77895751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104052168-T-G

77895983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104052396-G-C

77896052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104052461-A-G

http://identifiers.org/hco/13/GRCh38#77896139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104052543-C-A

77896154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104052558-T-A

77896155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104052559-G-T

77896286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104052697-T-A

77896289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104052700-A-G

77896292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104052703-A-G

http://identifiers.org/hco/13/GRCh38#77896427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104052819-C-A

77896427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104052819-C-T

77896437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104052829-G-A

http://identifiers.org/hco/13/GRCh38#77896461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104052850-C-A

http://identifiers.org/hco/13/GRCh38#77896492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104052881-C-A

77896492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 104052881-C-G

77896492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 104052881-C-T

77896642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053091-A-G

77896642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053091-A-T

http://identifiers.org/hco/13/GRCh38#77896829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104053278-C-A

77896829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053278-C-T

77896877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053340-C-T

77896925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053386-G-A

http://identifiers.org/hco/13/GRCh38#77896946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104053407-C-A

77896946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053407-C-G

77897011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053473-A-G

http://identifiers.org/hco/13/GRCh38#77897030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104053493-C-A

77897100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053557-C-T

77897146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053601-G-A

77897146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053601-G-T

77897329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053797-G-A

77897513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053883-G-C

http://identifiers.org/hco/13/GRCh38#77897539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104053907-C-A

77897539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053907-C-T

77897625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104053927-T-C

http://identifiers.org/hco/13/GRCh38#77897695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104054001-C-A

77897771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104054080-G-A

77897771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104054080-G-T

77897840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104054145-T-A

http://identifiers.org/hco/13/GRCh38#77897922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104054221-C-A

77897922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104054221-C-G

77897922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104054221-C-T

http://identifiers.org/hco/13/GRCh38#77898000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104054301-C-A

77898048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104054341-T-G

77898089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104054384-G-A

77898089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104054384-G-C

77898337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 104054639-G-A

77898337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 104054639-G-C

77898455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104054759-G-T

77898990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104055809-C-T

77899373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104056227-C-T

77899420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104056273-T-C

77899438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104056290-G-T

http://identifiers.org/hco/13/GRCh38#77899452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104056710-C-A

77899452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104056710-C-G

77899452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104056710-C-T

http://identifiers.org/hco/13/GRCh38#77899511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104056774-C-A

77899550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104056813-G-T

http://identifiers.org/hco/13/GRCh38#77899573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104056836-C-A

http://identifiers.org/hco/13/GRCh38#77899614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104056867-C-A

77899614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104056867-C-G

77899614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104056867-C-T

http://identifiers.org/hco/13/GRCh38#77899648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104056901-C-A

http://identifiers.org/hco/13/GRCh38#77899685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104056946-C-A

77899685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104056946-C-T

77899720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104056972-A-G

77899737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104057246-G-A

77899737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104057246-G-T

77899782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104057287-T-G

77899961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, missense_variant, synonymous_variant, undefined
orthologous variants: 104057469-C-T

77900019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057524-G-A

77900019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057524-G-T

77900027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057534-T-G

77900037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057543-G-A

77900037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057543-G-T

77900054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057563-A-G

77900065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057574-T-A

77900078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057587-T-C

77900098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057604-G-T

http://identifiers.org/hco/13/GRCh38#77900102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104057608-A-C

77900216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057730-A-G

77900274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057771-G-A

http://identifiers.org/hco/13/GRCh38#77900333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104057824-A-C

77900333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057824-A-T

77900386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057876-T-G

http://identifiers.org/hco/13/GRCh38#77900388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104057878-A-C

77900388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104057878-A-G

77900496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104058139-A-G

77900541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 104058237-G-A

77900574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 104058270-A-T

77900682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104058375-A-G

77900747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104058493-A-G

http://identifiers.org/hco/13/GRCh38#77900911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104058920-C-A

