38715326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30845944-G-T

38715330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30845949-G-A

38715367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30845984-G-A

38715367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30845984-G-C

38715367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30845984-G-T

38716722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30847804-T-C

38716775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30847858-C-T

http://identifiers.org/hco/6/GRCh38#38722533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30853667-C-A

38722549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30853682-A-G

38722553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30853686-A-G

38722554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30853687-A-G

http://identifiers.org/hco/6/GRCh38#38722652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#30853767-C-A

38722652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30853767-C-G

38722652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30853767-C-T

38722664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30853779-T-C

http://identifiers.org/hco/6/GRCh38#38722667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#30853782-C-A

38722667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30853782-C-T

38722753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30854272-A-G

38722761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30854280-A-G

38722761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30854280-A-T

38722762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30854281-T-C

38722766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30854285-A-G

38722781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30854300-G-A

38722781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30854300-G-T

38722828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30854352-G-A

38722828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30854352-G-C

38722828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30854352-G-T

38722845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30854380-G-A

38722845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30854380-G-T

38722862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30854425-C-G

38722882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30854445-C-G

38722882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30854445-C-T

http://identifiers.org/hco/6/GRCh38#38722888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30854451-C-A

38722888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30854451-C-G

http://identifiers.org/hco/6/GRCh38#38722958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30854569-C-A

38722958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30854569-C-G

38722958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30854569-C-T

38723110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 30854721-C-T

38723214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30854822-C-T

38723226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30854834-T-A

http://identifiers.org/hco/6/GRCh38#38723230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30854838-C-A

http://identifiers.org/hco/6/GRCh38#38723231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30854839-C-A

38723380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30854959-A-G

38723380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30854959-A-T

38723426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30855005-C-T

38725856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30855766-T-C

38726124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30855989-A-T

38726217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30856080-C-G

http://identifiers.org/hco/6/GRCh38#38726256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30856118-C-A

38726256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30856118-C-T

38726298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30856157-A-G

38726309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30856168-A-G

38726351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30856201-G-T

http://identifiers.org/hco/6/GRCh38#38726488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30857017-C-A

38727375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30858867-G-T

38729492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30859932-A-G

38729571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30860009-G-A

http://identifiers.org/hco/6/GRCh38#38729590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30860014-C-A

38729590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30860014-C-T

http://identifiers.org/hco/6/GRCh38#38729651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30860043-A-C

38729651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30860043-A-G

38729693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30860085-A-G

38729877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30862205-T-C

38729928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30862256-G-A

38729928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30862256-G-T

38729958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30862286-G-A

38729958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30862286-G-C

38729958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30862286-G-T

38730003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30862333-G-T

38734427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30863484-T-G

38734547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30863604-G-A

38734547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30863604-G-T

38734561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30863618-G-A

38734561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30863618-G-C

38734577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30863634-T-A

38734577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30863634-T-C

38734583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30863640-T-C

38734718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30863983-A-G

38734761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30864025-T-A

38734761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30864025-T-C

38734762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30864026-T-A

38734762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30864026-T-C

38734774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30864038-A-G

38734781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30864045-G-A

38734781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30864045-G-C

38735226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30865009-G-T

38735271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30865058-A-G

38735393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30865170-G-T

38735498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30865262-T-C

38735554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30865314-C-T

38735561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30865321-G-A

38735563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30865323-A-G

38736786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30867116-T-C

38736792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30867122-T-G

38736832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30867163-T-G

38737050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30867373-A-G

38737050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30867373-A-T

38737072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30867395-G-A

38737072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30867395-G-T

http://identifiers.org/hco/6/GRCh38#38737073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30867396-C-A

http://identifiers.org/hco/6/GRCh38#38737080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30867403-C-A

38737080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30867403-C-T

38737106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30867429-T-A

38737106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30867429-T-C

38737347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30867684-A-T

38737809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 30868598-G-A

38737809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 30868598-G-T

38737906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30868695-C-T

38737949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30868738-G-C

38741703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30872199-G-C

38741703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30872199-G-T

38741835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30872331-G-C

38742030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30873118-G-A

38742655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30873873-T-C

38742667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30873894-G-T

38742778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30873993-C-G

38742778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30873993-C-T

38750296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30874729-C-G

http://identifiers.org/hco/6/GRCh38#38750509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30875584-A-C

38750509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30875584-A-G

38750562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30875637-G-A

38750595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30875670-T-C

38750597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30875672-T-C

38756086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 30875974-T-C

38761595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30876861-C-G

38761595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30876861-C-T

38761797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30877038-A-G

http://identifiers.org/hco/6/GRCh38#38761845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30877086-C-A

38761845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30877086-C-T

38761891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30877137-G-A

38761891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30877137-G-T

38761899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30877145-T-C

38764052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30877341-G-A

38764052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30877341-G-T

38764267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30877809-G-A

38764267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30877809-G-T

38764315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30877845-G-C

38764315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30877845-G-T

http://identifiers.org/hco/6/GRCh38#38770565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30881112-C-A

38770622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30881172-T-G

38770628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30881178-G-T

38770630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30881180-G-A

38770630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30881180-G-T

http://identifiers.org/hco/6/GRCh38#38770663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30881212-C-A

http://identifiers.org/hco/6/GRCh38#38770665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30881214-C-A

38770728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30881286-C-T

38770832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30881387-G-T

http://identifiers.org/hco/6/GRCh38#38770867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30881422-A-C

38771018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30881616-T-G

38771081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30881672-T-C

38771112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30881703-G-A

http://identifiers.org/hco/6/GRCh38#38775693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30882215-A-C

http://identifiers.org/hco/6/GRCh38#38775807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30882325-C-A

38775807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30882325-C-T

http://identifiers.org/hco/6/GRCh38#38775997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30882515-C-A

http://identifiers.org/hco/6/GRCh38#38776005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30882523-C-A

38776005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30882523-C-T

38776016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30882536-T-A

38776016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30882536-T-C

38776050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30882569-A-G

38776062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30882587-T-A

38776062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30882587-T-C

38776062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30882587-T-G

http://identifiers.org/hco/6/GRCh38#38777029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30885176-C-A

38777053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30885200-A-G

38777059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30885206-A-G

38777072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30885217-T-C

38777081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30885226-A-G

38777235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30885914-G-A

38777441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30886468-T-C

38777873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30886746-G-A

38777987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30886864-T-C

38778001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30886878-A-G

38778084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30886969-T-C

38778138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30887048-A-G

38778138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30887048-A-T

38778141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30887051-C-T

38778242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30887152-G-T

38778277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30887189-T-G

http://identifiers.org/hco/6/GRCh38#38778338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30887199-C-A

