43475015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non coding transcript exon variant
orthologous variants: 24328773-G-A

43475015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non coding transcript exon variant
orthologous variants: 24328773-G-T

http://identifiers.org/hco/19/GRCh38#43475056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24328761-A-C

43475056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non coding transcript exon variant
orthologous variants: 24328761-A-G

http://identifiers.org/hco/19/GRCh38#43475129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24328697-C-A

43475129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328697-C-T

43475197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328629-G-A

43475197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328629-G-T

43475229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328597-G-A

43475229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328597-G-C

43475229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328597-G-T

43475250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328576-A-G

http://identifiers.org/hco/19/GRCh38#43475252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24328574-C-A

http://identifiers.org/hco/19/GRCh38#43475269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24328557-A-C

43475269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328557-A-G

43475269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328557-A-T

43475288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328538-T-C

43475298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328528-G-A

43475298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328528-G-C

43475298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328528-G-T

http://identifiers.org/hco/19/GRCh38#43475348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24328474-C-A

http://identifiers.org/hco/19/GRCh38#43475350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24328472-C-A

43475350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328472-C-G

43475350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328472-C-T

43475372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328453-A-G

43475383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328443-G-A

43475383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328443-G-T

http://identifiers.org/hco/19/GRCh38#43475384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24328442-A-C

43475384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328442-A-T

http://identifiers.org/hco/19/GRCh38#43475406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24328420-C-A

43475406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24328420-C-T

43475410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non_coding_transcript_exon_variant, stop_lost
orthologous variants: 24328416-T-C

43475534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24328278-G-A

http://identifiers.org/hco/19/GRCh38#43475556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24328256-A-C

43478025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326807-G-T

43478028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326804-T-A

43478057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24326773-C-G

43478057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24326773-C-T

43478143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326689-A-G

43478149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326683-G-A

43478149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326683-G-C

43478149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326683-G-T

43478176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326650-G-A

43478176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326650-G-T

43478226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326602-G-A

43478226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326602-G-T

43479102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326365-A-G

43479231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326264-T-A

43479231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326264-T-C

43479257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326243-A-G

http://identifiers.org/hco/19/GRCh38#43479276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24326224-A-C

43479276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326224-A-G

http://identifiers.org/hco/19/GRCh38#43479277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24326223-C-A

43479277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326223-C-G

43479277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326223-C-T

43479313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326193-G-A

43479313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326193-G-T

43479316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326185-G-A

43479316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326185-G-T

43479317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326184-A-G

43479321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326180-G-C

43479321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24326180-G-T

43479379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24326141-G-A

43479379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24326141-G-T

43479405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24326115-G-A

43479405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24326115-G-T

http://identifiers.org/hco/19/GRCh38#43479631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24325873-C-A

43479631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24325873-C-G

43479631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24325873-C-T

http://identifiers.org/hco/19/GRCh38#43479643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24325863-C-A

43479643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24325863-C-T

43482877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24325267-A-G

43486108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24324247-C-G

43486113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 24324242-A-G

43486151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24324212-G-T

43486155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 24324208-A-G

43486209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24324155-G-A

43486209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24324155-G-T

43486368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24324012-G-A

43486368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24324012-G-T

http://identifiers.org/hco/19/GRCh38#43486397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24323985-C-A

http://identifiers.org/hco/19/GRCh38#43486512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24323887-C-A

43486708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24323700-G-C

43486720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24323691-G-A

43486747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24323665-T-A

http://identifiers.org/hco/19/GRCh38#43486853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24323535-C-A

43486853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24323535-C-G

43486853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24323535-C-T

43486884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24323504-G-A

http://identifiers.org/hco/19/GRCh38#43487067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24323333-C-A

43487067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24323333-C-T

43487110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24323290-A-G

43487110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24323290-A-T

43487128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24323272-A-G

43494512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24319794-A-G

http://identifiers.org/hco/19/GRCh38#43494643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24319659-C-A

43494643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24319659-C-T

http://identifiers.org/hco/19/GRCh38#43494813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24319502-C-A

43494824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24319447-G-T

43494911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24319351-A-G

43494912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24319350-T-C

43495134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24319008-C-T

http://identifiers.org/hco/19/GRCh38#43495176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24318967-C-A

43495176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24318967-C-G

43495176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24318967-C-T

43495488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24318681-A-G

http://identifiers.org/hco/19/GRCh38#43495666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24318512-C-A

http://identifiers.org/hco/19/GRCh38#43495686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24318493-A-C

43495686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24318493-A-T

http://identifiers.org/hco/19/GRCh38#43495721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24318478-C-A

http://identifiers.org/hco/19/GRCh38#43496843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24317012-C-A