77901091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 104059107-G-A

77901094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 104059110-A-G

77901154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 104059170-T-C

77901154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 104059170-T-G

77901215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 104059231-G-T

77901248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059266-T-G

77901279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059298-T-G

77901296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059318-G-A

77901296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059318-G-T

77901301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059323-A-T

77901495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059488-G-A

77901502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059495-C-T

77901625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059612-C-T

77901643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059630-G-C

77901801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059778-C-T

http://identifiers.org/hco/13/GRCh38#77901845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104059807-C-A

77901928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059892-C-T

77901949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059913-T-C

77901996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104059950-T-C

77902272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104060207-T-A

77903360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 104060695-T-A

http://identifiers.org/hco/13/GRCh38#77903388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104060723-A-C

http://identifiers.org/hco/13/GRCh38#77903449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104060780-A-C

77903468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104060801-A-G

77903604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 104060937-G-A

http://identifiers.org/hco/13/GRCh38#77903622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104060955-C-A

77903628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104060961-G-A

77903628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104060961-G-T

77903637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104060970-G-A

77903668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104060990-T-A

77903681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104061002-A-G

77903850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104061132-G-A

77903896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104061289-T-C

77904197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104061716-G-A

77904296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104061825-G-A

77904302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104061831-G-A

77904302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104061831-G-T

77904518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104062041-C-T

77904899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104062347-T-C

http://identifiers.org/hco/13/GRCh38#77905102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104062551-C-A

77905166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104062614-C-T

77905578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104062991-A-G

77905697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104063107-A-G

77906217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104067743-G-A

http://identifiers.org/hco/13/GRCh38#77906337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104067855-C-A

77906422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104068165-G-A

77906567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104068318-G-A

77906628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104068379-C-T

77906825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104068568-C-T

77906900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104068632-G-C

77907454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104069245-C-T

77907465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104069653-C-T

77907469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104069657-A-T

77907752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104069984-T-A

77907786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070018-G-C

77907914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070145-A-G

77908057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070258-A-G

77908077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070278-A-G

http://identifiers.org/hco/13/GRCh38#77908102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104070303-C-A

77908317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070576-C-T

77908330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070589-A-G

77908331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070590-T-C

77908380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070637-T-A

77908413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070679-T-A

77908415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070681-T-A

77908415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070681-T-C

77908415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104070681-T-G

77908505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104070756-G-T

77908524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104070776-A-T

77908850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104071094-A-G

77908889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104071128-C-G

77908983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104071222-T-A

77908983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104071222-T-C

77908986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104071225-G-A

http://identifiers.org/hco/13/GRCh38#77909126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104071373-A-C

77909137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104071384-G-T

http://identifiers.org/hco/13/GRCh38#77909544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104071782-C-A

77909554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104071792-C-T

77909616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104071851-T-C

77909690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104071924-T-C

77909691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104071925-G-A

77909958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104072179-C-T

77910300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104072466-A-G

77910586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104072741-A-G

77910652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104072803-G-A

77910713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104072864-A-G

77910840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104072964-T-C

77911069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104073144-T-G

77911229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104073300-G-A

77911424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104073479-T-C

77911899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104073929-G-T

77912132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104074158-C-T

http://identifiers.org/hco/13/GRCh38#77912196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104074228-C-A

http://identifiers.org/hco/13/GRCh38#77912330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104074333-C-A

77912672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104074671-G-C

77912747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104074745-C-T

77912871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104074934-A-G

77913227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104075262-T-C

77913392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104075430-G-T

77913506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104075532-G-T

77913719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104075744-A-G

77913859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104075875-A-G

77913939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104075948-C-T

77914068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104076074-A-T

77914092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104076098-G-A

77914292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104076312-C-T

77914429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104076444-G-A

77914429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104076444-G-T

77914516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104076530-C-T

77914539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104076551-G-A

77914696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104076698-G-T

77914914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104076965-C-T

77915040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104077055-A-G

77915067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104077084-T-C

77915092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104077109-T-A

77915207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104077228-G-A

77915207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104077228-G-T

77915342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104077652-G-C

77916054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104078304-A-T

77916191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104078438-T-C

77916464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104078682-C-G

77916712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104078922-A-G

77916729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104078934-C-G

77916773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104078975-T-C

77916887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104079111-A-G

77916929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104079295-C-T

77917009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104079374-G-A

77917017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104079382-T-C

http://identifiers.org/hco/13/GRCh38#77917039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104079408-C-A

