http://identifiers.org/hco/16/GRCh38#19168125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#118047553-C-A

19168125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 118047553-C-T

19168240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118047443-G-A

19168240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118047443-G-C

http://identifiers.org/hco/16/GRCh38#19168366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118047310-A-C

http://identifiers.org/hco/16/GRCh38#19168405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118047272-C-A

19168422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118047255-G-A

19168422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118047255-G-C

19168422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118047255-G-T

19168425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118047252-G-A

19168425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118047252-G-T

19168546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118047148-C-T

19168553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118047141-T-C

http://identifiers.org/hco/16/GRCh38#19168758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118046942-C-A

19168758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118046942-C-T

http://identifiers.org/hco/16/GRCh38#19168795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118046907-C-A

19168795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118046907-C-T

19168962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118046753-C-G

19169051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118046666-G-A

19169250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118046468-C-T

19169340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118046386-T-G

19169562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118046154-G-A

19169595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118046129-C-T

19169650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118046082-G-T

http://identifiers.org/hco/16/GRCh38#19169733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#118046015-C-A

http://identifiers.org/hco/16/GRCh38#19169745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#118046003-C-A

19169781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118045969-A-G

http://identifiers.org/hco/16/GRCh38#19169864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118045897-C-A

19169865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045896-A-G

19169886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045875-G-A

19169886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045875-G-T

19169888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045873-G-A

19169888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045873-G-T

http://identifiers.org/hco/16/GRCh38#19169939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118045757-C-A

19169939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045757-C-T

http://identifiers.org/hco/16/GRCh38#19170058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118045589-C-A

19170070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045577-G-T

http://identifiers.org/hco/16/GRCh38#19170108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118045539-C-A

19170126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045526-T-C

http://identifiers.org/hco/16/GRCh38#19170173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118045498-C-A

http://identifiers.org/hco/16/GRCh38#19170177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118045494-C-A

19170268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045394-G-C

19170396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045304-C-T

19170419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045281-G-T

19170481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045211-T-C

19170511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045181-C-G

19170519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045171-G-T

19170567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045133-T-C

19170656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045043-C-G

19170656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045043-C-T

http://identifiers.org/hco/16/GRCh38#19170669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118045031-C-A

19170681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118045019-A-T

19172186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118042954-G-A

19172186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118042954-G-C

19172186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118042954-G-T

http://identifiers.org/hco/16/GRCh38#19172708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118042426-A-C

19172708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118042426-A-G

19172906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118042217-A-G

http://identifiers.org/hco/16/GRCh38#19172974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118042156-C-A

19173030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118042103-G-T

19173230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118041899-T-C

19173240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118041890-A-G

19173263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118041867-C-G

19173263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118041867-C-T

19173331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118041775-T-C

http://identifiers.org/hco/16/GRCh38#19173402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118041745-C-A

19173402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118041745-C-T

http://identifiers.org/hco/16/GRCh38#19173403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118041744-C-A

19173403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118041744-C-G

19173403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118041744-C-T

http://identifiers.org/hco/16/GRCh38#19173404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118041743-C-A

19173404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118041743-C-T

http://identifiers.org/hco/16/GRCh38#19173417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118041730-C-A

19173417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118041730-C-T

19173680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118041506-G-A

19174129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118041119-C-T

19174151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118041095-G-A

19174154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118041092-T-G

19174176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118041070-G-A

19174581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118040714-A-G

19177426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118038804-G-T

19177454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118038775-A-T

19177542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118038688-T-G

19177803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118038468-A-G

19177828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118038443-A-G

19178688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118037454-C-T

19179499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118037262-T-C

19179515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118037242-C-T

19180026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118036588-A-G

19180053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, undefined
orthologous variants: 118036561-T-C

19180053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, undefined
orthologous variants: 118036561-T-G

19180124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron variant
orthologous variants: 118036492-T-C

