92325683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806465-C-G

92325692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806456-C-G

92325692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806456-C-T

92325699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806449-G-A

92325738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806412-A-G

92325747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806403-C-G

92325759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806391-T-C

92325788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806362-T-C

92325788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806362-T-G

92325851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806320-G-A

92325851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806320-G-T

92325880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806288-T-C

92325953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806209-G-C

92325953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806209-G-T

92325954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806208-G-C

http://identifiers.org/hco/9/GRCh38#92325980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49806179-C-A

92325980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806179-C-G

92325980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806179-C-T

92325982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5 prime UTR variant
orthologous variants: 49806177-G-T

92326026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 49806136-G-A

92326026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 49806136-G-T

http://identifiers.org/hco/9/GRCh38#92326072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49806091-C-A

92326072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 49806091-C-T

http://identifiers.org/hco/9/GRCh38#92326081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49806082-C-A

92326081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 49806082-C-T

92326086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 49806077-G-A

92326086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 49806077-G-T

92326110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49806052-G-A

92326110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49806052-G-T

http://identifiers.org/hco/9/GRCh38#92326191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49805975-C-A

92326191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49805975-C-T

92326424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49805536-C-G

92326424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49805536-C-T

92326819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49805157-G-A

92327060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49804977-G-A

92327125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49804906-C-G

92328199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49804727-G-A

92328199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49804727-G-C

92328393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49804369-C-T

92332127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49803811-G-A

92332127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49803811-G-C

92332127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49803811-G-T

92332207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 49803736-G-A

92332305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 49803638-C-T

92335057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49802462-A-G

92337523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49801146-T-C

92337645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49801027-T-A

92337645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49801027-T-C

92337645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49801027-T-G

92337666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49801008-T-A

92337684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49800992-A-G

http://identifiers.org/hco/9/GRCh38#92337687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49800989-C-A

92337687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49800989-C-T

92342944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49798905-T-G

92343343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49798183-T-C

92344079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49796747-T-C

92344132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49796696-G-T

92345671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49794817-G-C

92345671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49794817-G-T

92345711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant
orthologous variants: 49794776-T-A

92345711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 49794776-T-C

92345711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant
orthologous variants: 49794776-T-G

92345717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant
orthologous variants: 49794770-T-C

92379590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49780969-G-C

92379651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49780917-A-T

92379670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49780916-A-G

92379670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49780916-A-T

http://identifiers.org/hco/9/GRCh38#92379708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49780879-A-C

92379708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49780879-A-T

92379728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49780859-A-G

92379728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49780859-A-T

92380254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49779805-G-A

92380383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49779688-C-T

92380464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49779606-C-T

92383797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49778225-G-C

92384111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49777769-G-A

92384472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49777456-T-C

92384599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49777357-A-G

92384675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49777282-A-G

92385184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776866-T-G

92385332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776725-A-G

92385367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776692-G-A

92385367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776692-G-T

92385368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776691-G-A

92385368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776691-G-T

92385371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776688-G-A

92385481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776576-C-G

92385481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776576-C-T

http://identifiers.org/hco/9/GRCh38#92385509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49776550-C-A

92385517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776542-G-T

92385567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776496-A-G

92385567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776496-A-T

92385586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776490-G-A

92385586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49776490-G-T

92385832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49776250-C-T

92385849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49776233-T-C

92386149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49774633-A-G

92386155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49774629-A-T

92387849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49773317-C-T

http://identifiers.org/hco/9/GRCh38#92387878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49773289-C-A

92388145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49773374-T-A

92388411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49773289-C-T

92389844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49771779-A-G

92390081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49771542-C-G

92390081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49771542-C-T

92390168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49771440-T-C

92390731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49770869-A-G

92391686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49770578-A-G

92391994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49770228-G-A

92392014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49770133-G-A

92392604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49769556-G-T

92393136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49769137-G-A

92399601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49766194-C-T

92399634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49766163-A-T

92399686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49766106-G-T

92399912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49765879-A-G

92400699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49765481-G-A

http://identifiers.org/hco/9/GRCh38#92400732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49765390-C-A

92401041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49764928-T-A

92401041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49764928-T-C

92401041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49764928-T-G

92401824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49764058-G-A

http://identifiers.org/hco/9/GRCh38#92401826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49764056-A-C

92401826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49764056-A-G

92401835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49764047-G-A

http://identifiers.org/hco/9/GRCh38#92401978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49763913-A-C

92402402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49763544-A-G

92403132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49762932-T-A

92403688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49762385-T-C

http://identifiers.org/hco/9/GRCh38#92403959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49762115-A-C

http://identifiers.org/hco/9/GRCh38#92404366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49761720-C-A