43496843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24317012-C-T

http://identifiers.org/hco/19/GRCh38#43496848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24317007-C-A

43496848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24317007-C-T

43496850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24317005-T-A

http://identifiers.org/hco/19/GRCh38#43496874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24316981-A-C

43496874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24316981-A-G

43496909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24316953-T-A

43496909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24316953-T-C

43496909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24316953-T-G

43497022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24316881-A-G

43497346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: 24316611-G-T

http://identifiers.org/hco/19/GRCh38#43497356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24316601-C-A

43497367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: 24316590-G-T

43497448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: 24316517-C-T

http://identifiers.org/hco/19/GRCh38#43497454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24316511-C-A

43497454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: 24316511-C-G

http://identifiers.org/hco/19/GRCh38#43497927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24316216-C-A

43497927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: 24316216-C-T

http://identifiers.org/hco/19/GRCh38#43497967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24316191-C-A

43497967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: 24316191-C-T

43497972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: 24316186-C-T

43498111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: 24316055-G-A

43499390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, undefined
orthologous variants: -G-T

43499545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: -G-C

43501502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron variant
orthologous variants: 24312644-A-G

43501714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24312453-A-T

http://identifiers.org/hco/19/GRCh38#43501756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24312414-C-A

43501756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24312414-C-T

http://identifiers.org/hco/19/GRCh38#43501831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24312339-C-A

http://identifiers.org/hco/19/GRCh38#43502028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24312169-A-C

43502032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24312165-G-T

43502036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24312161-G-A

http://identifiers.org/hco/19/GRCh38#43502059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24312137-C-A

http://identifiers.org/hco/19/GRCh38#43502079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24312124-C-A

43502084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24312119-G-C

43502084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24312119-G-T

43502086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24312117-G-A

43502086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24312117-G-T

http://identifiers.org/hco/19/GRCh38#43502110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24312093-C-A

43502110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 24312093-C-T

http://identifiers.org/hco/19/GRCh38#43502198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24312005-C-A

43502198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24312005-C-T

43502250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24311953-T-A

43502250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24311953-T-C

43502250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24311953-T-G

http://identifiers.org/hco/19/GRCh38#43502367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24311839-C-A

43502367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24311839-C-T

43503648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24311254-A-G

http://identifiers.org/hco/19/GRCh38#43503871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24311037-C-A

43503976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24310928-C-G

43504020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24310884-C-T

43504058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24310828-C-T

43504078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24310808-G-A

43504078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24310808-G-T

http://identifiers.org/hco/19/GRCh38#43504136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24310749-C-A

43504136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24310749-C-G

43504136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24310749-C-T

43504173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24310715-T-A

43504246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24310655-T-C

43504246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24310655-T-G

43504253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24310648-G-A

43504253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24310648-G-C

43504253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24310648-G-T

http://identifiers.org/hco/19/GRCh38#43504254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24310647-A-C

43504254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24310647-A-G

43504267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24310634-T-A

43504285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24310612-A-G

http://identifiers.org/hco/19/GRCh38#43504323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24310566-A-C

43504323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24310566-A-G

43504323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24310566-A-T

http://identifiers.org/hco/19/GRCh38#43504439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24310450-C-A

43504439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310450-C-T

http://identifiers.org/hco/19/GRCh38#43504465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24310424-C-A

43504465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310424-C-G

http://identifiers.org/hco/19/GRCh38#43504485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24310399-C-A

43504485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310399-C-G

43504485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310399-C-T

43504503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310385-T-C

43504503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310385-T-G

43504506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310382-G-A

http://identifiers.org/hco/19/GRCh38#43504548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24310349-C-A

43504548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310349-C-G

http://identifiers.org/hco/19/GRCh38#43504570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24310329-C-A

43504570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310329-C-G

43504570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310329-C-T

http://identifiers.org/hco/19/GRCh38#43504574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24310325-C-A

43504574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24310325-C-T

43504683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5 prime UTR variant
orthologous variants: 24310245-T-A

43504683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5 prime UTR variant
orthologous variants: 24310245-T-C

http://identifiers.org/hco/19/GRCh38#43504687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24310241-C-A

43504687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5 prime UTR variant
orthologous variants: 24310241-C-G

43504687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5 prime UTR variant
orthologous variants: 24310241-C-T

43504707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5 prime UTR variant
orthologous variants: 24310213-T-A

43504707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5 prime UTR variant
orthologous variants: 24310213-T-C

43504707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5 prime UTR variant
orthologous variants: 24310213-T-G

43504738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5 prime UTR variant
orthologous variants: 24310178-G-A

43504738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30499
most severe consequence: 5 prime UTR variant
orthologous variants: 24310178-G-T