http://identifiers.org/hco/10/GRCh38#25174937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21372582-C-A

25174937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21372582-C-T

25175011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21372656-G-A

25175011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21372656-G-T

25175036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21372699-G-A

25175042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21372705-G-A

25175042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21372705-G-C

25175042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21372705-G-T

http://identifiers.org/hco/10/GRCh38#25175054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21372717-C-A

25175054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21372717-C-G

25175054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21372717-C-T

25175399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21373045-T-A

25175399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21373045-T-C

25175399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21373045-T-G

25175966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21373612-G-A

25176207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21373853-T-G

25176239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21373885-G-A

25176290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21373936-C-T

25176579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374206-G-T

25176732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374396-A-G

25176807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374477-G-A

25177366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374969-C-T

25177452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21375071-G-C

http://identifiers.org/hco/10/GRCh38#25177478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21375104-A-C

25177689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21375305-C-T

25178006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21375609-A-G

25178116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21375823-C-T

25178318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376006-T-C

25178375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376055-G-A

25178756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376656-C-T

25182184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21377861-G-A

25182682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378437-T-A

25182700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378455-T-C

25182842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378711-G-C

25182842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378711-G-T

25183012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378875-T-C

25183034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378898-G-A

25183149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378993-G-A

http://identifiers.org/hco/10/GRCh38#25184634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21379173-C-A

25184634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21379173-C-T

25184969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21379508-A-G

25184980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21379519-G-T

25185293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21379779-C-T

25193543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382234-G-A

25193558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382249-G-A

25194165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382660-A-G

25197761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21383939-G-T

25197813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21383982-C-G

25198256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21384412-C-T

25198546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21384701-A-G

25198755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21384963-A-G

25198766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21384980-G-A

25198768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21384982-C-T

25198769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21384983-G-A

25198782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21384996-A-G

25198792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385007-C-G

25198885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385088-T-C

25198891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385094-G-A

25206555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385504-T-A

25206555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385504-T-C

25206555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385504-T-G

25206692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385616-T-G

25206704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385628-A-G

25206717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385641-G-T

25206740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385664-G-T

25206800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385724-G-A

25206800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385724-G-C

25206843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385765-C-T

25206872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385794-T-G

25206931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21385852-A-T

25207287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21386142-A-G

25207360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21386271-T-C

http://identifiers.org/hco/10/GRCh38#25207986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21386831-A-C

25208100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387086-A-G

25208101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387087-T-G

http://identifiers.org/hco/10/GRCh38#25208178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21387195-C-A

25208386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387553-T-A

25208471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387639-A-G

25208474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387642-T-G

25208538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387713-T-G

25208558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387822-T-G

25208564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387828-G-A

25208566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387830-G-A

25208568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387832-G-A

25208568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387832-G-C

25208572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387836-G-A

25208572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387836-G-C

25208606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387870-A-G

25208614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387878-T-C

25213917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394854-C-T

25217000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400649-G-A

25217258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400887-T-C

http://identifiers.org/hco/10/GRCh38#25217324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21400944-C-A

25217324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400944-C-T

25217604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401827-C-T

http://identifiers.org/hco/10/GRCh38#25217617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21401840-A-C

25217672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401895-T-C

25217820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21402015-C-G

http://identifiers.org/hco/10/GRCh38#25217879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21402073-A-C

25217969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21402128-C-G

25218018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21402177-C-T

25218117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21402262-T-C

25218179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21402325-C-T

25218250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21402395-G-A

25218250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21402395-G-T

25218457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21402593-G-A

25218501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21402630-G-C

http://identifiers.org/hco/10/GRCh38#25220613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21403732-C-A

25220631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21403750-C-T

25220756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21403870-G-C

25220872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21403959-A-G

25220928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404015-T-A

25220956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404038-T-C

25221016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404093-G-T

25221027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404104-T-C

25221230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404317-T-C

25221257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404343-A-G

25221637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404735-A-G

25221741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404875-A-G

25221806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404937-G-T

25221994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405126-G-A

25221995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405127-T-G

25222121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405251-C-T

25222122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405252-A-G

25222122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405252-A-T

25222137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405267-C-T

25222163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405293-C-G

25222163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405293-C-T

25222282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405408-C-T

25222321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405447-C-T

25222388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405511-C-T

http://identifiers.org/hco/10/GRCh38#25222429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21405544-C-A