38778338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30887199-C-T

http://identifiers.org/hco/6/GRCh38#38778354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30887214-C-A

38778354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30887214-C-T

38778402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30887262-A-G

38778402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30887262-A-T

38778536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30888039-T-G

http://identifiers.org/hco/6/GRCh38#38778562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30888063-C-A

http://identifiers.org/hco/6/GRCh38#38778563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30888064-A-C

38778563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30888064-A-G

http://identifiers.org/hco/6/GRCh38#38778595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30888096-C-A

38778805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30888398-G-T

38779156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889068-G-T

38779227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889140-A-G

38779499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889375-G-C

38779805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889448-C-G

38779805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889448-C-T

38779818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889461-C-T

38779854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889488-T-C

38779884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889518-A-G

http://identifiers.org/hco/6/GRCh38#38779933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30889565-A-C

38779933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889565-A-G

38779933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889565-A-T

38779950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889570-C-G

38779950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889570-C-T

38779975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30889595-G-A

38779984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30889604-T-C

38779996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30889616-A-T

38780054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30889674-G-A

http://identifiers.org/hco/6/GRCh38#38780134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30889752-C-A

38780214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30889832-T-C

38780809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30890041-C-T

38780822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30890054-A-T

http://identifiers.org/hco/6/GRCh38#38780826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30890058-A-C

38780826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30890058-A-T

38780903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30890124-G-A

38781146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30891099-G-A

38781146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30891099-G-C

38781166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30891121-G-A

http://identifiers.org/hco/6/GRCh38#38781261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30891221-A-C

38781261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30891221-A-T

38781339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30891299-A-T

38781343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30891303-C-G

38781512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30891477-A-G

38781512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30891477-A-T

38781805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30891748-G-A

38782830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30892579-C-G

38782904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30892640-A-G

http://identifiers.org/hco/6/GRCh38#38782926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30892656-C-A

38783067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30892817-T-C

38783067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30892817-T-G

http://identifiers.org/hco/6/GRCh38#38783069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30892819-C-A

38783069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30892819-C-G

38783112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30892862-A-G

http://identifiers.org/hco/6/GRCh38#38783237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30892971-C-A

38783240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30892974-A-G

38785028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30893280-G-A

38785277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30893452-G-C

38785312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30893476-C-T

38785464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30893605-T-C

38785904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30894184-A-G

38786149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30894674-A-G

38786856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30896152-T-C

38786856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30896152-T-G

38786859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30896155-G-C

38786883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30896179-T-G

38786947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30896243-T-C

http://identifiers.org/hco/6/GRCh38#38787081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30897904-C-A

http://identifiers.org/hco/6/GRCh38#38787235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30898048-A-C

38787497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30898275-G-A

38787529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30898300-C-G

38787670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30898515-T-G

38787680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30898525-A-T

38789160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30900296-A-T

38789277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30900573-A-T

38789516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902309-C-T

38789591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902377-A-G

38789677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902475-G-C

38789766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902569-G-T

38789777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902580-A-T

38789805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 30902607-T-C

38789805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 30902607-T-G

38789811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30902613-G-A

38789985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902785-T-A

38789985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902785-T-C

38789997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902798-G-C

38789997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902798-G-T

38790026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902857-T-C

38790029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902860-T-A

38790029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902860-T-C

38790030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902861-G-A

38790030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902861-G-T

http://identifiers.org/hco/6/GRCh38#38790031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30902862-C-A

38790031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902862-C-G

38790031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902862-C-T

38790106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30902939-T-A

38790172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30903005-G-A

38790179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30903012-A-G

38790179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30903012-A-T

38790196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30903029-A-G

38790206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30903039-A-G

38790213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30903046-T-C

38790219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30903052-A-G

38790261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30903076-G-A

38790390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30903206-T-C

http://identifiers.org/hco/6/GRCh38#38790429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30903245-C-A

38790432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30903248-T-C

38791088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30904858-A-G

http://identifiers.org/hco/6/GRCh38#38791330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30905124-C-A

38791416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905200-A-G

38791416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905200-A-T

http://identifiers.org/hco/6/GRCh38#38791424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30905208-A-C

38791424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905208-A-G

38791424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905208-A-T

http://identifiers.org/hco/6/GRCh38#38791485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30905270-C-A

38791485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905270-C-G

38791485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905270-C-T

38791505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905292-G-A

38791505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905292-G-C

38791505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905292-G-T

38791532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905330-T-C

38791587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30905389-A-G

38791639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30905441-G-T

38791681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30905483-A-G

38791747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905540-A-G

38791761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905554-G-A

38791761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905554-G-T

38791850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905640-G-A

38791852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905642-C-G

38791865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905655-A-G

38791888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905680-C-G

38792017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30905804-A-G

38792367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30906124-C-G

38792422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30906219-T-C

38792529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30906326-C-T

38792630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30906406-A-T

38803196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 30909172-G-A

38803308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30909284-T-C

http://identifiers.org/hco/6/GRCh38#38803309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: http://identifiers.org/mco/17/GRCm39#30909288-C-A

38803309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 30909288-C-G

38803338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30909315-A-G

http://identifiers.org/hco/6/GRCh38#38803348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30909325-C-A

38803348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30909325-C-T

http://identifiers.org/hco/6/GRCh38#38803413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30909377-C-A

http://identifiers.org/hco/6/GRCh38#38803414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30909378-C-A

38803414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30909378-C-T

38803420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30909384-G-T

38803438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30909402-A-G

38803495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30909455-G-A

38803772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30910048-C-T

38803792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30910071-G-T

38804006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30910423-G-T

38804276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30910702-A-G

38804420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30910841-T-C

38804731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30911102-A-G

38804791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30911200-A-G

38805193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30911619-T-C

38805212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30911638-G-A

38805389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30912830-A-G

38805389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30912830-A-T

38805408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30912849-G-T

http://identifiers.org/hco/6/GRCh38#38805431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30912873-C-A

38805453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30912895-A-G

38805460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30912902-T-G

38805493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30912935-A-T

38805508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30912950-G-A

38805608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30913047-G-A

38805609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30913048-G-A

38805609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30913048-G-T

38805638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30913078-G-T

38807464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30913940-A-T

38807483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30913958-A-G

http://identifiers.org/hco/6/GRCh38#38807554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30914033-A-C

38807554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30914033-A-G

38807554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30914033-A-T

38807588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30914062-T-C

38807639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30914113-T-A

38807639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30914113-T-C

38807669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30914143-T-C

38807728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30914202-A-G

38807745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30914219-G-A

38807745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30914219-G-T

38813456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30916142-G-A

38813520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30916208-G-A

38813526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30916214-G-A

38813673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30916318-A-G

38813696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30916335-G-A

http://identifiers.org/hco/6/GRCh38#38813977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30919295-C-A

