131855733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29418843-T-A

131855733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29418843-T-C

131855803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29418806-G-A

131856250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29418358-G-A

131856255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29418353-G-A

131856560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29417963-G-A

131856947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29417604-C-T

131857611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29417115-G-C

131857639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29417088-T-C

131857825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29416978-T-A

131857883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29416929-T-C

131860209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414723-G-A

131860209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414723-G-C

http://identifiers.org/hco/9/GRCh38#131860218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29414714-C-A

131860218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414714-C-T

131860271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414664-A-T

131860415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414617-T-C

131860422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414610-A-G

131860508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414545-T-C

131860508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414545-T-G

131860523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414526-G-A

131860523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414526-G-C

131860523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29414526-G-T

http://identifiers.org/hco/9/GRCh38#131860602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29414447-C-A

131860602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, missense_variant
orthologous variants: 29414447-C-T

http://identifiers.org/hco/9/GRCh38#131860668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29414381-C-A

131860668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, missense_variant
orthologous variants: 29414381-C-G

131860668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, stop_gained
orthologous variants: 29414381-C-T

131860708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29414353-G-T

131860853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29414213-G-A

131860904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29414170-C-G

131860904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29414170-C-T

http://identifiers.org/hco/9/GRCh38#131860942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29414132-C-A

131860942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29414132-C-T

131861250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29413899-C-T

131863054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29412870-G-A

131863159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29412766-G-C

131863584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29412530-C-T

131864007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29412297-G-C

131864007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29412297-G-T

131864690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29411814-T-A

131864690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29411814-T-C

131865044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29411477-T-C

http://identifiers.org/hco/9/GRCh38#131865048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29411473-C-A

131865075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29411448-A-G

131865217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29411315-C-T

131865626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29411152-T-C

131865642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29411136-C-T

131866044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29410743-C-T

131868932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29410495-G-A

131868933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29410494-G-A

131868971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29410459-A-G

131868991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29410439-T-A

131869078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29410359-G-C

131869191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29410240-T-C

131869251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29410182-G-A

131869269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29410164-C-G

131869269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29410164-C-T

http://identifiers.org/hco/9/GRCh38#131869465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29409938-C-A

131869465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29409938-C-T

http://identifiers.org/hco/9/GRCh38#131869511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29409880-C-A

131869511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29409880-C-G

131869511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29409880-C-T

131869791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29409616-G-A

131870104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29409336-C-T

131870545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29409056-G-A

131870603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29409004-A-G

http://identifiers.org/hco/9/GRCh38#131873035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29407469-A-C

131873089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29407418-A-G

131873651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29406894-G-A

131874622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29406062-A-T

131874696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29406012-A-T

131874866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29405867-T-C

131875328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29405596-G-A

http://identifiers.org/hco/9/GRCh38#131876119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29404749-A-C

131876119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29404749-A-G

http://identifiers.org/hco/9/GRCh38#131876140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29404717-A-C

131876321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29404544-G-A

131876638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29404308-G-A

131876638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29404308-G-C

131876732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29404224-C-T

131876792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29404168-C-T

131878603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29403398-C-T

131878638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29403365-A-T

131878811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29403206-T-C

131879041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29402990-T-C

131879334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29402736-G-A

131879724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29402439-C-T

131879966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29402235-C-T

131880551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29401760-T-C

131880663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29401675-G-C

131880725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29401625-G-A

131881059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29401315-A-T

131881148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29401226-T-G

http://identifiers.org/hco/9/GRCh38#131881504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29400967-A-C

131881505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29400966-G-A

131884134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29399398-G-A

131884134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29399398-G-C

131884134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29399398-G-T

http://identifiers.org/hco/9/GRCh38#131884238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29399350-A-C

131884452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29399172-T-A

131885252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, undefined
orthologous variants: 29398578-G-A

131885485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29398394-A-G

131885485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29398394-A-T

131885804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29398090-G-A

131886035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29397862-T-C

131886041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29397856-A-G

131886258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29397709-C-G

131886258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29397709-C-T

http://identifiers.org/hco/9/GRCh38#131886296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29397665-A-C

