http://identifiers.org/hco/16/GRCh38#56730254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94941304-C-A

56730258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941313-G-A

56730258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941313-G-T

http://identifiers.org/hco/16/GRCh38#56730263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94941318-C-A

56730263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941318-C-T

56730285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941340-G-A

56730285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941340-G-C

56730287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941342-G-A

56730287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941342-G-T

http://identifiers.org/hco/16/GRCh38#56730294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94941349-C-A

http://identifiers.org/hco/16/GRCh38#56730299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94941353-C-A

http://identifiers.org/hco/16/GRCh38#56730316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94941365-C-A

56730444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941416-G-A

56730690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941592-C-T

56730728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941631-A-G

56730728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94941631-A-T

56732211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94942169-G-A

56732661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94942660-A-G

56733001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94942898-A-G

56733546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94943353-C-T

56733759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94943483-T-G

http://identifiers.org/hco/16/GRCh38#56733900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94944613-A-C

56733934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94944643-A-T

56734153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94944873-T-A

56734153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94944873-T-G

http://identifiers.org/hco/16/GRCh38#56734244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94944948-C-A

56734665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94945552-G-T

http://identifiers.org/hco/16/GRCh38#56735421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94945995-A-C

56735421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94945995-A-T

56735490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94946028-G-A

56737243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94947016-C-G

56737570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94947314-A-G

56742868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94948676-C-T

56743169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94950545-A-G

56743169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94950545-A-T

56743267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94950650-A-T

56743329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94951419-C-T

http://identifiers.org/hco/16/GRCh38#56747913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94953978-C-A

56747913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94953978-C-G

56747913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94953978-C-T

56747915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94953980-T-A

56747915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94953980-T-C

56747915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94953980-T-G

56747926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94953991-G-A

56747926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94953991-G-C

56747926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94953991-G-T

56747933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94953998-T-A

56747933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94953998-T-C

56748111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94954171-G-T

http://identifiers.org/hco/16/GRCh38#56748126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94954186-C-A

http://identifiers.org/hco/16/GRCh38#56748198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94954256-C-A

56748198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94954256-C-G

56748213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94954270-T-A

56748213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94954270-T-C

http://identifiers.org/hco/16/GRCh38#56748215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94954272-C-A

56748373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 94954430-C-T

56748471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94954527-G-T

http://identifiers.org/hco/16/GRCh38#56748550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94954574-C-A

56748571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94954591-G-A

56748571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94954591-G-T

56748617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94954646-G-A

56748753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94954740-G-A

56749068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94955035-G-A

56749068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94955035-G-T

56749229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94955117-G-C

56749383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94955266-C-G

56749383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94955266-C-T

56749444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94955325-T-C

56750143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94956022-G-A

56750472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94956359-A-T

56750550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94956511-G-A

56751283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94957216-A-G

56751512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94957415-A-G

56751542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94957519-T-C

56751621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94957647-C-T

56751928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94958020-G-A

56751994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94958083-C-T

56752184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94958371-A-G

56752310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94958486-T-C

56752404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94958580-G-A

56752442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94958604-T-G

56752483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94958645-A-G

56757771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94969263-A-G

56758271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94969956-A-G

56758278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94969963-T-G

http://identifiers.org/hco/16/GRCh38#56758446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94970202-C-A

http://identifiers.org/hco/16/GRCh38#56758667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94970411-C-A

56758712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94970456-T-C

56758721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94970465-A-G

http://identifiers.org/hco/16/GRCh38#56758774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94970512-C-A

56758774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94970512-C-T

56758802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94970533-T-C

56758802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94970533-T-G

56758869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94970600-A-G

56758875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94970606-A-T

56759040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94970773-T-G

56759232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94970947-T-C

56759291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94971045-C-T

56759558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94971364-A-G

56760060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94971571-T-A

56761521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94973129-G-T

56761575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94973178-G-T

56761598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94973188-G-T

56761698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94973287-A-G

56762314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94973880-G-A

56763236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94974246-A-T

56763336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94974351-A-T

56763887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94974519-T-C

56763887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94974519-T-G

56763946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94974576-A-G

56764006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94974638-A-G

56764006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94974638-A-T

56764113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94974733-C-T

http://identifiers.org/hco/16/GRCh38#56764532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94974835-C-A

