http://identifiers.org/hco/6/GRCh38#33162720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34285633-C-A

33162720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285633-C-T

33162897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285489-A-G

33162918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285468-G-T

http://identifiers.org/hco/6/GRCh38#33162952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34285437-C-A

33162965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285425-G-T

33162970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285420-A-G

33162971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285419-G-A

33162971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285419-G-T

http://identifiers.org/hco/6/GRCh38#33162991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34285400-C-A

33162991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285400-C-T

http://identifiers.org/hco/6/GRCh38#33163036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34285380-C-A

33163036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285380-C-T

http://identifiers.org/hco/6/GRCh38#33163074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34285342-C-A

33163074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285342-C-T

33163137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285297-G-T

33163168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285281-A-G

33163168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285281-A-T

33163237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285216-T-G

33163266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285189-T-A

33163266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285189-T-G

http://identifiers.org/hco/6/GRCh38#33163273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34285182-A-C

33163273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285182-A-G

33163357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285088-T-A

http://identifiers.org/hco/6/GRCh38#33163366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34285079-C-A

33163366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285079-C-T

33163372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285073-G-A

33163372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34285073-G-T

http://identifiers.org/hco/6/GRCh38#33163508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34284952-C-A

33163508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34284952-C-T

33163529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34284926-C-T

33163598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34284855-T-C

33163642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34284811-C-G

33163685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34284773-A-G

33163685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34284773-A-T

33163742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34284716-G-A

http://identifiers.org/hco/6/GRCh38#33163823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34284635-A-C

33163832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284626-C-T

33163915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284544-G-T

33163928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284531-G-A

33163928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284531-G-T

33163948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284511-G-A

33163948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284511-G-C

33163948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284511-G-T

33163961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284497-G-A

33163961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284497-G-T

http://identifiers.org/hco/6/GRCh38#33163963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34284495-C-A

33164028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284429-G-A

33164196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284252-G-A

33164196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284252-G-T

http://identifiers.org/hco/6/GRCh38#33164206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34284242-C-A

33164206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34284242-C-T

http://identifiers.org/hco/6/GRCh38#33164237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34284214-A-C

33164388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34284063-T-C

33164426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34284025-G-A

33164463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34283988-A-G

33164463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34283988-A-T

33164608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283918-G-A

33164608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283918-G-T

33164704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283859-A-G

33164733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283846-G-C

33164733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283846-G-T

33164734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283845-G-A

33164734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283845-G-T

http://identifiers.org/hco/6/GRCh38#33164880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34283787-C-A

33164880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34283787-C-T

http://identifiers.org/hco/6/GRCh38#33164965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34283702-C-A

33164965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 34283702-C-T

33164969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34283698-T-G

http://identifiers.org/hco/6/GRCh38#33165057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34283630-C-A

33165057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283630-C-G

33165057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283630-C-T

http://identifiers.org/hco/6/GRCh38#33165115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34283577-C-A

33165115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283577-C-G

33165158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283535-T-A

33165434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34283342-C-T

http://identifiers.org/hco/6/GRCh38#33165688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34283124-A-C

33165688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34283124-A-G

33165688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34283124-A-T

33165763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34283049-A-G

33165830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282984-C-T

33165879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282941-G-A

33165898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282926-C-T

33166001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282818-C-G

33166007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282812-A-G

33166078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282740-G-C

33166078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282740-G-T

33166088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282721-G-A

33166088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282721-G-T

http://identifiers.org/hco/6/GRCh38#33166144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34282665-A-C

33166144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282665-A-G

33166250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282570-G-A

33166250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282570-G-T

33166270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282558-G-T

33166306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282521-T-C

33166306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282521-T-G

33166354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282488-T-C

33166501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282443-G-A

33166575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282364-G-A

33166593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282327-T-C

http://identifiers.org/hco/6/GRCh38#33166606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34282314-C-A

33166606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282314-C-T

http://identifiers.org/hco/6/GRCh38#33166704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34282205-C-A

