130365609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25954834-G-A

130365683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25954769-C-G

http://identifiers.org/hco/6/GRCh38#130365892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25954559-C-A

130365892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25954559-C-G

130365892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25954559-C-T

http://identifiers.org/hco/6/GRCh38#130366048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25954420-C-A

130366048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25954420-C-T

130366129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25954349-C-T

http://identifiers.org/hco/6/GRCh38#130366398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25954149-C-A

130366398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25954149-C-T

130366487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5 prime UTR variant
orthologous variants: 25954071-G-A

130366487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5 prime UTR variant
orthologous variants: 25954071-G-C

http://identifiers.org/hco/6/GRCh38#130366494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25954064-C-A

130366494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5 prime UTR variant
orthologous variants: 25954064-C-T

130366528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25954030-A-T

http://identifiers.org/hco/6/GRCh38#130366633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25953931-A-C

130366633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25953931-A-G

130366752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25953812-A-G

130366761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25953803-G-A

http://identifiers.org/hco/6/GRCh38#130367952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25952621-C-A

130367952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25952621-C-T

http://identifiers.org/hco/6/GRCh38#130368414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25952185-C-A

130368569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25951933-G-A

130368626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25951879-A-G

130368853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25951683-T-C

130368974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25951589-G-A

130369009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25951558-A-G

130369411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25951179-T-G

130369438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25951098-G-A

130369574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25950973-C-T

130369610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25950944-A-G

130369654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25950898-G-T

130370053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25950493-A-G

130370238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25950337-G-A

130370562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25950031-A-T

http://identifiers.org/hco/6/GRCh38#130370625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25949969-C-A

130370625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25949969-C-G

130370740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25949872-G-A

130370835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25949778-T-A

130370866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25949747-C-T

130371101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25949597-C-T

130371613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25948646-T-C

130371653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25948607-G-C

http://identifiers.org/hco/6/GRCh38#130371684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25948584-C-A

130371894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25948375-G-A

130372163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25948105-A-T

130373550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25945601-A-G

130373595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25945563-G-A

130373595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25945563-G-T

130373633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25945525-A-G

130374682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25938502-C-T

http://identifiers.org/hco/6/GRCh38#130374859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25938275-C-A

130375208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25937764-A-T

http://identifiers.org/hco/6/GRCh38#130375298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25937575-A-C

130375585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25937324-T-A

130375820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25937150-A-G

130375881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25937089-G-C

130375982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25936982-T-C

130376131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25936828-A-G

130377283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25935943-G-A

130377499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25935716-T-C

http://identifiers.org/hco/6/GRCh38#130377504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25935711-C-A

130377591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25935631-T-A

130377605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25935610-C-T

130377815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25935424-T-G

130378004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25935250-G-A

130378054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25935202-T-G

130378234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25935103-A-G

130379824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931952-G-A

130379869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931925-G-A

130379895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931904-T-C

130379956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931873-C-T

130379995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931835-G-A

130380126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931722-G-A

130380158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931673-A-T

130380164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931657-A-T

130380178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931644-G-T

130380230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931599-T-C

130380322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931508-G-A

130380340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931493-A-G

130380351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931482-G-A

130380486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25931327-C-T

130382909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25930375-A-T

130383007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25930285-C-G

130383011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25930282-G-A

130383062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25930251-T-A

130383062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25930251-T-G

130383119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25930194-A-G

130383120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25930193-G-T

130383174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25930151-C-T

130383246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25930085-G-A

130383280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25930050-C-T

http://identifiers.org/hco/6/GRCh38#130383330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#25929999-A-C

130383459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25929886-T-G

130383473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25929872-T-C

130383662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25929708-G-A

130383674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25929693-T-C

130384179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25929533-T-G

130384212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25929497-G-A

130384305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25929377-G-A

130384305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25929377-G-C

130385044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25929006-G-A

130385063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25928986-C-G

130385067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25928982-A-T

130385147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25928900-C-T

130385381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25928252-C-T

130385499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25928124-A-T

130385634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron_variant, undefined
orthologous variants: 25927990-T-A

130385636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron_variant, undefined
orthologous variants: 25927988-A-G

130385714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25927902-T-C

130386277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25927381-T-C

130386586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25927095-A-T

130386649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25927028-T-C

130386669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25927008-T-C

130386957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25926717-C-T

130387216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25926456-C-T

130387663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25926355-T-C

http://identifiers.org/hco/6/GRCh38#130387859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25926151-C-A

130388561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25918792-A-G

130388867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25918482-C-G

http://identifiers.org/hco/6/GRCh38#130389385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25917638-C-A

130389385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25917638-C-T

http://identifiers.org/hco/6/GRCh38#130390379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25916125-C-A

130390572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25915813-T-C

130390637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25915748-C-T

130390858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25915535-A-G

130391121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25915307-C-T

130391152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25915278-T-C

130391172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25915261-G-C

http://identifiers.org/hco/6/GRCh38#130391237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25914118-A-C

130391277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25914078-G-C

130391444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25913920-A-G

130391444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25913920-A-T

130392104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25913643-T-C

130392104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25913643-T-G

130392236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25913520-A-T

http://identifiers.org/hco/6/GRCh38#130392616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25913075-A-C

130392616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25913075-A-G

130392628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25913063-C-T

130393295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25912436-G-C

130393677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25912063-T-C

130393797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25911880-A-G

130394503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25911035-T-C

130394883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25910674-G-C

http://identifiers.org/hco/6/GRCh38#130394905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25910653-A-C

130395012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25910568-C-T

http://identifiers.org/hco/6/GRCh38#130395145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25910358-A-C