38813977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30919295-C-T

38814005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30919323-A-G

http://identifiers.org/hco/6/GRCh38#38814026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30919336-C-A

38814026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30919336-C-T

38814102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30919409-T-C

38814160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30919464-A-G

38814160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30919464-A-T

38814627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920276-T-C

38814895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920470-G-A

38815022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920570-G-A

38815059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920607-T-A

http://identifiers.org/hco/6/GRCh38#38815337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30920712-C-A

38815338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920713-T-C

http://identifiers.org/hco/6/GRCh38#38815342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30920717-C-A

38815342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920717-C-G

38815342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920717-C-T

38815356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920731-T-C

http://identifiers.org/hco/6/GRCh38#38815386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30920749-C-A

38815386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920749-C-G

38815386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920749-C-T

38815434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920785-G-A

38815434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30920785-G-T

38815852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30922096-T-C

38822890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30923681-G-T

38823020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30923811-G-A

38823020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30923811-G-C

38823065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30923880-G-T

38823122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30923935-A-G

http://identifiers.org/hco/6/GRCh38#38823128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30923941-C-A

38823131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30923944-T-A

38823147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30923960-A-G

38823558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30925355-A-G

38823558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30925355-A-T

38823594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30925391-A-G

http://identifiers.org/hco/6/GRCh38#38823598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30925395-A-C

38823640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30925437-G-A

38823670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30925467-G-A

38823702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30925500-G-A

38823702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30925500-G-T

http://identifiers.org/hco/6/GRCh38#38825537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30926549-C-A

http://identifiers.org/hco/6/GRCh38#38825620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30926612-C-A

38825620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30926612-C-G

38825631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30926623-T-G

38825673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30926662-T-G

38825721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30926703-G-A

38825827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30926814-A-G

38825935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30926919-C-G

http://identifiers.org/hco/6/GRCh38#38826010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30927114-A-C

38826045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30927147-A-G

38826077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30927179-G-T

38826178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30927287-C-T

38826193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30927302-A-G

38826214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30927323-A-G

38826346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30927455-A-T

38826382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30927491-A-G

38826491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30927599-A-G

38826491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30927599-A-T

38827716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30929038-C-T

38827720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30929042-A-T

38827906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30929155-G-T

http://identifiers.org/hco/6/GRCh38#38828136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30929426-C-A

38828136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30929426-C-T

38828192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30929484-T-C

38828217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30929509-G-A

38828288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 30929580-T-C

38828331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30929622-T-A

38828331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30929622-T-C

38828331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30929622-T-G

http://identifiers.org/hco/6/GRCh38#38828336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30929627-A-C

38828896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30929851-T-A

38828909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30929864-C-G

38829300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30930252-G-T

38832184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30931110-T-A

38832195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30931121-A-G

38832195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30931121-A-T

38832235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30931160-T-G

http://identifiers.org/hco/6/GRCh38#38832346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30931271-C-A

http://identifiers.org/hco/6/GRCh38#38832347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30931272-A-C

38832371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30931296-A-G

38832388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30931313-G-A

38832388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30931313-G-C

38832397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30931322-C-T

http://identifiers.org/hco/6/GRCh38#38832411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30931336-A-C

38832573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30931501-G-C

38832573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30931501-G-T

38832910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30931589-C-T

38834656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30932084-T-C

http://identifiers.org/hco/6/GRCh38#38834689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30932118-A-C

38834689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30932118-A-G

http://identifiers.org/hco/6/GRCh38#38834759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30932198-A-C

38837536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30934064-A-G

38837728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30934253-T-C

http://identifiers.org/hco/6/GRCh38#38837835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30934360-A-C

38837835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30934360-A-G

38837938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30934450-A-G

http://identifiers.org/hco/6/GRCh38#38838128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30934610-C-A

38838128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30934610-C-G

http://identifiers.org/hco/6/GRCh38#38838156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30934638-C-A

38838190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30934672-A-G

38838498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30934994-A-G

38838537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30935036-T-A

38838664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30935322-G-A

38839124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30935776-G-C

38842262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30936713-T-G

38842589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30937692-A-G

38842591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30937694-A-G

38842623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30937755-T-C

38842680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30937818-A-G

38842683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30937821-G-A

38842683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30937821-G-T

38842744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30937882-A-T

http://identifiers.org/hco/6/GRCh38#38842777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30937915-C-A

38842807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30937945-C-T

38842817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30937955-G-A

38842831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30937969-T-A

38842837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30937975-A-G

38842840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30937978-T-C

38842840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30937978-T-G

38842962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30938113-T-C

38845449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30939844-A-G

http://identifiers.org/hco/6/GRCh38#38845487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30939890-C-A

38845487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30939890-C-T

http://identifiers.org/hco/6/GRCh38#38845491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30939894-C-A

38845531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30939931-T-C

38845582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30939981-C-T

38845615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30940014-C-T

38845646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30940045-A-T

38845748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30940147-G-A

38845788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30940187-T-C

38845844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30940244-G-A

http://identifiers.org/hco/6/GRCh38#38845855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30940255-C-A

38845860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30940260-A-G

38845860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30940260-A-T

38846312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30940570-C-T

38846420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30940693-C-T

38848681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30941906-T-G

38848723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30941948-G-C

38849430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30943186-C-G

38849789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30943664-A-G

38849825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30943700-T-C

38849997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30943871-A-G

38850050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30943924-G-A

38850050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30943924-G-T

http://identifiers.org/hco/6/GRCh38#38850443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30944232-C-A

38850484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30944274-T-C

38850552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30944341-G-T

http://identifiers.org/hco/6/GRCh38#38850560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30944349-C-A

38850859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945045-A-G

38850859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945045-A-T

38850863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945058-C-T

38850868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945065-T-C

38850874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945086-A-G

38850946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945196-G-A

38850946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945196-G-C

38851205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945427-A-G

38851316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945515-G-T

38851380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945588-G-A

38851435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945635-G-T

38851540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945729-A-G

38851540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30945729-A-T

38851644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30945832-T-C

38851644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30945832-T-G

38852640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947078-T-C

38852675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947108-G-A

http://identifiers.org/hco/6/GRCh38#38852680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30947114-C-A

38852680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947114-C-T

38852795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30947238-T-A

38852802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947245-A-G

38852855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947294-G-A

38852876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947315-G-A

38852876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947315-G-C

38852905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947346-T-G

38853045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947479-T-A

38853045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947479-T-C

http://identifiers.org/hco/6/GRCh38#38853049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30947483-C-A

http://identifiers.org/hco/6/GRCh38#38853143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30947997-C-A