33166704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282205-C-T

33166736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34282173-C-T

33166778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34282131-T-C

33166793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34282116-G-A

33166793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34282116-G-T

33166868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282041-G-A

33166868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282041-G-T

33166877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282035-A-G

33166900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282013-C-T

33166916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34282005-G-A

http://identifiers.org/hco/6/GRCh38#33166947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34281975-C-A

33166959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281963-G-A

33166959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281963-G-T

33167013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281913-T-A

33167021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281910-G-A

33167145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281789-T-C

33167370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281587-C-T

http://identifiers.org/hco/6/GRCh38#33167371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34281586-C-A

33167371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281586-C-T

33167375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281582-C-T

http://identifiers.org/hco/6/GRCh38#33167381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34281576-C-A

33167381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281576-C-T

http://identifiers.org/hco/6/GRCh38#33167586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34281391-C-A

33167586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281391-C-G

33167586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281391-C-T

http://identifiers.org/hco/6/GRCh38#33167604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34281378-A-C

33167604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281378-A-T

33167605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281377-G-C

33167605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281377-G-T

33167652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281357-T-A

33167710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281318-T-G

33167752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281284-T-A

33167754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281282-G-T

33167758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281278-G-C

33167760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281276-G-A

33167760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281276-G-T

33167772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281264-C-G

33167781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281254-G-A

33167839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34281200-G-A

33167886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281155-G-A

33167900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281141-G-A

33167920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281123-C-T

33167936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281066-C-T

33167944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281042-T-C

33167944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281042-T-G

33167959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281027-G-A

33167959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281027-G-C

33167959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34281027-G-T

33167970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280988-G-T

http://identifiers.org/hco/6/GRCh38#33167972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34280986-C-A

33167972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280986-C-T

33167977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280981-G-A

33167977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280981-G-T

http://identifiers.org/hco/6/GRCh38#33167985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34280970-C-A

33167985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280970-C-T

http://identifiers.org/hco/6/GRCh38#33168050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34280908-A-C

http://identifiers.org/hco/6/GRCh38#33168149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34280839-C-A

33168299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280764-G-A

http://identifiers.org/hco/6/GRCh38#33168336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34280750-C-A

33168442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280698-C-T

http://identifiers.org/hco/6/GRCh38#33168458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34280680-A-C

33168481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280657-G-T

33168526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34280627-C-T

33168608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280551-T-A

33168640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280527-C-T

33168641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280526-A-G

33168707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34280488-G-T

http://identifiers.org/hco/6/GRCh38#33168732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34280463-C-A

33168764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34280431-A-G

33168782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280413-G-T

33168867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280330-C-T

33168930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280269-C-T

33169049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280151-T-C

33169052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280148-G-A

33169052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280148-G-T

http://identifiers.org/hco/6/GRCh38#33169084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34280130-C-A

http://identifiers.org/hco/6/GRCh38#33169240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34280045-C-A

http://identifiers.org/hco/6/GRCh38#33169268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34280023-C-A

33169268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34280023-C-T

http://identifiers.org/hco/6/GRCh38#33169302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34279991-C-A

33169302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279991-C-T

http://identifiers.org/hco/6/GRCh38#33169332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34279959-C-A

33169332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279959-C-T

http://identifiers.org/hco/6/GRCh38#33169362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34279943-C-A

33169362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279943-C-G

33169362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279943-C-T

33169497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34279805-A-G

33169498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34279804-A-T

http://identifiers.org/hco/6/GRCh38#33169574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34279766-C-A

http://identifiers.org/hco/6/GRCh38#33169598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34279743-A-C