25222429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405544-C-G

25222474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405576-T-C

http://identifiers.org/hco/10/GRCh38#25222492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21405594-C-A

25222564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405700-G-A

25222617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405775-G-A

25222640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405796-G-A

25222756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405886-A-G

25222770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405900-G-A

25222959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21406060-G-C

25222963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21406064-A-G

25223013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21406108-C-T

25223364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407446-A-G

http://identifiers.org/hco/10/GRCh38#25223484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21407560-A-C

25223662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407722-T-C

25223701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407753-T-C

25223772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407822-A-G

25223947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407982-C-T

25224017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408049-C-T

25224292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408360-G-A

25224556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408605-T-A

25224610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408865-A-G

25224958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409191-G-A

25225897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409872-G-A

25225897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409872-G-T

25226094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410039-C-T

http://identifiers.org/hco/10/GRCh38#25226379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21410309-A-C

25226379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410309-A-G

25226522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410556-A-T

25226545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410579-C-T

25227205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21411170-G-C

25227333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21411277-A-T

25227401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21411340-A-G

25227626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21411535-A-G

25228093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412065-C-T

25228421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412329-G-T

25228749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412618-A-G

25228754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412623-G-A

25231771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415296-A-G

25232030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415464-C-G

http://identifiers.org/hco/10/GRCh38#25232140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21415574-A-C

25232140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415574-A-G

25232146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415580-C-T

25232357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415790-A-G

25232557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415990-T-C

25232595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416053-C-T

25232858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416295-C-T

25232887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416359-C-T

25232931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416403-T-C

25233011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416468-G-T

25233119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416577-G-A

25233188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416646-T-C

25233195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416653-G-T

25233218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416676-C-G

25235103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21419043-G-A

25235125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21419069-G-C

25235134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21419073-A-G

25235270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21419215-T-A

25235288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21419248-C-T

25235346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21419323-T-C

25235396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21419377-T-C

25236549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421837-G-A

25237777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21423210-C-T

http://identifiers.org/hco/10/GRCh38#25237808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21423241-C-A

http://identifiers.org/hco/10/GRCh38#25237943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21423348-A-C

25237943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21423348-A-T

http://identifiers.org/hco/10/GRCh38#25240077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21425875-C-A

25240259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426078-A-G

25240386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426183-G-A

25240518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426302-A-G

25240521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426305-G-A

25240603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426351-G-A

25240724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426445-T-A

25240824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426543-A-G

25240925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426642-C-T

25241108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426809-T-C

25241108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426809-T-G

25241836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426932-T-G

http://identifiers.org/hco/10/GRCh38#25242146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21427237-C-A

25242347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427424-A-G

25242859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427942-G-A

25242965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428046-T-A

25246553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428901-G-C

25246589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428933-A-G

25253824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21430753-T-A

25254558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431011-C-G

25254926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431336-C-T

25255088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431499-A-G

25255207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431624-G-C

25255537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434205-C-G

25255537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434205-C-T

25255539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434207-G-T

25255858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434488-T-A

http://identifiers.org/hco/10/GRCh38#25255886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21434520-A-C

25255886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434520-A-G

25255924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434549-T-C

25255981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434598-G-T

25256289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434870-T-G

25256295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434876-C-T

http://identifiers.org/hco/10/GRCh38#25257382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

25257382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

25257685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

25257796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

25257821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

25257821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

25258111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21436672-T-C

25258271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21436803-A-G

25261767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21438519-A-G

25262546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21439342-T-C

25264415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21439701-C-T

25265836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21440547-C-G

25265836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21440547-C-T

25266130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21441012-A-G

25266312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21441184-C-T

25266344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21441222-C-T

25266371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21441249-T-C

25266378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21441256-G-T

25266642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21441399-T-G

25266678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21441434-C-T

http://identifiers.org/hco/10/GRCh38#25266693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21441448-C-A

25266783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21441536-A-G

25270089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21442556-T-C

25270287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21442738-A-T

25270437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21442886-G-A

25270516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21442964-T-C

25270669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21443098-C-T

25270908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21443289-G-A

25271068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21443421-C-G

http://identifiers.org/hco/10/GRCh38#25271389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21443711-A-C

