77650510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 81745798-A-G

77650752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81746011-A-G

77650767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81746023-G-A

77651010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81746248-C-T

77651193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81746349-A-G

77651360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81746474-G-C

77651408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81746521-A-G

77651419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81746532-T-C

77651552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81746841-G-A

http://identifiers.org/hco/6/GRCh38#77651696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81746966-A-C

77651910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81747150-G-C

77652157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81747364-T-C

77652167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81747374-G-T

77652374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81747560-G-C

77652637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750004-A-G

77652674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750041-C-T

77652942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750292-G-A

77652966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750316-T-C

77652966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750316-T-G

77653009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750340-T-G

77653037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750371-C-G

77653107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750438-C-T

77653234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750570-T-C

http://identifiers.org/hco/6/GRCh38#77653496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81750838-C-A

77653496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750838-C-T

77653540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750879-T-C

77653540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81750879-T-G

77653671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81751022-T-A

77653995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81751361-T-C

77653998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81751364-A-G

77654031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81751397-C-G

77654061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81751427-G-C

77654152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81751531-T-C

77654176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81751558-A-G

77654268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81751650-T-C

77655565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81753270-A-G

77655566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81753271-T-C

77656267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81753982-C-T

77656354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81754051-A-G

77656810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81754461-T-G

77657442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81754983-C-T

77657481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81755001-G-A

77657596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81755119-T-C

77657611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81755129-T-A

77668006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81755243-A-T

77668734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81755915-T-C

http://identifiers.org/hco/6/GRCh38#77669121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81756383-C-A

77669368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81758221-T-C

http://identifiers.org/hco/6/GRCh38#77669375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81758228-A-C

77669444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81758281-G-C

http://identifiers.org/hco/6/GRCh38#77669541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81758374-A-C

77669645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81758464-T-G

77669705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81758520-T-G

77670198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81759023-A-G

77670328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81759103-A-G

77670595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81759156-C-T

77670705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81759240-G-A

77670761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81759295-C-G

77670960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81759510-T-C

77670977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81759526-G-C

77671145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81759665-C-T

77671453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81759916-G-T

http://identifiers.org/hco/6/GRCh38#77671635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81760074-C-A

77671635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81760074-C-T

77673070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81762033-G-T

77673380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81762492-A-G

http://identifiers.org/hco/6/GRCh38#77673985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81763064-A-C

77674096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81763158-A-G

77674253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81763318-A-G

77674253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81763318-A-T

77674924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81763757-C-T

77675163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81763969-T-G

77675166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81763972-A-G

77680797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81764816-A-G

77680918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81764919-G-A

77680918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81764919-G-T

77681135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81765154-C-T

77681141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81765160-C-G

77686864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81767726-G-T

77686867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81767729-C-T

77686912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81767773-A-G

77686912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81767773-A-T

77687038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81767892-C-G

77687157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81768003-T-A

77687159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81768005-A-G

77687437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81768235-G-T

77687989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81768757-C-G

77688330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81769132-G-A

77688442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81769233-A-G

77688589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81769363-G-T

77688693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81769465-T-A

77688828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81769657-G-T

77689058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81769894-C-T

77689460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81770290-C-G

77689460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81770290-C-T

77689632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81770844-T-A

77689811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81770986-C-T

77689835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81771300-A-G

77689835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81771300-A-T

77689943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81771407-G-A

77689943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81771407-G-C

77690026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81771487-T-C

77690036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81771497-G-A

77690036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81771497-G-T

http://identifiers.org/hco/6/GRCh38#77690513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81772040-C-A

77690513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81772040-C-T

77690539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81772068-G-A

77690573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81772102-A-T

77690632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81772150-A-G

77690783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: 81772300-A-G

77690851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: 81772368-A-G

http://identifiers.org/hco/6/GRCh38#77690875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81772392-C-A

77690875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: 81772392-C-T

77690917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81772429-A-G

77691001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81772496-A-G

77691002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81772497-G-A

77691102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81772621-G-T

77691503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81773102-A-G

77691522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81773121-C-G

77693230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81781227-G-A

77693293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81781285-A-T

77693334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81781327-A-G

77693569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81781544-G-A

77693747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81781708-C-T

77693835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81781799-G-A

77693911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81781877-G-A

77693911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81781877-G-C

77701244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81782862-G-C

77701305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81782916-G-C

77701306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81782917-C-G

77701998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81783444-T-A

http://identifiers.org/hco/6/GRCh38#77702264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81783719-C-A

77702274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81783729-T-C

77702386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81783838-A-G

77702533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81784446-A-G

77702590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81784497-T-C

77702729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81784666-C-T

77702744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81784681-A-G

http://identifiers.org/hco/6/GRCh38#77702909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81784847-C-A