77917109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104079514-A-G

77917482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104079894-C-T

77917904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104080274-T-C

77918014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104080331-A-G

http://identifiers.org/hco/13/GRCh38#77918050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104080387-C-A

77918217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: synonymous variant
orthologous variants: 104080556-G-A

77918384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: missense variant
orthologous variants: 104080720-G-A

77918384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: missense variant
orthologous variants: 104080720-G-C

77918384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: synonymous variant
orthologous variants: 104080720-G-T

77918418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: synonymous variant
orthologous variants: 104080754-G-A

http://identifiers.org/hco/13/GRCh38#77918632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104080970-C-A

77918632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 104080970-C-T

77918665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081003-A-G

77918669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081007-G-A

77918728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081057-G-A

http://identifiers.org/hco/13/GRCh38#77918775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104081105-A-C

77918775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081105-A-G

http://identifiers.org/hco/13/GRCh38#77918812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104081141-C-A

77918812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081141-C-T

77918835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104081164-C-T

http://identifiers.org/hco/13/GRCh38#77918838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104081167-C-A

77918838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104081167-C-G

77918851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104081173-G-A

77918851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104081173-G-T

77918852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104081174-G-A

77918880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron variant
orthologous variants: 104081200-T-G

77919193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081372-A-G

77919193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081372-A-T

77919201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081380-G-A

77919201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081380-G-T

http://identifiers.org/hco/13/GRCh38#77919223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104081394-C-A

77919223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081394-C-T

77919247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081418-G-A

77919247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081418-G-T

77919276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081441-T-C

77919298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081458-T-C

77919314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081476-A-G

http://identifiers.org/hco/13/GRCh38#77919319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104081481-A-C

77919323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081485-T-C

http://identifiers.org/hco/13/GRCh38#77919351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104081513-A-C

http://identifiers.org/hco/13/GRCh38#77919381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104081543-A-C

http://identifiers.org/hco/13/GRCh38#77919399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, stop_gained
orthologous variants: http://identifiers.org/mco/14/GRCm39#104081567-C-A

77919429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 104081597-C-T

77919573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, stop_gained
orthologous variants: 104081755-T-A

http://identifiers.org/hco/13/GRCh38#77919680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104081870-C-A

77919680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104081870-C-T

77919714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104081904-T-C

77919826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104081988-A-G

http://identifiers.org/hco/13/GRCh38#77919837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104082000-C-A

77919837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104082000-C-G

77919837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104082000-C-T

http://identifiers.org/hco/13/GRCh38#77919870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104082035-C-A

http://identifiers.org/hco/13/GRCh38#77919898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104082057-C-A

77919898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104082057-C-T

77920027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104082196-G-A

77920027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104082196-G-T

77920469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104082564-A-G

77920701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104082749-G-T

77920845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104082896-T-C

http://identifiers.org/hco/13/GRCh38#77921196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104084072-A-C

77921275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104084159-A-G

http://identifiers.org/hco/13/GRCh38#77921397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104084295-C-A

77921397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104084295-C-G

http://identifiers.org/hco/13/GRCh38#77921562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104084461-A-C

77921562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104084461-A-G

77921922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104085466-C-T

77921950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104085494-T-G

77921962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104085506-C-T

http://identifiers.org/hco/13/GRCh38#77921976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104085516-A-C

77922338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104085872-T-C

77922404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104085939-A-G

77922539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104086064-G-A

77923516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104087402-T-C

77924088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104087990-G-A

77924103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104088006-A-G

77928217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104093695-A-G

77928441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104093927-T-A

77928857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104094347-T-C

77929021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104094516-G-A

77929051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104094539-G-A

77929298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104095039-A-G

77929348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104095089-C-T

77929431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104095188-G-A

77930514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104102513-G-C

77931008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104102992-A-G

77932011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104113014-G-T

77932084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104113078-G-T

77932182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104113174-T-C

http://identifiers.org/hco/13/GRCh38#77932195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104113187-C-A

