http://identifiers.org/hco/2/GRCh38#215939620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72188653-C-A

215939624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: non coding transcript exon variant
orthologous variants: 72188658-G-A

215941552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72197489-A-G

215941931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: non coding transcript exon variant
orthologous variants: 72197822-G-A

215942200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198046-C-T

215942276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198081-A-G

215942533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198338-T-A

215942558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198366-T-C

215942805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72198606-A-G

215942859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72198645-T-A

215942948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72198741-G-C

215942985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72198778-C-G

215943029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72198822-G-A

215943077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72198879-C-T

215943185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72198987-T-A

215943185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72198987-T-C

215943185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72198987-T-G

215943189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72198991-T-G

215943292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72199082-T-C

http://identifiers.org/hco/2/GRCh38#215944397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72199576-C-A

http://identifiers.org/hco/2/GRCh38#215944474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72199668-C-A

215944585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72199766-A-G

215944652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72199836-A-G

215944664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72199850-A-T

215944683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72199869-G-A

215944683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72199869-G-T

http://identifiers.org/hco/2/GRCh38#215944685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72199871-C-A

215944685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72199871-C-T

http://identifiers.org/hco/2/GRCh38#215944702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72199887-C-A

215944734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72199917-G-A

215944734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72199917-G-T

215944745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72199928-T-C

215944757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72199940-C-T

215944781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 72199967-C-G

215944781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 72199967-C-T

http://identifiers.org/hco/2/GRCh38#215944839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72200025-C-A

215944839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72200025-C-T

215944889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72200070-G-A

215944905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72200086-A-G

215945000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72200181-G-A

http://identifiers.org/hco/2/GRCh38#215945091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72200234-C-A

http://identifiers.org/hco/2/GRCh38#215945092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72200235-C-A

215945440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201359-T-C

215945441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201360-A-G

http://identifiers.org/hco/2/GRCh38#215945454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72201373-C-A

215945456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201375-G-A

215945456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201375-G-T

215945458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201377-C-T

215945488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201404-G-A

215945488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201404-G-T

215945549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201460-A-G

215945809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201805-G-C

215945811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201807-G-T

215945838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201848-G-A

215945838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201848-G-T

215945874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201872-G-T

215945912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201903-G-A

215945931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201922-A-T

215946046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202000-A-G

http://identifiers.org/hco/2/GRCh38#215946182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72202135-C-A

215946390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202326-C-G

http://identifiers.org/hco/2/GRCh38#215946490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72202416-A-C

215946496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202422-C-T

215946549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202453-A-G

215946560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202464-T-A

215946561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202465-G-A

215946832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202724-A-G

215946887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202778-G-A

215946887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202778-G-T

http://identifiers.org/hco/2/GRCh38#215946923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72202805-A-C

215946928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202810-T-C

215946938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202820-T-C

215947066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72203274-T-C

215947866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72204619-C-T

http://identifiers.org/hco/2/GRCh38#215948000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72204903-C-A

215948166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205064-T-C

215948346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205230-T-C

215951257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207052-T-A

215951257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207052-T-C

215951456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207244-C-T

215951516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207298-G-A

215951557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207339-C-T

215951587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207364-A-G

215951595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207372-A-G

215951742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207510-G-A

215960871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210292-A-G

215960962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210396-G-A

215961040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210467-T-C

215961042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210469-G-C

215961122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72210550-T-C

215961122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72210550-T-G

http://identifiers.org/hco/2/GRCh38#215961170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72210598-C-A

215961241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72210668-A-G

215961862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212430-C-T

215962131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212673-T-G

215962264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212813-C-T

215962265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212814-T-G

215962272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212821-C-T

215962341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212912-G-A

http://identifiers.org/hco/2/GRCh38#215962587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72213130-A-C

215967172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72213559-G-A

215967432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214537-T-C

215967625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214727-C-T

215967676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214780-A-G

215969117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215335-G-C

http://identifiers.org/hco/2/GRCh38#215969149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72215367-A-C

215971700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219102-G-A

215971701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219103-G-A

http://identifiers.org/hco/2/GRCh38#215971804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72219210-A-C

215971804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72219210-A-G

215971856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219259-T-A

http://identifiers.org/hco/2/GRCh38#215971889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72219292-C-A

215971889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219292-C-T

215971890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219293-G-A

215972056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219405-G-A

215972177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219500-C-G

http://identifiers.org/hco/2/GRCh38#215972186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72219509-A-C

215972271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219610-T-A

215972944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220679-T-A

215972944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220679-T-C

215972952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220687-G-A

215973398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221352-A-T

215973459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221399-G-A

215973485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221419-G-C

215973540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221475-G-C

215973588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221526-T-C

215973777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221691-C-T

http://identifiers.org/hco/2/GRCh38#215973939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72221850-C-A

215974000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221913-C-T

215974045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221955-T-C

215974357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72222216-G-C

215974363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72222220-G-A

215974490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222349-T-G

215974602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222466-G-C

215974754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222572-G-C

215974754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222572-G-T

215974973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222745-G-A

215974973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222745-G-C

215974973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222745-G-T

215975006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222777-A-G

215975006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222777-A-T

215975008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222779-T-G

215975197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222879-A-G

215975197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222879-A-T

215975226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222907-T-C

215979959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72223532-T-A

215979959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72223532-T-C

215979959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72223532-T-G

215980310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72223761-G-A

215980310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72223761-G-C

http://identifiers.org/hco/2/GRCh38#215981861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72225016-A-C