38853143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947997-C-T

38853341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 30948210-A-G

38853428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30948280-T-C

38854025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948599-C-T

38854042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948616-A-G

38854052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948626-A-G

38854111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948671-A-G

38854420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948954-A-T

38854473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30949016-T-C

38854479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30949022-A-G

38854551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30949098-A-G

38857544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30950014-G-A

38857623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30950093-T-C

38857712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30950182-T-C

38857748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30950218-G-C

38857748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30950218-G-T

38857770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30950268-G-A

38857770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30950268-G-T

38857799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30950297-T-C

38857799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30950297-T-G

38859910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30954295-G-A

38859969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30954350-T-G

38859978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30954359-T-C

38860069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30954472-G-A

38860152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30954642-G-A

38860313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30954857-G-T

38860365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30954911-A-G

38860416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30954963-G-A

38860416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30954963-G-T

38860477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30955023-A-G

38860477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30955023-A-T

38860481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30955027-A-G

38860481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30955027-A-T

38860489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30955035-T-C

38860510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30955056-A-G

38860618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30955164-A-G

38860643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30955189-T-C

38860648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30955194-G-A

38860648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30955194-G-T

38860746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30955268-G-C

38862292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30956237-G-A

38862292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30956237-G-C

38862406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30956351-G-C

38862406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30956351-G-T

http://identifiers.org/hco/6/GRCh38#38862418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30956363-A-C

38862492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30956428-A-G

38862568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30956491-G-A

38862568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30956491-G-T

38862622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30956529-A-G

38862634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30956538-A-G

38863694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30958363-C-T

38863753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30958421-A-T

38863780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30958449-T-C

38863795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30958462-G-T

38863805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30958474-G-A

http://identifiers.org/hco/6/GRCh38#38863806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30958475-A-C

38863806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30958475-A-T

38863807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30958476-A-G

38863817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30958486-A-G

38863886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30958555-G-A

38863931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30958600-T-C

38864555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30959162-A-G

38866384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30959879-A-G

38866433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30959959-A-G

38866605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30960115-T-C

38866735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30960244-A-G

38866889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30960402-A-T

38867783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30961393-A-G

38867957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30961569-T-C

38868034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30961601-A-G

38868157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30961725-T-A

38868506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30962368-A-G

38868667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30962534-A-G

38868667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30962534-A-T

38868703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30962574-C-G

38868703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30962574-C-T

38868709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30962580-C-G

38868815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30962674-C-T

38868819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30962678-C-T

38869512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963245-A-G

38869590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963331-C-T

http://identifiers.org/hco/6/GRCh38#38869592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30963333-C-A

38869592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963333-C-G

38870418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30963505-C-G

http://identifiers.org/hco/6/GRCh38#38870496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30963583-A-C

38870496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30963583-A-G

38870673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963748-A-G

38870675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963750-A-G

38870675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963750-A-T

38870681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963756-T-C

38870692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963767-G-A

http://identifiers.org/hco/6/GRCh38#38870693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30963768-C-A

38870693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963768-C-G

38870740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963810-G-T

38870756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963825-C-G

38870894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963963-A-G

38870902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30963970-G-A

38871721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30965027-C-T

38871750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30965045-C-T

38871876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30965174-G-A

38871940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30965211-G-C

38871940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30965211-G-T

http://identifiers.org/hco/6/GRCh38#38872475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30965671-C-A

38872490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30965686-A-G

38872568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30965764-G-A

38872592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30965788-T-C

38872881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30966085-G-A

38872884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30966088-T-A

38872884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30966088-T-C

38872884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30966088-T-G

38872925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30966140-T-A

38873081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30966296-C-G

38873081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30966296-C-T

http://identifiers.org/hco/6/GRCh38#38873259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30966844-A-C

38873259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30966844-A-G

38873308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30966893-A-G

38873310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30966895-A-G

38873372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30966957-T-G

38873384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30966969-T-A

38873384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30966969-T-C

38873386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30966971-T-A

38873386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30966971-T-G

http://identifiers.org/hco/6/GRCh38#38873425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30967015-C-A

38873425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967015-C-T

http://identifiers.org/hco/6/GRCh38#38873429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30967019-C-A

http://identifiers.org/hco/6/GRCh38#38873524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30967113-C-A

38873524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967113-C-G

38873524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967113-C-T

38875367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967243-C-G

38875410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967286-G-T

38875413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967289-T-C

38875450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967322-G-A

38875450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967322-G-T

38875638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30967529-T-C

38875639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30967530-G-A

38875926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967796-T-A

38875927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967797-A-G

38876127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30967968-C-T

38876371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30968143-C-T

http://identifiers.org/hco/6/GRCh38#38876727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30968488-A-C

38876888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30968602-T-C

38882765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30970296-A-T

38882804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30970332-G-T

http://identifiers.org/hco/6/GRCh38#38882885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30970396-A-C

38882904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30970415-A-G

http://identifiers.org/hco/6/GRCh38#38882936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30970447-C-A

38882936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30970447-C-G

38882971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30970482-G-A

38882971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30970482-G-T

38883049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30970560-T-C

38883189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30970883-T-C

38883267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30970966-A-G

http://identifiers.org/hco/6/GRCh38#38883274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30970973-A-C

38883302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971001-C-G

38883302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971001-C-T

38883375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30971074-C-T

38883420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30971119-A-G

38883465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971164-C-T

http://identifiers.org/hco/6/GRCh38#38883546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30971346-A-C

http://identifiers.org/hco/6/GRCh38#38883573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30971415-C-A

http://identifiers.org/hco/6/GRCh38#38883737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30971669-C-A

38883755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971687-T-G

38883770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971702-T-C

38883774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971706-A-G

38883774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971706-A-T

http://identifiers.org/hco/6/GRCh38#38883865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30971785-C-A

38883865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971785-C-T

38883884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30971804-T-C

http://identifiers.org/hco/6/GRCh38#38883914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30971834-C-A

38883914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30971834-C-T

38883974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30971894-T-C

http://identifiers.org/hco/6/GRCh38#38884017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30971937-A-C

38884017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971937-A-G

38884017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971937-A-T

38884018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971938-T-C

38884019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30971939-A-G

38885849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30972867-T-C

38885961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30973011-C-G

38886115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30973154-T-C

38886115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30973154-T-G

38886426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30973449-C-G

http://identifiers.org/hco/6/GRCh38#38886659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30973833-C-A

