120457000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 128858549-G-A

http://identifiers.org/hco/10/GRCh38#120457114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128858650-C-A

120457114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: non coding transcript exon variant
orthologous variants: 128858650-C-G

120457255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128858787-G-A

120457255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128858787-G-C

120457255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128858787-G-T

120457270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128858802-A-G

120457270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128858802-A-T

http://identifiers.org/hco/10/GRCh38#120457359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128858891-C-A

120457359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 128858891-C-G

120457359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 128858891-C-T

http://identifiers.org/hco/10/GRCh38#120457411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128858927-C-A

120457411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128858927-C-T

http://identifiers.org/hco/10/GRCh38#120457424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128858940-C-A

120457460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128858976-T-A

120457460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128858976-T-C

120457476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128858992-G-A

120457476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128858992-G-T

http://identifiers.org/hco/10/GRCh38#120457509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#128859025-C-A

120457509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128859025-C-T

120457631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128859189-C-G

120457631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128859189-C-T

120457815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128859388-C-T

120458052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128859596-C-T

120458118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128859646-G-A

120458206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128859693-A-T

120458515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128860006-G-A

120458515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128860006-G-T

http://identifiers.org/hco/10/GRCh38#120458654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128860188-C-A

120458794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128860330-G-A

120459059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128860595-C-G

120459059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128860595-C-T

120459085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128860621-A-G

120459210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128860781-T-A

120459396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128860934-C-T

120459611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128861144-G-A

120459615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128861149-A-G

120459812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128861591-T-C

120460036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128861803-C-G

http://identifiers.org/hco/10/GRCh38#120460082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128861849-C-A

120460082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128861849-C-T

120460083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128861850-G-A

120460083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128861850-G-T

120460101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128861868-A-G

http://identifiers.org/hco/10/GRCh38#120460124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128861892-C-A

120460451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128862163-C-T

120460495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128862201-A-G

120462178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128862673-T-G

120462288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128862790-G-C

120462329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128862953-G-A

120462329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128862953-G-C

120462329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128862953-G-T

120462331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128863131-G-C

120462332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128863132-G-A

120462737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128863582-C-G

120462737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128863582-C-T

120462750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128863594-A-G

120463364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128864021-C-G

120464183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128864391-C-G

120464375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128864515-G-T

120464657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128864787-G-A

120464657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128864787-G-T

120464735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128864828-T-C

120464946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865038-A-G

120465079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865162-T-C

120465103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865186-G-C

120465103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865186-G-T

120465126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865214-A-G

120465437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865438-G-A

120465829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865852-G-A

120465878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865897-C-T

120465912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865925-C-T

120465923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865936-A-G

http://identifiers.org/hco/10/GRCh38#120465941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128865963-C-A

120465967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128865993-T-G

http://identifiers.org/hco/10/GRCh38#120466050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128866075-C-A

http://identifiers.org/hco/10/GRCh38#120466106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128866118-A-C

http://identifiers.org/hco/10/GRCh38#120466119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128866131-C-A

120470622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128873439-G-A

http://identifiers.org/hco/10/GRCh38#120470736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128873583-A-C

120470736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128873583-A-T

120470817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128873851-G-A

120470834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128873868-C-T

120470948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128874005-G-T

120471192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128874238-T-G

120471459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128874844-C-T

120471591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128874968-A-G

120471889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128875278-C-G

120471903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128875293-T-C

120471959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128875343-C-G

120472408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128875759-G-A

120472408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128875759-G-C

120472408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128875759-G-T

120472416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128875766-T-C

120472695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128876012-A-G

120472921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128876215-A-G

120472923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128876217-G-A

120472930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128876292-G-C

http://identifiers.org/hco/10/GRCh38#120472955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128876315-A-C

120473141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128876479-A-G

120473173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128876512-A-G

120473377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128876704-G-A

http://identifiers.org/hco/10/GRCh38#120473448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128876773-A-C