92404705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49761377-G-T

92404976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49760944-G-T

92405272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49760313-A-G

http://identifiers.org/hco/9/GRCh38#92407545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49759634-A-C

92407976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49758998-A-G

92409208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49757443-A-G

92409247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49757385-G-A

92409272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49757360-T-C

92409272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49757360-T-G

http://identifiers.org/hco/9/GRCh38#92409435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49757179-A-C

92409435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49757179-A-G

92409704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49756933-G-T

92410350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49755374-G-A

92410883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49754911-A-G

http://identifiers.org/hco/9/GRCh38#92413686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49747426-C-A

92413686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49747426-C-T

http://identifiers.org/hco/9/GRCh38#92414104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49747023-C-A

92414882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49746110-A-G

92414969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49746023-A-G

92415072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49745919-A-G

92415086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49745904-A-T

92415171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant
orthologous variants: 49745827-T-C

92415309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant
orthologous variants: 49745698-C-G

92415309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant
orthologous variants: 49745698-C-T

92415539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49745484-A-G

92415577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49745465-T-C

http://identifiers.org/hco/9/GRCh38#92416602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49743904-A-C

92417145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 49743363-A-G

92417146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant
orthologous variants: 49743362-G-A

92417691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49742838-T-C

92417874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49742731-A-G

http://identifiers.org/hco/9/GRCh38#92417972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49742669-C-A

92418988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49741678-T-G

http://identifiers.org/hco/9/GRCh38#92419247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49741418-C-A

92420212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49739893-G-A

92420446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49739678-T-C

92421054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49739045-T-A

92421761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49738384-T-A

92422196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49738028-G-A

92422607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49737701-G-A

92423052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49737399-T-C

http://identifiers.org/hco/9/GRCh38#92423170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49737291-C-A

92423626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49736793-T-C

92423757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49736678-T-C

92423923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49736568-C-T

92424026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49736457-T-C

92424166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49736323-A-G

92425411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49735460-A-G

92426580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49734236-G-A

92454454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49722401-T-G

92456465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49720820-T-C

92456496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49720793-G-T

http://identifiers.org/hco/9/GRCh38#92456840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49720505-A-C

92456840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49720505-A-G

92456840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49720505-A-T

92456953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49720394-T-G

92457126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49720239-T-C

92457167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49720215-A-G

92457427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 49719966-G-C

http://identifiers.org/hco/9/GRCh38#92459129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49717803-C-A

92459129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49717803-C-T

92459781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49717219-T-C

92460558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49716924-G-T

92460577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49716905-A-G

92460597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49716892-T-C

http://identifiers.org/hco/9/GRCh38#92460661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49716836-C-A

92462327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49715461-G-A

92462351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49715443-C-T

92462751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49715079-T-C

92463189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49714512-C-T

92463683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49714324-G-A

92464233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49713081-G-A

92464289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49713037-G-C

92464314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49713015-C-T

92464483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712868-T-C

92464671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712699-G-A

http://identifiers.org/hco/9/GRCh38#92464754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49712621-C-A

92464754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712621-C-T

http://identifiers.org/hco/9/GRCh38#92464756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49712619-C-A

92464756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712619-C-T

92464788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712578-T-C

http://identifiers.org/hco/9/GRCh38#92464803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49712563-C-A

92464803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712563-C-G

92464803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712563-C-T

http://identifiers.org/hco/9/GRCh38#92465161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49712154-C-A

92465161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712154-C-G

92465161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712154-C-T

92465165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712150-A-G

92465206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49712114-A-G

92465429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49711510-A-T

92466017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49711138-G-A

92466025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49711130-G-A

92466231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49711043-T-C

http://identifiers.org/hco/9/GRCh38#92466260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49711024-A-C

92466299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49710993-G-T

92466372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49710920-G-A

92466372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49710920-G-T

http://identifiers.org/hco/9/GRCh38#92466643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49710445-C-A

92466643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49710445-C-T

92466705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49710399-T-C

92466705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49710399-T-G

http://identifiers.org/hco/9/GRCh38#92466711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49710393-C-A

92466711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49710393-C-T

92467475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49710206-G-A

http://identifiers.org/hco/9/GRCh38#92467640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49710057-C-A

92468265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49709908-A-G

92468576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49709636-T-C

92468859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49709066-C-T

92469820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49708124-A-G

92469888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49708052-G-T

http://identifiers.org/hco/9/GRCh38#92470513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49707653-A-C

http://identifiers.org/hco/9/GRCh38#92470592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49707582-C-A