56765363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94975756-T-C

56765437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94975828-A-G

56765441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94975832-A-G

56765444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94975835-G-A

56765451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94975842-C-T

56765490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94975880-A-G

56765492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94975882-A-G

56765505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94975895-T-C

56765985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94976481-A-T

56766423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94976916-A-G

56766959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94977338-A-G

56767234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94977587-G-A

56767337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94977654-G-T

56767390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94977704-A-T

56767516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94977822-G-C

56767593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94977872-C-T

56767659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94977933-A-G

56769420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94978801-T-C

56769454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94978818-C-T

56769559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94978915-A-G

56769564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94978920-A-G

56770086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94979417-C-G

56770591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94980137-T-C

56770705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94980253-G-A

56770705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94980253-G-C

56770760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94980306-G-A

56770859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94980438-C-G

56770859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94980438-C-T

56770957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94980592-A-G

56771077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94980700-C-T

56771195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94980818-C-T

56771333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94981619-T-C

http://identifiers.org/hco/16/GRCh38#56771540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94982203-C-A

56771624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94982292-G-T

http://identifiers.org/hco/16/GRCh38#56771833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94982900-A-C

56771940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94982994-T-C

56772072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94983045-G-T

56772242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94983219-T-C

56772837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94983718-A-G

56773238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94983861-C-G

56773238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94983861-C-T

56773253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94983891-G-A

56773869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94984608-A-G

56773950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94985294-T-C

56774771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94986160-G-A

56775935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94986876-C-G

http://identifiers.org/hco/16/GRCh38#56776202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94987378-C-A

56776274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94987463-C-T

http://identifiers.org/hco/16/GRCh38#56776427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94987724-A-C

56776816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94988094-C-T

56776844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94988141-G-C

56777276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94988785-C-T

56777363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94989004-T-C

56777408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94989137-T-C

http://identifiers.org/hco/16/GRCh38#56777479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94989207-C-A

56777479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94989207-C-T

56777708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94989410-A-T

56778141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94989836-A-G

56778371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94990088-C-T

56779142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94990315-G-A

56779142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94990315-G-C

56779217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94990366-C-G

56779261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94990413-C-T

56779517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94991192-G-A

56779542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94991217-T-C

56780755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94992419-C-T

56780798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94992463-C-T

56780839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94992503-G-T

56780849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94992513-C-T

56780908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94992559-C-T

56780966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94992606-T-G

56781440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94993069-A-T

56781481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 94993110-A-G

56781911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94993544-C-G

56781911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94993544-C-T

56782184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94993818-T-C

56782342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94993973-G-A

56782345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94993976-G-A

56782345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94993976-G-T

56782376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94994008-G-T

56782554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94994209-T-C

56782561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94994216-T-C

56783017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94994632-G-A

http://identifiers.org/hco/16/GRCh38#56783052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94994671-C-A

56783052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94994671-C-T

56783202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94994811-T-C

56783400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94995011-G-T

http://identifiers.org/hco/16/GRCh38#56783410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94995021-A-C

56783541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94995155-G-C

56783541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94995155-G-T

56783552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94995169-G-A

56783816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94995429-G-A

56783818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94995431-T-A

http://identifiers.org/hco/16/GRCh38#56783819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94995432-C-A

56784311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94995878-C-T

56784329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94995896-A-G

http://identifiers.org/hco/16/GRCh38#56784476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94996046-C-A

56784608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94996177-T-C

56784701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94996257-A-G

56784809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94996360-C-G

56785165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94996722-C-T

56785280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94996815-T-C

56785346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94996894-T-G

56785487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94997027-G-A

56785640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94997177-G-C

56785663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94997200-A-G

56786119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94997558-C-G

56786261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94997698-G-A

56786262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94997699-G-A

56786520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94997938-A-G

56786534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94997952-G-A

56786535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94997953-A-T

56786756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94998157-C-T

56787255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94998569-C-G

56787318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94998629-G-A

56787383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94998700-A-T

56787491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94998793-G-T

56787837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999122-C-T

56787887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999161-A-T

56788025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999298-A-G

56788184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999443-T-C

56788275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999543-G-A

56788285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999553-C-G

56788285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999553-C-T

56788287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999555-T-A

56788287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999555-T-C

56788509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999946-T-C

56788509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94999946-T-G

56789233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95000595-G-A

56789267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95000628-T-C

http://identifiers.org/hco/16/GRCh38#56789302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95000665-C-A