38886659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30973833-C-T

38886679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30973855-T-C

38886718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30973894-G-A

38886754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30973912-T-A

38886754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30973912-T-G

38886910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30974067-A-G

38887301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30975228-G-A

38890609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30975626-A-T

38890735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30975760-G-A

38894554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30976848-G-A

38894554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30976848-G-T

38894609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977118-T-G

38894618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977127-A-G

38894683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977198-A-G

38894697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30977215-C-G

38894697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30977215-C-T

38894785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30977303-A-G

38894785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30977303-A-T

38894808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30977326-A-G

http://identifiers.org/hco/6/GRCh38#38894838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30977356-C-A

38894838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30977356-C-G

38894838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30977356-C-T

http://identifiers.org/hco/6/GRCh38#38894875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30977393-C-A

38894875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977393-C-T

38894892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977410-T-G

38894893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977411-G-A

38894896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977414-T-C

http://identifiers.org/hco/6/GRCh38#38894914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30977432-C-A

38894914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977432-C-T

38894918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977436-T-C

38894922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977440-T-C

38895299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30977869-G-C

38895593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30978116-A-G

38895602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30978125-C-G

38895687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30978213-C-T

38895944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30978374-G-T

38896023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30978534-T-G

38896051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30978562-T-C

38896051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30978562-T-G

38896103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30978614-T-C

38896240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30978755-C-G

38896251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30978766-G-A

38896252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30978767-G-A

38898210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30979942-A-G

38898302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30980024-G-C

38898332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30980054-A-G

38898332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30980054-A-T

38898375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30980097-A-G

http://identifiers.org/hco/6/GRCh38#38898384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30980106-C-A

38898440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30980155-A-G

38898504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30980216-G-T

38899703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30981540-G-A

38899703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30981540-G-T

38899707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30981544-C-T

38899708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30981545-A-G

38899718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30981554-A-T

38899783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30981622-G-A

38899811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30981650-A-G

38899826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30981665-T-A

38899898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30981737-A-G

38899964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30981797-G-A

38899964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30981797-G-T

http://identifiers.org/hco/6/GRCh38#38899984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30981808-C-A

38905343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30983776-C-G

38905343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30983776-C-T

38905400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30983826-G-A

38905502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30983931-A-G

38905646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30984076-G-T

38906237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30984554-A-G

38906237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30984554-A-T

38906244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30984561-T-C

38906266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30984582-G-A

38906266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30984582-G-T

38906390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30984706-T-G

38906467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30985285-G-A

38906467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30985285-G-T

38906531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30985355-T-C

http://identifiers.org/hco/6/GRCh38#38906535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30985359-C-A

38906535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30985359-C-T

38906685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30985564-A-G

38907204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30985908-G-C

38907290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30986010-C-T

http://identifiers.org/hco/6/GRCh38#38907366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30986069-C-A

38907366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30986069-C-T

38907387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30986083-A-G

38907409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30986101-T-A

38907454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30986133-A-G

38907511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30986188-A-G

38907539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30986216-A-G

38907603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30986283-T-C

http://identifiers.org/hco/6/GRCh38#38907674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30986372-C-A

http://identifiers.org/hco/6/GRCh38#38907805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30986507-C-A

38907805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30986507-C-T

38907848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30986579-A-G

38907848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30986579-A-T

38907862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30986595-G-T

38907876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30986609-A-G

38907908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30986717-G-A

http://identifiers.org/hco/6/GRCh38#38907933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30986750-A-C

38908078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30986895-A-G

http://identifiers.org/hco/6/GRCh38#38908081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30986898-A-C

38908120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 30986937-A-G

38908120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 30986937-A-T

http://identifiers.org/hco/6/GRCh38#38908148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30986956-C-A

38908148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30986956-C-T

http://identifiers.org/hco/6/GRCh38#38908391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30987207-A-C

38908392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30987208-T-C

http://identifiers.org/hco/6/GRCh38#38908523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30987493-A-C

38909106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988043-C-T

38909112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988049-C-T

38909258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988194-G-A

38909276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988218-C-T

38909368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988336-A-G

http://identifiers.org/hco/6/GRCh38#38909393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30988468-C-A

38909393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988468-C-G

38909393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988468-C-T

38909401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988478-G-A

38909401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988478-G-T

http://identifiers.org/hco/6/GRCh38#38909408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30988485-C-A

38909408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988485-C-G

38909437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30988533-G-A

38909437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30988533-G-T

38909611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30988710-C-G

http://identifiers.org/hco/6/GRCh38#38909748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#30988885-A-C

38909810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988954-T-C

38909810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30988954-T-G

38910070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30989220-G-A

38910386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30989703-G-A

38910436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30989748-G-C

38910436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30989748-G-T

38910761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30990130-A-G

38910761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30990130-A-T

38910881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30990288-C-T

38910922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30990346-A-G

38911199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30990560-T-C

38911333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30990664-G-A

38911362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30990669-T-C

38911445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30990748-T-G

38911457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30990760-T-C

38911530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30990833-A-G

38911625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30990921-G-A

http://identifiers.org/hco/6/GRCh38#38913727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30992399-C-A

38913727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992399-C-T

38913739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992412-G-A

38913739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992412-G-T

http://identifiers.org/hco/6/GRCh38#38913759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30992428-A-C

38913759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992428-A-G

38913759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992428-A-T

38913832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992486-T-G

38913833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992487-G-A

38913833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992487-G-C

38913904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30992558-T-G

38913972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992626-A-G

http://identifiers.org/hco/6/GRCh38#38914017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30992675-A-C

http://identifiers.org/hco/6/GRCh38#38914056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30992727-C-A

38914056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992727-C-T

http://identifiers.org/hco/6/GRCh38#38914080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30992781-C-A

38914092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992793-G-C

38914092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992793-G-T

38914095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992796-A-G

38914095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992796-A-T

38914228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992915-A-G

38914245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992927-T-C

38914613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993243-G-A

38915068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993795-G-C

38915071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993798-A-G

38915100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993830-T-G

38915111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993841-A-G

38915111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993841-A-T

38915128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993856-G-A

38915128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993856-G-T

http://identifiers.org/hco/6/GRCh38#38915131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30993860-C-A

38915131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993860-C-T

http://identifiers.org/hco/6/GRCh38#38915149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30993878-A-C

38915149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993878-A-G

38915263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30993982-G-A

38915263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30993982-G-C

38915416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994197-A-G

38915433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994214-A-G

38915507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994304-A-G

38915595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994393-A-G

38915595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994393-A-T

38915788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994679-G-T

http://identifiers.org/hco/6/GRCh38#38916024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#30995413-A-C