77702909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81784847-C-G

77703188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81785097-A-G

http://identifiers.org/hco/6/GRCh38#77703217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81785110-C-A

77703217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81785110-C-G

77703259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81785155-G-T

77703631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81785705-C-G

77703826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81785878-G-C

77703854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81785903-A-G

77703856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81785905-A-T

http://identifiers.org/hco/6/GRCh38#77704036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81786112-A-C

77704036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81786112-A-G

77727130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81798482-T-C

77727219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81798572-T-C

77727312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81798657-T-C

77727367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81798718-T-C

77727374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81798725-T-C

77727427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81798842-A-G

77727654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799083-A-G

77727689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799115-A-T

http://identifiers.org/hco/6/GRCh38#77727759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81799231-C-A

77727759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799231-C-G

77727793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799268-T-C

77727793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799268-T-G

77727886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799330-T-A

77728201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799641-C-G

77728201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799641-C-T

77728206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799646-A-G

77728206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799646-A-T

77728242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799682-G-A

77728307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799755-C-T

77728337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799784-G-A

77728337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799784-G-C

77728496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799879-G-A

77728496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799879-G-C

77728566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81799948-G-A

77728648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800032-C-T

77728788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800175-G-A

77728789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800176-G-T

http://identifiers.org/hco/6/GRCh38#77728832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81800229-C-A

77728891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800293-T-G

77728920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800326-G-T

77728953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800366-G-A

77728998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800414-C-T

77729004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800420-G-T

77729010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800426-G-C

77729064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800458-G-T

77729458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800711-A-G

http://identifiers.org/hco/6/GRCh38#77729515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81800767-C-A

77729515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800767-C-G

77729519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800771-A-G

77729607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800864-G-A

77729607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800864-G-C

77729704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81800956-A-G

77729756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81801007-C-T

77729832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81801079-G-A

77729880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81801134-A-G

77736961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81801205-T-C

77737186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81801427-G-A

77737262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81801502-A-G

77737374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81801568-G-T

77737638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81801856-C-T

77737765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81801978-T-G

77737783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81801989-A-G

77737876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81802070-A-T

77738031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81802823-G-T

http://identifiers.org/hco/6/GRCh38#77738041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81802833-A-C

77738189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81802983-A-T

77738301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81803088-T-C

77738390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81803176-T-A

77740718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81803826-G-A

77740755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81803867-T-C

77740938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81804021-G-A

77741304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81804310-T-C

77741329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81804327-G-A

77741329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81804327-G-T

http://identifiers.org/hco/6/GRCh38#77755296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81805866-C-A

77755429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81805999-T-C

77757435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81808589-T-C

77757480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81808633-A-G

77761030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81809055-T-A

77761030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81809055-T-C

77761030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81809055-T-G

77761031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81809056-A-G

http://identifiers.org/hco/6/GRCh38#77761187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81809211-C-A

77761187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 81809211-C-T

77761270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: 81809296-T-C

http://identifiers.org/hco/6/GRCh38#77761278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81809304-C-A

77761278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: 81809304-C-G

77761278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: 81809304-C-T

77761293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: 81809314-A-G

77761387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: 81809408-A-T

http://identifiers.org/hco/6/GRCh38#77761516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81809537-A-C

77761530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: 81809551-A-T

77761569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: 81809590-C-T

http://identifiers.org/hco/6/GRCh38#77761599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81809620-C-A

77761599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: 81809620-C-T

77761646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: 81809667-G-A

77761650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: 81809671-C-T

http://identifiers.org/hco/6/GRCh38#77761752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81809777-C-A

77761752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81809777-C-T

77761779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81809802-G-T

77761933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81809957-C-T

77761998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81810024-A-T

77762042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81810069-G-A

77766044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81821130-A-G

77766132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81821223-G-A

77766132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81821223-G-T

77766200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81821280-T-G

http://identifiers.org/hco/6/GRCh38#77766941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81821796-C-A

77767744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81822487-T-A

http://identifiers.org/hco/6/GRCh38#77767830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81822571-A-C

77767863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81822602-A-G

77768081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81822828-A-G

77768081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81822828-A-T

77768132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81822879-G-A

77779040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81826559-G-A

77779154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81826690-T-C

77779311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81826848-A-G

77779327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81826864-A-G

77783617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81828481-C-T

77783639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81828508-G-A

77783639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81828508-G-C

http://identifiers.org/hco/6/GRCh38#77783742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81828662-A-C

77783849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81828752-G-A

http://identifiers.org/hco/6/GRCh38#77783989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81829452-C-A

77784113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81829552-A-G

77784140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81829573-T-C

http://identifiers.org/hco/6/GRCh38#77784162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81829597-C-A

http://identifiers.org/hco/6/GRCh38#77784233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81829671-A-C

http://identifiers.org/hco/6/GRCh38#77784252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81829690-A-C