25272109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21444100-C-T

25272248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21444224-G-A

25272398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21444320-A-G

25272581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21444508-T-G

25272770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21444697-C-T

http://identifiers.org/hco/10/GRCh38#25272974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21444900-C-A

25273077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445001-A-G

25273166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445077-C-T

25273212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445123-A-G

25273212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445123-A-T

http://identifiers.org/hco/10/GRCh38#25273289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21445191-A-C

25273652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445856-T-C

25274193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446083-T-C

25274307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446191-C-T

25274793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446678-G-C

25274825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446715-C-T

25275010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446831-T-G

25275038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446845-T-C

25275038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446845-T-G

25275098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446865-A-G

25275372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21447117-A-G

25275377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21447122-G-A

25275722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21448991-T-A

25275722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21448991-T-G

25275773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449043-A-G

25275978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449240-A-G

25276192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449451-A-G

25276331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449590-T-G

25276790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449997-C-T

25276846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21450041-T-C

25276856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21450051-A-G

25287906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21450837-G-A

25288235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21451196-G-A

25288294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21451258-G-T

25288371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21451326-C-G

25288472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21451424-G-A

25288693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21451637-G-A

25288818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21453722-C-G

25292716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458930-C-T

25292844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459079-G-T

25293068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459294-T-C

25293173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459410-C-T

25294112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459664-G-A

http://identifiers.org/hco/10/GRCh38#25294158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21459710-C-A

25294468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459979-C-T

25294588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460086-A-G

25295017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460383-G-A

25295017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460383-G-T

25295022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460388-G-C

25295319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460651-C-T

25296053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

25296473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

25296477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

25296481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/10/GRCh38#25296485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

25296485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

25296626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

25296761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

25296877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/10/GRCh38#25297077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21470955-C-A

25297244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21471113-C-G

25297244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21471113-C-T

25297386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21471229-A-G

25297386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21471229-A-T

25297400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21471243-G-A

25298121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

25298245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

25300235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479311-C-T

25300439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479510-T-G

25300472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479543-A-G

25300705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479756-T-C

25300784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479831-C-T

http://identifiers.org/hco/10/GRCh38#25300807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21479854-A-C

25300807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479854-A-G

25300869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479872-C-T

25300903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479905-T-C

25300967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479967-T-G

25301106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21480063-T-C

25301392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21480335-G-A

25301515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21480478-G-A

http://identifiers.org/hco/10/GRCh38#25301595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21480588-A-C

25301690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21480664-C-G

25301735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21480707-C-T

25301819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21480791-A-G

25301875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21480847-T-C

25302043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21480987-A-G

25302531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21481467-G-A

25302659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21481597-T-C

25302695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21481634-G-A

25302787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21481751-A-G

25302866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21481866-A-G

25302964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21481958-A-G

25302985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21481980-T-C

25303006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482001-C-T

25303039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482031-A-G

25303109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482110-A-T

25303197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482227-A-G

25303472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482659-C-T

25303526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482713-C-T

25303610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482785-G-A

25303610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482785-G-T

http://identifiers.org/hco/10/GRCh38#25303825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21482967-A-C

25303876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483012-T-G

25304177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483239-G-T

25305719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21484127-T-G

25305735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21484143-C-T

25306142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21484559-C-G

25306143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21484560-T-G

25306361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21484782-C-T

25326430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502324-G-T

25326461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502355-G-C

http://identifiers.org/hco/10/GRCh38#25326532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21502411-C-A

25326783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502647-G-T

http://identifiers.org/hco/10/GRCh38#25327218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21502777-A-C

25327218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502777-A-G

25327401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502908-A-G

25327727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504515-G-A

25327934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504662-T-C

25328123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504852-A-G

25328141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504869-G-A

25328469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21505481-T-G

http://identifiers.org/hco/10/GRCh38#25332894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21506300-C-A

25333172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21506581-T-C

25333225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507806-C-G

25333343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507920-C-G

http://identifiers.org/hco/10/GRCh38#25333498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21508054-C-A