131886411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29397615-C-T

131886958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29397010-C-T

131887037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29396965-G-A

131887310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29396723-C-G

131887310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29396723-C-T

131887403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29396633-C-G

131887814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29396239-A-G

131887816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29396237-A-G

131889447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29394795-T-A

http://identifiers.org/hco/9/GRCh38#131889502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29394744-C-A

131889628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29394630-G-A

131889920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29394378-A-G

131890113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29394250-A-T

131890348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29394056-T-C

131890609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29393453-A-G

131890618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29393444-T-C

131890668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29393392-C-T

131890696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29393366-A-G

131891728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29392336-A-G

131891945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29392169-A-T

131891990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29392124-G-C

131892111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29392059-T-C

131892142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29392027-G-A

131892229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29391939-G-A

131892229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29391939-G-C

131892229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29391939-G-T

131892283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29391912-T-C

131892436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29391774-T-C

131892478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29391738-T-A

http://identifiers.org/hco/9/GRCh38#131893270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29391011-A-C

131893299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390982-T-G

131893325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390956-G-A

131893335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390946-A-G

131893461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390741-C-T

131893533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390666-T-C

131893904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, missense_variant
orthologous variants: 29390317-A-G

131893995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 29390226-G-A

131894016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390207-C-T

131894049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390169-G-A

131894049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390169-G-C

131894065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390151-T-A

131894065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390151-T-C

131894066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29390150-G-T

131894424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29389876-T-C

131894640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29389717-A-G

131895062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29389465-A-G

131895118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29389425-A-G

131895673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29389031-C-T

131895703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29389007-T-C

131898955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29386509-C-T

131898956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29386508-G-A

http://identifiers.org/hco/9/GRCh38#131899282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29386231-C-A

131899285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29386228-C-T

131899303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29386209-T-G

131899360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29386160-C-T

131899479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29386035-C-T

131899793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29385765-A-G

131899794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29385764-T-C

http://identifiers.org/hco/9/GRCh38#131900255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29385304-C-A

131900255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29385304-C-T

131900349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29385242-T-C

131900800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29384909-T-C

131900800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29384909-T-G

http://identifiers.org/hco/9/GRCh38#131901157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29384749-C-A

131901157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29384749-C-T

131901656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29384234-T-C

131901751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29384132-G-T

131902262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29383663-T-C

http://identifiers.org/hco/9/GRCh38#131902305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29383619-C-A

131902305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29383619-C-T

131902336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29383588-G-T

131902727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29383178-A-G

131905378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29382131-A-G

131909211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29380357-T-C

131909294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29380276-A-G

131909732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29379834-T-C

131909759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29379810-A-G

http://identifiers.org/hco/9/GRCh38#131909992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29379588-C-A

131910024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29379557-A-G

131910084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29379502-C-T

131910383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29379080-G-T

131910612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29378855-A-T

131910631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29378836-G-A

131910648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29378820-C-G

131910793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29378678-C-T

131911236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29378272-G-C

131911285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29378221-T-C

131911508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29378026-A-T

131911717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29377834-T-C

131911773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29377778-C-T

http://identifiers.org/hco/9/GRCh38#131912661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29376891-C-A

131912661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29376891-C-T

131913152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29376397-A-G

131913162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29376387-T-A

131913350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29376209-C-T

131915794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29375621-A-G

131916058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29375397-T-G

131916143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29375316-A-G

131916196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29375263-G-A

131916362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29375079-G-A

131916427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29375019-G-T

http://identifiers.org/hco/9/GRCh38#131916442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29375004-C-A

131916459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374988-A-G

131916658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374833-C-T

131916758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374745-T-A

131916758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374745-T-C

131916787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374718-T-C

131916792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374713-T-C

131916845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374661-A-G

131916998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374564-C-T

131917078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374495-G-A

131917206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374375-G-A

131917463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29374159-G-A

131918027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29373673-A-G

131918256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29373500-G-A

http://identifiers.org/hco/9/GRCh38#131918293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29373463-C-A

131918297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29373459-G-T

131918513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29373248-A-T

http://identifiers.org/hco/9/GRCh38#131918962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29372928-A-C

131919254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29372726-T-A

131919254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29372726-T-C

131926097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29366470-G-A

http://identifiers.org/hco/9/GRCh38#131926234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29366352-C-A