77784252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81829690-A-T

77784294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81829732-G-A

77784318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81829756-C-T

77784662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81830093-T-C

77784832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81830266-G-T

77784938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81830393-C-T

77785212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81830677-G-A

77785212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81830677-G-T

77785354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81830823-T-A

77785354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81830823-T-C

77785356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81830825-T-C

77785476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81831109-G-C

77785542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81831167-T-C

77785582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81831205-G-A

77804883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81836474-A-G

77805173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81836757-G-T

77805194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81836778-A-T

77805308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81836876-C-G

77805568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81837345-T-C

77805857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81837637-T-A

77805952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81837726-C-T

77806071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81837834-A-G

77806283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81838056-A-G

77808964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81839051-T-C

77808978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81839065-G-A

http://identifiers.org/hco/6/GRCh38#77809005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81839092-A-C

77809195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81839259-G-A

77809527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81839561-A-G

77809527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81839561-A-T

77810122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81840067-G-A

77810479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81840428-C-T

77810642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81840587-T-A

77810702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81840647-T-G

77810877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81840813-A-T

77810936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81840869-G-A

77810963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81840888-A-T

77810990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81840915-A-G

77811102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81841026-A-G

77811200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81841124-C-T

http://identifiers.org/hco/6/GRCh38#77811207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81841132-C-A

77811207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81841132-C-G

77815156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848426-A-G

77815173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848443-C-G

77815187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848452-A-G

77815193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848458-A-G

77815198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848463-T-C

77815291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848555-T-A

http://identifiers.org/hco/6/GRCh38#77815388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81848640-C-A

77815388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848640-C-T

77815473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848724-G-A

77815510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848757-T-C

77815523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848770-A-G

77815615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81848845-C-T

77815876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81849135-A-G

77815948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81849189-G-T

77815951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81849192-A-G

77816097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81849322-A-G

77823045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81856937-T-C

77827392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81858776-T-A

77827392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81858776-T-C

77827684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81859043-C-T

77827735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81859081-C-T

77827989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81859330-T-C

77827990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81859331-A-G

http://identifiers.org/hco/6/GRCh38#77828657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81860933-A-C

77828657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81860933-A-G

http://identifiers.org/hco/6/GRCh38#77828811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81861069-C-A

77828811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81861069-C-T

77828944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: 81861192-A-G

77829241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81861511-A-G

77829257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81861643-C-G

77829291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81861677-A-G

77829507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81861888-A-G

77829521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81861902-G-T

77829638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81862017-A-G

77829991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81862335-T-G

http://identifiers.org/hco/6/GRCh38#77830136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81862475-A-C

77830302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81862682-G-A

77836378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81866341-A-G

77836450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81866412-C-T

http://identifiers.org/hco/6/GRCh38#77836538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81866486-C-A

77836745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81866676-T-C

77837042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81866965-A-G

77846400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81874251-C-G

77846683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81874556-C-G

77846858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81874703-G-C

77846894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81874739-G-T

77846980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81874822-C-T

77847058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81874899-G-T

77847196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81875041-G-T

77847198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81875043-G-A

http://identifiers.org/hco/6/GRCh38#77847214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81875059-C-A

77847214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81875059-C-T

77847885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81875715-A-G

77847894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81875724-A-G

77848092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81875901-A-G

77848108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81875918-A-G

77848181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81875996-G-A

77848571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81876540-G-T

77848871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81876849-A-G

77849006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81876982-A-G

http://identifiers.org/hco/6/GRCh38#77849385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81877768-C-A

77849465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81877830-G-A

77849555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81877918-A-G

77849751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878119-A-G

77849792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878160-T-C

77849848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878229-A-G

77849864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878245-T-G

77850048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878414-A-G

77851821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878485-G-A

77851883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878553-G-A

77851883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878553-G-T

77851957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878616-T-C

77852049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878705-T-C

77852221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81878872-G-A

http://identifiers.org/hco/6/GRCh38#77852225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81878878-A-C

77853266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81881521-T-C

77853432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81881679-A-G

77853436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81881683-T-G

77853497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81881750-C-T

77853579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81881842-C-T

77853640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81881889-T-G

77853716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81881957-T-C

77853754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81881989-G-A

77853769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81882001-A-G

77853769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81882001-A-T

77856107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81884256-C-T

77856175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81884312-G-A

77856280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81884392-T-A

77856301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81884415-A-G

77856473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81884592-T-C

77856475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81884594-A-G

77857187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81887918-G-A

77857493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81888209-G-A

77857493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81888209-G-C

77857556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81888242-G-T

77857897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81888370-G-A

77858152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81888590-G-A

77859837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81890204-C-G

http://identifiers.org/hco/6/GRCh38#77859995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81890364-A-C