38916024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995413-A-G

38916024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995413-A-T

38916116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995461-A-G

38916241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995590-G-A

38916249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995595-G-T

38916407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995763-A-G

38916535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995891-A-G

38916539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995895-T-C

38916963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997337-C-T

38916974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997345-G-A

38917536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998295-T-C

38917552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998327-T-A

38917552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998327-T-G

38918080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30998852-G-C

38918953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30999811-A-G

38919056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30999900-T-C

38920662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31000600-G-T

38920879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31000863-T-C

http://identifiers.org/hco/6/GRCh38#38920895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31000879-A-C

38920895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31000879-A-T

38920907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31000910-T-C

38920909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31000912-G-T

38921277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001253-A-G

38921306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001285-T-C

38921308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001287-C-G

38921308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001287-C-T

38921497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31001486-T-G

38922873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31002820-T-C

38922993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31002974-A-G

http://identifiers.org/hco/6/GRCh38#38923036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31003016-C-A

38923041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31003020-T-C

38923100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31003079-G-T

38923172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31003151-G-A

38923236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31003232-A-G

38923384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31003366-T-C

38923397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31003373-T-A

38923437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31003389-G-A

38923437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31003389-G-T

http://identifiers.org/hco/6/GRCh38#38923459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31003406-C-A

38923459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31003406-C-T

38923782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003813-T-C

38923897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003904-A-G

38923897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003904-A-T

38924087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31004077-A-G

38924922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31004982-T-C

http://identifiers.org/hco/6/GRCh38#38925018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31005079-C-A

38925554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005330-G-A

38925919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005991-T-G

38925929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005995-A-G

38925973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006031-T-C

38926028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006089-T-C

38926044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006108-C-T

38926045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006109-T-C

http://identifiers.org/hco/6/GRCh38#38926358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31007265-C-A

http://identifiers.org/hco/6/GRCh38#38926361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31007268-C-A

38926361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007268-C-T

38926658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007649-A-G

38929161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009482-G-T

http://identifiers.org/hco/6/GRCh38#38929200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31009521-A-C

38929217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009538-C-T

http://identifiers.org/hco/6/GRCh38#38929294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31009601-A-C

38929294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009601-A-G

38929294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009601-A-T

38929354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31009648-G-T

38929436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31009725-C-T

38929470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31009758-T-C

38929642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31009932-T-A

38929642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31009932-T-C

38929677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009969-T-A

38929677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009969-T-G

38930346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011039-G-A

38930378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011070-G-C

38930950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012418-T-C

38931017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012497-G-A

http://identifiers.org/hco/6/GRCh38#38931587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31012962-C-A

38931675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013053-A-T

38931680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013058-A-G

http://identifiers.org/hco/6/GRCh38#38931690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31013068-C-A

38931690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013068-C-G

38931690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013068-C-T

38931725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013104-G-A

38931725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013104-G-C

38931725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013104-G-T

38931728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013110-A-G

38931749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013131-G-T

http://identifiers.org/hco/6/GRCh38#38931765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31013147-C-A

38931781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013577-G-A

38931791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013587-T-C

38931807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31013603-G-A

38931807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31013603-G-T

38931951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31013747-T-G

38932136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014092-T-A

38932136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014092-T-C

38932136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014092-T-G

38932315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014474-T-C

38932508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014654-T-C

38932796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014893-A-G

38932801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014897-G-A

38932834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014930-A-G

38932883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31014943-C-T

http://identifiers.org/hco/6/GRCh38#38933031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31014987-C-A

38933031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014987-C-T

http://identifiers.org/hco/6/GRCh38#38933058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31015010-C-A

38933101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015051-A-G

38933336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015256-T-C

38933389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015288-C-G

http://identifiers.org/hco/6/GRCh38#38933406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31015305-C-A

38933501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31015377-T-G

http://identifiers.org/hco/6/GRCh38#38935499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31018966-C-A

38935499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018966-C-T

38935511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018978-T-A

38935511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018978-T-C

38935532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019000-G-A

38935532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019000-G-T

http://identifiers.org/hco/6/GRCh38#38935553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31019021-A-C

38935553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019021-A-G

38935594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 31019460-G-A

38935702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019568-T-C

38935705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31019571-G-A

38935729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019595-G-A

38935733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019599-T-C

http://identifiers.org/hco/6/GRCh38#38935756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31019646-C-A

38935756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019646-C-T

http://identifiers.org/hco/6/GRCh38#38935770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31019660-C-A

38935802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019687-T-C

http://identifiers.org/hco/6/GRCh38#38935836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31019721-C-A

38935836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019721-C-G

38935896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019779-C-T

38936070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019966-C-G

38936070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019966-C-T

38936350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31020378-G-A

38936350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31020378-G-C

38936350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31020378-G-T

38936371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31020404-T-C

38936434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020489-A-G

38936938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021061-A-G

38936941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021064-T-A

38936948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021071-T-C

http://identifiers.org/hco/6/GRCh38#38937707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31021767-A-C

http://identifiers.org/hco/6/GRCh38#38937845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31021929-C-A

38937849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021933-A-G

38937849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021933-A-T

38937892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021968-T-G

http://identifiers.org/hco/6/GRCh38#38937918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31021981-C-A

38937918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021981-C-G

38937918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021981-C-T

38937919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021982-T-C

38938013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31022076-G-A

http://identifiers.org/hco/6/GRCh38#38938075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31022138-A-C

http://identifiers.org/hco/6/GRCh38#38938119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31022182-C-A

38938229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022292-G-A

38938229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022292-G-T

38938942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31023111-T-C

38939103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023273-G-A

38939103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023273-G-T

38942699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023802-A-G

38942742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023844-C-G

38942852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023936-G-A

38943609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024634-C-T

38943623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024648-G-A

38943705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024716-T-C

38943707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024718-G-T

38943871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024812-G-A

38944022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024953-T-C

38944193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31025053-A-G

38944296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025154-C-T

38944452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025310-T-G

38944487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025352-G-C

38944511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025586-C-T

38944786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025823-G-C

38944788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025825-G-A

38944815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025844-T-G

38944858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025886-C-T

38945510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31026222-T-C

38945643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026354-G-A

38945643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026354-G-C

38945707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026418-T-G

38945708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026419-G-T

38945715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026426-A-G

38945794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026885-T-A

38945857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026943-G-C

38945940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027024-A-T

http://identifiers.org/hco/6/GRCh38#38945955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31027039-A-C

38945964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027048-G-A

38945973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027057-C-T

38948113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027391-G-C

38948635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027980-C-T

38948718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028063-A-G

38948775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028117-C-G

38948823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028170-C-G

38948853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028198-G-A

http://identifiers.org/hco/6/GRCh38#38949316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31029107-A-C

