19645255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 70260342-T-C

19645255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 70260342-T-G

http://identifiers.org/hco/19/GRCh38#19645343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70260256-C-A

19645343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 70260256-C-T

19645366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 70260233-T-C

19645504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70260095-A-G

19645613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70260014-T-C

19645638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259992-G-A

19645690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70259940-G-T

19645733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70259897-C-G

19645733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70259897-C-T

19645803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259827-G-C

19645828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259807-G-A

19645828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259807-G-C

19645831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259804-G-C

19645831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259804-G-T

http://identifiers.org/hco/19/GRCh38#19646011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70259620-C-A

19646052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259585-T-C

19646052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259585-T-G

19646207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 70259549-C-G

19646380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259385-T-C

19646390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259375-T-C

19646390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259375-T-G

19646402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259352-T-G

19646847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258746-T-G

19646877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258721-T-A

19646902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258695-G-A

19646902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258695-G-T

19646903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258694-G-T

http://identifiers.org/hco/19/GRCh38#19646906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70258691-C-A

19646925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258673-T-G

19646928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258670-A-G

http://identifiers.org/hco/19/GRCh38#19646936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70258662-C-A

19646961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258648-G-A

19646961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258648-G-T

http://identifiers.org/hco/19/GRCh38#19647002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70258609-C-A

19647002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258609-C-T

19647389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258229-G-A

19647389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258229-G-C

19647389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258229-G-T

http://identifiers.org/hco/19/GRCh38#19647579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70258045-C-A

19647590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258034-G-C

19647713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 70257914-T-C

http://identifiers.org/hco/19/GRCh38#19647729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70257898-C-A

19647729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70257898-C-G

19647729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70257898-C-T

19647765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70257862-G-T

http://identifiers.org/hco/19/GRCh38#19647805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70257826-A-C

19647805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257826-A-G

http://identifiers.org/hco/19/GRCh38#19647849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70257779-C-A

19647849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257779-C-T

19648066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257439-C-G

19648066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257439-C-T

http://identifiers.org/hco/19/GRCh38#19648169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70257343-A-C

19648170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257342-T-C

19648171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257341-T-C

19648179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257332-G-A

19648179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257332-G-C

19648209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70257303-C-T

19649667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70256384-T-A

19649667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70256384-T-C

19649698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70256351-G-A

http://identifiers.org/hco/19/GRCh38#19650033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70256056-C-A

19650033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70256056-C-T

http://identifiers.org/hco/19/GRCh38#19650035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70256054-C-A

http://identifiers.org/hco/19/GRCh38#19650214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70255922-C-A

19650214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255922-C-T

19650337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255868-G-A

19650337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255868-G-C

19650337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255868-G-T

19650360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255845-G-A

19650360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255845-G-T

http://identifiers.org/hco/19/GRCh38#19650384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70255818-C-A

19650384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255818-C-T

19650523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255744-G-A

http://identifiers.org/hco/19/GRCh38#19650524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70255743-C-A

http://identifiers.org/hco/19/GRCh38#19650550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70255733-C-A

19650581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255712-G-A

19650581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255712-G-T

19650636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255653-A-G

19650674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255622-G-T

http://identifiers.org/hco/19/GRCh38#19651047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70255305-C-A

19651156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255186-T-G

19651263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255091-G-A

19651263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255091-G-T

19651284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255068-G-T

19651328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255039-G-A

19651328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255039-G-C

19651328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255039-G-T

19651337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255030-G-A

19651337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255030-G-T

19651360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255006-T-C

19651360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70255006-T-G

19651394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70254991-A-G

19651494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70254900-A-T

19651653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70254809-C-T

19652848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253424-T-A

19652848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253424-T-C

19652848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253424-T-G

19652854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253418-G-T

19652877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253390-G-A

19652877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253390-G-T

19652882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253385-T-C

19653034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253324-T-C

19653124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253236-T-A

19653124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253236-T-C

19653207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253172-A-G

http://identifiers.org/hco/19/GRCh38#19653367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70253037-A-C

19653367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253037-A-G

http://identifiers.org/hco/19/GRCh38#19653374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70253030-C-A

19653374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70253030-C-T

19653447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252964-G-A

19653447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252964-G-T

19653663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252808-G-A

19653663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252808-G-T

19653913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70252641-G-A

19653913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70252641-G-T

19653952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252602-G-T

19654373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252242-G-C

19654389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252234-G-T

19654419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252206-T-A

19654495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252173-G-A

19654495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252173-G-T

19654740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251926-G-A

19654740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251926-G-T

19654744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251923-G-A

19654744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251923-G-T

19654745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251922-G-A

19654745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251922-G-T

19654887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251776-T-A

19654887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251776-T-G

19654959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251709-C-T

19654991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251672-A-G

19654993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70251670-A-G

19655288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70251402-G-A

http://identifiers.org/hco/19/GRCh38#19655667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70251021-A-C

http://identifiers.org/hco/19/GRCh38#19655719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70250963-C-A

19655719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250963-C-T

19655724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250957-G-T

19655747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250913-C-T

http://identifiers.org/hco/19/GRCh38#19655835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70250752-C-A

19655835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250752-C-T

19655991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250532-A-G

http://identifiers.org/hco/19/GRCh38#19656000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70250523-A-C

19656201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250337-G-A

19656285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250279-G-T

http://identifiers.org/hco/19/GRCh38#19656513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70250122-C-A

19656513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250122-C-T

http://identifiers.org/hco/19/GRCh38#19656540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70250094-C-A

19656540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250094-C-T

19656583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250055-C-T

19656595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250043-G-T

19656757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70249882-G-T

19656885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70249761-G-A

19657010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70249617-T-C

19657182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249446-A-G

19657182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249446-A-T

19657228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249404-G-A

19657228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249404-G-C

19657394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70249241-A-G

19657444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249196-A-G

19657451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249193-C-G

19657451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249193-C-T

http://identifiers.org/hco/19/GRCh38#19659527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70246842-C-A

19659549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246821-G-A

19659549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246821-G-C

19659886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron variant
orthologous variants: 70246498-G-A

19660040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246348-C-T

19661649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245782-C-T

19661770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245719-A-T

19662056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70245526-G-A

19662056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70245526-G-C

19662056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70245526-G-T

19662330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70245276-A-G

http://identifiers.org/hco/19/GRCh38#19662342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#70245264-C-A

19662342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70245264-C-T

19662355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245251-C-G

19662377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245222-G-T

19662581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245066-C-T

19662743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244920-C-T

19662990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244528-G-T

19663132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 70244425-G-A

19663132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 70244425-G-C

19663132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 70244425-G-T

http://identifiers.org/hco/19/GRCh38#19663155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#70244402-C-A

19663155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 70244402-C-G

19663167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 70244390-G-A

19663167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 70244390-G-C

19663201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 70244374-G-A

http://identifiers.org/hco/19/GRCh38#19663252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#70244306-C-A

19663252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70244306-C-T

19663393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70244167-T-A

19663512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 70244048-G-A

19663563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 70243997-A-G

19663607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 70243953-G-A

19663607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 70243953-G-T

http://identifiers.org/hco/19/GRCh38#19663645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#70243915-C-A

19663645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 70243915-C-G

19663645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24215
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 70243915-C-T