49308772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59786248-C-T

49309004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59786021-G-A

49309028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59786016-T-G

49309131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785934-T-C

http://identifiers.org/hco/13/GRCh38#49309318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59785842-C-A

49309318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785842-C-T

http://identifiers.org/hco/13/GRCh38#49309393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59785807-C-A

49309452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785748-T-C

49309576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785665-G-A

49309576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785665-G-T

49309585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785656-G-T

49309734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785506-G-T

49309841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785425-T-G

49310010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785287-A-G

49310057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785240-G-T

http://identifiers.org/hco/13/GRCh38#49310287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59785057-C-A

49310287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59785057-C-T

http://identifiers.org/hco/13/GRCh38#49310382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59784975-C-A

49310382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59784975-C-G

49310382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59784975-C-T

49310503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59784883-G-A

49310503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59784883-G-T

49310703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59784715-G-T

49310792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59784630-G-A

49310792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 3 prime UTR variant
orthologous variants: 59784630-G-C

49310815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: undefined
orthologous variants: 59784611-C-G

49310917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: missense variant
orthologous variants: 59784509-A-G

49315346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59784185-G-A

49315346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59784185-G-C

49319564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59781965-T-C

49319564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59781965-T-G

49319997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59781607-A-T

49320208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59781442-A-T

49320353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59781357-G-A

http://identifiers.org/hco/13/GRCh38#49321185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59780641-A-C

49321373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59780369-T-C

49321482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59780214-T-C

49321536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59780167-G-A

49321590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59780143-C-T

49321799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59779971-T-G

49321844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59779938-A-G

49321924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59779863-G-A

http://identifiers.org/hco/13/GRCh38#49326691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59778869-C-A

49326691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59778869-C-T

49326899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59778667-T-G

49326915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59778640-G-A

49326952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59778598-C-T

49331867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59776718-A-G

49331869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59776716-T-A

49331869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59776716-T-C

49331873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59776712-G-A

49331873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59776712-G-T

49331923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59776668-G-A

49331926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59776665-T-C

49335994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59771069-G-A

49336059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59771010-C-T

49336180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59770906-G-C

49336227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59770858-A-G

49336493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59770641-G-T

49336871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59769407-A-G

49336877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59769401-G-A

49337174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59769111-C-T

49337299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59769051-T-C

49337391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59768971-A-T

49337532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59768846-T-C

49338970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766916-C-T

49339161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766770-G-A

49339161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766770-G-C

49339384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766629-G-T

49339446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766580-T-C

49339599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766424-T-C

49339624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766402-G-A

49339624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766402-G-T

49339665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766366-A-G

49339805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766236-G-A

49339805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766236-G-T

49339815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766226-T-C

http://identifiers.org/hco/13/GRCh38#49339853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59766196-C-A

49339853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59766196-C-T

49340195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59765880-G-A

49340257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59765807-C-T

49340316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59765758-A-G

49340518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59765602-C-T

49340590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59765537-A-T

49344276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59764167-A-G

49344666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59763637-C-G

49344666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59763637-C-T

49344674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59763629-A-T

49344678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59763623-C-T

49344801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59763428-T-C

49344862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59763365-T-C

49344926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59763298-T-C

http://identifiers.org/hco/13/GRCh38#49345082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59763147-A-C

49345111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59763118-C-G

49345280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59762718-C-G

49345331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59761449-C-T

http://identifiers.org/hco/13/GRCh38#49345503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59761299-C-A

49345575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59761225-G-C

49345889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59760924-T-C

49346051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59760785-C-T

49346305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59760582-T-A

http://identifiers.org/hco/13/GRCh38#49346311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59760575-C-A

http://identifiers.org/hco/13/GRCh38#49346394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59760498-C-A

49349913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59758054-T-C

49350285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59757571-T-C

http://identifiers.org/hco/13/GRCh38#49350351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59757508-A-C