38949376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029161-G-A

38949445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31029227-C-G

38949577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31029359-A-G

38949581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029362-G-A

http://identifiers.org/hco/6/GRCh38#38949583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31029364-A-C

38949583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029364-A-T

38949585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029366-T-A

38949594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029376-T-G

38949631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029410-T-C

http://identifiers.org/hco/6/GRCh38#38949770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31029657-C-A

38949838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029713-T-C

38949880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029756-C-T

38950357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031310-A-G

http://identifiers.org/hco/6/GRCh38#38950381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31031330-A-C

38950381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031330-A-T

38950403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031351-A-G

38951058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031708-T-G

38951154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031802-G-A

38951166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031815-T-C

38951189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031837-A-G

38951189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031837-A-T

http://identifiers.org/hco/6/GRCh38#38951223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31031871-C-A

38951223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031871-C-T

38951253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31031902-T-G

http://identifiers.org/hco/6/GRCh38#38951438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31032122-C-A

38951438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31032122-C-G

38951485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31032169-A-G

38951557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31032245-C-T

38951577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31032261-T-C

38951609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31032284-G-T

38952046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31032825-T-G

38971419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31034481-A-G

http://identifiers.org/hco/6/GRCh38#38971463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31034524-A-C

38971463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31034524-A-G

38971463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31034524-A-T

http://identifiers.org/hco/6/GRCh38#38971542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31034586-C-A

38971542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31034586-C-T

38971669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31034683-T-A

38971669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31034683-T-C

38971669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31034683-T-G

38971723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034749-G-A

38971723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034749-G-C

38971723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034749-G-T

38971729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034766-T-C

http://identifiers.org/hco/6/GRCh38#38971798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31034843-A-C

38971798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034843-A-T

38971853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034896-T-C

38971853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034896-T-G

http://identifiers.org/hco/6/GRCh38#38971872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31034915-C-A

38971872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034915-C-T

38971899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034965-G-A

38971899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034965-G-C

38971899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31034965-G-T

http://identifiers.org/hco/6/GRCh38#38972713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31035822-C-A

38972713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31035822-C-G

http://identifiers.org/hco/6/GRCh38#38972888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31035989-C-A

38972888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31035989-C-G

38973438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036617-G-A

38973529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036870-G-A

38973529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036870-G-T

38973580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036957-A-T

38973626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036997-A-G

38973693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31037066-T-C

38973725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31037098-C-T

38973860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037251-G-A

38973860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037251-G-T

http://identifiers.org/hco/6/GRCh38#38974033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31037531-A-C

38974055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037553-C-G

38974172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037828-C-G

http://identifiers.org/hco/6/GRCh38#38974296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31038021-C-A

38974296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038021-C-T

http://identifiers.org/hco/6/GRCh38#38974317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31038036-A-C

38974317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038036-A-G

38974339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038058-A-G

38974339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038058-A-T

38974380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31038099-C-T

38974565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038282-G-T

38974577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038294-G-A

38975024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039507-G-A

38975300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039776-C-T

38975354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039825-C-T

38975443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039910-G-A

38975445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039912-T-G

http://identifiers.org/hco/6/GRCh38#38975449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31039916-C-A

38975450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039917-A-G

38975620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040081-A-G

38975691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040155-A-G

38975786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040234-G-A

38975791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040239-A-G

38975952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040405-T-C

38975968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040419-A-G

38976922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041423-A-T

38977293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041819-C-T

38979124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31043994-G-A

38979139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31044009-G-A

38979158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31044025-C-T

38979326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31044172-C-T

38979636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045017-T-C

38979758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045139-G-C

38980092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045468-G-A

38980164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045641-G-A

38980312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045774-T-G

38981186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048242-A-G

38981257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048299-A-T

38981290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048329-C-T

38981297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048336-A-G

38981688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048854-A-G

38981723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048873-T-A

38981724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048874-A-G

38982256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049542-G-C

38982256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049542-G-T

38982265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049551-G-A

38982265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049551-G-T

http://identifiers.org/hco/6/GRCh38#38982325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31049726-C-A

38982325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049726-C-G

38982325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049726-C-T

38982342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31049743-T-C

38982342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31049743-T-G

38982354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31049755-A-G

38982402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31049803-T-C

38982426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31049827-T-C

38982470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31049871-A-G

38982539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049928-G-A

38982539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049928-G-T

38982552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049941-T-C

38982709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31050126-G-A

38983313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051340-C-T

38983340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051367-C-T

38983341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051368-G-A

38983416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051456-T-C

38983693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051749-G-T

38983744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051791-T-C

38983902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051953-A-G

38984062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052113-A-T

38984172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052478-G-T

38984180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052491-A-G

38984180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052491-A-T

38984196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052520-T-A

38984196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052520-T-C

38984208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 31052532-T-C

38984208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 31052532-T-G

38984214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31052538-A-G

38984223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31052547-G-A

38984223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31052547-G-C

38984223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31052547-G-T

38984289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31052613-A-G

38984354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052680-T-C

38984932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31053243-T-C

38984938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31053251-A-G

38985164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31053484-T-C

38985206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31053526-G-A

38985516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054088-A-G

38985622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054184-T-C

http://identifiers.org/hco/6/GRCh38#38985845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31054399-C-A

38985845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054399-C-T

38985863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054417-G-T

38985966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054530-A-G

http://identifiers.org/hco/6/GRCh38#38986019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31054582-C-A

38986129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054689-C-T

38986203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054742-C-G

38986319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054836-C-G

38986319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054836-C-T

38987258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056357-G-A

38987271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056370-G-A

38987378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056457-A-G

38987486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056571-C-G

38988251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057572-C-G

http://identifiers.org/hco/6/GRCh38#38988383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31057722-A-C

38988383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057722-A-G

38988501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057837-T-C

38988607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057939-T-C

38988631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057962-C-T

38989004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31058282-A-G

38989070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31058375-T-C

38989116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31058419-T-C

38989658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31058973-T-C

38989771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059270-C-G

38990122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31059637-A-G

38990180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31059695-C-T

38990296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059968-T-C

http://identifiers.org/hco/6/GRCh38#38990380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31060052-A-C

38990496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060163-C-G

38991024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31060790-C-G

38991180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31060937-T-C

38991599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31061332-A-T

http://identifiers.org/hco/6/GRCh38#38991636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31061368-C-A

38991726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31061420-C-T

http://identifiers.org/hco/6/GRCh38#38991807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31061491-C-A

