identifiers.org/hco/1/GRCh38#24425727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135214439-C-A

24425727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135214439-C-T

24425731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135214435-T-C

24425769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135214397-G-T

24425792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135214375-T-C

24425827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135214339-C-T

http://identifiers.org/hco/1/GRCh38#24425836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135214334-C-A

24425922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135214285-T-C

24427278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135212618-G-A

24427291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135212605-C-T

24427448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135212443-T-C

24427648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135212266-A-G

24439861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135210169-G-A

http://identifiers.org/hco/1/GRCh38#24440114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135209896-C-A

24440114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135209896-C-T

http://identifiers.org/hco/1/GRCh38#24440280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135209738-C-A

24440280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135209738-C-T

24440282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135209736-G-A

24440282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135209736-G-T

24440294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135209724-G-A

24440294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135209724-G-T

24440546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135208652-A-G

24440603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135208594-G-A

http://identifiers.org/hco/1/GRCh38#24440621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135208576-C-A

24440630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135208567-C-T

http://identifiers.org/hco/1/GRCh38#24440634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135208564-C-A

24440634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135208564-C-T

24440637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135208561-T-A

24440834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135208414-G-A

24440992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135208286-C-T

http://identifiers.org/hco/1/GRCh38#24441008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135208271-C-A

24441128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135208160-C-T

24441446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135208029-T-A

http://identifiers.org/hco/1/GRCh38#24441492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135207984-C-A

24441492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135207984-C-T

24441687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135207795-A-G

24441754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135207741-C-G

24441754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135207741-C-T

24442154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135206917-C-T

24442178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135206893-T-A

http://identifiers.org/hco/1/GRCh38#24442202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135206869-C-A

http://identifiers.org/hco/1/GRCh38#24442253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135206822-C-A

24442290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135206782-G-A

24442290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135206782-G-T

24442301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135206771-A-T

24443460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135206585-T-A

24444000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135205950-G-A

24444043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135205899-T-A

24444085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135205821-G-A

24444211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135205711-G-A

24444539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135205440-A-G

24444917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135205071-T-C

24445063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204908-G-A

24445063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204908-G-T

24445079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204898-A-G

http://identifiers.org/hco/1/GRCh38#24445117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135204861-A-C

24445187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135204799-A-G

http://identifiers.org/hco/1/GRCh38#24445316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135204686-C-A

24445316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204686-C-T

http://identifiers.org/hco/1/GRCh38#24445359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135204644-C-A

24445361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204642-A-G

24445378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204641-G-T

24445385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204634-G-A

24445385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204634-G-T

24445626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204433-T-C

24445636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204423-C-T

24445808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204262-G-C

24448294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135204025-C-T

24448433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135203903-A-T

24448456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135203889-T-C

24448607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135203757-T-C

24449473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135201786-C-T

24449519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135201740-G-A

24449519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135201740-G-C

http://identifiers.org/hco/1/GRCh38#24449674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135201595-C-A

24449674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135201595-C-G

24450288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135201330-G-T

24452155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135200643-G-A

24452251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135200543-A-G

24452300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135200462-G-A

24452300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135200462-G-C

24452479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135200291-G-A

24452521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135200253-C-T

24452534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135200240-G-A

24452534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135200240-G-T

24452607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135200168-C-G

24452838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135199886-C-T

24452843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135199881-C-G

24452843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135199881-C-T

24453417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135199281-A-T

24453492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135199206-G-A

24453492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135199206-G-T

24453561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135199160-A-G

http://identifiers.org/hco/1/GRCh38#24455555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135196454-A-C

24455576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135196430-A-T

http://identifiers.org/hco/1/GRCh38#24455718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135196296-C-A

24455753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135196266-T-C

http://identifiers.org/hco/1/GRCh38#24456032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135196030-C-A

24456032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135196030-C-T

24456035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135196027-C-T

24456122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135195966-T-C

24456275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 135195813-T-G

24457139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135195583-G-A

24457371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135195379-A-G

24457518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135195223-G-A

24457635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135195126-G-C

24457635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135195126-G-T

24457702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135195061-C-G

24457702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135195061-C-T

http://identifiers.org/hco/1/GRCh38#24457948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135194898-C-A

24457948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194898-C-T

24457969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194877-T-C

24458080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194807-C-T

24458421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194608-A-G

24458482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194560-A-G

24458499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194543-G-A

24458568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194481-G-A

24458568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194481-G-T

24458709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194392-G-A

24458738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194362-G-A

24458742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194358-T-C

24458754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194346-G-C

24458754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194346-G-T

http://identifiers.org/hco/1/GRCh38#24458855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135194275-C-A

24458855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194275-C-T

24458864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194266-G-A

24458864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194266-G-T

24458934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135194198-A-G

24458960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135194172-C-T

http://identifiers.org/hco/1/GRCh38#24458961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135194171-A-C

24459038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194113-G-T

24459067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194075-T-C

http://identifiers.org/hco/1/GRCh38#24459071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135194071-C-A

24459097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194058-G-A

24459097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135194058-G-T

24460437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135193109-T-G

24460438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135193108-T-C

24460438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135193108-T-G

24460477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135193066-G-A

24460477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135193066-G-T

24460483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135193058-G-A

24460506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135193035-C-T

24460602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135192945-T-C

http://identifiers.org/hco/1/GRCh38#24460630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135192923-C-A

24460630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135192923-C-T

http://identifiers.org/hco/1/GRCh38#24460681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135192877-C-A