56789302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95000665-C-T

56789469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95000811-G-T

56789548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95000872-G-C

56791068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95001909-A-G

56791118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95001958-C-G

56791501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95002624-C-T

56791773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95002872-G-A

56793184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95003231-G-A

56793184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95003231-G-T

56794455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95005822-C-T

56794581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95005996-T-C

56794594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95006009-G-A

56794608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95006023-G-T

56795212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95006443-A-G

56797535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95007417-T-C

56797670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95007541-A-G

http://identifiers.org/hco/16/GRCh38#56798414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95007840-C-A

56798414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95007840-C-T

56799310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95008404-A-G

http://identifiers.org/hco/16/GRCh38#56799560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95008668-A-C

56800230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95008985-A-G

56800257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95009012-A-G

56800308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95009067-C-G

56800308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95009067-C-T

56800947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95009915-T-G

56801112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95010051-C-G

56801839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95010474-G-A

56801946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95010578-C-G

56801949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95010581-C-T

56802246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95010851-G-A

56803035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95011606-A-G

56803081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95011637-A-G

56803093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95011648-C-T

56803326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95011834-G-A

56803417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95011938-A-T

56803471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95011985-T-A

http://identifiers.org/hco/16/GRCh38#56805593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95013206-A-C

56805629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 95013242-C-T

56805675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95013281-G-A

56808871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95013399-A-G

56809173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95013699-C-T

56809174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95013700-C-T

56809571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95014309-G-A

56810160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95014845-A-G

56811043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95015482-C-T

http://identifiers.org/hco/16/GRCh38#56811383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95015877-C-A

56811383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95015877-C-T

56811393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95015887-C-T

56811592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95016072-T-A

56811594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95016074-C-G

56811986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95016439-G-A

56811986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95016439-G-T

56812324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95016750-A-G

56812324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95016750-A-T

56813156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95017463-G-A

56813316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95017624-A-G

56813317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95017625-T-C

http://identifiers.org/hco/16/GRCh38#56813461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95017772-C-A

56813723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95018024-A-G

56814557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95018434-C-T

56814709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95018651-A-G

56814834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95018777-T-C

56814873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95018855-T-A

56814873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95018855-T-C

56814879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95018868-G-A

56814946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95018935-C-T

56815202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95019184-A-G

56818644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95019277-G-A

56818717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95019349-C-G

56818717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95019349-C-T

56818747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95019379-G-T

56818756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95019388-G-T

56818764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95019397-A-G

http://identifiers.org/hco/16/GRCh38#56818776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95019413-C-A

56818843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95019478-G-T

56818844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95019479-T-C

56819146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95019754-T-G

56819228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95019834-G-C

56819644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95020113-A-G

56819647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95020116-G-C

56819707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95020163-T-C

56819751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95020194-G-A

56819867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95020374-A-G

56820041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95020528-A-G

56820181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95020652-C-T

56820728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95020859-C-T

56820897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95021072-C-T

56821318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95021471-G-T

56821369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95021511-C-T

56821380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95021521-G-T

http://identifiers.org/hco/16/GRCh38#56821393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95021533-C-A

56821393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95021533-C-T

56821394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95021534-G-A

56821394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95021534-G-T

56821473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95021619-T-G

56821542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95021687-G-A

56821633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95021778-G-A

56821633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95021778-G-T

56821652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95021797-A-G

56821728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95021862-T-C

56821771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95021905-A-T

56822058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95022137-C-T

56822924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95022413-C-G

56823384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95022773-G-T

http://identifiers.org/hco/16/GRCh38#56823617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95023000-C-A

56823617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023000-C-T

56823632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023015-G-A

56823632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023015-G-T

56823865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023359-A-G

56823866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023360-G-A

56823960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023449-T-G

56824042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023519-G-A

56824064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023539-A-G

56824126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023601-C-T

56824405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023881-C-G

56824539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95023990-A-T

http://identifiers.org/hco/16/GRCh38#56824575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95024026-A-C