33169598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279743-A-G

33169720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279670-G-A

33169939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279510-G-A

33170213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279296-G-A

33170213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279296-G-T

33170281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279246-G-C

33170311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279242-G-T

33170312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279241-C-T

33170345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34279208-G-A

33170345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34279208-G-T

33170403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279136-G-T

33170438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279101-G-T

33170441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279098-G-A

33170441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279098-G-T

33170442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279097-G-A

33170488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279030-T-G

33170500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279018-T-G

33170503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279008-C-T

33170512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278999-G-C

33170515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278996-G-A

33170515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278996-G-T

33170517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278994-G-A

33170517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278994-G-T

33170525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278986-T-C

33170634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278879-G-T

33170640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278873-G-A

33170641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278872-T-G

33170727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278834-G-A

33170727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278834-G-C

33170727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278834-G-T

http://identifiers.org/hco/6/GRCh38#33170989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34278599-A-C

33171047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278569-G-A

33171095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278529-G-T

http://identifiers.org/hco/6/GRCh38#33171180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34278429-A-C

33171188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278421-A-G

33171216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278373-G-A

33171242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278347-G-A

33171258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278331-C-T

33171316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34278273-C-T

33171488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34278123-C-T

33171579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34278032-G-A

33171579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34278032-G-T

33171599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278011-T-C

33171608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278002-G-A

33171616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277995-T-A

33171618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277993-A-G

33171640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277964-A-G

http://identifiers.org/hco/6/GRCh38#33171729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34277888-C-A

33171729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34277888-C-T

http://identifiers.org/hco/6/GRCh38#33171830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34277788-C-A

33171830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277788-C-T

http://identifiers.org/hco/6/GRCh38#33171858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34277756-A-C

http://identifiers.org/hco/6/GRCh38#33171934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34277696-C-A

33171934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277696-C-T

33171952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277675-G-T

33171993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277640-T-A

33171993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277640-T-G

33171997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277636-T-A

33171997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277636-T-G

33172002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277631-C-T

33172066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34277565-C-G

33172148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277449-A-G

33172191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277416-A-G

33172191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277416-A-T

33172247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277373-C-T

33172275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277353-G-C

http://identifiers.org/hco/6/GRCh38#33172296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34277332-C-A

33172296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34277332-C-T

33172311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34277317-T-A

33172361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34277267-A-G

http://identifiers.org/hco/6/GRCh38#33172492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34277156-A-C

33172594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277065-G-T

http://identifiers.org/hco/6/GRCh38#33172722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34276955-A-C

33172722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276955-A-G

http://identifiers.org/hco/6/GRCh38#33172748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34276931-C-A

33172748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276931-C-T

33172848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276831-A-G

33172908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276768-G-T

http://identifiers.org/hco/6/GRCh38#33172924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34276745-C-A

33173044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276660-C-T

33173094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34276611-C-G

33173117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34276588-G-A

33173122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276584-G-A

33173122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276584-G-C

33173156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276543-G-A

33173156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276543-G-T

33173161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276537-G-T

33173208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276489-G-A

33173208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276489-G-T

33173243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276465-G-T

http://identifiers.org/hco/6/GRCh38#33173249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34276459-C-A

33173249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276459-C-T

http://identifiers.org/hco/6/GRCh38#33173251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34276457-C-A

33173253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276455-G-T

33173364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34276409-C-T

33173428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276344-A-T

33173451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276320-G-C

33173451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276320-G-T

33173472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276307-G-A

33173472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276307-G-T

http://identifiers.org/hco/6/GRCh38#33173602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34276184-A-C

33173602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276184-A-G

33173602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276184-A-T

33173680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276142-G-A

33173680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276142-G-C

33173680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276142-G-T

33173720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34276102-T-C

33173747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 34276075-T-C

33173757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276066-A-T

33173758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276065-A-T

http://identifiers.org/hco/6/GRCh38#33173788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34276036-C-A

33173788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276036-C-T

33173792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276032-C-T

33173793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276031-T-G

33173817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276002-G-A

33173824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276000-T-C

33173824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276000-T-G

http://identifiers.org/hco/6/GRCh38#33173832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34275992-A-C

33173851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275965-G-C

33173936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275874-G-C

33173983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275597-G-C

http://identifiers.org/hco/6/GRCh38#33174021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34275551-C-A

