14838335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3513791-T-A

14838335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3513791-T-C

14838360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 3513766-T-A

14838360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 3513766-T-C

14838462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3513666-G-A

14838462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3513666-G-T

http://identifiers.org/hco/10/GRCh38#14838487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#3513643-C-A

14838487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3513643-C-T

14838529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3513604-A-G

14838701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3513432-G-T

14838711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3513429-G-A

14838711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3513429-G-T

14838762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3513389-G-C

http://identifiers.org/hco/10/GRCh38#14838785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3513366-C-A

http://identifiers.org/hco/10/GRCh38#14840285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3511933-C-A

14840285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3511933-C-T

14840347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3511916-G-A

14840347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3511916-G-T

14840756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3511483-G-A

14840759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3511480-G-T

14840863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3511386-A-T

14841042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3511228-G-T

14841491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3510674-G-A

14841615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3510551-T-C

14841809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3510355-C-T

14841979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3510197-T-C

http://identifiers.org/hco/10/GRCh38#14842001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3510171-C-A

14842001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3510171-C-G

14842001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3510171-C-T

http://identifiers.org/hco/10/GRCh38#14842063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3510126-C-A

14842094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3510095-A-T

14842156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3510033-T-C

14842268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3509906-C-T

14842285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3509889-A-G

14842292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3509882-G-A

14842292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3509882-G-T

14842309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 3509865-G-A

http://identifiers.org/hco/10/GRCh38#14842315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3509859-C-A

14842315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3509859-C-T

14842377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3509797-G-A

14842648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3509526-G-T

14842793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3509381-G-A

14842806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3509368-C-T

14842825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3509349-T-C

14842858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3509316-G-A

14842914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3509265-G-A

14842914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3509265-G-C

http://identifiers.org/hco/10/GRCh38#14842964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3509215-C-A

14843273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3508875-C-T

http://identifiers.org/hco/10/GRCh38#14843533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3508622-A-C

14843559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3508596-G-A

14843650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3508505-C-T

14843679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3508476-G-T

14843860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3508295-T-G

14844145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3508026-T-C

14844186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3507986-G-T

http://identifiers.org/hco/10/GRCh38#14844197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3507975-C-A

14844197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3507975-C-T

14844330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3507844-T-C

14844337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3507837-G-A

14844337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3507837-G-T

14844436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3507734-T-C

14844504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3507674-T-A

14844504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3507674-T-G

14844724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3507466-A-G

14844758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3507432-G-T

14845024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3507170-T-C

14845042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3507152-A-G

14845098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3507103-C-G

14845098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3507103-C-T

14845147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3507057-T-C

14845225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3507000-T-C

14845285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506947-T-A

14845353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506867-T-C

14845441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506778-G-A

14845441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506778-G-T

14845510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506714-A-G

14845529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506695-A-G

http://identifiers.org/hco/10/GRCh38#14845676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3506686-C-A

http://identifiers.org/hco/10/GRCh38#14845682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3506680-C-A

14845682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506680-C-T

http://identifiers.org/hco/10/GRCh38#14845807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3506673-C-A

14845807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506673-C-T

14845876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506622-T-A

14845903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506594-G-A

14845903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506594-G-T

14845991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506519-T-A

14845991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506519-T-C

14845991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506519-T-G

14846192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506326-A-G

14846192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506326-A-T

14846330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506200-A-G

14846414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506121-A-G

14846508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506042-A-G

14846508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3506042-A-T

14846587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505961-T-A

http://identifiers.org/hco/10/GRCh38#14846694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3505855-C-A

14846694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505855-C-T

14846764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505785-G-A

14846764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505785-G-C

14846764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505785-G-T

14846765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505784-C-T

14846865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505688-A-G

14846884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505672-A-T

14846915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505641-G-A

14846915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505641-G-T

14846968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3505594-G-A

http://identifiers.org/hco/10/GRCh38#14847103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3505464-C-A