25333539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508082-A-G

25333608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508123-G-A

25333637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508150-A-G

25333852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508368-T-C

25333876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508392-C-T

25333933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508447-C-T

25334039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508531-C-G

25334295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508976-A-G

25334304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508996-A-T

25334391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21509083-T-G

http://identifiers.org/hco/10/GRCh38#25334448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21509141-C-A

25334448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21509141-C-T

25334625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21509318-A-G

25334669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21509360-C-G

25334799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21509473-A-T

25334868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21509542-T-C

25335012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21509727-A-G

25335527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21510249-T-C

25335624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21510342-A-G

25335868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21510609-C-T

http://identifiers.org/hco/10/GRCh38#25339360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21513555-A-C

25339433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21513625-T-C

25339706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21513896-A-G

25340079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514237-T-A

25340118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514272-G-T

25340137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514290-C-T

25340152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514305-C-T

25340154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514307-T-C

25340344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514481-T-C

25341917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21518168-C-T

25342044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21518055-T-C

25342113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21517986-G-C

25342167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21517933-T-G

25342305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21517823-G-A

25342305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21517823-G-C

25342457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21517715-C-T

25342580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21517598-C-G

25342598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21517580-A-G

25343262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514851-G-A

25343280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514814-G-A

25343349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514747-T-C

http://identifiers.org/hco/10/GRCh38#25343364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21514732-A-C

25345776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21518426-C-T

25345929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21518542-C-G

25346323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21518884-A-G

25346427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21518988-T-C

25346457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21519013-T-C

25346591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21519122-G-A

25346591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21519122-G-T

25346633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21519173-G-A

25346839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21519490-G-A

25346849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21519498-T-C

25347884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21520169-C-T

25347909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21520192-T-C

25348188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21520496-T-C

25348229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21520514-C-G

http://identifiers.org/hco/10/GRCh38#25348257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21520542-C-A

25348257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21520542-C-G

http://identifiers.org/hco/10/GRCh38#25348657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21521065-A-C

25348698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21521106-A-T

http://identifiers.org/hco/10/GRCh38#25348738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21521113-C-A

http://identifiers.org/hco/10/GRCh38#25349024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21521412-C-A

25349024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21521412-C-G

25349024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21521412-C-T

25349366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21521616-A-T

25349413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21521644-G-A

25350003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522021-C-G

25350089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522554-C-T

25350131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522589-A-T

25350172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522632-G-A

25350294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522750-A-G

http://identifiers.org/hco/10/GRCh38#25350775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21523593-C-A

25350775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21523593-C-T

25350839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21523673-A-G

25350988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524477-G-T

25351130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524602-C-T

25351131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524603-C-T

25351379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524816-G-A

25351701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525064-T-C

25351713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525076-T-C

25364549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534741-A-T

25364656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534839-G-T

25364770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534952-T-C

25364827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535008-G-A

25364864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535041-C-T

25364871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535047-G-A

25365028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535289-T-C

25365052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535411-A-T

http://identifiers.org/hco/10/GRCh38#25365069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21535421-A-C

25365111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535458-A-G

25365303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535629-G-A

25365303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535629-G-T

25365361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535687-T-G

25365441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535766-T-C

25365562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535887-C-G

25365631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535950-A-G

25365739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21536055-T-G

25365777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21536094-A-G

25365813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21536129-G-C

25365859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21536210-C-T

25365915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21536266-T-C

25366100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21536423-A-G

25366244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21536548-A-G

25394137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21548290-C-G

http://identifiers.org/hco/10/GRCh38#25394283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21548419-C-A

25394283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21548419-C-T

25394284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21548420-A-G

25394410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21548551-A-G

http://identifiers.org/hco/10/GRCh38#25394440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21548580-A-C

25394571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21548724-A-T

25394630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21548858-C-T

25394636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21548910-A-G

http://identifiers.org/hco/10/GRCh38#25394719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21549055-C-A

25394785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21549113-C-T

25394863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21549184-G-A

25394965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21549284-T-C

25394997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21549314-G-T

25395038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21549361-T-G

http://identifiers.org/hco/10/GRCh38#25395306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21549528-C-A

25395483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21549704-A-G

25395544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21549745-A-G

25395581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21549782-G-A

25395761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21557965-C-T

25395809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558012-G-A

25395809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558012-G-T

25395810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558013-T-C

25395810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558013-T-G

http://identifiers.org/hco/10/GRCh38#25395833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21558034-C-A