33174021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34275551-C-T

http://identifiers.org/hco/6/GRCh38#33174108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34275465-C-A

33174108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275465-C-G

http://identifiers.org/hco/6/GRCh38#33174155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34275428-C-A

33174155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275428-C-T

33174226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34275357-G-C

33174255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275334-A-G

33174255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275334-A-T

33174259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275330-A-G

33174287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275282-G-T

33174288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275281-G-A

33174288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275281-G-C

33174288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275281-G-T

33174302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275267-C-T

33174318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275254-G-A

33174326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275248-G-A

http://identifiers.org/hco/6/GRCh38#33174428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34275143-C-A

33174428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275143-C-G

33174428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275143-C-T

33174433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275138-A-T

33174546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34275058-G-A

33174685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274966-C-T

http://identifiers.org/hco/6/GRCh38#33174714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34274948-C-A

33174714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274948-C-T

33174746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274929-G-C

33174784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274903-T-C

http://identifiers.org/hco/6/GRCh38#33174799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34274889-A-C

33174990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274761-C-T

33175270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274542-C-T

33175351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274486-T-A

33175351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274486-T-C

33175351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274486-T-G

33175379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274465-G-A

33175379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274465-G-T

33175400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274436-A-G

http://identifiers.org/hco/6/GRCh38#33175440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34274400-C-A

33175540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274328-A-G

33175596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34274275-G-A

33175733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274145-G-A

33175762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274114-G-A

33175762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274114-G-C

33175762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274114-G-T

http://identifiers.org/hco/6/GRCh38#33175763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34274113-C-A

33175763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274113-C-T

http://identifiers.org/hco/6/GRCh38#33175777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34274098-A-C

33175995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273904-C-T

33176145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273608-G-A

33176211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273368-G-A

33176211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273368-G-C

33176231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273349-G-A

33176231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273349-G-C

33176231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273349-G-T

33176476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34273132-C-T

33176479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34273129-G-A

33176502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273106-G-A

33176529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273082-G-A

33176545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273066-C-T

33176589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34273021-G-T

http://identifiers.org/hco/6/GRCh38#33176601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34273009-A-C

33176814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272796-C-T

33176827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272786-T-A

33176862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272751-T-G

33176873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272730-G-A

33176952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272617-G-T

33176953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272616-G-A

33177075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272524-C-T

33177249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272361-A-T

33177254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272356-G-A

33177254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272356-G-T

33177350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272272-C-T

33177351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272271-C-T

33177357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272267-T-G

33177375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272249-C-T

33177484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272140-G-A

33177506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272099-G-A

33177506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272099-G-T

33177519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272092-T-A

33177519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272092-T-C

33177594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34272018-G-T

33177634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34271982-G-C

33177644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34271976-C-T

33177792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34271811-G-A

33177792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34271811-G-T

33177803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 34271800-C-T

http://identifiers.org/hco/6/GRCh38#33177806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34271797-C-A

33177806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34271797-C-T

33177853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34271742-G-A

33177853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34271742-G-T

http://identifiers.org/hco/6/GRCh38#33177918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34271679-A-C

33177918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271679-A-G

33177918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271679-A-T

http://identifiers.org/hco/6/GRCh38#33177930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34271667-C-A

33177930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271667-C-T

http://identifiers.org/hco/6/GRCh38#33177947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34271651-C-A

33177947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271651-C-T

http://identifiers.org/hco/6/GRCh38#33177948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34271650-A-C

33177948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271650-A-G

33177948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271650-A-T

http://identifiers.org/hco/6/GRCh38#33178036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34271584-C-A

33178036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271584-C-T

33178043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271577-A-G

33178044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271576-G-C

33178102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271519-C-T

33178103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271518-T-A

33178104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271517-C-T

33178127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271494-C-T

33178133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 34271488-G-A

33178151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant
orthologous variants: 34271470-G-A

33178151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant
orthologous variants: 34271470-G-C

