63276030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31246673-T-C

63276055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31246648-A-G

http://identifiers.org/hco/6/GRCh38#63276065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31246639-C-A

63276065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31246639-C-T

63276079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31246625-A-G

http://identifiers.org/hco/6/GRCh38#63276161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31246544-C-A

63276342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31246357-A-T

63276569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31246134-G-A

http://identifiers.org/hco/6/GRCh38#63276667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31246037-C-A

63276673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31246031-C-T

63276733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31245978-A-G

http://identifiers.org/hco/6/GRCh38#63276820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31245893-C-A

63276890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31245784-T-C

http://identifiers.org/hco/6/GRCh38#63276966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31245708-C-A

63277000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31245676-C-G

63277258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31245423-T-C

63277343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31245339-G-A

63277343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31245339-G-T

63277404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31245272-G-A

http://identifiers.org/hco/6/GRCh38#63277464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31245201-C-A

63277464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31245201-C-T

63277471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31245194-A-T

http://identifiers.org/hco/6/GRCh38#63277505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31245159-C-A

63277505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31245159-C-T

63278733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31244783-T-C

http://identifiers.org/hco/6/GRCh38#63278743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31244773-A-C

63278754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31244762-T-C

63279082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31244439-C-T

63279323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3 prime UTR variant
orthologous variants: 31244231-A-G

63279440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31244119-G-C

63279476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31244088-C-T

http://identifiers.org/hco/6/GRCh38#63279507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31244066-A-C

63279507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31244066-A-G

63279596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31243977-T-C

http://identifiers.org/hco/6/GRCh38#63279864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31243732-C-A

63279864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31243732-C-T

63279870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31243726-T-C

63279870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31243726-T-G

63280000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31243624-G-T

http://identifiers.org/hco/6/GRCh38#63280337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31243293-A-C

63280337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 31243293-A-G

63280337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 31243293-A-T

63280508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 31243122-A-G

63280508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 31243122-A-T

63280537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 31243093-C-T

http://identifiers.org/hco/6/GRCh38#63280549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31243081-A-C

63280549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 31243081-A-G

63280656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 31242974-T-C

63280712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 31242918-T-G

63280733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 31242897-T-G

63280772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 31242858-G-A

63280825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 31242805-T-C

63280960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 31242670-G-A

63280960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 31242670-G-C

63281056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 31242574-A-G

63281204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron_variant, missense_variant
orthologous variants: 31242426-C-T

63281272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31242342-T-G

63281350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31242307-G-A

63281350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31242307-G-T

63281367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31242290-T-A

63281695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31240935-C-G

http://identifiers.org/hco/6/GRCh38#63282048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31240645-C-A

63282048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31240645-C-T

63282162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31240559-T-C

63282771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31239048-T-C

63282935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31238891-T-G

63283045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31238777-A-G

http://identifiers.org/hco/6/GRCh38#63283145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31238691-A-C

63283176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31238665-C-T

63283492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31238344-A-G

63283555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31238288-A-G

63285277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31236324-A-G

http://identifiers.org/hco/6/GRCh38#63285784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31235836-C-A

63285784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31235836-C-T

63285792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31235828-T-A

63285792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31235828-T-C

63285815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31235805-G-A

63285815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31235805-G-T

63285883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31235731-A-G

http://identifiers.org/hco/6/GRCh38#63286013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31235624-C-A

63286013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31235624-C-T

63286042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31235601-T-C

63286491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31235278-A-G

http://identifiers.org/hco/6/GRCh38#63286551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31235212-A-C

http://identifiers.org/hco/6/GRCh38#63286807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31234846-C-A

http://identifiers.org/hco/6/GRCh38#63286982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31234678-C-A

63287175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31234483-T-C

63287176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31234482-G-T

63287204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31234454-A-G

63287727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31234240-G-A

63288411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31233737-A-G

63288423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31233721-A-G

63288478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31233670-A-G

63288611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31233548-C-T

63288626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31233533-C-T

63289059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31233122-T-C

63289082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31233102-G-A

63289095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31233090-G-A

63289099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31233086-T-C

63289247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31232931-T-A

63289361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31232815-C-T

63289368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31232808-A-T

63289434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31232741-T-C

63289492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31232683-G-C

63289547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31232628-G-T

63289929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31231877-G-A

63290004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31231791-G-C

63290050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31231742-T-G

63292104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230712-C-T

63292176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230651-T-C

63292380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230529-C-G

63292393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230516-G-T

63292419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230490-T-C

http://identifiers.org/hco/6/GRCh38#63292491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31230419-A-C