38991821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31061505-A-T

http://identifiers.org/hco/6/GRCh38#38996616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31062983-C-A

38996616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31062983-C-T

38996635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063007-G-A

38997030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063321-T-A

http://identifiers.org/hco/6/GRCh38#38997119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31063408-C-A

38997157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063454-G-T

http://identifiers.org/hco/6/GRCh38#38997304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31063638-A-C

38997578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063884-G-A

38997781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064015-A-G

38998122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064070-T-A

38998141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064089-A-G

38998524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064479-G-A

38998529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064484-C-T

38998640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064573-G-A

38998763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064736-G-A

38998883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064852-G-A

http://identifiers.org/hco/6/GRCh38#38999988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31065804-A-C

39000277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066093-A-G

39000331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066172-A-G

39000349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066190-T-C

39001961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066367-C-G

http://identifiers.org/hco/6/GRCh38#39001969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31066375-C-A

39002010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066420-G-T

39002143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066519-G-A

39002575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066996-T-G

39002653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067085-A-G

39002654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067086-T-C

39003095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067695-G-A

39003209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067804-G-A

39003331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067919-T-C

39003476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31068078-A-G

39008380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070155-A-G

39008473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070249-T-C

39008487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070263-C-G

39008487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070263-C-T

39008618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070355-T-C

http://identifiers.org/hco/6/GRCh38#39008663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31070395-C-A

39008729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070490-G-A

39008729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070490-G-T

39008732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070493-T-A

39008732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070493-T-C

39008732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070493-T-G

http://identifiers.org/hco/6/GRCh38#39008735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31070496-A-C

39008735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070496-A-G

39008735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070496-A-T

39008753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070539-T-A

39008772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070560-T-C

39008877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31070665-T-G

39008880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31070668-A-G

39008880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31070668-A-T

39008901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31070689-G-A

39008923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31070711-T-C

39010800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31072490-C-T

39010840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31072530-T-C

http://identifiers.org/hco/6/GRCh38#39011012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31072636-A-C

39011143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31072742-T-G

39011190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31072790-C-T

39011409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31072917-G-A

http://identifiers.org/hco/6/GRCh38#39011658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31073161-A-C

39011658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073161-A-G

39011730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073233-A-G

39011732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073235-G-C

http://identifiers.org/hco/6/GRCh38#39012117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31073622-C-A

39012117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073622-C-T

39012145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073651-A-G

39012146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073652-G-A

39012146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073652-G-T

http://identifiers.org/hco/6/GRCh38#39012241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31073801-C-A

39012349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31073909-A-G

39012440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31074871-T-C

39012564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31074995-T-C

39012668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075100-G-A

39012692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075120-A-G

39012733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075161-G-A

39012733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075161-G-T

39012746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075173-G-A

39012746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075173-G-C

39012860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075265-T-C

39012895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075300-A-G

39013120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076066-C-T

39013150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076095-T-A

39013178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076123-T-C

39013208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076153-T-C

39013270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076197-G-C

39013293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076220-A-G

39013338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076264-A-G

39013393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076316-T-C

39013400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076324-A-G

39013438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076363-C-G

39013438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076363-C-T

39013471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076396-A-G

39013960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076693-A-G

39014009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076736-C-T

39014045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076769-A-G

39014150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31077091-A-G

39015891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31077621-C-T

39016052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31077800-C-T

39016057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31077805-A-G

39016615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078022-G-C

39016615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078022-G-T

39016709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078263-G-A

39016960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078804-C-T

39017122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078972-G-A

39017122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078972-G-T

39017165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079015-G-C

39017190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079038-G-T

39017272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079121-G-T

39017292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079144-G-A

39017316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079169-G-A

39017316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079169-G-C

39017358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079209-G-A

39017469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079320-T-C

39017741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079576-G-A

39017766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079601-G-A

39017895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31079759-G-C

39018116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31080176-C-T

39018150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31080231-A-G

39018210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31080296-C-G

39018399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31080537-C-G

39018399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31080537-C-T

39018421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31080585-C-T

39018503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31080855-G-A

39018503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31080855-G-T

39018629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31081020-C-T

39018637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31081029-T-G

39018710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31081091-G-T

http://identifiers.org/hco/6/GRCh38#39018798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31081167-A-C

39018923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31081283-G-T

39019243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31081750-C-T

39019244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31081751-G-A

39019772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083117-A-G

39019774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083119-G-A

39019774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083119-G-T

39019792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083137-A-T

39019895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083237-G-A

39020004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083324-G-A

39020181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083479-T-G

39020297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083600-T-C

39020396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083695-G-A

39021245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31083902-C-T

39021677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31084802-G-A

39021954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31085502-G-T

39022987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31085720-G-A

39023102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31085837-C-G

39023797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086421-C-T

39024126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31086742-C-T

39024404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31087002-A-G

39024991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31087982-A-G

http://identifiers.org/hco/6/GRCh38#39024992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31087983-A-C

39025006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31087997-C-G

39025599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31089352-C-G

39026474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090193-T-C

39026492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31090211-G-T

http://identifiers.org/hco/6/GRCh38#39026517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31090236-C-A

39026598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31090338-A-G

39026657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense variant
orthologous variants: 31090397-C-T

http://identifiers.org/hco/6/GRCh38#39026806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31090633-A-C

39026806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31090633-A-G

39026806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31090633-A-T

39026863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31090689-A-G

39028657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31092477-A-G

39028898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31092721-G-A

39028898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31092721-G-C

39029278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31093078-C-T

39029311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31093104-C-G

39029711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31093469-G-C

39029740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31093497-C-G

http://identifiers.org/hco/6/GRCh38#39029865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31093589-C-A

http://identifiers.org/hco/6/GRCh38#39029953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31093670-C-A

39029993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31093710-A-G

39029993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31093710-A-T

39030034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31093751-G-A

39030034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31093751-G-T

39030090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: intron variant
orthologous variants: 31093802-G-A

39030199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: missense variant
orthologous variants: 31093910-C-T

39030260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: synonymous variant
orthologous variants: 31093971-G-A

39030260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: synonymous variant
orthologous variants: 31093971-G-C

39030314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: synonymous variant
orthologous variants: 31094025-T-A

39030320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: synonymous variant
orthologous variants: 31094031-A-G

39030432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3 prime UTR variant
orthologous variants: 31094147-A-G

39030432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3 prime UTR variant
orthologous variants: 31094147-A-T

http://identifiers.org/hco/6/GRCh38#39030436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31094151-C-A

39030451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3 prime UTR variant
orthologous variants: 31094165-G-T

http://identifiers.org/hco/6/GRCh38#39030551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2952
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31094257-C-A