13910146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118479241-C-T

13910205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118479296-G-T

13910233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118479323-C-T

13910313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118479396-A-G

13910327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118479408-T-C

13910490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480058-G-A

13910490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480058-G-T

13910533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118480101-G-A

13910533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118480101-G-T

13910548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 118480116-A-G

13910554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118480122-A-G

13910554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118480122-A-T

13910627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480203-G-T

13910632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480208-G-T

13910657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480216-G-T

13910710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480275-A-G

13910728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480295-G-A

13910728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480295-G-C

13911577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482552-C-T

http://identifiers.org/hco/21/GRCh38#13911580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118482555-C-A

13911608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482575-A-T

13911636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482603-G-T

13911655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482621-T-C

http://identifiers.org/hco/21/GRCh38#13911665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118482631-C-A

13911665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482631-C-T

13911685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482655-C-T

13911709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482679-G-A

13911709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482679-G-C

13911709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482679-G-T

13911771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118482740-A-G

13911791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482759-T-C

13911791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482759-T-G

13914114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482990-G-A

13914132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483008-C-T

13914849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483053-G-C

13914916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483115-C-T

13915061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483234-C-T

13915065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483238-G-A

13915065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483238-G-T

13915155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483318-A-G

13915232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118483385-A-G

13915234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118483387-T-C

13915234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118483387-T-G

13915291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118483447-G-T

http://identifiers.org/hco/21/GRCh38#13915451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483608-C-A

13915451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483608-C-T

13915457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483613-A-G

13915468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483621-T-C

13915472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483625-T-A

http://identifiers.org/hco/21/GRCh38#13915499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483653-A-C

http://identifiers.org/hco/21/GRCh38#13915535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483687-C-A

13915535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483687-C-T

http://identifiers.org/hco/21/GRCh38#13915556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483708-C-A

http://identifiers.org/hco/21/GRCh38#13915599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483747-A-C

13915599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483747-A-T

13915620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483768-T-A

13915721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483863-T-C

13915721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483863-T-G

13915818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483952-A-G

13915818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483952-A-T

http://identifiers.org/hco/21/GRCh38#13915898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118484007-A-C

13915898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484007-A-G

13916307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484200-T-C

http://identifiers.org/hco/21/GRCh38#13916308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118484201-C-A

13916321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484214-G-A

13916321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484214-G-T

13916353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484272-C-T

13916359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484278-G-T

13916475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484420-T-A

http://identifiers.org/hco/21/GRCh38#13916648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118484518-C-A

13916648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484518-C-G

13916648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484518-C-T

13916684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484541-T-A

13916684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484541-T-C

13916684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484541-T-G

13916740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118484592-G-A

13916740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118484592-G-T

13916744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484596-T-C

13916744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484596-T-G

13916767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118484619-G-A

13916767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118484619-G-T

13916855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118484707-G-A

13916855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118484707-G-C

13916855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118484707-G-T

13916936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118484791-T-A

13916936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118484791-T-C

13916969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484821-T-A

13916969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484821-T-C

13916969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484821-T-G

13916981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484833-A-G

13917003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484856-A-G

13917414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485289-A-T

13917422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485306-T-G

13917454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485351-A-G

13917463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485360-G-T

13917522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485436-T-C

13917677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118485582-A-G

13917677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118485582-A-T

13917747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118485652-T-C

13917867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485775-T-C

13921859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118486847-A-G

13921966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118486957-G-A

13921966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118486957-G-T

13922002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118486992-A-G

http://identifiers.org/hco/21/GRCh38#13922012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118487002-C-A

13922012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487002-C-T

13922040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487029-G-C

13922125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487116-G-A

13922254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487230-T-A

13922287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487245-T-C

13922739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487652-G-T

13922805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487724-C-T

13922806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487725-A-G

13925327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488685-T-A

13925327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488685-T-C

13925336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488694-G-A

13925336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488694-G-C

13925336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488694-G-T

13925387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488744-A-G

13925400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488802-A-T

http://identifiers.org/hco/21/GRCh38#13925422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118488880-C-A

13925422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488880-C-T

13925445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488913-T-C

http://identifiers.org/hco/21/GRCh38#13925520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118488986-C-A

13925527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488993-A-G

13925909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489037-G-A

13927268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118492684-G-A

13927268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118492684-G-C

13927288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118492697-A-T

13927294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118492703-T-C

13927427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118492834-T-C

13927427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118492834-T-G

13930630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118496715-A-G

13930864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497116-T-C

13930936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497153-A-T

13931484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497624-T-C

http://identifiers.org/hco/21/GRCh38#13931497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118497637-A-C

http://identifiers.org/hco/21/GRCh38#13931533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118497695-C-A

13931765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498052-A-G

13931952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498382-C-T

13932268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118498842-G-T

13932342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118498922-A-G

13932402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498980-T-C

13933827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118499889-T-C

13933827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118499889-T-G

http://identifiers.org/hco/21/GRCh38#13933853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118499915-C-A