77859995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81890364-A-T

77860069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81890428-C-T

77860084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81890444-T-C

77860151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81890513-G-A

77860228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81890599-T-C

77860240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81890612-A-T

77860277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81890651-C-T

77860305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81890678-G-A

77861095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81891116-A-G

77870425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81892654-G-A

77870450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81892674-A-G

77870772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81892980-A-G

77871001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81893189-A-G

77871343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81893464-A-G

77875319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81893914-G-C

77875388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81893982-G-A

77875585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81894176-A-G

77875585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81894176-A-T

77875668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81894257-A-G

77875936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81894510-T-C

77875993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81894565-A-T

77877288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81896908-A-G

77877290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81896910-A-G

77877532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897141-C-T

77877668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897281-G-C

77877668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897281-G-T

http://identifiers.org/hco/6/GRCh38#77877714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81897312-C-A

77877842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897427-A-G

77877862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897444-A-G

77877894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897476-G-A

77877983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897553-T-A

77877999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897565-A-T

77878002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897568-G-A

77878129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897741-G-A

77878132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897744-A-G

77878160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897773-C-T

77878243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897856-G-A

http://identifiers.org/hco/6/GRCh38#77878245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81897858-C-A

77878253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897866-C-T

77878254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897867-T-G

77878342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897955-C-T

77878378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81897990-T-G

77878615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81898608-G-A

77878692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81898677-C-T

77879825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81899039-C-T

77879836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81899054-G-C

77879930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81899140-C-G

77879955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81899163-C-T

77879973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81899181-T-C

77880752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron_variant, undefined
orthologous variants: 81899685-G-A

77880826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81899758-G-A

77880871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81899801-T-C

77880937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81899866-G-A

77880992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81899916-G-T

77880999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81899923-A-T

http://identifiers.org/hco/6/GRCh38#77881157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81900067-C-A

77881473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81900357-T-C

77881577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81900442-G-C

77881660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81900750-G-T

http://identifiers.org/hco/6/GRCh38#77882014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81901103-A-C

77882014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81901103-A-G

77882144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81901277-C-T

77882341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81901508-C-T

77882441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81901616-T-G

http://identifiers.org/hco/6/GRCh38#77882448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81901623-C-A

77882467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81901643-C-T

77882470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81901646-G-A

77897320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81901871-A-G

77897321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81901872-A-G

77897520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81902064-A-G

77897622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81902166-A-G

77897877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81902425-C-T

77897936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81902483-G-C

77898152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81902681-T-G

77898153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81902682-T-C

77898183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81902711-A-G

77898364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81902882-C-T

77898572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81903101-T-C

77898756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81903285-C-G

77898875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81903427-G-A

77898875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81903427-G-C

http://identifiers.org/hco/6/GRCh38#77899041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81903576-C-A

77899041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81903576-C-T

77899122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81903675-T-C

77899147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81903700-C-G

http://identifiers.org/hco/6/GRCh38#77922126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81906351-C-A

77922193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81906418-A-G

77922241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81906466-T-C

http://identifiers.org/hco/6/GRCh38#77922409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81906636-A-C

77922555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81906784-A-G

77922711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81907131-A-T

http://identifiers.org/hco/6/GRCh38#77922946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81907417-C-A

77922946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81907417-C-T

77922969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81907458-C-G

http://identifiers.org/hco/6/GRCh38#77923012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81907501-C-A

77923012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: intron variant
orthologous variants: 81907501-C-T

77923114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: 81907597-G-A

77923114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: 81907597-G-T

77923174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: 81907657-A-G

77923201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: 81907684-A-T

http://identifiers.org/hco/6/GRCh38#77923217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81907700-C-A

http://identifiers.org/hco/6/GRCh38#77923255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81907738-A-C

http://identifiers.org/hco/6/GRCh38#77923379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81907854-C-A

http://identifiers.org/hco/6/GRCh38#77923392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81907867-A-C

77923394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81907869-T-C

77923399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81907874-G-A

77923399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81907874-G-T

77923459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81907923-C-T

http://identifiers.org/hco/6/GRCh38#77923494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81907958-C-A

77923494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81907958-C-T

77923501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81907962-T-G

77923504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81907965-A-G

77923531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81907992-A-G

http://identifiers.org/hco/6/GRCh38#77923575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81908035-A-C

77923575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81908035-A-G

http://identifiers.org/hco/6/GRCh38#77923706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#81908155-C-A

77923722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81908160-T-C

77923722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81908160-T-G

77923805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81908226-C-T

77923806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81908227-A-G

77923882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81908292-T-C

77924196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43638
most severe consequence: 3 prime UTR variant
orthologous variants: 81908600-T-C