132643642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125798620-A-G

132644117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125798987-A-G

132644130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125798999-G-A

132644160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125799031-A-G

132644279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125799116-A-G

132644393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125799229-A-G

132644438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125799286-T-C

http://identifiers.org/hco/2/GRCh38#132644624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125799640-C-A

132644719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125799741-T-A

132644719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125799741-T-C

132644724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125799746-A-G

132644762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125799775-T-G

http://identifiers.org/hco/2/GRCh38#132644842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125799849-C-A

132644842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125799849-C-G

http://identifiers.org/hco/2/GRCh38#132644860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125799867-C-A

132645117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 125800123-A-G

132645231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 125800237-G-A

132645255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 125800261-G-A

132645255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 125800261-G-T

132645429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 125800438-G-A

132645495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 125800507-C-T

132645499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 125800511-C-T

http://identifiers.org/hco/2/GRCh38#132645518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125800533-C-A

132645574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 125800589-G-A

132645574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 125800589-G-T

132645671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125800689-T-G

http://identifiers.org/hco/2/GRCh38#132645740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125800766-C-A

132645740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125800766-C-G

132645740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125800766-C-T

132645765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125800791-A-G

http://identifiers.org/hco/2/GRCh38#132645789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125800815-C-A

132645789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125800815-C-T

132645868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125800899-T-G

132645972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125801010-C-G

132645991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125801025-T-C

132645991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125801025-T-G

132645992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125801026-T-G

132646012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 125801040-A-G

http://identifiers.org/hco/2/GRCh38#132646040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125801068-C-A

132646074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 125801102-T-C

http://identifiers.org/hco/2/GRCh38#132646120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125801148-A-C

132646180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 125801208-G-A

132646231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 125801259-G-A

132646332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125801360-G-A

132646332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125801360-G-T

http://identifiers.org/hco/2/GRCh38#132646489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125801541-C-A

132646489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125801541-C-T

132646516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125801568-A-G

132647615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125804215-G-A

132647615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125804215-G-C

132648075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125804665-T-G

132648088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125804678-G-A

132648101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125804691-G-A

132650881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125808881-G-A

132651074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125809085-T-A

132651074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125809085-T-C

132651276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125809305-C-T

132651326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125809402-G-C

132651326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125809402-G-T

132651731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125810134-G-T

132651752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125810152-A-T

132651754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125810154-T-G

132651761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125810161-C-T

132651762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125810162-G-A

132652267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811307-A-T

132652272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811312-G-A

132652284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811324-T-C

132652316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811357-G-A

132652330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811369-G-A

132652330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811369-G-T

132652518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811545-G-A

132652606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811635-G-A

132652737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811763-C-T

132652738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811764-G-A

132652773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811793-G-C

132652822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811848-C-T

132652854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811880-T-C

132652854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125811880-T-G

132655053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125819604-C-G

132655163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125819717-A-G

http://identifiers.org/hco/2/GRCh38#132655172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125819726-A-C

132655186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125819742-G-C

132655210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125819763-A-G

132655507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125820054-G-A

http://identifiers.org/hco/2/GRCh38#132656213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125820655-A-C

132656227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125820670-C-G

132656682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125821142-A-G

132656850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125821298-T-G

132656859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125821304-C-T

132657337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125822129-G-T

132657613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125822780-C-T

132657672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125823244-T-C

132657729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125823296-G-A

132657793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125823357-C-T

132657825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125823389-T-C

132658262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125824231-A-G

132658604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125824545-A-G

132658783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125825034-T-C

132658843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125825116-G-A

132658852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125825123-A-G

http://identifiers.org/hco/2/GRCh38#132658876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125825148-A-C

132658876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125825148-A-T

132659010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125825268-C-G

132659269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125825496-C-T

132659329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125825561-A-G

132660019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125826377-C-T

132660031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125826389-A-G

132660031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125826389-A-T

132660069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125826425-T-C

132660154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125826496-T-C

http://identifiers.org/hco/2/GRCh38#132660202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125826544-C-A

132660202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125826544-C-T

http://identifiers.org/hco/2/GRCh38#132660238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125826582-C-A

132660346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125826701-G-A

132660346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125826701-G-C

132660457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125826816-A-G

132660515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125826878-T-C

http://identifiers.org/hco/2/GRCh38#132660557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125826929-C-A

132660592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827198-A-G

132660621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827227-G-T

132660705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827300-A-G

http://identifiers.org/hco/2/GRCh38#132660712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125827307-C-A

132660876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827423-T-C

http://identifiers.org/hco/2/GRCh38#132660993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125827527-A-C

132660993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827527-A-G

132661047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827578-C-T

132661093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827625-C-T

132661175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827682-C-G

132661175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827682-C-T

132661179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827686-G-T

132661204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827717-G-A

132661255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125827770-A-G

http://identifiers.org/hco/2/GRCh38#132661646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125828131-C-A