25395833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558034-C-G

25395833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558034-C-T

25395876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558075-T-C

http://identifiers.org/hco/10/GRCh38#25395976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21558175-C-A

25395988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21558187-A-G

http://identifiers.org/hco/10/GRCh38#25396023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21558222-C-A

25396023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558222-C-T

http://identifiers.org/hco/10/GRCh38#25396132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21558348-C-A

25396133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558349-T-A

25396133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558349-T-C

25396198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558418-A-G

25396427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558632-G-A

25396866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558760-C-G

25397063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558921-T-G

25397074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558932-G-A

25397147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558976-C-G

25397166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558995-A-G

http://identifiers.org/hco/10/GRCh38#25397176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21559005-A-C

25397191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559020-G-T

25397279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559099-A-G

25397287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559107-C-G

25397361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559190-G-A

25397425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559256-C-G

25397425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559256-C-T

25397789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559569-A-G

25397809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559594-C-G

25397851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559620-G-T

25397922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559713-A-G

25397922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559713-A-T

25398028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559811-C-T

25398029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21559812-A-T

25398407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21560213-C-T

25398472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21560282-T-C

25398485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21560295-C-T

25398603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21560413-C-T

25398679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21560510-C-T

25399954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21561298-C-T

25399955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21561299-C-T

25399969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21561313-A-G

25400038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21561384-A-T

25400213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21561673-A-T

25400376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21561842-A-G

25400814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21562260-G-A

http://identifiers.org/hco/10/GRCh38#25400979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21562423-A-C

25401888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21563253-T-A

25402924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21564471-A-G

25402960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21564507-A-T

25403006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21564556-A-G

25403028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21564578-G-A

http://identifiers.org/hco/10/GRCh38#25403266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21573275-A-C

25403479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21573429-A-G

25403489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21573439-C-G

25403528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21573479-T-A

http://identifiers.org/hco/10/GRCh38#25403743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21573666-A-C

25404286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21574151-A-G

25411203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21580958-T-C

25411308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21581055-A-G

25411308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21581055-A-T

25411598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21581313-T-C

25412101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21581499-G-C

25412101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21581499-G-T

25412155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21581551-A-G

25412246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21581630-T-C

http://identifiers.org/hco/10/GRCh38#25412282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21581666-A-C

25412353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21581737-C-G

25412353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21581737-C-T

25412383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21581767-T-C

http://identifiers.org/hco/10/GRCh38#25412398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21581782-C-A

25412519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21581907-T-G

25412572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21581960-G-T

http://identifiers.org/hco/10/GRCh38#25412573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21581961-C-A

25413417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21582366-T-C

http://identifiers.org/hco/10/GRCh38#25413548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21582488-A-C

25413548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21582488-A-G

25413602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21582542-T-G

25413626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21582567-T-C

25413627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21582568-A-G

25413689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21582631-C-T

25413753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21582687-T-A

25413753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21582687-T-C

http://identifiers.org/hco/10/GRCh38#25414046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21595510-C-A

25414165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21595625-A-G

25414221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21595686-G-A

25414258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21595723-G-A

25414258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21595723-G-T

25414259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21595724-G-A

25414263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21595728-T-C

25414373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21595838-G-A

25414492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21595915-G-A

25414520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21595942-T-C

25414548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21595970-G-A

25414627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596057-G-A

25414798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596208-C-T

25414906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596302-G-C

25414997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596355-G-T

25415007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596370-A-G

25415011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596374-T-C

http://identifiers.org/hco/10/GRCh38#25415099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21596462-A-C

25415447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596830-G-A

25415470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596853-C-T

25415533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596923-T-C

25415534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596924-C-G

25415543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596933-C-T

25415570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21596958-T-C

25415620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597009-A-G

http://identifiers.org/hco/10/GRCh38#25415692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21597159-A-C

25415692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597159-A-G

25415707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597214-G-C

25415769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597278-A-G

25415866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597373-C-T

25416205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597566-G-T

25416254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597614-A-G

25416310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597663-T-C

25416360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597683-C-T

25416427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597746-C-T

25416450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597766-T-G

25416456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597772-A-G

25416513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597827-G-C

http://identifiers.org/hco/10/GRCh38#25416621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21597924-A-C

http://identifiers.org/hco/10/GRCh38#25416664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21597963-C-A