14847116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3505449-T-C

14847152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3505414-A-G

14847348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3505228-G-A

14847348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3505228-G-T

14847498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3505073-T-C

14847732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3504831-A-G

14847772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3504796-A-G

14847837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3504745-C-G

14848058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3504510-G-A

14848076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3504491-C-T

14848256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3504293-C-G

14848256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3504293-C-T

14848474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3503952-A-T

14848568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3503863-G-A

14848568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3503863-G-C

14848568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3503863-G-T

14848675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3503754-A-G

14849596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3502300-G-T

14849605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 3502291-A-G

14849676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3502223-G-A

14849676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3502223-G-C

14849676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3502223-G-T

14849677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3502222-T-C

14849695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3502210-A-G

14849726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: missense variant
orthologous variants: 3502168-G-A

14849959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3501939-T-C

14849970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3501928-T-A

14850011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3501908-T-C

14850173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3501706-G-A

14850485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3501409-A-T

14850510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3501380-G-A

14850524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3501367-G-A

http://identifiers.org/hco/10/GRCh38#14850683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3501240-C-A

14850683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3501240-C-T

14850697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3501224-G-T

14850731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3501176-C-T

14850735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3501172-T-C

14850773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3501135-A-G

14850938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3500979-T-C

14850938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3500979-T-G

14851122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3500439-T-G

http://identifiers.org/hco/10/GRCh38#14851140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3500421-A-C

14851244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3500321-A-G

http://identifiers.org/hco/10/GRCh38#14851253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3500312-C-A

14851253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 3500312-C-T

14851388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3500208-A-T

14851448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3500168-A-G

http://identifiers.org/hco/10/GRCh38#14851451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3500165-C-A

14851451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3500165-C-G

14851451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3500165-C-T

14851452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3500164-T-A

14851526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3500112-T-G

14851547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3500096-T-C

14851917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3499863-A-G

14852227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3499545-G-A

14852241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3499531-C-G

14852241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3499531-C-T

14852294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3499374-A-T

14852346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3499246-A-G

14852505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3499083-A-G

14853176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3498208-A-T

14854027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3497848-A-G

14854180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3497699-A-G

14854337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3497550-G-T

14854383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3497512-A-T

14854387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3497508-A-G

14854390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3497505-A-G

14855833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 3495643-G-A

14855833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 3495643-G-T

14856014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3495470-G-C

14856014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3495470-G-T

14856026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3495458-A-G

14856180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3495301-A-G

14856402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron variant
orthologous variants: 3495124-G-A

14866467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3493285-A-G

14866629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3493129-C-T

http://identifiers.org/hco/10/GRCh38#14866666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3493054-A-C

14866738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3492979-G-A

14866846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3492883-G-A

14866941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3492821-T-C

http://identifiers.org/hco/10/GRCh38#14867018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3492780-C-A

14867018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3492780-C-G

14867018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3492780-C-T

http://identifiers.org/hco/10/GRCh38#14867019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3492779-A-C

14867113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3492738-C-T

14867158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3492693-C-T

14867167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3492684-T-A

14867245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3492606-G-C

14867344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3492537-A-G

14867344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3492537-A-T

14867401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3492484-A-G

14867755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3492126-C-G

14867755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3492126-C-T

14867841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3492040-T-C

http://identifiers.org/hco/10/GRCh38#14867944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3491923-A-C

14869907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3491400-A-G

14870223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3491137-A-G

14870269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3491092-T-A

14870560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3490848-A-T

14870561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3490847-T-C

14870699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3490699-T-C

http://identifiers.org/hco/10/GRCh38#14870708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3490692-A-C

14870708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3490692-A-G

http://identifiers.org/hco/10/GRCh38#14870711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3490689-C-A

14871490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3490138-G-A

14871490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3490138-G-T

14871509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3490124-T-C

14871592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3490040-G-A

14871592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29526
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 3490040-G-T