2542108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71855792-A-G

2542513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71852803-T-A

2542649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71852652-T-C

2542709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71852593-G-A

2542816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71852502-A-G

2542835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71852487-A-G

http://identifiers.org/hco/18/GRCh38#2543232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71852126-C-A

2543369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851948-A-G

2543518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851816-C-G

2543665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851666-T-C

2543855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851496-G-A

2543863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851472-G-A

2543886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851449-C-T

2543887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851448-T-C

2543913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851415-A-G

2544118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851256-G-T

2544126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851248-A-T

2544139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851237-A-G

2544139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851237-A-T

2544141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851235-A-G

2544151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851225-A-T

2544172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851206-A-T

2544192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851186-T-A

2544192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851186-T-C

2544203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71851176-G-A

2544203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71851176-G-T

2544205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71851174-T-C

2544242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71851137-A-G

2544247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71851132-T-C

2544260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71851119-A-T

2544261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71851118-T-A

2544261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71851118-T-C

2544283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71851096-A-G

http://identifiers.org/hco/18/GRCh38#2544335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71851043-C-A

2544335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71851043-C-G

2544410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71850751-G-A

2544410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71850751-G-T

2544525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71850654-T-A

2544535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71850644-T-C

2544604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71850575-G-A

2544604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71850575-G-C

2544604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71850575-G-T

2544663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71850526-G-A

2544684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71850505-T-C

2544888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71850283-T-C

2544892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71850279-T-C

2544923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71850247-G-A

2545232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71849944-T-C

2545245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71849932-A-G

2545265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71849912-A-G

2546865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71849545-G-A

2546865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71849545-G-C

2546912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71849498-T-C

2546924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71849490-C-T

2546990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71849422-G-A

http://identifiers.org/hco/18/GRCh38#2547315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71848780-A-C

2547315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71848780-A-G

2547318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71848777-A-G

2547339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71848756-T-C

http://identifiers.org/hco/18/GRCh38#2547350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71848745-C-A

2547350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71848745-C-T

http://identifiers.org/hco/18/GRCh38#2547392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71848703-C-A

2547401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71848694-T-C

2547422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71848673-C-T

2547437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71848658-C-G

2547468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71848627-T-A

2547468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71848627-T-C

http://identifiers.org/hco/18/GRCh38#2547508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71848588-C-A

2547508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71848588-C-T

2547537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71848559-T-A

2547543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71848542-G-A

2547543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71848542-G-T

2547927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71848149-T-C

2547964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71848115-T-C

2548035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847983-A-G

2548081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847940-C-T

2548101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847920-C-T

2548118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847901-T-G

2548128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847891-C-T

2548183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847838-A-G

2548197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847824-G-C

2548262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847756-C-T

2548369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847654-T-A

2548369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847654-T-C

2548369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847654-T-G

http://identifiers.org/hco/18/GRCh38#2548426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71847599-A-C

2548426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847599-A-G

2548471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847552-G-C

2548516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847509-C-G

2548879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847265-C-T

2549031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847122-C-G

2549067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71847091-A-G

2550071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845943-C-G

2550161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845852-G-A

2550173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845840-G-C

2550181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845832-A-T

2550206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845809-T-C

2550474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845723-A-G

2550530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845672-C-T

2550760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845483-G-A

2550778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845461-T-C

2550804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845439-A-G

2550804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845439-A-T

2550825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845420-A-G

2550838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71845407-T-C

2551346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844933-T-G

2551371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844910-G-T

2551376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844905-A-T

2551399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844882-T-A

2552271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844681-G-C

2552411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844556-T-C

2552579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844375-G-T

2552587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844367-G-C

2552587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844367-G-T

2552590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844364-G-T

2552603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844351-T-C

2552618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844344-T-G

2552619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844343-G-A

2552619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844343-G-C

2552619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844343-G-T

2552631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71844331-T-A

2552701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71844274-C-T

http://identifiers.org/hco/18/GRCh38#2552711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71844264-C-A