25416664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597963-C-G

25416695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597991-A-G

25416696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21597992-C-G

25416733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598021-C-G

25416733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598021-C-T

25416807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598096-A-G

25416958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598232-G-A

25416994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598269-T-C

25417012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598287-T-C

25417107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598366-C-T

25417172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598430-G-A

25417403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598660-G-A

25417403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598660-G-T

25417514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598792-A-T

25417573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598842-C-G

25417950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599139-G-A

25418065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599253-G-A

25418099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599286-G-T

http://identifiers.org/hco/10/GRCh38#25418161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21599341-A-C

25418197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599379-C-T

25418311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599507-G-T

25418583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599756-A-T

25418599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599766-T-C

25418663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599832-G-A

25418693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599872-A-G

25418693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599872-A-T

http://identifiers.org/hco/10/GRCh38#25418699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21599878-A-C

25418699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21599878-A-G

http://identifiers.org/hco/10/GRCh38#25418726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21599904-C-A

25418923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600071-G-T

25432366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600322-T-G

25432415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600360-C-T

25432532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600477-G-A

25432689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600619-C-T

25432831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600768-A-G

http://identifiers.org/hco/10/GRCh38#25432951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21600874-C-A

25432956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600879-T-A

25432965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600888-A-G

25433003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600895-T-C

25433142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21601025-T-G

25433201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21601087-A-G

25433411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21601293-C-T

25433537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21601379-T-C

25434542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21608282-A-G

25434625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21608353-A-G

25434952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21615404-T-C

http://identifiers.org/hco/10/GRCh38#25434961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21615413-C-A

25434962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21615414-A-G

25434987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21615426-C-T

25435501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21615664-G-T

25435509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21615672-G-A

25435785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21615876-G-A

25435801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21615892-G-T

25435947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616031-G-A

25436018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616093-T-A

25436144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616235-G-C

25436436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616391-T-A

25436484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616438-C-T

25436497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616451-T-C

25436570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616525-A-G

25436598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616553-T-C

25436607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616576-G-A

25436898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617370-G-A

25436898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617370-G-T

25436909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617381-A-G

25436982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617453-A-G

25437023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617495-G-T

25437057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617527-G-A

25437077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617539-C-T

25437543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617677-T-C

25437582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617738-A-G

25437928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618072-G-C

25438087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618220-C-G

25438087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618220-C-T

25438114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618256-G-T

25438270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618380-A-G

25438579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618809-G-C

25438721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618954-T-A

25438721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618954-T-C

25438839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619129-T-C

25438859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619149-T-A

25439874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619589-C-T

25439933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619648-G-A

25439985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619697-C-T

25440159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619865-G-A

25440331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620030-T-A

25440402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620104-T-A

25440682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620353-G-T

25440695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620367-T-C

25440830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620507-G-T

25440836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620513-G-A

25440912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620584-C-T

25441064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620726-C-G

25441065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620727-C-G

25441153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620812-T-C

25441166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620825-C-T

25441374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21621010-G-A

http://identifiers.org/hco/10/GRCh38#25441410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21621048-C-A

25442125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21621504-C-G

25442247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21621625-G-A

25442275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21621653-C-T

25442357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21621730-G-A

25442367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21621740-A-G

25442442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21621815-G-A

25442660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21622009-C-G

25442800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21622141-T-C

25442844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21622185-A-G

25444783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21622994-A-G

25444864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623419-T-G

25445064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623605-T-C

25445151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623687-A-G

25445164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623701-T-C

25445167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623704-G-A

25445167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623704-G-T

25445423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21624058-G-C

25445617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21624249-T-A

25445882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21624427-G-A

25446894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625367-G-C

25446996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625469-T-G

25447132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625597-T-C

25447168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625640-A-G

25451412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21637699-G-A

25451577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21637853-A-G

25451594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21637870-G-A

25451720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638004-C-T

25451726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638017-A-G

25451822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638114-A-G

25451837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638128-C-T

25452393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638308-A-G

25452515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638420-G-T

25452664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638531-G-A

25453124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638787-C-G

25453124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638787-C-T

25453594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21639225-G-A

25453845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21639677-T-G

http://identifiers.org/hco/10/GRCh38#25453965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21639799-C-A