120474283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128878143-A-T

120474338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128878190-C-G

120474362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128878215-A-G

120474408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128878261-T-G

120474913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128880158-G-A

120474913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128880158-G-T

120474957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128880202-A-G

120474987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128880232-G-A

120475012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128880257-C-T

120475027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128880273-G-A

120475217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128880462-T-A

120475463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881059-G-A

120475679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881268-G-C

120475930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881384-C-T

120475998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881436-C-T

120476045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881480-T-C

120476050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881485-G-A

120476077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881510-A-G

120476100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881545-T-G

120476111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881557-G-A

120476119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881565-G-A

120476207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881719-C-T

120476260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881772-T-C

120476300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128881822-C-G

120476436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128882095-G-A

120476653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128882262-G-A

120476658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128882267-G-T

120476950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128882862-A-G

120477114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128883032-A-G

120477143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128883060-A-G

120477145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128883062-T-G

120477152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128883069-C-T

120477431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128883331-A-G

120477625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128883455-G-T

120477763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128883550-G-C

120477765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128883552-C-G

120477863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128883651-A-G

120477995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128883733-A-T

120478008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128883746-G-A

120478137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128883863-A-T

120478154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128883875-G-A

120478280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128883958-G-A

http://identifiers.org/hco/10/GRCh38#120478658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128884286-C-A

120478660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128884288-C-T

120478665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128884289-G-A

http://identifiers.org/hco/10/GRCh38#120478694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128884315-C-A

120478694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128884315-C-G

http://identifiers.org/hco/10/GRCh38#120478711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128884332-C-A

http://identifiers.org/hco/10/GRCh38#120478714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128884335-C-A

120479512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128885092-T-C

120479621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128885216-C-T

120479630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128885225-G-C

120479956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128885902-C-G

120480041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128885987-A-T

120485065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128889625-A-G

120485211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128889757-C-G

120485239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128889784-C-G

120485239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128889784-C-T

120485340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128889860-C-T

120485342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128889862-G-A

120485364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128889884-T-C

120485604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128890070-C-T

120486106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128890552-A-G

120486129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128890570-G-A

120486136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128890577-G-T

120486143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128890584-G-T

120486341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128890762-C-T

120486397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128890816-G-T

120486859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128891188-T-C

120487228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128891549-T-A

120487278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128891600-G-A

120487388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128891708-G-A

120487403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128891721-G-A

120488512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128892322-A-G

120489099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128892807-T-A

120489173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128892878-T-C

120489630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128893240-C-T

120490099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128893865-C-G

120490249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894000-G-A

120490329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894061-G-A

120490521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894209-T-C

120490538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894226-C-T

120490691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894398-C-T

120490832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894526-A-G

120490839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894533-A-G

120490872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894568-G-A

120490872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894568-G-T

120491005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894687-G-A

120491025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128894707-G-C

120491126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128895002-G-T

120491167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128895033-G-A

120491317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128895174-G-A

120491328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128895214-T-C

120491455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128895585-C-T

http://identifiers.org/hco/10/GRCh38#120491525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128895658-A-C

120491525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128895658-A-T

120492082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128896307-A-G

120492208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128896436-G-A

120492308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128896533-A-G

120492527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128896746-G-A

120492594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128896802-T-C

120492684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128896938-A-G

120492721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128896984-C-T

120492963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128897291-C-T

120492969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128897297-C-G

120492969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128897297-C-T

120493160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128897549-G-C

120493213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128897618-C-G

120493549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128898331-G-T

http://identifiers.org/hco/10/GRCh38#120493575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128898357-C-A

120493638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128898412-A-G

http://identifiers.org/hco/10/GRCh38#120493661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128898437-C-A

120493661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128898437-C-G

http://identifiers.org/hco/10/GRCh38#120493672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128898448-C-A

120493672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128898448-C-T

120493690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128898466-A-G

120493746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128898553-G-T

120494080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128898820-A-T

120494169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128898908-T-C

120494172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128898911-C-T

120494308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128899000-G-A

120494308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128899000-G-T

120494372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128899059-A-G

120494444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128899128-A-G

120494541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128899219-C-T

120494555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128899231-G-A

120494609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128899268-G-C

120494854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128899690-G-A

http://identifiers.org/hco/10/GRCh38#120495185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128900161-A-C

120495290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128900275-G-C

120495396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128900379-C-G

120495533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128900488-G-T

120495773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128900710-C-T

120497086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128901999-G-T

120497225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128902104-G-A

120497413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128902278-C-T

120497439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128902304-G-C

120498362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128903304-A-G

120498470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128903410-G-C

120499129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128903770-G-C

120499149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128903791-C-G

http://identifiers.org/hco/10/GRCh38#120499259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128903898-A-C