77932414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104113373-T-A

77932496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104113625-A-G

77932543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104113670-G-T

77932568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104113689-C-T

77932661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104113787-G-A

77932703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104113829-A-G

77939465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104114416-A-G

77939568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104114518-G-A

77939684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104114638-G-A

77939684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104114638-G-T

77939686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104114640-A-G

77941273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104116805-G-A

77941303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104116833-T-G

77941318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104116848-T-C

77942681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104119215-C-G

http://identifiers.org/hco/13/GRCh38#77942694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104119230-A-C

77942742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104119263-A-G

http://identifiers.org/hco/13/GRCh38#77943028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104119528-A-C

77943082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104119583-G-C

77943121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104119622-A-G

77943132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104119633-T-G

http://identifiers.org/hco/13/GRCh38#77943281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104119760-C-A

77943579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104120032-C-G

77944086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104120532-G-A

http://identifiers.org/hco/13/GRCh38#77944140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104120581-A-C

77944182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104120623-G-A

77944231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104120668-T-G

77944292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104120729-A-G

77944300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104120737-G-T

77944591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104121008-C-T

77944676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104121065-C-T

http://identifiers.org/hco/13/GRCh38#77944739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104121105-C-A

http://identifiers.org/hco/13/GRCh38#77944751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104121117-C-A

http://identifiers.org/hco/13/GRCh38#77944762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104121128-C-A

77944809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104121173-A-T

77944818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104121182-G-C

77944818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104121182-G-T

77944880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 104121247-A-G

http://identifiers.org/hco/13/GRCh38#77944921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104121288-C-A

77945377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104121676-G-T

77945404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104121703-C-T

77945626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104121911-G-A

77945721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104122000-C-T

77945835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104122111-T-C

77946158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104122379-G-A

77946318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104122513-G-C

77946803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104122983-C-T

77946805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104122985-C-T

77946847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104123033-T-C

77946847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104123033-T-G

77946894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104123078-C-T

77946935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104123112-C-T

77946962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104123181-A-G

77947023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104123242-G-A

77947058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104123283-C-T

77947061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104123286-T-C

http://identifiers.org/hco/13/GRCh38#77947082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104123308-A-C

77947135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104123355-G-A

77952726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104129112-C-T

77952850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104129237-G-A

77952922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104129307-G-T

http://identifiers.org/hco/13/GRCh38#77953185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104129543-A-C

77953254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104129631-T-C

77953317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104129695-G-A

77953482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104129848-G-A

77953551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104129913-A-T

77953835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104130340-A-G

77954065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104130573-C-T

77954128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104130648-G-C

77954142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104130662-C-T

77954143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104130663-A-G

77954198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104130707-T-C

77954250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104130751-G-T

77954536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104131045-G-A

77966474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104133135-G-A

77966698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104133347-G-A

77966698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104133347-G-T

77966789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104133440-C-T

77966971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104133604-A-G

77966999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104133632-T-C

77967004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104133663-T-C

77967171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104134010-G-A

77967221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104134060-T-C

http://identifiers.org/hco/13/GRCh38#77967313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104134138-C-A

77967328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104134152-T-C

77967331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104134155-G-A

77967517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104134539-T-C

77967625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104134698-G-C

77968006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104135038-A-G

77968127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104135249-A-G

77968127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104135249-A-T

http://identifiers.org/hco/13/GRCh38#77968194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104135319-C-A

77968194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104135319-C-T

77968235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104135360-G-A

77968549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104136005-C-T

77968902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104136279-G-T

77969013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104136393-T-C

77969099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104136423-G-C

77969430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104136735-T-A

77969470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104136775-G-A

http://identifiers.org/hco/13/GRCh38#77970098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104137519-A-C

77970119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104137540-C-T

http://identifiers.org/hco/13/GRCh38#77970169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104137592-C-A

77970169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104137592-C-T

77970257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104137692-A-G

http://identifiers.org/hco/13/GRCh38#77970279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104137714-C-A

77970279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: 104137714-C-G

http://identifiers.org/hco/13/GRCh38#77970298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#104137733-A-C