131926234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29366352-C-T

131926355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29366229-T-C

131926596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29365959-A-G

131926975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29365617-T-C

131936194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29364255-T-A

131936220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29364226-A-G

131936221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29364225-G-C

131936224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29364222-T-A

131936514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29364016-C-T

131936520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29364010-C-T

131936583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29363951-T-C

131936702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29363849-C-T

131936704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29363847-G-A

http://identifiers.org/hco/9/GRCh38#131937265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29363319-A-C

131937462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29363167-C-T

131937500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29363130-C-T

131938503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29362355-C-T

131939330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29361447-A-G

http://identifiers.org/hco/9/GRCh38#131939488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29361289-A-C

131939488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29361289-A-G

131941074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29360640-G-A

131941279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29360476-A-G

131941631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29360203-C-T

http://identifiers.org/hco/9/GRCh38#131942147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29360021-A-C

131942355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29359845-C-T

131942832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29359418-G-A

131943371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29358896-T-C

131943661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29358605-C-T

131944062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29358244-C-G

131945066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29357341-T-C

131945075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29357332-A-G

http://identifiers.org/hco/9/GRCh38#131945603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29356954-A-C

131946660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29356315-G-A

131946683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29356300-G-A

131946683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29356300-G-C

131946878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29356149-T-C

131947203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29355846-T-A

131947209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29355840-G-T

131947738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29355309-T-C

131948082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29354974-T-C

131948136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29354921-A-G

131948143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29354911-T-G

131950496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29352854-G-A

131950496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29352854-G-T

131950600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29352773-T-C

131950712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29352662-T-C

131950774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29352602-G-A

131951634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29351737-T-A

131951745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29351673-T-C

131952128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29351370-A-G

131952669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29350596-T-G

131952976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29350332-C-T

131953221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29350090-G-A

131953293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29349936-T-C

131953333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29349893-T-G

131953564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29349698-A-G

131954235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29349458-A-G

131958888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29345678-G-A

131959118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29345512-C-T

http://identifiers.org/hco/9/GRCh38#131959178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29345491-A-C

131959363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29345346-T-C

http://identifiers.org/hco/9/GRCh38#131959946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29344803-C-A

131959946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29344803-C-T

131960217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29344537-G-A

131960268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29344486-G-A

131960320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29344461-C-T

131960417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29344391-C-T

131960667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29344244-C-G

131960770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29344170-G-C

131960770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29344170-G-T

131961037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29343964-T-C

131961169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29343849-G-C

131961611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29343475-A-G

131963493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29341888-G-A

131963625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29341761-G-A

131963639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29341747-A-G

131963787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29341591-G-C

131963810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29341568-T-C

131964048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29341340-T-C

http://identifiers.org/hco/9/GRCh38#131964624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29340977-A-C

131964973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29340637-T-C

131964999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29340611-T-C

131966685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29339196-G-A

131966721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29339165-A-T

131969386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29338009-T-C

131969406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29337989-T-C

131969656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29337768-C-T

131969686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29337718-G-A

131969688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29337716-G-C

131971444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29336077-A-G

131971463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29336063-C-T

131971536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29335998-C-T

131971571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29335970-A-G

131971650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29335938-G-A

131971692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29335917-T-C

131976948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29334002-T-G

131977172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29333702-C-G

131977172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29333702-C-T

131977187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29333687-C-T

131977219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29333674-G-C

131977512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29333396-C-G

131977552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29333356-G-A

131977552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29333356-G-C

131977582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29333347-G-T

131978066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29332770-G-A

131978183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29332696-A-G

131978554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29332329-A-G

131978822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331877-A-G

131978826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331873-T-C

131978826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331873-T-G

131979040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331689-C-G

131979414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331349-C-G

131979481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331283-T-A

131979481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331283-T-C

http://identifiers.org/hco/9/GRCh38#131979483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29331281-C-A

131979584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331213-G-A

131979584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331213-G-C

131979595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331202-G-A

131979657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29331138-C-G

131980195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29330722-A-G

131980195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29330722-A-T

131980585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29330343-T-C

131980600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29330329-T-C

131980600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29330329-T-G

131980801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29330152-A-G

http://identifiers.org/hco/9/GRCh38#131981066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29329895-C-A