120499259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128903898-A-G

120499417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128904100-T-C

120499434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128904120-A-T

120499436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128904122-C-T

120499565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128904336-T-C

120499763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128904604-A-G

120499821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128905091-G-A

120499821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128905091-G-T

120500029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128905264-A-G

120500132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128905359-G-A

120500161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128905388-G-C

120500282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128905813-C-T

120500328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128905860-G-A

120500421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128905949-C-T

120500432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128905959-T-C

120500591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128906086-G-A

http://identifiers.org/hco/10/GRCh38#120500597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128906092-C-A

120501130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128906616-A-G

120501213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128906692-T-C

120501344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128906830-G-T

120501434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128907027-A-G

120501898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128907654-G-C

120502004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128907724-A-T

120502701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128908358-T-C

120502717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128908373-A-T

120503112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128908620-G-A

http://identifiers.org/hco/10/GRCh38#120503439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128908930-C-A

http://identifiers.org/hco/10/GRCh38#120503440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128908931-C-A

120503440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128908931-C-T

http://identifiers.org/hco/10/GRCh38#120503496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128909006-C-A

120503497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909007-T-C

120503508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909037-T-G

120503520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909049-C-T

120503521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909050-C-G

http://identifiers.org/hco/10/GRCh38#120503582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128909116-C-A

120503582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128909116-C-T

120503585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128909119-G-A

120503763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909291-C-T

120503937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909467-T-C

120503941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909471-T-A

120504001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909531-T-C

120504017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909546-G-T

120504049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909575-G-A

120504049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909575-G-C

120504049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909575-G-T

120504068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909594-A-G

120504068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909594-A-T

120504069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909595-G-T

120504759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128909753-G-C

120505135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128910404-A-G

120505296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128910554-T-C

120505348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128910596-T-C

120505361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128910609-A-T

120505534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128910751-C-G

120505534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128910751-C-T

120505775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128911069-C-T

120505910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128911191-C-T

http://identifiers.org/hco/10/GRCh38#120506259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128911538-C-A

120506383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128911663-G-T

120506683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128912274-A-G

120506687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128912278-G-A

120506799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128912399-C-T

120506836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128912422-G-T

120506894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128912481-G-A

120507382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128913028-C-T

120507474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128913351-T-G

120507651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128913572-T-A

120507660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128913583-A-G

120507671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128913594-C-T

120507681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128913627-C-T

120507809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128913775-C-T

120507865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128913868-T-C

http://identifiers.org/hco/10/GRCh38#120508019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128914020-C-A

120508019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128914020-C-G

120508069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128914066-C-T

120508402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128914380-G-C

120508597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128914517-G-T

120508646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128914563-G-A

120508792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128914715-G-T

120510966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128915541-G-A

120510972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128915547-A-G

120511090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128915682-G-A

120511090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128915682-G-C

120511126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128915718-T-C

120511329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128915886-C-G

120511581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128916116-T-C

120511586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128916121-G-A

http://identifiers.org/hco/10/GRCh38#120511596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128916131-A-C

120511602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128916137-C-G

120511750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128916266-G-A

120511751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128916267-C-T

120512933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128916746-T-C

120513102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128916865-C-T

120513140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128916904-A-G

120513140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128916904-A-T

120513177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128916928-C-T

120513328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128917046-G-A

120513797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128917885-A-G

120513836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128917919-G-A

120513836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128917919-G-T

http://identifiers.org/hco/10/GRCh38#120514000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128918081-A-C

120514000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 128918081-A-G

120514393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128918354-C-T

120514789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128918690-G-A

120514789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128918690-G-T

120515003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128918865-G-A

120515100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128918933-G-A

120515239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128919128-G-A

120515601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128919473-G-A

120515692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128919569-T-A

120516220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128920073-T-A

120516220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128920073-T-C

120516264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128920118-T-C

120516264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128920118-T-G

120516496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128920298-T-C

120516524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128920337-A-G

120516817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128920661-T-G

120517113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128921373-A-T

120517283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128921541-A-G

120517310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128921563-G-A

120517369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128921617-G-A

120517448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128921693-C-T

120517645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128921888-G-T

http://identifiers.org/hco/10/GRCh38#120517860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128922087-C-A

