31846997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152775953-G-A

31847162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152776115-G-T

31847359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152776310-T-G

31847495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152776436-C-T

31847514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152776457-A-T

31847543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152776485-A-T

31847897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777111-G-T

31847904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777118-G-A

31847904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777118-G-T

http://identifiers.org/hco/20/GRCh38#31847907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152777121-C-A

31847907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777121-C-T

http://identifiers.org/hco/20/GRCh38#31847978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152777185-C-A

31848124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777339-T-A

31848251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777443-G-A

31848251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777443-G-T

http://identifiers.org/hco/20/GRCh38#31848260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152777452-C-A

31848260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777452-C-G

31848260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777452-C-T

31848273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777471-G-A

31848273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777471-G-C

31848273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777471-G-T

http://identifiers.org/hco/20/GRCh38#31848300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152777497-C-A

31848300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777497-C-T

http://identifiers.org/hco/20/GRCh38#31848303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152777500-C-A

31848303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152777500-C-T

31848492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, missense_variant
orthologous variants: 152777653-G-A

31848514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, missense_variant
orthologous variants: 152777677-T-C

31848521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152777684-A-G

31848568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 152777728-G-C

31848568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 152777728-G-T

http://identifiers.org/hco/20/GRCh38#31848659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152777790-C-A

31848659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152777790-C-G

31848681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152777794-G-A

31848681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152777794-G-T

31848691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152777804-C-G

31848707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152777820-G-A

31848749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152777862-C-T

31848854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 152777946-C-G

http://identifiers.org/hco/20/GRCh38#31849053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152778085-C-A

31849053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152778085-C-G

31849053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152778085-C-T

31849576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152778550-T-A

31849576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152778550-T-C

http://identifiers.org/hco/20/GRCh38#31849651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152778571-A-C

31849651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152778571-A-T

31849652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152778572-G-A

31849652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152778572-G-T

http://identifiers.org/hco/20/GRCh38#31849781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152778655-C-A

31849781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152778655-C-T

http://identifiers.org/hco/20/GRCh38#31849838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152778704-C-A

31849838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152778704-C-T

http://identifiers.org/hco/20/GRCh38#31849934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152778775-C-A

31849934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152778775-C-T

31850021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152778886-T-C

31850021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152778886-T-G

31850272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152780328-G-A

31850463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152780515-T-C

http://identifiers.org/hco/20/GRCh38#31850567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152780608-C-A

31850567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152780608-C-T

http://identifiers.org/hco/20/GRCh38#31850575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152780616-C-A

31850575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152780616-C-T

31850642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: missense variant
orthologous variants: 152780683-G-A

http://identifiers.org/hco/20/GRCh38#31850662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152780704-C-A

http://identifiers.org/hco/20/GRCh38#31850712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152780745-A-C

http://identifiers.org/hco/20/GRCh38#31850722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152780757-C-A

31850722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152780757-C-T

31850761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152780790-G-C

31850761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152780790-G-T

http://identifiers.org/hco/20/GRCh38#31850762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152780791-C-A

31850802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152780831-G-A

31850802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152780831-G-T

http://identifiers.org/hco/20/GRCh38#31850834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152780848-C-A

31850856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, stop_gained
orthologous variants: 152780865-C-T

31850880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152780889-G-A

31860013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152783951-T-C

31860013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152783951-T-G

31860858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152784629-G-C

http://identifiers.org/hco/20/GRCh38#31861065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152784782-C-A

http://identifiers.org/hco/20/GRCh38#31861109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152784823-C-A

31861109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152784823-C-T

31861261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152784977-G-A

31861261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152784977-G-T

31861271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152784987-G-A

31861271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152784987-G-C

31861271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152784987-G-T

31861272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152784988-G-A

31861272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152784988-G-C

31861272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152784988-G-T

http://identifiers.org/hco/20/GRCh38#31861297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152785000-C-A

31861297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152785000-C-G

31861297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152785000-C-T

http://identifiers.org/hco/20/GRCh38#31861387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152785086-C-A

31861387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152785086-C-T

31861460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152785158-G-A

31861460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152785158-G-T

31861568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152785266-G-A

31861568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152785266-G-C

31861568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152785266-G-T

http://identifiers.org/hco/20/GRCh38#31861658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152785356-C-A

31861658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, missense_variant
orthologous variants: 152785356-C-G

31861658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152785356-C-T

http://identifiers.org/hco/20/GRCh38#31861784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152785455-C-A