92470592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49707582-C-T

http://identifiers.org/hco/9/GRCh38#92470648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49707527-A-C

http://identifiers.org/hco/9/GRCh38#92470870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49707317-C-A

92470903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49707285-G-A

92470903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49707285-G-T

92470980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49707210-A-G

92474675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49705339-A-G

92474821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 49705214-A-G

92474925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 49705111-G-A

92474925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 49705111-G-C

http://identifiers.org/hco/9/GRCh38#92474937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49705099-C-A

92474937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49705099-C-T

92474942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49705094-G-A

92474942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49705094-G-T

http://identifiers.org/hco/9/GRCh38#92474992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49705045-C-A

92475356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49704537-A-T

92475447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49704208-C-G

92479265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49701183-C-T

92479480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49700994-T-C

92479493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49700962-A-G

92479493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49700962-A-T

92479538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49700920-C-T

92479855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49700651-G-A

92479905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49700601-T-C

92481053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49699558-A-T

92481319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49699212-A-G

92481319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49699212-A-T

92482146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49698334-T-A

92482279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49698206-G-T

92482717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49697756-T-C

92482786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49697689-A-G

92482810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49697665-A-G

92483660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49697225-A-G

92483716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49697176-A-G

92483875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49697029-C-G

92484074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49696844-G-C

92484363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49696595-G-A

92484494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49696409-G-A

92486350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49695149-G-A

92486370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49695137-A-G

92488183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49693485-G-C

92489309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49691843-T-C

92489750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49690813-A-G

92490285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49688880-A-G

92490358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49688812-T-C

92490580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49688594-C-T

92490654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49688526-A-G

92493659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49687096-G-T

92493962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49686823-G-A

92493962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49686823-G-C

92493962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49686823-G-T

92495584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49685501-G-A

92496473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant
orthologous variants: 49684747-G-T

92500661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49683922-T-C

92501376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49683321-G-T

92501589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49683149-G-A

92501623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49683116-T-C

92501870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49682932-C-T

92502714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49682288-G-A

http://identifiers.org/hco/9/GRCh38#92502739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49682271-A-C

92502739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49682271-A-G

92508268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49680555-G-A

92508268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49680555-G-T

92508464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49680382-G-A

92508497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49680246-T-G

92509653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 49679311-A-G

http://identifiers.org/hco/9/GRCh38#92510073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49677760-C-A

92510073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49677760-C-G

92510073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49677760-C-T

92510149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49677681-A-G

92510199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49677653-T-C

92510582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49677415-T-A

92511498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49676870-G-T

92511610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49676754-G-A

92511720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49676643-T-C

http://identifiers.org/hco/9/GRCh38#92512551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49675836-A-C

92514034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49674651-A-G

92514635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 49674542-G-A

92514903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49674262-G-C

92514941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 49674224-T-A

92515004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 49674176-C-T

92515023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49674157-T-C

92515220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49673963-G-T

92515512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49673680-T-C

92516566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49673320-T-C

http://identifiers.org/hco/9/GRCh38#92517096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49672508-A-C

http://identifiers.org/hco/9/GRCh38#92517170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49672434-C-A

92517250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49672351-G-C

92517250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49672351-G-T

92517313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49672299-A-T

http://identifiers.org/hco/9/GRCh38#92517589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49672064-C-A

92517589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49672064-C-G

92517758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49671893-A-G

92518217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49671326-C-T

92521558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49669268-T-C

92522670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49668478-C-G

92522685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49668466-A-G

92522700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49668451-T-A

92522700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 49668451-T-G

92522915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49668249-A-G

92522918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49668246-T-G

92522986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49668184-G-T

92522998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49668172-T-C

92532769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49661238-C-G

92533009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49661048-A-T

92533463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49660854-C-T

92533578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49660755-C-T

http://identifiers.org/hco/9/GRCh38#92534129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49660097-C-A

92534157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49660056-G-C

92534264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49659962-G-T

http://identifiers.org/hco/9/GRCh38#92534375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49659858-C-A

92534911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49659403-C-G

92534911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49659403-C-T

92534968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49659343-T-A

http://identifiers.org/hco/9/GRCh38#92535789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49658621-C-A

http://identifiers.org/hco/9/GRCh38#92535888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49658525-C-A

92536173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49658246-A-T

92536535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49657934-A-G

92536535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49657934-A-T

92536537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49657932-G-A

http://identifiers.org/hco/9/GRCh38#92538414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49656486-C-A

92538414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49656486-C-G

92538414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49656486-C-T

92538559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49656104-A-G

http://identifiers.org/hco/9/GRCh38#92538718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49655961-C-A

92562589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49646253-T-C

http://identifiers.org/hco/9/GRCh38#92563797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49643731-C-A