2552711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71844264-C-T

2552719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71844256-T-C

2552727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71844248-T-C

2552730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71844245-T-G

2552791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71844185-A-G

2552803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71844173-A-G

2554727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71843662-T-C

http://identifiers.org/hco/18/GRCh38#2554772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71843618-A-C

2554775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71843615-G-A

2554775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71843615-G-T

http://identifiers.org/hco/18/GRCh38#2554842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/17/GRCm39#71843548-A-C

2554891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71843499-C-G

2554983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71843407-C-G

2554983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71843407-C-T

2554986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71843404-T-C

2555007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71843383-T-C

http://identifiers.org/hco/18/GRCh38#2555023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71843367-A-C

2555044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71843341-A-G

2555045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71843340-G-C

2555067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71843318-G-C

2555067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71843318-G-T

http://identifiers.org/hco/18/GRCh38#2563684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71840749-C-A

2563728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840705-T-C

2563729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840704-G-A

2563729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840704-G-T

2563787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840651-T-C

2563801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71840637-G-A

2563801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71840637-G-T

2563841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71840597-C-T

http://identifiers.org/hco/18/GRCh38#2563843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71840595-A-C

2563936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840479-G-A

2563936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840479-G-T

2563955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840460-A-G

2563955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840460-A-T

http://identifiers.org/hco/18/GRCh38#2563962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71840453-A-C

2563962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840453-A-T

2563987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840443-T-A

2563987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840443-T-C

2563987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840443-T-G

2564002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840428-T-C

2564007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840423-A-G

2564409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71840394-A-G

2565095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71839128-T-C

http://identifiers.org/hco/18/GRCh38#2565103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71839120-C-A

2565103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71839120-C-G

2565138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71839077-G-A

2565138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71839077-G-T

2565145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71839070-G-A

2565146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71839069-G-A

2565149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71839066-G-T

2565156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71839059-A-G

2565185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71839031-A-T

http://identifiers.org/hco/18/GRCh38#2565260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71838974-C-A

2565260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838974-C-T

2565266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838968-A-G

2565277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838957-T-A

2565313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838935-A-G

2565549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838773-G-T

2565615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838691-T-A

http://identifiers.org/hco/18/GRCh38#2565619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71838687-C-A

2565619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838687-C-G

2565619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838687-C-T

2565620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838686-A-T

2565747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838570-G-T

2566165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71838514-T-C

2566397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71837809-A-G

2566767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71836505-T-C

2566859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71836420-C-T

2566965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71836314-T-G

http://identifiers.org/hco/18/GRCh38#2566983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71836296-A-C

http://identifiers.org/hco/18/GRCh38#2567010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71836269-A-C

2567083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71836196-A-G

2567130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71836148-A-G

2567237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71836024-T-C

2567244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71836017-A-G

2567276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71835894-G-A

2567276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71835894-G-T

2567296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71835853-T-C

2567376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71835690-G-A

2567376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71835690-G-T

2567393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71835666-T-C

2567393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71835666-T-G

2567425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71835634-G-A

2567425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71835634-G-T

http://identifiers.org/hco/18/GRCh38#2567685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71835413-C-A

2567685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron variant
orthologous variants: 71835413-C-T

http://identifiers.org/hco/18/GRCh38#2567697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71835401-C-A

2567852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron variant
orthologous variants: 71835257-T-G

2568081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: intron variant
orthologous variants: 71835037-G-A

http://identifiers.org/hco/18/GRCh38#2571239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71834128-C-A

2571240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71834127-T-C

2571240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71834127-T-G

2571356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71834030-T-C

2571396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71834007-G-A

2571396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71834007-G-C

2571396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71834007-G-T

http://identifiers.org/hco/18/GRCh38#2571465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71833924-C-A

2571465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71833924-C-G

2571465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24726
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71833924-C-T