19180213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118036431-G-A

19180213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118036431-G-T

19180279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118036356-G-A

19180279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118036356-G-T

19180293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118036305-T-C

19180308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118036290-C-T

19180346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118036246-C-G

19180365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118036218-T-C

19180431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118036152-C-T

19183422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118033758-G-A

19183686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118033515-C-T

19183812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118033389-A-G

19183968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118033233-G-A

19184157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033044-G-A

19184206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033010-T-A

19184713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118030936-C-T

19184742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118030910-T-C

19184744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118030908-G-A

19184744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118030908-G-C

http://identifiers.org/hco/16/GRCh38#19184875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118030770-A-C

19185025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118030619-T-C

19197270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118028053-A-G

19210617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118019742-A-G

http://identifiers.org/hco/16/GRCh38#19210834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118019512-C-A

http://identifiers.org/hco/16/GRCh38#19211030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118019279-C-A

19211248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 118019012-C-T

19211312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 118018954-G-A

19211312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 118018954-G-T

http://identifiers.org/hco/16/GRCh38#19211581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118017289-C-A

19211581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118017289-C-T

http://identifiers.org/hco/16/GRCh38#19211598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118017276-A-C

19218094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118013628-G-T

http://identifiers.org/hco/16/GRCh38#19218241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118013498-A-C

19218356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118013413-T-C

19218453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118013318-A-G

19218673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118013116-A-G

19218761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118013031-G-A

http://identifiers.org/hco/16/GRCh38#19218849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118012914-C-A

19218851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118012912-G-A

19218851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118012912-G-C

19219893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118012817-A-G

19219952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118012749-G-A

19219953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118012748-G-C

http://identifiers.org/hco/16/GRCh38#19220020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118012681-C-A

http://identifiers.org/hco/16/GRCh38#19220037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118012664-C-A

19220037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118012664-C-T

19220212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118012502-G-A

http://identifiers.org/hco/16/GRCh38#19220647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118011847-A-C

19220647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118011847-A-G

19220669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118011826-C-T

http://identifiers.org/hco/16/GRCh38#19220709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118011755-A-C

19220719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118011740-A-G

19220724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118011735-A-G

19220868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118011553-T-C

19221214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118011402-A-G

19221618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118010862-C-T

19221759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118010748-T-C

19221776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118010732-T-C

19221838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118010672-T-C

19221876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118010631-T-C

http://identifiers.org/hco/16/GRCh38#19221980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118010526-C-A

19222164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118010333-G-A

19222314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118010190-G-C

http://identifiers.org/hco/16/GRCh38#19222830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118009810-C-A

19222870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118009764-T-C

19222930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118009410-A-G

19222933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118009407-T-C

19222933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118009407-T-G

19222998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118009342-G-A

19223277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118008968-G-A

19223277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118008968-G-T

19223282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118008963-A-G

19223346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118008917-A-G

19223478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118008799-G-A

19223479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118008798-T-C

19223622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118008633-C-G

http://identifiers.org/hco/16/GRCh38#19223988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118008310-A-C

http://identifiers.org/hco/16/GRCh38#19224225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118008105-C-A

19224554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118007533-T-C

19224554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118007533-T-G

19224630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118007454-C-T

19224636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118007448-A-G

19224649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118007435-T-G

19224706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118007378-G-A

19224859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118007227-C-G

19224859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118007227-C-T

19225017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118007071-T-C

19225335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118006697-T-C

19228596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118004934-A-G

19228743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118004803-A-G

19228749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118004795-C-T

19229011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118004533-C-T

19229066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118004485-C-T

19229595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118003914-G-C

19229613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118003896-T-G

19229641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118003839-G-A

19229699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118003746-C-G

19230007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118003454-T-C

19230211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118003280-C-T

19233071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118002274-T-C

19233125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118002205-G-A

19233125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118002205-G-C

19233306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118002014-G-A

19233306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118002014-G-T

19234753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118001556-A-G

19234941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118001375-A-G

19235113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118001212-C-G

19235113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118001212-C-T

19235300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118001026-T-C

19238695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118000061-A-G

19238695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118000061-A-T

19242959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117999221-C-T

19242968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117999212-C-T

19243054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117999125-C-T

19243111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117999075-T-G

19243364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117998359-A-G

19243794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117998069-G-C

http://identifiers.org/hco/16/GRCh38#19243822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117998045-A-C