24460681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135192877-C-T

24463630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191835-C-G

24463714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191482-G-A

24463881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191312-A-G

http://identifiers.org/hco/1/GRCh38#24463911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135191293-C-A

24463911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191293-C-G

24463960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191259-G-A

24463960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191259-G-C

24463960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191259-G-T

http://identifiers.org/hco/1/GRCh38#24463974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135191245-C-A

24463974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191245-C-G

24463974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191245-C-T

24463988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191231-G-A

24464001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135191215-T-C

24464148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135191067-T-C

http://identifiers.org/hco/1/GRCh38#24464155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135191060-C-A

24464155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135191060-C-G

24464180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135191034-G-C

http://identifiers.org/hco/1/GRCh38#24464249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135190957-C-A

24464249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135190957-C-T

http://identifiers.org/hco/1/GRCh38#24464360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135190846-C-A

24464384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135190822-G-T

24464409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135190797-T-C

24464476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135190755-A-G

http://identifiers.org/hco/1/GRCh38#24464937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135182575-C-A

24464937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135182575-C-T

24464968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135182544-C-T

24465089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135182417-A-G

24465166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135182343-T-C

24465201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135182309-A-G

24465481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135182036-G-A

http://identifiers.org/hco/1/GRCh38#24465685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135181875-A-C

24465685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135181875-A-G

24465745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135181817-G-A

24465745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135181817-G-T

24465780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135181782-A-G

24468499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135180245-C-T

24468500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135180244-C-G

24468609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135180148-A-G

24468662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135180101-G-A

24468830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135180029-G-T

24468835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135180024-T-C

24468866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135179993-T-G

http://identifiers.org/hco/1/GRCh38#24468888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135179972-C-A

24468888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135179972-C-T

24468930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135179927-G-A

24468953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135179912-G-A

24468953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135179912-G-C

24469156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135179711-C-G

24469156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 135179711-C-T

24469187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179682-A-G

http://identifiers.org/hco/1/GRCh38#24469235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135179636-C-A

24469235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179636-C-T

http://identifiers.org/hco/1/GRCh38#24469246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135179625-C-A

http://identifiers.org/hco/1/GRCh38#24469247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135179624-C-A

24469247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179624-C-T

24469318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179555-T-C

24469431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179464-T-A

24469431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179464-T-G

24469493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179407-G-T

24469494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179406-A-T

http://identifiers.org/hco/1/GRCh38#24469517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135179384-C-A

24469572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179327-A-G

24469572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179327-A-T

http://identifiers.org/hco/1/GRCh38#24469589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135179310-A-C

24469589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179310-A-G

24469610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179289-T-C

24469616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179283-T-G

24469658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179239-A-G

24469689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179222-G-A

24469689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179222-G-T

24469694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179217-A-G

24469698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179213-T-C

24469710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179201-T-G

24469879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179052-G-T

24469900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179033-T-A

24469912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135179021-G-A

http://identifiers.org/hco/1/GRCh38#24470040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135178939-C-A

24470044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135178935-T-C

24470123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135178880-A-G

24470138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135178865-A-G

24470407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135178623-G-A

24470568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135178476-T-C

24470712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135178373-T-C

24470715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135178370-T-C

24470829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135178260-T-C

24470829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135178260-T-G

http://identifiers.org/hco/1/GRCh38#24471050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135178035-C-A

24471072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135178013-G-A

http://identifiers.org/hco/1/GRCh38#24471122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135177970-C-A

http://identifiers.org/hco/1/GRCh38#24471196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135177899-C-A

24471196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177899-C-T

24471215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177883-A-G

24471215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177883-A-T

24471254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177849-A-G

24471267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177836-A-G

24471270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177833-A-G

24471270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177833-A-T

24471272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177831-T-C

24471302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177801-A-G

24471315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177788-T-C

24471395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177778-A-G

24471398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177775-A-G

24471401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177772-T-C

24471401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177772-T-G

24471477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177755-A-G

http://identifiers.org/hco/1/GRCh38#24471503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135177749-C-A

http://identifiers.org/hco/1/GRCh38#24471504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135177748-C-A

24471504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177748-C-T

24471601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177693-T-A

24471601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177693-T-G

24471701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177601-G-T

24471715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177587-C-T

24471761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177543-A-G

24471797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177496-G-C

24471797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177496-G-T

http://identifiers.org/hco/1/GRCh38#24471864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135177469-A-C

24471864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177469-A-G

24471889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177451-G-T

24471890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177450-A-G

24471900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177440-G-T

http://identifiers.org/hco/1/GRCh38#24471906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135177434-C-A

24471906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177434-C-T

24471930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177416-T-C

http://identifiers.org/hco/1/GRCh38#24471968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135177378-C-A

24471975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177370-A-G

24471975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177370-A-T

http://identifiers.org/hco/1/GRCh38#24472104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135177279-C-A

24472104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177279-C-T

24472143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177239-T-C

24472145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177237-A-T

http://identifiers.org/hco/1/GRCh38#24472159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135177223-C-A

24472263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177131-A-G

24472296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177104-G-A

24472296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177104-G-T

http://identifiers.org/hco/1/GRCh38#24472357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135177051-C-A

24472357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135177051-C-T

http://identifiers.org/hco/1/GRCh38#24472448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135176969-C-A

http://identifiers.org/hco/1/GRCh38#24472490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135176791-C-A

24472546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135176739-G-C

24472546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135176739-G-T

24472560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135176725-G-T

24472582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135176691-A-G

24472701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135176461-G-A

24472701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135176461-G-T