56825679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95025031-T-C

56826013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95025331-T-A

56826159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95025468-G-A

56826159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95025468-G-C

56828760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95027190-T-A

56828914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95027322-G-T

56828947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95027357-T-C

http://identifiers.org/hco/16/GRCh38#56828960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95027370-C-A

56828960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95027370-C-T

56829070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: synonymous variant
orthologous variants: 95027481-C-T

56829229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95027614-G-A

56829229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95027614-G-C

56829229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95027614-G-T

56829362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95027714-G-A

56829399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95027751-G-A

56829524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95027864-A-G

56829814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95028141-G-C

56829912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95028214-G-A

56830088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95028362-C-T

56830368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95028561-G-A

56830459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95028638-G-A

http://identifiers.org/hco/16/GRCh38#56830519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95028683-C-A

56830519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95028683-C-G

56830519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95028683-C-T

56830548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: missense variant
orthologous variants: 95028716-T-G

56830700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95028868-G-A

56830700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95028868-G-T

56831073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95029164-T-C

56831358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95029428-G-A

http://identifiers.org/hco/16/GRCh38#56831419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95029485-A-C

56831419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95029485-A-G

56831483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95029634-G-C

56831483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95029634-G-T

56831513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95029660-C-G

56831513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95029660-C-T

http://identifiers.org/hco/16/GRCh38#56831532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95029728-C-A

56831532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95029728-C-G

56831532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95029728-C-T

56831546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95029778-T-C

http://identifiers.org/hco/16/GRCh38#56831586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95030014-C-A

56831586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030014-C-T

http://identifiers.org/hco/16/GRCh38#56831591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95030019-C-A

56831619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030048-G-A

56831619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030048-G-C

56831619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030048-G-T

56831650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030079-A-G

56831739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030148-A-G

56831755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030164-A-G

56831755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030164-A-T

56831804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030202-G-A

56831810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030208-G-A

56831812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030210-A-G

56831820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030218-G-A

56831820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030218-G-C

56831820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95030218-G-T

56832080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95030438-C-T

56832203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95030698-T-C

56832251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95030744-G-A

56832251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95030744-G-T

56832378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95030871-G-C

56832569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95031150-T-C

56832866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95031421-C-T

56832889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95031427-G-A

56832889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95031427-G-T

56833074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95031641-G-A

56833074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95031641-G-T

56833143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95031793-C-T

http://identifiers.org/hco/16/GRCh38#56833449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95032105-C-A

56833449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95032105-C-T

56833460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95032116-G-T

http://identifiers.org/hco/16/GRCh38#56833475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95032126-C-A

56833475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95032126-C-T

56833795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95032375-A-G

56833876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95032439-T-C

56833997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95032540-A-G

56833997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95032540-A-T

56834021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95032564-G-A

56834021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95032564-G-T

56834357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95032888-A-G

56834477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95033008-T-C

56834552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95033058-G-A

56834552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95033058-G-T

http://identifiers.org/hco/16/GRCh38#56834580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95033097-C-A

56834582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95033099-A-G

56835061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95033487-A-G

56835803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034087-T-A

56836367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034288-T-C

56836367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034288-T-G

56836435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034339-A-T

56836460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034363-G-A

56836460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034363-G-C

56836460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034363-G-T

56836515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034409-G-C

56836515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034409-G-T

http://identifiers.org/hco/16/GRCh38#56836576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95034445-C-A

56836737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034603-T-A

56836737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034603-T-G

http://identifiers.org/hco/16/GRCh38#56836745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95034611-C-A

56836745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034611-C-T

56836782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034620-G-A

56836782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034620-G-T

56836828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034649-G-T

56836841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034662-T-G

56836863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034677-G-T

56836932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034749-G-A

56836932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034749-G-C

56836938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95034755-A-G

http://identifiers.org/hco/16/GRCh38#56837544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95035471-A-C

56837544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95035471-A-T

56837558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95035482-T-G

56837623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: synonymous variant
orthologous variants: 95035547-C-T

56837629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: missense variant
orthologous variants: 95035553-C-G