92564036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49643502-T-C

92564036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49643502-T-G

92564986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49642780-A-G

92582542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49640670-A-T

http://identifiers.org/hco/9/GRCh38#92582643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49640597-C-A

92582643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49640597-C-T

92583003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49640267-G-A

92583125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49640099-G-A

92583519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49639481-C-T

92583908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49639071-G-A

92583917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49639062-A-G

http://identifiers.org/hco/9/GRCh38#92583927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49639052-A-C

92584059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49638925-G-A

92584102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49638881-C-T

92585916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49637218-A-T

92585943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49637194-G-C

92588871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49635163-T-C

92590953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49633317-A-G

92591071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49633216-C-G

92593452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49631978-A-G

92594101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49631717-G-A

92594101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49631717-G-C

92594101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49631717-G-T

92594401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49631480-C-T

92594554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49631330-C-T

92596964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49627515-C-T

http://identifiers.org/hco/9/GRCh38#92600415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49626472-C-A

92600541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49626383-G-C

92600591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49626335-G-T

http://identifiers.org/hco/9/GRCh38#92600637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49626293-C-A

92600637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49626293-C-T

http://identifiers.org/hco/9/GRCh38#92601231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49625717-C-A

92601424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49625541-G-A

92601489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49625489-T-C

92607427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49621873-G-A

92607574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49621747-G-A

92608126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49621205-A-G

92608182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49621151-G-A

92608328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49621001-A-G

92608522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49620847-C-G

92609249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49620103-A-G

92610538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49619596-T-C

92610798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49619371-T-C

92610798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49619371-T-G

92611423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49619135-A-G

92611423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49619135-A-T

92611819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49618768-G-A

92611819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49618768-G-T

92611869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49618728-T-C

92612022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron_variant, undefined
orthologous variants: 49618600-C-T

92612791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: intron variant
orthologous variants: 49617988-G-A

92613066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: missense variant
orthologous variants: 49617764-T-C

92613457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3 prime UTR variant
orthologous variants: 49617397-G-T

http://identifiers.org/hco/9/GRCh38#92613461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49617393-C-A

92614091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3 prime UTR variant
orthologous variants: 49616849-T-A

92614173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3 prime UTR variant
orthologous variants: 49616789-G-T

http://identifiers.org/hco/9/GRCh38#92614243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49616719-C-A

92614243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3 prime UTR variant
orthologous variants: 49616719-C-T

http://identifiers.org/hco/9/GRCh38#92614412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49616587-C-A

92615076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49615964-T-A

92615076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49615964-T-C

92615120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49615920-T-C

http://identifiers.org/hco/9/GRCh38#92615121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49615919-C-A

92615121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49615919-C-T

92615152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49615891-G-A

92615152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49615891-G-T

92615409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 49615640-A-G

http://identifiers.org/hco/9/GRCh38#92616229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49614955-C-A

92616229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614955-C-G

92616249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614937-G-A

92616249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614937-G-C

92616249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614937-G-T

92616282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614915-C-G

92616282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614915-C-T

92616349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614843-G-A

92616781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614422-G-C

92616781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614422-G-T

http://identifiers.org/hco/9/GRCh38#92616873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49614336-C-A

92616881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614328-C-G

92616887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614322-T-C

92616900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614308-T-A

92616900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614308-T-C

92616933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614256-C-G

92616933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614256-C-T

92616981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614211-G-A

92616981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49614211-G-T

92618685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612920-C-T

92618953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612715-G-A

92618953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612715-G-C

92618953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612715-G-T

92618970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612696-G-A

92618970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612696-G-T

92618973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612693-G-A

92618973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612693-G-T

92619048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612616-T-C

http://identifiers.org/hco/9/GRCh38#92619107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49612555-C-A

92619107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612555-C-T

92619212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612474-G-A

92619212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612474-G-T

http://identifiers.org/hco/9/GRCh38#92619338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49612287-C-A

92619338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612287-C-T

92619651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612034-G-A

92619651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612034-G-T

http://identifiers.org/hco/9/GRCh38#92619671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49612014-A-C

92619671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49612014-A-G

http://identifiers.org/hco/9/GRCh38#92619730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49611963-C-A

92619800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49611936-T-A

92619800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49611936-T-C

http://identifiers.org/hco/9/GRCh38#92619803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49611933-C-A

92619803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49611933-C-T

92619872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49611867-G-T

http://identifiers.org/hco/9/GRCh38#92620130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49611669-C-A

92620130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49611669-C-T

http://identifiers.org/hco/9/GRCh38#92620361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#49611531-C-A

92620361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49611531-C-T

92620404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32933
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49611500-T-C