13933853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118499915-C-T

http://identifiers.org/hco/21/GRCh38#13933913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118499975-A-C

13933928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118499990-T-C

13933928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118499990-T-G

http://identifiers.org/hco/21/GRCh38#13933994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500083-C-A

13933994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118500083-C-T

13934033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118500122-T-C

13934111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118500200-T-C

13934216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118500305-T-C

http://identifiers.org/hco/21/GRCh38#13934219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500308-C-A

13934219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118500308-C-G

13934219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118500308-C-T

http://identifiers.org/hco/21/GRCh38#13937537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500320-A-C

13937617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118500400-T-C

13937750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118500539-T-A

13937762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118500551-T-A

13937762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118500551-T-C

13937762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118500551-T-G

13937792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118500581-T-A

13937792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118500581-T-G

13937813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118500602-C-T

http://identifiers.org/hco/21/GRCh38#13937865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500654-A-C

13937865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118500654-A-G

13938124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500906-T-C

13938124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500906-T-G

13938178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500955-A-G

http://identifiers.org/hco/21/GRCh38#13938455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118501204-A-C

13938455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501204-A-G

13938455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501204-A-T

13938581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501311-G-A

13938581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501311-G-T

13938677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501402-T-A

13939167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502610-A-G

13939192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502635-T-A

13939339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502790-T-C

13939339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502790-T-G

13939340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502791-T-C

13939340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502791-T-G

13939366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502815-T-A

13939366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502815-T-C

13939367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502816-T-C

13939382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502831-G-A

13939382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502831-G-C

13939382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502831-G-T

13939398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118502847-T-A

13939440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502889-G-A

13939440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502889-G-T

13939517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502983-A-G

13939630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118503049-A-G

13939630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118503049-A-T

13940821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510282-T-A

13940821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510282-T-C

http://identifiers.org/hco/21/GRCh38#13940825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118510286-C-A

13940825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510286-C-T

13940840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510301-T-C

13940842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510303-G-A

13940842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510303-G-T

13940865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510317-C-T

http://identifiers.org/hco/21/GRCh38#13940903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118510355-A-C

13940903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510355-A-G

13940931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510383-T-C

http://identifiers.org/hco/21/GRCh38#13940950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118510402-C-A

13940950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510402-C-T

13940961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510410-A-G

13940961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118510410-A-T

13943830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118511061-T-C

13943844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118511075-G-A

13943844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118511075-G-C

13943844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118511075-G-T

13943884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511115-G-A

13943884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511115-G-T

13943934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511164-T-C

http://identifiers.org/hco/21/GRCh38#13943965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118511195-A-C

13943965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511195-A-G

http://identifiers.org/hco/21/GRCh38#13944069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118511292-A-C

13944089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511313-A-G

13944103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511327-G-A

13944198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511417-G-C

13944329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511526-T-C

13944342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511539-T-C

13944354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511551-C-T

13944491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511693-T-G

http://identifiers.org/hco/21/GRCh38#13945027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512028-A-C

13945040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 118512041-T-A

13945040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 118512041-T-C

13945056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118512057-C-T

13945059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118512060-T-A

13945059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118512060-T-C

http://identifiers.org/hco/21/GRCh38#13945078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512079-C-A

13945078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118512079-C-G

13945078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118512079-C-T

http://identifiers.org/hco/21/GRCh38#13945124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512119-A-C

13945124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118512119-A-G

13945124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118512119-A-T

13945139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118512134-A-G

13945139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118512134-A-T

13945223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512197-G-A

13945223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512197-G-T

13945239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512213-A-G

13945239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512213-A-T

13945241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512215-G-A

13945241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512215-G-T

13945252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512234-T-A

http://identifiers.org/hco/21/GRCh38#13945276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512259-C-A

13945276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512259-C-T

13945287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512270-A-G

13945303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512286-C-T

http://identifiers.org/hco/21/GRCh38#13945325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512304-C-A

13945341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512320-C-T

13945371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512348-C-T

13945373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512350-C-T

13948410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513413-A-G

13948446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513450-A-T

13948487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513479-T-G

13948643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513631-C-T

http://identifiers.org/hco/21/GRCh38#13948695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118513673-A-C

13948695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513673-A-G

13948779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513748-T-G

13948835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513800-A-G

13948837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513802-C-T

13950952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516541-T-A

13950952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516541-T-C

13950952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516541-T-G

13951004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516595-T-C

13951025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516613-A-G

13951027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516615-T-G

13951063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516643-G-A

13951063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516643-G-T

13951090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118516670-T-G

13951159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516745-A-G

13951192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516773-T-C

13951242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118516818-G-A

13951264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118516840-C-T

13951342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516917-G-C

13951342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516917-G-T

13951349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516924-T-C

13951404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516955-T-A

13951404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516955-T-C

13951404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516955-T-G

13951586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517136-C-G

13951611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517161-C-G

http://identifiers.org/hco/21/GRCh38#13951685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517231-C-A