25453965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21639799-C-G

25454072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21639896-C-T

25454100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21639928-A-G

25454324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21640891-C-T

25454332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21640899-G-A

25454332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21640899-G-T

25454419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21640994-A-G

25454422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21640997-G-C

25454532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21641101-G-A

25454694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21641250-A-G

25454713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21641270-T-A

25454946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21641512-T-C

25454946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21641512-T-G

25455052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21641622-T-G

25455116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21641686-G-C

25455773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642305-G-A

25455773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642305-G-T

25455827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642351-A-G

25455865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642401-T-A

25455865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642401-T-G

25455907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642448-T-C

http://identifiers.org/hco/10/GRCh38#25455913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21642454-C-A

25456053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642595-G-A

25456053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642595-G-T

http://identifiers.org/hco/10/GRCh38#25456083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21642624-C-A

25456083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642624-C-T

25456094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642635-T-C

25456225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642771-C-G

25456249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21642796-G-C

25456415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642913-T-C

25456460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642952-G-T

25456476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642968-T-C

25456688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21643184-T-C

25456772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21643265-A-T

25458660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647200-C-G

25458754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647289-A-G

http://identifiers.org/hco/10/GRCh38#25458810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21647336-A-C

25458810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647336-A-G

25458810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647336-A-T

http://identifiers.org/hco/10/GRCh38#25458841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21647367-C-A

25458867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647384-A-T

25459031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647526-G-A

25459033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647528-A-G

25459058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647551-G-A

25459064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647557-G-A

25459064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647557-G-T

25459269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647763-G-A

25459401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21647883-G-A

http://identifiers.org/hco/10/GRCh38#25459711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21648194-C-A

25459736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21648222-G-A

25459846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21648333-T-A

25459975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21648461-T-C

25463617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21648988-C-T

25463692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21649063-C-T

http://identifiers.org/hco/10/GRCh38#25463854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21649170-A-C

25463893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21649204-G-C

25463907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21649218-G-A

25463956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21649275-T-G

http://identifiers.org/hco/10/GRCh38#25464069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21649554-C-A

25464069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21649554-C-T

25464126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21649611-G-A

25464147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21649630-A-G

25464184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21649667-G-C

25464307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21649786-G-A

25464319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21649798-C-G

http://identifiers.org/hco/10/GRCh38#25464596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21650314-C-A

25464912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21650646-T-C

25465249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21651053-T-A

25465373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21651137-T-G

http://identifiers.org/hco/10/GRCh38#25465434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21651195-C-A

25466395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21653532-T-C

25466608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21653727-A-G

25466608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21653727-A-T

25466641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21653759-G-C

25466641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21653759-G-T

25466755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21653872-T-G

25468434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21654005-A-T

25468463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21654034-G-T

25468470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21654041-G-A

25468554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21654125-C-G

25469096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21654637-T-A

25469159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21654691-G-A

25469159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21654691-G-C

25469209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21654739-A-G

25469264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21654797-C-T

http://identifiers.org/hco/10/GRCh38#25469282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21654815-A-C

25470115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21662759-C-T

25470177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21662822-T-A

25470727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21662900-T-C

25470774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21662947-C-T

25470831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21663005-A-G

25470925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21663115-C-T

25470935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21663125-C-T

25474889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21663394-G-A

25474891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21663396-A-T

25474952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21669331-G-A

25474994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21669368-G-A

25475227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21669584-G-C

25475228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21669585-A-G

25475233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21669590-G-A

25475233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21669590-G-T

25475281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21669637-G-A

25475298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21669654-T-C

25475369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21669716-G-T

25475868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21670676-A-G

25475981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21670789-G-C

25476005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21670813-G-A

25476005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21670813-G-T

25476300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21671093-T-C

25476448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21671208-C-T

25477989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21671817-T-C

25477994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21671822-T-C

25478007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21671835-T-C

25478081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21671895-G-C

25478119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21671937-G-C

25478127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21671945-C-T

http://identifiers.org/hco/10/GRCh38#25478382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23689
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21672193-A-C