49350398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59757463-T-C

49350401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59757460-A-G

49350469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59757399-C-T

49350510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59757359-G-A

49350510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59757359-G-C

49350651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59757254-G-T

49350692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59757235-A-G

49351024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 59756905-T-C

http://identifiers.org/hco/13/GRCh38#49351073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59756847-C-A

49351073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 59756847-C-T

http://identifiers.org/hco/13/GRCh38#49351079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59756841-C-A

49351079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 59756841-C-T

http://identifiers.org/hco/13/GRCh38#49351181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59756740-A-C

49351220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59756706-A-T

49351276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59756665-G-A

49351399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59756584-T-A

49351714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59756180-T-G

49351798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59756101-T-A

49352344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59755583-G-T

49352348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59755579-T-C

49352404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59755530-A-G

http://identifiers.org/hco/13/GRCh38#49352933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59754588-A-C

49353082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59754437-G-A

49353148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59754363-T-G

49353541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59752125-T-C

49353593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59752080-C-T

49353594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59752079-C-T

49353650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59752050-C-T

49353732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59752000-C-T

49353931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59751826-T-C

49353931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59751826-T-G

49353941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59751816-T-A

49353976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59751779-T-G

49354001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59751754-A-G

49354218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59751543-C-G

49354242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59751523-G-A

http://identifiers.org/hco/13/GRCh38#49355040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59749578-C-A

49355040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59749578-C-T

49355088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59749528-G-A

49355088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59749528-G-C

49355739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59749232-G-A

49355739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59749232-G-T

49356037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59748983-T-C

49356274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59748158-A-G

49356389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, undefined
orthologous variants: 59748052-T-C

49356553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59747928-C-T

49356616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59747872-G-A

49356664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59747823-C-G

49357480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59745654-T-C

49357595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59745542-G-A

http://identifiers.org/hco/13/GRCh38#49357805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59745382-A-C

49358068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59745122-C-T

49358122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59745075-C-T

49358264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59744937-T-C

49359230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59744302-C-T

49359368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59744134-G-A

49359600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59743922-A-T

http://identifiers.org/hco/13/GRCh38#49359607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59743915-C-A

49359607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59743915-C-T

49359656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59743883-T-C

49359747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: missense variant
orthologous variants: 59743797-G-A

49359747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: missense variant
orthologous variants: 59743797-G-C

49359851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59743693-G-T

49359888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59743656-A-T

49360055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59743520-G-C

49360071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59743502-C-T

49360072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59743501-G-A

49368334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59741910-A-G

http://identifiers.org/hco/13/GRCh38#49368770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59741661-A-C

49368775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59741656-T-A

49372099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: -C-T

49372397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59739149-T-C

49375031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59738280-G-A

http://identifiers.org/hco/13/GRCh38#49375284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59738023-A-C

49375290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59738017-C-T

49376053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59737627-A-G

http://identifiers.org/hco/13/GRCh38#49377211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59736922-A-C

49377211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59736922-A-T

http://identifiers.org/hco/13/GRCh38#49377261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59736889-C-A

49377382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59736794-T-C

49377383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59736793-T-C

49377392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59736778-T-C

http://identifiers.org/hco/13/GRCh38#49377430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59736740-C-A

49380135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59736616-G-A

49380331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59736349-A-G

49380539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59736173-G-T

49380948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59735824-A-G

49381852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59735153-G-T

http://identifiers.org/hco/13/GRCh38#49381866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59735139-A-C

http://identifiers.org/hco/13/GRCh38#49382122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59734985-A-C

49382174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59734945-A-G

49382294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59734831-G-A

49382401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59734724-A-G

http://identifiers.org/hco/13/GRCh38#49382406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59734708-C-A

49382407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron variant
orthologous variants: 59734707-A-T