215981935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225077-A-G

215982005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225148-G-A

215982654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72225415-G-A

215982654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72225415-G-T

215982850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72225613-A-G

215982861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72225621-G-A

215983013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225760-C-T

215983111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225949-G-A

http://identifiers.org/hco/2/GRCh38#215983140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72225978-C-A

215983140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225978-C-T

215983222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226059-A-G

215983282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72226117-T-C

215983356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226195-C-T

http://identifiers.org/hco/2/GRCh38#215983547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72226365-C-A

215983547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226365-C-G

215983695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226428-T-A

215983735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226479-A-T

215983783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72226528-T-C

215983799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226559-G-C

215983950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226675-G-T

215983965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226690-A-T

215983966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226691-T-A

215994719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229276-G-T

215994795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229357-G-A

215996360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 72231256-G-A

215996360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72231256-G-C

215996592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72231485-G-A

215996592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72231485-G-T

http://identifiers.org/hco/2/GRCh38#215997241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72233026-C-A

215997241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72233026-C-T

215997246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72233031-C-G

http://identifiers.org/hco/2/GRCh38#215997384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72233161-A-C

215997617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72233367-A-G

215997997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234638-T-G

215998459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234764-C-T

215998634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234890-G-C

215998634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234890-G-T

215998664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72234911-T-C

215999092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235301-T-A

216000075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235716-C-T

216000123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72235758-G-T

216001505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

216001534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-T

216001963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237513-C-T

216001976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237531-C-T

216002089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237646-T-C

216002126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237683-T-C

216002419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72237958-G-A

216002572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72238090-C-T

216002624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72238117-T-C

216002694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72238179-T-C

216002694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72238179-T-G

216003468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72238731-T-G

216003521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72238784-T-C

216003658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72238916-C-G

216004037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72239321-C-G

216004143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72239454-A-G

216004583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72239884-C-T

216004807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72240093-C-T

216005078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72240343-T-G

216005410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72240727-A-T

216005843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72240990-A-T

http://identifiers.org/hco/2/GRCh38#216005863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72241010-C-A

216005868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72241015-T-A

216005868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72241015-T-C

216005868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72241015-T-G

216006554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242062-A-G

216006645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242150-G-A

http://identifiers.org/hco/2/GRCh38#216006770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72242273-A-C

216006770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242273-A-G

http://identifiers.org/hco/2/GRCh38#216006771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72242274-C-A

216006771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242274-C-G

216006853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242350-C-T

http://identifiers.org/hco/2/GRCh38#216006870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72242367-C-A

216007081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242567-T-C

216007110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242595-G-C

216007136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242620-T-G

216007243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242721-T-C

216007246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242724-T-A

216007262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242740-C-G

216007274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72242752-T-C

216007602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72243005-G-A

216010765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72243778-T-C

216011329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72248577-G-A

216011624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72248880-T-C

216011692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72249473-C-T

216011885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72249672-C-T

216012012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72249907-C-T

216012029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72249923-A-G

http://identifiers.org/hco/2/GRCh38#216012052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72249947-A-C

216012096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72250019-T-C

216012375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72250261-C-T

216012444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72250338-T-C

216012713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72250767-G-A

216013095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72251079-A-G

216013095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72251079-A-T

http://identifiers.org/hco/2/GRCh38#216013136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72251117-C-A

216013214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72251163-G-A

216013214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72251163-G-T

216013425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72251334-G-T

216013449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72251358-T-G

216013484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72251393-G-C

216013484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72251393-G-T

http://identifiers.org/hco/2/GRCh38#216013500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72251409-C-A

216013500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72251409-C-T

216013593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72251463-T-C

216013623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72251490-G-A

216013637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72251504-A-G

216013637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72251504-A-T

216013661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72251526-G-T

216013750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72251576-G-T

216013754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72251580-T-C

216013954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72251784-A-T

216014209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72252072-T-G

216014306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72252164-T-G

216014345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72252203-G-T

216017566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72253892-G-A

216019324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72256627-C-T

216019377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72256663-G-A

216020021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72256964-G-A

216020028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72256971-A-G

216020060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72257005-T-A

216020060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72257005-T-C

216022654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72258727-A-G

http://identifiers.org/hco/2/GRCh38#216024138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72261276-C-A

216024141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72261279-T-A

216024303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, undefined
orthologous variants: 72261380-G-A

216033475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72295479-A-T

http://identifiers.org/hco/2/GRCh38#216033564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72295583-C-A

216033569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72295588-G-T

216033577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72295591-T-G

216033700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72295714-G-T

216033794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72295799-C-G

216033803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72295808-C-T

216033929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72295921-G-T

216033930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72295922-G-A

216033942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72295934-C-T

216034050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72295973-G-C

http://identifiers.org/hco/2/GRCh38#216034078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72296002-A-C

216034084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72296008-A-G

216034094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72296018-G-T