131981387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29329582-A-G

131981584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29329433-G-A

131981584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29329433-G-C

131981684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29329312-G-C

131982310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29328787-G-C

131982406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29328721-T-C

131982727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29328491-C-T

131982728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29328490-C-T

131983398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29327430-T-C

131983791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29327021-A-G

131983943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29326874-A-G

http://identifiers.org/hco/9/GRCh38#131984022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29326788-C-A

131984775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29326193-T-C

131984884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29326103-T-C

http://identifiers.org/hco/9/GRCh38#131987849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29323941-A-C

131988049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: -G-A

http://identifiers.org/hco/9/GRCh38#131989626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29322447-C-A

131989626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29322447-C-T

131989765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29322313-T-A

http://identifiers.org/hco/9/GRCh38#131990197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29321944-A-C

131991114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29320906-T-C

131991275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29320742-A-T

131991688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29320376-G-C

131993035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29319628-C-T

131993197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29319503-T-A

131997181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29317533-G-C

131997325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29317424-C-T

131998152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316758-C-T

http://identifiers.org/hco/9/GRCh38#131998281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29316643-C-A

131998281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316643-C-G

131998281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316643-C-T

http://identifiers.org/hco/9/GRCh38#131998336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29316601-A-C

131998420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316565-A-G

131998453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316544-G-C

131998456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316541-T-C

131998558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316442-G-C

131998692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316308-T-C

131998855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316168-T-C

131998956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316057-G-C

131998956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316057-G-T

131998972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29316041-A-T

131999624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29315469-G-A

132001720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29314227-A-G

132001762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29314193-A-G

132001782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29314174-G-A

132001782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29314174-G-T

132002347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29313775-T-C

132002372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29313749-T-G

132002907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29313632-A-G

132002907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29313632-A-T

132003387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29313052-G-C

http://identifiers.org/hco/9/GRCh38#132003411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29313028-C-A

132003411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29313028-C-T

132004078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29311976-G-A

132004717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29311407-C-T

132004880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29311096-G-A

132004979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29310912-G-C

132005181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29310746-C-T

132005182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29310745-G-A

132005204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29310724-G-T

132005369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29310567-G-A

132005701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29310256-A-G

132005782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29310106-C-T

http://identifiers.org/hco/9/GRCh38#132005791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29310097-A-C

132006143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29309750-G-A

132006196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29309701-G-A

132006202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29309695-C-T

132006336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29309604-G-C

132006467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29309479-A-G

http://identifiers.org/hco/9/GRCh38#132006517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29309439-C-A

132006706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29309272-G-T

132006898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29309139-T-C

132006898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29309139-T-G

132007001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29309091-C-T

132007002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29309090-T-C

132007642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29308621-T-C

http://identifiers.org/hco/9/GRCh38#132007888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29308437-C-A

132008332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29308035-T-C

http://identifiers.org/hco/9/GRCh38#132011153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29305976-A-C

132011183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29305946-T-G

132011892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29305443-A-G

132011942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29305389-T-C

132011984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29305349-G-T

132012111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29305222-G-C

132012848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29304755-A-T

132013069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29304514-T-G

132013345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29304218-T-C

132013633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29303843-G-C

132013848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron variant
orthologous variants: 29303677-C-T

http://identifiers.org/hco/9/GRCh38#132014378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29303487-A-C

http://identifiers.org/hco/9/GRCh38#132014536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29303344-A-C

132014826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29303089-A-G

132015045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29302900-G-A

132015048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29302897-T-A

http://identifiers.org/hco/9/GRCh38#132015167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29302801-A-C

132015170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29302798-A-G

132015193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29302776-T-C

132015377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29302600-T-C

http://identifiers.org/hco/9/GRCh38#132015441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29302536-A-C

132015547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29302209-C-T

132016429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29301374-G-A

132017273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29300561-G-A

132017566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29300267-C-G

132017747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29300113-C-T

132017776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29300092-G-T

132017871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29299997-T-C

http://identifiers.org/hco/9/GRCh38#132017968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29299908-A-C

132018013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29299873-C-T

132018073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29299819-G-C

132018870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29298732-G-A

132019043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29298656-G-T

132019208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29298540-T-C

132020459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29298152-G-A

132020494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29298112-A-G

132020521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29298085-A-G

132021457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297264-G-A

132021461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297260-G-A

132021461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297260-G-C

132021461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297260-G-T

132021463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297258-G-A

132022532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29295783-C-T

132022586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29295726-A-G

132022605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29295709-A-G

132024549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294178-T-C

132026174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29292519-T-C

http://identifiers.org/hco/9/GRCh38#132026295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29292403-C-A