120517860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128922087-C-T

120517980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128922203-G-A

120518031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128922252-A-G

120518038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128922259-G-A

120518360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128922522-G-A

120518706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128922866-T-C

http://identifiers.org/hco/10/GRCh38#120518797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128923173-C-A

120518797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923173-C-T

http://identifiers.org/hco/10/GRCh38#120518941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128923318-C-A

120518941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923318-C-T

120518955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923332-G-A

120518958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923335-G-T

120518979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923355-G-A

http://identifiers.org/hco/10/GRCh38#120518981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128923357-C-A

120518981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923357-C-T

120519230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923623-T-C

120519332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923727-T-A

http://identifiers.org/hco/10/GRCh38#120519359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128923754-C-A

120519521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923843-G-T

120519613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923869-T-C

120519619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923875-C-T

120519621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923876-C-T

120519862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924109-G-A

120520151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924446-C-T

120520173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924468-G-A

120520438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128923621-G-T

120520531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924719-A-G

http://identifiers.org/hco/10/GRCh38#120520861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128924980-C-A

http://identifiers.org/hco/10/GRCh38#120520862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128924981-A-C

120520865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128924984-G-C

120521154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925256-T-C

120521178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925273-G-A

120521178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925273-G-C

http://identifiers.org/hco/10/GRCh38#120521200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128925294-C-A

120521200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925294-C-G

120521200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925294-C-T

http://identifiers.org/hco/10/GRCh38#120521214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128925308-C-A

120521214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925308-C-T

120521245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925342-G-A

120521245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925342-G-T

120521388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925507-A-G

120521390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925509-G-A

http://identifiers.org/hco/10/GRCh38#120521394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128925513-C-A

120521530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925641-A-G

120521717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925851-G-A

120521717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925851-G-T

http://identifiers.org/hco/10/GRCh38#120521793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128925927-C-A

120521793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925927-C-T

120521846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128925981-A-T

http://identifiers.org/hco/10/GRCh38#120521899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128926026-A-C

120521995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926123-G-T

120522025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926151-T-C

120522186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926309-A-G

http://identifiers.org/hco/10/GRCh38#120522320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128926443-A-C

120522320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926443-A-G

http://identifiers.org/hco/10/GRCh38#120522549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128926645-C-A

120522549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926645-C-T

120522621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926716-G-A

120522636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128926732-C-T

120522795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128927016-T-C

120523001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128927196-A-G

120523462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128927668-C-G

120523539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128927744-G-A

120523646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928108-C-T

http://identifiers.org/hco/10/GRCh38#120523706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128928237-C-A

120523816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928358-T-C

120523900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928430-G-T

120523917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928447-G-C

120523955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928484-C-T

120524068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928599-A-T

120524098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928629-G-C

120524172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928703-A-T

120524242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928770-C-T

120524248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928776-T-C

120524407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928939-G-A

120524464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128928966-G-A

120524518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128929016-C-T

120524523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128929021-A-G

120524583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128929097-A-T

120524906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128929376-T-C

120524930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128929400-T-C

120525163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128929638-G-T

http://identifiers.org/hco/10/GRCh38#120525493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128931012-C-A

120525767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128931257-C-T

http://identifiers.org/hco/10/GRCh38#120525788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128931278-A-C

120525866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128931554-A-G

120525868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128931556-C-T

120525897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128931586-C-T

120526362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128931996-G-A

120526581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128932177-G-C

120526741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128932300-G-T

120527000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128932533-A-G

120527970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128933677-G-A

120528970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128934397-C-T

120537891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940867-C-T

120537904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940880-A-G

120537992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940968-T-C

120537992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940968-T-G

120537998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940974-C-G

120537998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940974-C-T

120538002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940978-C-G

120538004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940980-C-G

120538004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940980-C-T

http://identifiers.org/hco/10/GRCh38#120538008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128940984-C-A

120538008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940984-C-G

120538008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940984-C-T

120538010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940986-C-G

120538010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940986-C-T

120538016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940992-C-G

120538017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940993-T-C

120538020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128940996-C-G

120538048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128941024-C-G

120538048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128941024-C-T

120538107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128941102-G-A

120538107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128941102-G-T

120538332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128941322-G-A

120538332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128941322-G-C

120538454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128941442-C-G

120538724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128941638-T-C

120538946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128941857-C-T

120539184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128942066-C-G

120539192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128942074-G-A

120539355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128943399-G-C

120539437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128943477-C-T

120539452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128943489-A-T

120539655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128943694-A-G

120539761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128943804-C-T

http://identifiers.org/hco/10/GRCh38#120539978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128943960-C-A