31861784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152785455-C-T

31861982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152785605-A-G

31862018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152785626-C-G

http://identifiers.org/hco/20/GRCh38#31862046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152785655-C-A

http://identifiers.org/hco/20/GRCh38#31862205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152785830-C-A

http://identifiers.org/hco/20/GRCh38#31862463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152786003-A-C

31862463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152786003-A-G

31862463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152786003-A-T

http://identifiers.org/hco/20/GRCh38#31862542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152786050-C-A

31862542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron variant
orthologous variants: 152786050-C-T

31862784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786281-A-G

http://identifiers.org/hco/20/GRCh38#31862792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152786289-C-A

31862792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786289-C-T

31862854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786358-T-A

31862854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786358-T-G

31862864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786368-G-A

31862864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786368-G-T

http://identifiers.org/hco/20/GRCh38#31863066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152786566-C-A

31863066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786566-C-G

31863066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786566-C-T

31863128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786624-G-T

31863158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786648-T-G

31863426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152786972-G-A

31863488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152787029-G-A

31863488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152787029-G-C

31863488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152787029-G-T

http://identifiers.org/hco/20/GRCh38#31863552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152787068-C-A

31863552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152787068-C-T

http://identifiers.org/hco/20/GRCh38#31863612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152787116-C-A

31863612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152787116-C-T

31863638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152787142-A-T

31863652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152787156-A-G

http://identifiers.org/hco/20/GRCh38#31863787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152787290-C-A

31863787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152787290-C-T

31863833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152787321-G-T

31864103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152787522-G-A

31864108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152787527-T-G

http://identifiers.org/hco/20/GRCh38#31864312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152787641-C-A

31864312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152787641-C-G

31864312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152787641-C-T

31864340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 152787669-T-C

31864340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 152787669-T-G

31864493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152787815-A-G

31864621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152787920-G-A

31864621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152787920-G-T

31864707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152788003-A-G

31864720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152788016-T-C

31864896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152788148-C-T

31865030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152788288-G-A

31865030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152788288-G-C

31865040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152788298-C-T

http://identifiers.org/hco/20/GRCh38#31865095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152788347-C-A

31865327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152788516-T-C

31865336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152788525-C-T

31865403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152788601-C-T

31865556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152788897-C-T

31866368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152790182-T-A

31866486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152790282-C-T

http://identifiers.org/hco/20/GRCh38#31866649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152790442-C-A

31866929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152790747-T-A

31866929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152790747-T-C

31867030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152790919-C-T

http://identifiers.org/hco/20/GRCh38#31867077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152790964-C-A

31867077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 152790964-C-T

31867169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791056-T-C

31867170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791057-G-T

31867236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791125-A-G

http://identifiers.org/hco/20/GRCh38#31867255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152791144-C-A

31867255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791144-C-G

31867255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791144-C-T

31867282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791172-G-A

31867282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791172-G-C

31867587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791476-A-G

31867622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791515-G-A

31867622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791515-G-C

31867622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152791515-G-T

31869116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152792181-C-G

http://identifiers.org/hco/20/GRCh38#31869124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152792189-C-A

31869500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152792477-T-C

http://identifiers.org/hco/20/GRCh38#31869648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152792621-C-A

31869648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152792621-C-G

31869769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152792719-G-T

31869864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152792825-G-A

31869864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152792825-G-T

http://identifiers.org/hco/20/GRCh38#31870031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#152792963-C-A

31870031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152792963-C-G

31870031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152792963-C-T

http://identifiers.org/hco/20/GRCh38#31870075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#152793007-C-A

31870075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152793007-C-T

31870081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152793013-G-T

31870085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152793017-G-A

31870085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152793017-G-C

31870085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152793017-G-T

31870087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152793019-G-A

31870087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152793019-G-T

http://identifiers.org/hco/20/GRCh38#31870093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#152793025-C-A

31870093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152793025-C-T

31870147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152793091-G-T

31870192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152793122-G-A

31870270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152793200-G-A

http://identifiers.org/hco/20/GRCh38#31870285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152793215-A-C

31870285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152793215-A-G

http://identifiers.org/hco/20/GRCh38#31870286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152793216-C-A

31870286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152793216-C-T

31870372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152793310-C-G

31870372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152793310-C-T

31870384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152793322-G-A

31870384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152793322-G-C

31870384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152793322-G-T

31870387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152793325-G-A

31870387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152793325-G-T

http://identifiers.org/hco/20/GRCh38#31870427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#152793363-C-A

31870427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152793363-C-T

31870517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 152793443-G-A

31870517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 152793443-G-C

31870517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 152793443-G-T

31870659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152793610-G-A

31870659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152793610-G-T