132026465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29292273-T-G

132026475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29292263-T-A

132026920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29291024-T-C

132027283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29290681-G-A

132028940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29289853-G-T

132029193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29289447-T-C

132029670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29288974-C-T

132030284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29288425-T-C

132030448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29288266-G-A

132030462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29288256-A-T

132031312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286879-C-T

132031322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286875-C-G

132031379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286824-T-C

http://identifiers.org/hco/9/GRCh38#132031790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29286560-C-A

132031807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286543-G-A

132031807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286543-G-T

132031875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286480-G-C

132032122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29286260-G-A

132032124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29286258-A-G

132032304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286109-T-C

132032407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286010-T-C

132032683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29285767-G-A

132032937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29285572-T-C

132033843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284665-A-G

132033851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284657-G-T

132034059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284448-A-G

132034311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284201-T-C

132034479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29284035-A-G

132034512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284002-A-G

132036880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279905-T-A

http://identifiers.org/hco/9/GRCh38#132036927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29279859-A-C

132036944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279844-G-A

132036967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279831-G-C

132037018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279805-G-C

132037067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279776-G-A

132037159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279719-C-G

132037159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279719-C-T

132037255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279639-C-T

132037280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279615-C-T

132037289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279606-T-C

132037418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279503-T-C

132037482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279440-T-G

132037785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279156-T-C

132037839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29279105-A-G

132038470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29278817-G-A

132038515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29278772-G-A

132038578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29278699-T-C

132038757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29278540-T-G

132038812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29278498-G-A

http://identifiers.org/hco/9/GRCh38#132038901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29278417-A-C

132038959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29278359-G-A

http://identifiers.org/hco/9/GRCh38#132039200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29278125-A-C

132039774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29277598-A-G

132039801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29277574-C-G

132039847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29277533-C-T

132040182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29277219-G-A

132040182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29277219-G-C

132040378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29277019-T-C

132040418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29276988-C-T

http://identifiers.org/hco/9/GRCh38#132040493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29276918-C-A

132040739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29276693-G-A

132040744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29276688-G-A

132040791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29276655-G-A

132040817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29276630-G-A

132040893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29276562-G-T

132040896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29276559-G-C

132041550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29275972-C-G

132041557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29275965-G-T

132041842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29275709-C-T

132042565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29275107-A-G

http://identifiers.org/hco/9/GRCh38#132042607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#29275067-A-C

132042676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29275001-G-A

132042872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29274823-G-T

132042888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29274809-T-C

132043172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29274575-G-A

132044988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29272513-T-C

132044989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29272512-G-A

132045024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29272476-A-G

132045045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29272455-C-T

http://identifiers.org/hco/9/GRCh38#132045283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29272224-C-A

http://identifiers.org/hco/9/GRCh38#132047400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29270086-C-A

132047482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29270006-G-A

132047547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29269946-A-G

132047699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29269806-T-G

132047725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29269780-T-G

132048367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29269278-G-A

132048499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29269146-T-C

132048741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29268906-G-A

132048781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29268866-C-T

132048784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29268772-G-A

132049091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29268456-G-C

132049110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29268439-C-T

132049629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29267906-G-A

132049783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29267761-C-T

132049911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29267637-G-C

132049912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29267636-A-G

132050328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266478-G-A

132050758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266112-G-A

132050883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265987-T-C

132051342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265538-T-C

132051533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265313-T-C

132051544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265300-G-A

132051621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265229-T-C

132051861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265012-G-A

132052185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29264733-A-T

132053485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29263909-G-A

132053906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29263560-A-G

132054008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29263504-C-G

132054862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29263446-A-T

132055093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29263249-C-T

132055258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29263112-T-C

132055373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29262624-G-C

132055383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29262614-C-T

132056111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29261944-G-C

132056985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29261218-G-A

http://identifiers.org/hco/9/GRCh38#132057566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29260661-A-C

132058935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29259613-C-G

132058935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29259613-C-T

132058987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29259558-C-G

132059090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29259457-A-G

http://identifiers.org/hco/9/GRCh38#132059093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29259454-C-A