120540593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128945428-G-T

120540681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128945515-G-A

120540859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128945667-G-A

120540992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128945782-A-G

http://identifiers.org/hco/10/GRCh38#120545158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128945799-C-A

120545319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128945964-A-G

120545582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128946403-C-T

120545669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128946478-C-G

120546391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128946621-T-A

120546450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128946675-A-G

120546661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128946853-G-C

http://identifiers.org/hco/10/GRCh38#120546698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128946884-A-C

120546924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128947110-G-A

120547025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128947196-T-C

120547042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128947213-C-T

120547093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128947265-C-T

120547108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128947290-T-C

120547109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128947291-T-C

120547145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128947336-A-G

120547152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128947343-T-G

120547208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128947414-T-C

120547710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128948260-T-C

120547710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128948260-T-G

120551914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128956494-T-G

120552407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128957230-G-C

120552426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128957279-T-A

120552426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128957279-T-G

120552565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128957440-C-T

120552752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128957608-C-T

120555146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128958520-T-C

120555313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128958670-G-A

120555459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128958845-G-A

120555500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128958888-A-G

120555897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128959310-C-G

120556055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128959448-C-T

120556094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128959487-T-C

120556174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128959563-G-C

120556295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128959704-T-A

120556422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128959827-G-A

http://identifiers.org/hco/10/GRCh38#120556495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128959893-A-C

120556930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128960534-G-T

120557196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128961115-C-T

120557241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128961206-A-G

120557241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128961206-A-T

120557417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128961382-T-C

120557419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128961384-C-T

120557423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128961388-C-T

120557517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128961482-T-A

120558008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128961954-T-C

120567282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968039-C-G

120567336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968092-C-G

120567347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968103-A-G

120567367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968123-G-A

120567535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968255-A-G

120567620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968325-T-C

120567799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968469-A-G

120567925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968594-G-A

120568036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968711-T-A

120568082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968753-A-T

120568086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968757-G-A

120568102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128968776-G-A

120568168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128969063-G-A

120568168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128969063-G-T

120568431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128969781-T-C

120569272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128970287-T-C

120570249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128972972-G-C

120570249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128972972-G-T

120570559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128975237-G-A

120570797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128975467-T-C

120570907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128975551-A-G

120570915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128975559-T-G

120571038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128975700-T-A

120571089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128975753-G-A

120571231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128975903-C-T

120571589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128976660-C-T

120571742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128976768-T-C

120571746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128976772-G-A

120571923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128976952-G-A

120571954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128976983-T-C

120571984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128977012-G-A

120572069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128977097-C-G

120572234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128977273-T-C

120572536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128977631-G-A

120572536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128977631-G-C

120572863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128977949-C-T

120573453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128978318-A-G

120573565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128978414-A-G

120573948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128978764-T-C

120574040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128978855-G-A

120574130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128978945-A-T

http://identifiers.org/hco/10/GRCh38#120574166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128978982-A-C

120574166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128978982-A-T

120574240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128979011-C-T

http://identifiers.org/hco/10/GRCh38#120574348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128979121-C-A

120574348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128979121-C-T

120574907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128980851-T-C

http://identifiers.org/hco/10/GRCh38#120575026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128980967-C-A

120575026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128980967-C-T

http://identifiers.org/hco/10/GRCh38#120575032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128980973-C-A

120575171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128981111-G-A

http://identifiers.org/hco/10/GRCh38#120575183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128981123-C-A

120575192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128981132-C-G

120575192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: 128981132-C-T

120575368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128981298-A-G

120575739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128981602-G-A

120575787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128981651-G-T

http://identifiers.org/hco/10/GRCh38#120576939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128981805-C-A

120576939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128981805-C-G

120576939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128981805-C-T

120577006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128981873-C-T

120577093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128981964-A-G

120577111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128981976-A-G

120577148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128982014-G-A

120577199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128982064-A-G

120577214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128982079-G-A

120577394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128982481-G-A

120577409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128982493-G-A

120578217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128982561-A-G

120578711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983039-A-G

120578806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983128-G-A

120578885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983206-T-C

120578964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983291-C-G

120579086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128983411-G-T

120579106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128983431-C-G

120579106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128983431-C-T

120580642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983528-T-C

120580681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983568-G-A

120580681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983568-G-C

http://identifiers.org/hco/10/GRCh38#120580843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128983721-C-A