56837757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95035680-G-C

http://identifiers.org/hco/16/GRCh38#56838928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95036188-C-A

56838928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95036188-C-T

http://identifiers.org/hco/16/GRCh38#56839000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95036264-C-A

56839000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: missense variant
orthologous variants: 95036264-C-G

56839088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, missense_variant
orthologous variants: 95036352-G-A

56839197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95036401-T-A

56839206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95036410-G-A

56839206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95036410-G-T

56839232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95036433-G-A

56839232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95036433-G-C

56839232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95036433-G-T

56839243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95036444-T-A

56839243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95036444-T-G

56839245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron variant
orthologous variants: 95036446-T-G

56839438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95036852-A-G

56839503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95036905-G-A

http://identifiers.org/hco/16/GRCh38#56839657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95037067-A-C

http://identifiers.org/hco/16/GRCh38#56839666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95037076-C-A

56839716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 95037405-G-C

56839716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 95037405-G-T

56839949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95037254-T-C

http://identifiers.org/hco/16/GRCh38#56839950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95037253-A-C

56839991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95037210-G-A

56839991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95037210-G-T

56840020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95037184-G-A

56840020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95037184-G-T

56841480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95037954-G-A

56841509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95037977-G-A

56841648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95038104-G-A

56841702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95038158-T-C

56841776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95038232-G-A

56842168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95038565-C-T

56843505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95040198-C-T

56843877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95040626-G-T

56843985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95040771-A-G

56844172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95040938-A-G

56844209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95040973-A-G

56844226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95040990-G-A

56844612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95041326-G-T

http://identifiers.org/hco/16/GRCh38#56844639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95041352-C-A

56844639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95041352-C-T

56844662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95041375-A-G

56845064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95041797-A-G

56845064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95041797-A-T

http://identifiers.org/hco/16/GRCh38#56845134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95041861-C-A

56845142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95041869-T-C

http://identifiers.org/hco/16/GRCh38#56845446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95042027-C-A

56845477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042057-G-A

56845477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042057-G-T

http://identifiers.org/hco/16/GRCh38#56845500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95042071-C-A

56845506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042077-G-A

56845506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042077-G-T

56845566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042135-T-C

56845575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042146-C-T

http://identifiers.org/hco/16/GRCh38#56845602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95042168-C-A

56845755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042261-G-T

http://identifiers.org/hco/16/GRCh38#56845806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95042305-C-A

56845943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042398-G-T

http://identifiers.org/hco/16/GRCh38#56845966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95042423-C-A

56845982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042435-G-A

56845984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042437-A-G

56845998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042448-T-C

56846863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042853-C-T

56847009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042973-A-G

56847015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95042979-G-A

http://identifiers.org/hco/16/GRCh38#56847135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95043062-C-A

56847135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043062-C-G

56847135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043062-C-T

56847181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043091-T-C

56847618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043479-A-G

56847643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043505-A-G

http://identifiers.org/hco/16/GRCh38#56847753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95043598-C-A

56847753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043598-C-T

http://identifiers.org/hco/16/GRCh38#56847774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95043619-C-A

56847774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043619-C-T

56847958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043769-G-A

56847983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043798-T-C

56848008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043843-G-A

56848008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95043843-G-T

http://identifiers.org/hco/16/GRCh38#56848016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95043849-C-A

http://identifiers.org/hco/16/GRCh38#56848027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95043860-C-A

http://identifiers.org/hco/16/GRCh38#56848105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95043925-C-A

http://identifiers.org/hco/16/GRCh38#56848196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95044019-C-A

56849354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044179-G-A

http://identifiers.org/hco/16/GRCh38#56849361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95044186-C-A

56849382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044207-G-T

56849438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044261-G-A

56849502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044322-T-A

56849519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044342-G-T

56849542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044353-G-A

56849542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044353-G-T

56849567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044373-G-T

56849767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 95044520-G-T

56849885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044635-G-C

56849965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044721-G-T

http://identifiers.org/hco/16/GRCh38#56850032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95044784-C-A

56850114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044834-G-A

56850114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044834-G-T

56850167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044878-G-A

56850167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28958
most severe consequence: 3 prime UTR variant
orthologous variants: 95044878-G-T