132059188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29259363-G-A

132059271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29259264-G-A

132059592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29258943-G-A

132059599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29258936-G-T

132059606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29258929-C-T

132059952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29258612-C-T

132059967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29258597-C-T

132060092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29258486-T-C

132061139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257923-G-A

132061139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257923-G-T

132061242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257820-G-A

132061399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257691-T-C

132062208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29256024-T-C

132062273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255966-C-T

http://identifiers.org/hco/9/GRCh38#132062546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29255701-C-A

132063113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255520-T-C

132063209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255439-T-C

132063455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255217-A-T

132063467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255205-T-C

132063490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255182-C-T

132064986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252434-T-C

132065016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252396-C-T

http://identifiers.org/hco/9/GRCh38#132065019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29252393-C-A

132065108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252310-G-A

132065170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252264-T-C

132065176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252258-C-T

http://identifiers.org/hco/9/GRCh38#132065226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29252223-C-A

http://identifiers.org/hco/9/GRCh38#132065454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29252035-C-A

132065475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252015-C-T

132065479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252012-G-C

132065484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252007-T-A

132065543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251958-G-A

132065616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251884-G-T

132065619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251881-G-A

132065622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251878-T-G

132065911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251708-T-C

132065930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251689-T-C

132066050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251571-C-T

http://identifiers.org/hco/9/GRCh38#132066299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29251377-C-A

132066299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251377-C-T

132066746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251069-C-T

132066823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251002-T-C

http://identifiers.org/hco/9/GRCh38#132067262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29250669-C-A

132069678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248999-A-T

132070861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/9/GRCh38#132070862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

132071148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

http://identifiers.org/hco/9/GRCh38#132071266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

132071266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

132072933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29245675-G-A

132072946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29245665-G-C

132073039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29245573-G-A

132073146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29245432-T-C

132073204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29245373-T-A

132073204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29245373-T-C

132073234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29245340-A-G

http://identifiers.org/hco/9/GRCh38#132073236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29245338-C-A

132073236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29245338-C-T

http://identifiers.org/hco/9/GRCh38#132073279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29245301-C-A

132073423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29245120-T-G

132073425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29245118-G-T

132073438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29245103-G-A

132073438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29245103-G-T

132073479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29245062-T-C

132073479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29245062-T-G

132073588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29244952-A-G

132073611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29244617-T-A

132073611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29244617-T-G

132074026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29243480-T-G

132074206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29243306-A-T

132074848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29242717-A-G

132074969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29242609-G-A

132074983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29242595-G-C

132075122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29242443-G-T

132075986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29241221-T-C

132075995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29241212-G-A

132076036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29241191-A-T

132076137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29241094-G-C

132076156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29241076-G-A

132076252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29241003-T-G

132076687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29240644-A-G

132076865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29240497-G-A

132076865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29240497-G-C

132076871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29240491-C-T

132077049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29240346-G-C

132077150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29240231-T-C

http://identifiers.org/hco/9/GRCh38#132077305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29240117-C-A

132077305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29240117-C-T

132077597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29239846-A-G

132077847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29239151-C-T

132077923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29239081-T-A

132078151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29238869-T-G

http://identifiers.org/hco/9/GRCh38#132078189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29238831-A-C

132078189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29238831-A-T

132078237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29238791-G-A

132078273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29238760-C-T

http://identifiers.org/hco/9/GRCh38#132078506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29238473-C-A

132078506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29238473-C-T

132078534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29238446-A-T

132078754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29238165-T-C

132078754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29238165-T-G

132079103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237547-G-T

132079176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237490-G-C

132079234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237427-G-A

132079234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237427-G-C

http://identifiers.org/hco/9/GRCh38#132079500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29237197-C-A

132079500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237197-C-G

132079500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237197-C-T

http://identifiers.org/hco/9/GRCh38#132079539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29237160-A-C

132079539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237160-A-G

http://identifiers.org/hco/9/GRCh38#132079556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29237143-C-A

132079556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237143-C-T

http://identifiers.org/hco/9/GRCh38#132079569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#29237130-A-C

132079570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237129-G-T

132079602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29237097-G-A

132079602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29237097-G-C

132079623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29237076-C-T

132079780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29236919-T-C

132079851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2377
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29236848-G-A