19243864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117998004-T-A

19243864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117998004-T-C

19243878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117997981-G-A

19244034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117997826-G-A

19244123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117997742-T-C

19244682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117997224-A-G

19244896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117997036-T-C

19244900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117997032-G-A

19244905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117997027-G-A

19244915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117997017-T-C

19245163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117996870-C-T

19245273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117996774-G-A

http://identifiers.org/hco/16/GRCh38#19245286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117996759-A-C

19245286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117996759-A-G

19245358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117996685-C-T

19245529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117996548-G-C

19252712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117993762-T-C

19252787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117993695-G-T

19254748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117991445-G-A

19257458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989671-G-T

19257494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989643-A-T

19257517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989621-T-C

19257583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989565-C-T

19257756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989430-G-T

http://identifiers.org/hco/16/GRCh38#19258809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117988609-C-A

19259143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988278-G-T

http://identifiers.org/hco/16/GRCh38#19259265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117988192-A-C

19259265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988192-A-G

19259398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988082-A-G

19259432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988051-G-A

19259479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988010-G-A

http://identifiers.org/hco/16/GRCh38#19260838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117987243-A-C

19260848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987233-G-C

19261050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986935-A-G

19261277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986722-C-T

19261421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986570-T-G

19261852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986249-G-A

19261852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986249-G-T

http://identifiers.org/hco/16/GRCh38#19262035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117986109-A-C

19262430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985922-A-G

19262595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985783-A-T

http://identifiers.org/hco/16/GRCh38#19262922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117985458-C-A

19263027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985351-G-A

19263033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985345-T-A

19263951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985237-C-T

19264008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985180-G-T

http://identifiers.org/hco/16/GRCh38#19264036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117985153-C-A

19264084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985105-G-A

http://identifiers.org/hco/16/GRCh38#19264216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117984848-C-A

19264306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984763-G-A

19264367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984702-T-G

19264419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984650-A-T

19264429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984641-A-G

19264443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984624-T-G

19264492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984583-A-G

19264548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984554-T-C

19264570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984539-G-A

19264964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984055-A-G

19265032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984000-A-G

19265207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983828-C-T

19265293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983741-A-G

19265401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983631-A-G

19265468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983567-T-C

http://identifiers.org/hco/16/GRCh38#19265497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117983536-A-C

19265497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983536-A-G

19265649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983383-G-A

19266354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981940-C-T

http://identifiers.org/hco/16/GRCh38#19266480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117981673-A-C

19266541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981576-G-A

19266541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981576-G-T

19266743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981409-G-A

19266743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981409-G-C

19266743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981409-G-T

http://identifiers.org/hco/16/GRCh38#19266771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117981382-C-A

19266771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981382-C-T

19266777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981376-A-G

19266814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981340-G-C

19266814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981340-G-T

19266954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 117981199-T-C

http://identifiers.org/hco/16/GRCh38#19267044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117981109-C-A

19267044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 117981109-C-T

http://identifiers.org/hco/16/GRCh38#19267100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117981053-A-C

19267100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117981053-A-G

19267100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117981053-A-T

19267104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117981049-G-A

19267104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117981049-G-C

19267104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117981049-G-T

19267473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980715-G-A

19267473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980715-G-C

19267473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980715-G-T

19267480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980708-G-A

19267480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980708-G-C

19267480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980708-G-T

http://identifiers.org/hco/16/GRCh38#19267508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117980677-C-A

19267508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980677-C-G

19267508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980677-C-T

19267546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980639-G-T

http://identifiers.org/hco/16/GRCh38#19267653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117980535-C-A

19267653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980535-C-T

19267748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980442-T-C

http://identifiers.org/hco/16/GRCh38#19267781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117980409-A-C

19267781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980409-A-T

19267797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980393-G-A

19267830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980361-G-T

19267882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980311-T-C

19267909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980284-T-C

http://identifiers.org/hco/16/GRCh38#19267932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117980261-A-C

19267946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980247-G-A

19268246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117980025-G-T

19268272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24119
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117979999-A-G