130395170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25910310-C-G

130395293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25910177-T-G

130395358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25910101-C-T

130396111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25909392-A-G

130400573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25904344-G-T

130400622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25904292-T-C

130400705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25904224-T-C

130400775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25904154-G-A

http://identifiers.org/hco/6/GRCh38#130403501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25903229-C-A

130406561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25901937-T-C

130406617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25901781-T-G

130406622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25901776-A-G

130406667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25901736-C-T

130409209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25900345-T-A

130409639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25896979-T-C

130410336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25896329-A-G

130411307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25895494-T-A

130411310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25895491-A-G

130411327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25895474-A-G

130411580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25895243-G-T

130411912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25894936-C-T

130414976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25892840-A-G

130415210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25892662-G-A

130415252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25892618-C-T

130415579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25892285-G-A

130415579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25892285-G-T

130415600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25892268-G-A

130415629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25892242-C-G

130415688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25892152-T-C

130416246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25890752-A-G

130419808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25888040-T-C

130422060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25885493-C-T

130422650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25885118-T-A

130423082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25884659-G-A

130423164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25884580-C-T

http://identifiers.org/hco/6/GRCh38#130423255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25884492-C-A

130423271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25884476-G-T

http://identifiers.org/hco/6/GRCh38#130430307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25874416-C-A

130430307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25874416-C-G

130430342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25874451-G-A

130430470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25874586-T-A

130430616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25874724-G-A

130430617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25874725-G-A

130430742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25874847-C-T

130430878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25874935-T-C

130430993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25875025-A-G

130431050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25875081-G-A

130431068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25875099-C-T

130431161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25875181-C-G

130431223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25875240-C-T

130431349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25875352-A-T

130431357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25875360-T-A

130431534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25875534-G-A

130431804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25875803-A-G

130431936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25875934-C-T

130432354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25876264-G-A

130432354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25876264-G-T

130433890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877198-G-T

130433984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877292-T-A

130434080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877373-C-T

130434375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877551-A-G

130434385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877561-G-A

130434535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877733-G-A

130434593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877794-C-G

130434611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877825-G-A

130434653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877862-A-G

130434777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877994-G-A

130434777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25877994-G-C

130435034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25878255-G-A

http://identifiers.org/hco/6/GRCh38#130436432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25878984-A-C

130436432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25878984-A-G

130436432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25878984-A-T

130436466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25879016-G-A

130436522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25879059-C-T

130437081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25879254-G-T

130437088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25879261-T-C

http://identifiers.org/hco/6/GRCh38#130437089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25879262-C-A

130437108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25879281-G-A

130437108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25879281-G-T

http://identifiers.org/hco/6/GRCh38#130437147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25879319-C-A

130437164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25879336-C-T

http://identifiers.org/hco/6/GRCh38#130437219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25873865-C-A

130437219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873865-C-T

130437238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873840-T-C

130437238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873840-T-G

130437250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873828-T-C

130437372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873699-C-T

130437422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873645-G-A

130437422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873645-G-T

http://identifiers.org/hco/6/GRCh38#130437445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25873622-C-A

130437445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873622-C-G

130437446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873621-T-C

130437759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873334-T-C

130437838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25873265-T-A

130438437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25872728-G-A

http://identifiers.org/hco/6/GRCh38#130438481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25872684-A-C

130438646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25872524-G-A

130438646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25872524-G-C

130438776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25872241-G-A

130438792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25872208-G-A

130438792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25872208-G-T

http://identifiers.org/hco/6/GRCh38#130438806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25872194-A-C

130438856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25872147-A-G

130438903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25872095-T-C

130438904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25872094-T-C

130438962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25871974-G-A

130438962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25871974-G-T

130439082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25871861-G-C

130439287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25871655-G-A

130439359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25871584-T-C

130439360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25871583-G-A

130439360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25871583-G-T

130439372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25871571-A-G

130439379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25871564-A-T

130439380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25871563-A-G

http://identifiers.org/hco/6/GRCh38#130439450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25871498-C-A

130439584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25871375-G-T

130439585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25871374-A-G

130439656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25871315-A-T

130439724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25871240-G-A

130439856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25871139-G-A

130440162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25870637-A-G

130440362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: intron variant
orthologous variants: 25870318-G-A

130440498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: missense variant
orthologous variants: 25870190-G-T

130440512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: synonymous variant
orthologous variants: 25870176-G-A

130440512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: synonymous variant
orthologous variants: 25870176-G-T

130440846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: missense variant
orthologous variants: 25869842-T-A

130440996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: missense variant
orthologous variants: 25869692-A-T

130441110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: missense variant
orthologous variants: 25869578-G-A

130441110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: missense variant
orthologous variants: 25869578-G-C

130441113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: missense variant
orthologous variants: 25869575-C-T

130441155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: missense variant
orthologous variants: 25869533-C-G

130441155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: missense variant
orthologous variants: 25869533-C-T

130441518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: missense variant
orthologous variants: 25869170-G-A

130441545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: missense variant
orthologous variants: 25869143-C-T

130441983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25868706-G-T

130442074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25868618-A-G

130442082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25868610-A-G

http://identifiers.org/hco/6/GRCh38#130442089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#25868603-C-A

130442089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25868603-C-G

130442090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25868602-A-G

130442244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25868446-A-G

130442244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25868446-A-T

130442330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25868363-T-C

130442330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25868363-T-G

130442331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25868362-G-T

130442961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25867788-T-C

130443022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21075
most severe consequence: 3 prime UTR variant
orthologous variants: 25867720-G-A