49382521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59734642-A-G

49382585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59734579-T-C

49382585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59734579-T-G

49382589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59734575-G-T

49382627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59734536-A-T

49382645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59734518-A-T

49382667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59734497-A-G

http://identifiers.org/hco/13/GRCh38#49382703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59734482-A-C

49383029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59734145-C-T

49386345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59730835-C-T

49386389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59730452-G-A

49386682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59730192-C-T

http://identifiers.org/hco/13/GRCh38#49388111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59729695-A-C

49388116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59729690-G-C

49388254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59729565-T-A

http://identifiers.org/hco/13/GRCh38#49388284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59729521-A-C

49388456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59729193-T-C

49388517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59729128-A-G

49388563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59729080-T-C

49388576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59729067-T-G

49388711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59728929-G-A

49388828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59728821-T-A

49388934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59728736-T-C

49388989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59728686-C-T

49389243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59728428-G-A

49389243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59728428-G-C

http://identifiers.org/hco/13/GRCh38#49389269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59728404-C-A

49389269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59728404-C-T

49389277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59728396-T-C

49394160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59723609-T-C

http://identifiers.org/hco/13/GRCh38#49396713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59722124-A-C

49397641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59720610-C-T

49397832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59720413-C-T

49397924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59720085-C-T

49398659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59719305-T-A

49398900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59718998-T-C

http://identifiers.org/hco/13/GRCh38#49398937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59718966-A-C

http://identifiers.org/hco/13/GRCh38#49399030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59718858-C-A

http://identifiers.org/hco/13/GRCh38#49399035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59718853-A-C

49399477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59718135-T-C

http://identifiers.org/hco/13/GRCh38#49399518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59718094-C-A

49399682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59717938-A-G

49399814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59717819-G-T

49399930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59717758-T-C

49400075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59717639-G-C

49400109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59717607-G-A

49400211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59717504-T-C

49400299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59717421-T-C

49400312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59717408-G-A

49401014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59716740-T-A

http://identifiers.org/hco/13/GRCh38#49401194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59716571-C-A

49401194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59716571-C-T

49401352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59716417-C-T

49401377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59716392-G-A

49401377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59716392-G-T

49401474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59716299-A-G

49401707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59716063-T-A

49401707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59716063-T-C

49401760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59716010-G-A

49402410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59715417-G-A

http://identifiers.org/hco/13/GRCh38#49429959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59701978-C-A

49430032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59701916-C-T

49433217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59699243-T-C

49433329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59699140-T-C

49433846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59698669-C-T

49434091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59696683-T-C

49434123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59696651-T-C

49434148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59696626-G-A

49434148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59696626-G-T

49434167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59696607-A-G

49434194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59696570-A-G

http://identifiers.org/hco/13/GRCh38#49434312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59696437-C-A

49434312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59696437-C-G

49434316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59696433-A-G

49434368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59696383-G-A

49434736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59695967-C-T

http://identifiers.org/hco/13/GRCh38#49434833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59695876-A-C

49434994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59695731-T-C

49435186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59695647-G-A

49435433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59694804-T-C

49435689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59694498-T-C

49435806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59694368-C-T

49435901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59694270-G-A

49435901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59694270-G-C

49435923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59694251-G-C

49435945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59694244-A-T

49435956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59694234-C-T

49436104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59694141-C-T

49436383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59693766-A-T

49436757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59693472-T-C

49437211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59693209-T-A

49442522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59680009-T-C

49442523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59680008-G-T

http://identifiers.org/hco/13/GRCh38#49442810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59679798-A-C

http://identifiers.org/hco/13/GRCh38#49442811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59679797-A-C

49443001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59679678-T-A

49443051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59679628-G-A

49443051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59679628-G-C

49443051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59679628-G-T

49443379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59678995-T-C

49443477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59678913-C-T

49443649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59678739-A-G

49443889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59678537-T-C

49443997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59678451-G-A

49443997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59678451-G-C

49444019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59678429-G-T

49444050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20290
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59678398-G-T