63292491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230419-A-G

63292597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230317-T-C

63292618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230299-G-A

63292657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230260-T-G

63292872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230065-G-A

63292892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230045-T-A

63292892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31230045-T-C

63293342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31229919-G-A

63293448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31229817-A-T

63293460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31229805-C-T

63293540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31229726-G-C

63293574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31229697-A-G

http://identifiers.org/hco/6/GRCh38#63293624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31229647-C-A

63293699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31229572-A-G

63293704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron_variant, missense_variant
orthologous variants: 31229567-T-C

63293718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron_variant, missense_variant
orthologous variants: 31229553-G-A

63293763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron_variant, missense_variant
orthologous variants: 31229508-T-A

63293763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron_variant, missense_variant
orthologous variants: 31229508-T-C

63293788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron_variant, missense_variant
orthologous variants: 31229483-A-G

63293873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31229421-A-G

63294027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31229262-T-C

63294049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31229240-C-T

63294393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228975-T-A

63294552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228844-A-G

63294665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228811-T-G

63294762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228719-T-G

63294812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228674-G-T

63294842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228648-T-C

63294861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228629-T-A

63294861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228629-T-C

63294861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228629-T-G

http://identifiers.org/hco/6/GRCh38#63294877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31228613-C-A

63294877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228613-C-T

63294883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228607-C-G

63294883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228607-C-T

63294918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: stop gained
orthologous variants: 31228572-G-C

63294941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: synonymous variant
orthologous variants: 31228549-C-T

63294962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: synonymous variant
orthologous variants: 31228528-T-A

63294962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: synonymous variant
orthologous variants: 31228528-T-C

63295037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 31228453-T-C

http://identifiers.org/hco/6/GRCh38#63295072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31228419-C-A

63295072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228419-C-T

63295155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228366-A-G

63295169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31228356-G-T

63295623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31227241-T-C

63295636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31227228-A-G

63295711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31226643-C-T

63295837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31226530-T-C

63295889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31226491-T-A

63295951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31226199-G-A

63296000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31226151-G-A

63296000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31226151-G-T

63296056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31226097-G-A

63296056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31226097-G-T

63296145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31226032-A-G

http://identifiers.org/hco/6/GRCh38#63296269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31225856-C-A

63296349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31225778-T-A

63296402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31225734-T-C

63296428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31225711-G-A

63296428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31225711-G-T

63296586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31225610-A-G

63296850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31225376-T-C

63306155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31224605-T-C

63306757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31224010-C-G

63308518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31222272-T-C

63308536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31222252-T-C

63308574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31222214-G-T

63308657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31222108-T-C

63308676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31222089-T-G

63308688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31222077-A-G

63308713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31222054-G-T

63308914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31221840-C-G

63309041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31221722-C-T

63309119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31221644-A-T

63309170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31221594-C-T

63309270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31221472-A-G

http://identifiers.org/hco/6/GRCh38#63316497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31218472-A-C

http://identifiers.org/hco/6/GRCh38#63316534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31218439-C-A

63316571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31218379-T-C

63318041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217683-G-A

63318041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217683-G-C

63318249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217521-A-G

63318355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217423-A-G

63318419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217358-C-G

63318468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217308-G-T

63318535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217239-T-C

63318545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217229-A-T

63318551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217223-C-T

63318559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217215-C-T

63318629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31217020-T-A

63318740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31216758-G-A

63318778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31216720-C-T

63318786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31216712-T-C

63319050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31216470-C-G

63319128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31216391-G-A

63319333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31216210-G-A

63319553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31215904-T-C

63319621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31215835-T-A

63319621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31215835-T-C

63319795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31215670-C-T

63319814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31215658-T-C

63319872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31215601-T-C

63319921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron_variant, missense_variant
orthologous variants: 31215552-A-G

63319964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 31215505-G-T

http://identifiers.org/hco/6/GRCh38#63320003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31215467-A-C

63320003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31215467-A-G

63320005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31215465-G-A

63320005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31215465-G-T

63320121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: 5 prime UTR variant
orthologous variants: 31215355-A-T

63320284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31215191-T-C

http://identifiers.org/hco/6/GRCh38#63320326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#31215149-C-A

63320346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31215130-G-C

63320690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31214844-G-A

63320899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31214672-C-T

63321139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31214447-G-A

63321163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31214423-G-T

63321179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21016
most severe consequence: intron variant
orthologous variants: 31214407-A-G