132661738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125828222-G-C

132661781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125828246-G-A

132662586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125830527-G-A

132662615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125830545-G-T

132663029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125830953-A-T

132663073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125830998-G-T

http://identifiers.org/hco/2/GRCh38#132663381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125831368-C-A

132663420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125831411-T-C

132663490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125831477-G-C

132663731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125831808-G-A

132663786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125831856-G-C

132663854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125831922-T-G

http://identifiers.org/hco/2/GRCh38#132664072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125832130-C-A

132664072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125832130-C-T

132664125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125832201-G-A

132664399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125832495-T-C

132664400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125832496-A-T

132664466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125832562-C-T

132664557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125832652-G-A

132664795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125832890-A-G

132665135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125833219-T-C

http://identifiers.org/hco/2/GRCh38#132665339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125833445-A-C

http://identifiers.org/hco/2/GRCh38#132665444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125833544-C-A

132665444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125833544-C-T

132665545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125833653-C-G

132665545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125833653-C-T

http://identifiers.org/hco/2/GRCh38#132665546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125833654-C-A

132665731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125833840-C-T

http://identifiers.org/hco/2/GRCh38#132665892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125833992-C-A

132666100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125834190-A-G

132666307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125834393-G-A

132666307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125834393-G-C

132666517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125835897-T-C

132666633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125836018-A-G

132666640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125836025-A-G

132666795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125836149-G-A

132666795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125836149-G-T

132666899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125836244-G-T

http://identifiers.org/hco/2/GRCh38#132666907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125836251-C-A

http://identifiers.org/hco/2/GRCh38#132666927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125836270-C-A

132666927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125836270-C-T

132667116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125836380-A-G

132667216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125836482-G-T

132667256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125836522-T-C

132667297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125836974-C-G

http://identifiers.org/hco/2/GRCh38#132667316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125836996-C-A

132667385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125837072-C-T

132667428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125837113-A-G

132667485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125837170-C-T

132667526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125837208-T-C

132667728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125837380-G-T

132668072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125837723-C-T

132668186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125837853-A-T

132668321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838062-T-A

132668321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838062-T-C

http://identifiers.org/hco/2/GRCh38#132668322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125838063-C-A

132668322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838063-C-G

132668322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838063-C-T

132668485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 125838213-G-A

132668485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 125838213-G-T

http://identifiers.org/hco/2/GRCh38#132668530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125838258-C-A

132668546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838274-C-T

132668552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838280-C-T

132668566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838308-T-C

http://identifiers.org/hco/2/GRCh38#132668577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125838319-C-A

132668577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838319-C-G

132668577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838319-C-T

http://identifiers.org/hco/2/GRCh38#132668585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125838327-A-C

132668787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838515-C-T

132669011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838723-C-T

132669216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125838935-C-T

132669483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125839188-G-A

132669518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125839223-G-A

132669556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125839261-G-A

http://identifiers.org/hco/2/GRCh38#132669577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125839285-C-A

132669717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125839410-T-C

132669780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125839473-G-A

132669780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125839473-G-T

132670008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 125839703-A-T

132670034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 125839729-G-T

http://identifiers.org/hco/2/GRCh38#132670124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125839820-C-A

132670124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 125839820-C-T

http://identifiers.org/hco/2/GRCh38#132670190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125839892-C-A

132670190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 125839892-C-G

132670190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 125839892-C-T

132670281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125839987-G-A

132670281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125839987-G-C

132670281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125839987-G-T

132670403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125840112-G-C

132670544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125840220-G-A

132670564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125840239-C-T

132670605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125840280-G-A

132671062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125840686-A-G

132671062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125840686-A-T

132671071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125840695-T-C

http://identifiers.org/hco/2/GRCh38#132671083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125840707-C-A

132671083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron_variant, undefined
orthologous variants: 125840707-C-T

http://identifiers.org/hco/2/GRCh38#132671114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125840725-C-A

132671114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125840725-C-T

132671159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: intron variant
orthologous variants: 125840765-G-A

132671193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5 prime UTR variant
orthologous variants: 125840798-G-T

http://identifiers.org/hco/2/GRCh38#132671207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125840812-C-A

132671404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5 prime UTR variant
orthologous variants: 125840997-G-A

132671404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5 prime UTR variant
orthologous variants: 125840997-G-T

http://identifiers.org/hco/2/GRCh38#132671428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#125841023-C-A

132671428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5 prime UTR variant
orthologous variants: 125841023-C-G

132671428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5 prime UTR variant
orthologous variants: 125841023-C-T

132671516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 125841108-G-A

132671516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 125841108-G-C

132671516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 125841108-G-T

http://identifiers.org/hco/2/GRCh38#132671553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#125841145-C-A

132671553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28431
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 125841145-C-T