120580843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983721-C-T

120581060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983902-C-T

120581066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983908-G-A

120581066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983908-G-C

120581066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983908-G-T

120581073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128983915-G-A

120581262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128984014-G-C

120581281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128984033-G-A

120581423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128984123-A-G

120581425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128984125-T-C

120581443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128984147-G-A

http://identifiers.org/hco/10/GRCh38#120581455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128984158-C-A

120581519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128984223-G-C

120581660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128984319-A-G

120581747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128984404-C-T

http://identifiers.org/hco/10/GRCh38#120581773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#128984421-A-C

120581773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128984421-A-G

http://identifiers.org/hco/10/GRCh38#120581774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#128984422-C-A

120581943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128984571-T-C

120582128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128984714-G-A

120582259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128984832-G-C

120582354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128984919-T-C

120583022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128986278-A-G

120583093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128986358-A-G

120583116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128986381-C-T

120583151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128986416-T-C

120583225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128986506-T-C

120583272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128986582-A-G

120583466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128986770-A-G

http://identifiers.org/hco/10/GRCh38#120583622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128986879-C-A

120583622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128986879-C-T

120583993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128987226-A-T

120584194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128987395-C-T

120584329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128987523-C-G

120584554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128987751-C-G

120584636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128987846-T-C

120584842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128988027-T-C

120585130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128988291-G-A

120585334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128988505-G-C

120585413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128988886-T-A

120585568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989026-A-G

120585662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989124-G-C

120585712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989168-C-T

120585874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989287-A-T

120585952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989374-C-T

120586026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989412-T-G

120586636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989579-C-T

120586831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989769-T-C

120587093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989894-G-A

120587093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989894-G-C

http://identifiers.org/hco/10/GRCh38#120587145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128989929-C-A

120587149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989933-A-G

120587149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989933-A-T

120587214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128989984-G-T

http://identifiers.org/hco/10/GRCh38#120587240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128990010-C-A

120587240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128990010-C-T

http://identifiers.org/hco/10/GRCh38#120587277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128990043-C-A

120587313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128990079-A-T

http://identifiers.org/hco/10/GRCh38#120587322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128990088-C-A

http://identifiers.org/hco/10/GRCh38#120587349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128990123-C-A

120587349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128990123-C-T

120587356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128990130-G-T

http://identifiers.org/hco/10/GRCh38#120587366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128990139-C-A

120587366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128990139-C-G

120587366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128990139-C-T

http://identifiers.org/hco/10/GRCh38#120587395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128990168-C-A

120587395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128990168-C-T

120587443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128990210-A-G

http://identifiers.org/hco/10/GRCh38#120587487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128990252-C-A

120587487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128990252-C-T

120587562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128990327-C-T

120587671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128990645-T-A

120587699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128990667-G-A

120587898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128990834-C-T

120588407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128991777-T-C

120588689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128992056-A-G

120589182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128992439-G-A

120589182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128992439-G-T

120589191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128992472-G-A

120589191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128992472-G-T

120589212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128992493-A-G

120589216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128992497-G-T

120589240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128992522-T-C

120589290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128992567-G-A

120589290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128992567-G-C

120589409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128992686-G-A

120589487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128992764-C-T

120589522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128992799-G-A

120589539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128992816-A-G

120589575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128992853-G-T

120589588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128992866-G-A

120589588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128992866-G-T

120589634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128992905-G-A

120589634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128992905-G-T

120589763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128993052-G-A

120589763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128993052-G-T

120589888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128993174-G-A

http://identifiers.org/hco/10/GRCh38#120589918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#128993206-C-A

120589958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128993234-G-A

120590246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128993333-T-A

120590425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128993475-G-A

120590425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128993475-G-C

120590575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128993613-A-G

120590597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128993635-T-C

120591286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128993923-C-T

120591395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128994030-T-C

120591580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128994466-A-G

120591834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23531
most severe consequence: 3 prime UTR variant
orthologous variants: 128994716-T-C