13951775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517328-A-T

13951839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517393-C-T

13951919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517471-C-T

13952043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517567-C-T

13952079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517601-T-A

13952079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517601-T-C

13952200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517715-T-C

13952246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517757-G-A

13952254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517765-A-T

13952297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517801-G-C

http://identifiers.org/hco/21/GRCh38#13952386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517889-C-A

13952443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517920-T-A

13952464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517942-A-G

13952540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518001-T-A

13952656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518111-C-T

13952680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518131-C-T

13957527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528396-A-G

http://identifiers.org/hco/21/GRCh38#13957595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118528461-C-A

13957595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528461-C-T

13957662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528523-G-A

13957949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528791-T-G

13957994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528837-G-A

13957994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528837-G-C

13957994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528837-G-T

http://identifiers.org/hco/21/GRCh38#13958013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118528849-C-A

13958013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528849-C-T

13958092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528906-T-C

http://identifiers.org/hco/21/GRCh38#13958175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118528991-C-A

13958216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529037-G-A

13958216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529037-G-T

13958247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529065-T-C

13958300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529263-G-T

http://identifiers.org/hco/21/GRCh38#13958302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118529265-C-A

13958302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529265-C-G

13958302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529265-C-T

13958324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529284-T-C

13958325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529285-G-A

13958325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529285-G-T

13958333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529297-A-G

13958375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529337-T-C

http://identifiers.org/hco/21/GRCh38#13958410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118529368-A-C

http://identifiers.org/hco/21/GRCh38#13960727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118529605-C-A

13960727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529605-C-T

13960745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529623-A-G

13960780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529661-T-A

13960780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529661-T-C

13960780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529661-T-G

13960865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529766-T-A

13960865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529766-T-C

13967046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118530899-T-C

http://identifiers.org/hco/21/GRCh38#13967115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118530941-A-C

13967185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531015-G-T

http://identifiers.org/hco/21/GRCh38#13967259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118531060-C-A

13967261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531062-T-C

13967264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531071-A-G

13967349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531142-A-G

13967374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118531158-G-A

13967374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118531158-G-T

13967421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118531214-A-G

13967427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118531221-T-A

13967427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118531221-T-C

13967427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118531221-T-G

13967441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118531231-G-A

13967441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118531231-G-C

13967441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118531231-G-T

13971175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533165-G-A

13971175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533165-G-T

13971284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533274-G-T

13971313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533302-C-G

13971313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533302-C-T

13971608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533372-G-T

13971633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533397-T-A

13971918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533633-G-T

13971932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533647-G-A

13971932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533647-G-T

13971941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533656-G-A

13971941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533656-G-T

http://identifiers.org/hco/21/GRCh38#13971945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118533660-C-A

13971945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533660-C-G

13971945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533660-C-T

13972013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533721-G-A

13972013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533721-G-T

13972076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533784-A-G

13972116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533820-T-A

13972116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533820-T-G

http://identifiers.org/hco/21/GRCh38#13972121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118533825-A-C

13972121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533825-A-G

13972126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533830-G-A

13972126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533830-G-T

13972127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533831-T-A

13972127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533831-T-C

13972377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118534011-C-T

13972378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118534012-A-G

13975238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118535953-G-A

13975256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118535971-A-G

13975256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118535971-A-T

13975258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118535973-C-T

13975278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118535993-C-T

http://identifiers.org/hco/21/GRCh38#13975411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118536125-C-A

13975411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536125-C-T

http://identifiers.org/hco/21/GRCh38#13975416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118536130-C-A

13975419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536133-A-G

13975435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536148-T-A

13975435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536148-T-C

13975435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536148-T-G

13975455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536168-T-A

13975455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536168-T-G

13975471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536185-G-A

13975471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536185-G-C

13975471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536185-G-T

13975485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536199-T-C

13975489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536203-T-A

13975489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536203-T-C

13975490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536204-G-A

13975490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536204-G-T

http://identifiers.org/hco/21/GRCh38#13975496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118536209-C-A

13975496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536209-C-T

13975539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118536251-T-G

13975671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536384-G-A

13975671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536384-G-T

13979054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538122-C-G

13979054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538122-C-T

13979159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538199-G-T

13979204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538244-T-G

http://identifiers.org/hco/21/GRCh38#13979211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118538251-A-C

13979215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538255-C-G

13979215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538255-C-T

13979347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538384-G-A

13979648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538695-G-A

13979648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538695-G-T

http://identifiers.org/hco/21/GRCh38#13979662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118538709-C-A

13979662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538709-C-T

13979666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538722-G-A

http://identifiers.org/hco/21/GRCh38#13979758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118538830-C-A

13979758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118538830-C-G

13979758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118538830-C-T

13979821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118538893-T-C

13979854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118538968-G-A

13979854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42024
most severe consequence: non coding transcript exon variant
orthologous variants: 118538968-G-T