33178251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271366-T-G

http://identifiers.org/hco/6/GRCh38#33178406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34271219-C-A

33178406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271219-C-T

33178430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271195-C-T

33178474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: synonymous variant
orthologous variants: 34271151-G-A

33178474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: synonymous variant
orthologous variants: 34271151-G-T

33178514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271111-G-A

33178514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34271111-G-T

http://identifiers.org/hco/6/GRCh38#33178640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34271014-C-A

33178664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270991-C-T

33178756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270899-A-T

33178794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270866-C-G

33178794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270866-C-T

33178814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270847-G-A

33178814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270847-G-C

33178814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270847-G-T

33178815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270846-T-G

33178902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270794-G-A

http://identifiers.org/hco/6/GRCh38#33178923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34270775-C-A

33179007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270690-G-A

33179064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270648-G-A

33179095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense variant
orthologous variants: 34270617-G-A

33179145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270567-G-A

33179289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 34270447-G-A

33179305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270431-T-A

33179339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270402-C-T

33179368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270351-C-G

33179368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270351-C-T

http://identifiers.org/hco/6/GRCh38#33179391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34270327-C-A

http://identifiers.org/hco/6/GRCh38#33179431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34270290-C-A

33179431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 34270290-C-G

33179431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 34270290-C-T

33179453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense variant
orthologous variants: 34270268-T-A

33179453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense variant
orthologous variants: 34270268-T-C

http://identifiers.org/hco/6/GRCh38#33179485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34270236-C-A

33179485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 34270236-C-T

33179512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270208-G-A

33179512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270208-G-T

http://identifiers.org/hco/6/GRCh38#33179539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34270184-A-C

33179539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270184-A-G

33179540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270183-G-T

http://identifiers.org/hco/6/GRCh38#33179603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34270123-C-A

33179603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270123-C-T

http://identifiers.org/hco/6/GRCh38#33179604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34270122-C-A

http://identifiers.org/hco/6/GRCh38#33179636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34270095-C-A

http://identifiers.org/hco/6/GRCh38#33179658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34270081-C-A

33179658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270081-C-G

33179702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270043-G-A

33179702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270043-G-C

33179706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34270039-C-T

33179736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense variant
orthologous variants: 34269998-T-C

33179771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense variant
orthologous variants: 34269963-G-T

http://identifiers.org/hco/6/GRCh38#33179789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34269945-C-A

33179789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense variant
orthologous variants: 34269945-C-T

33179806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: splice acceptor variant
orthologous variants: 34269928-C-T

33179809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 34269925-A-G

33179810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 34269924-G-C

33179810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 34269924-G-T

33179822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269914-A-G

33179908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269843-G-C

33179908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269843-G-T

http://identifiers.org/hco/6/GRCh38#33179974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34269793-C-A

33179974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269793-C-G

33180031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269740-C-T

33180067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269703-T-C

http://identifiers.org/hco/6/GRCh38#33180098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34269675-C-A

33180106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269667-C-T

http://identifiers.org/hco/6/GRCh38#33180112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34269661-C-A

33180112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269661-C-G

33180112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269661-C-T

33180136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269636-G-T

33180162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269575-T-A

33180183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269549-A-G

33180183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269549-A-T

http://identifiers.org/hco/6/GRCh38#33180211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34269517-C-A

33180211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269517-C-T

33180223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269503-C-G

33180313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: missense variant
orthologous variants: 34269413-C-T

33180335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 34269391-G-C

http://identifiers.org/hco/6/GRCh38#33180640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34269106-C-A

33180640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269106-C-T

33180641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269105-C-T

33180644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269102-G-A

33180644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269102-G-T

33180656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34269092-A-G

33180751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268996-G-T

33180762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268985-G-A

33180796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268957-C-G

33180844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268917-A-T

http://identifiers.org/hco/6/GRCh38#33180884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34268885-C-A

33180884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268885-C-T

33180906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268863-G-A

33180922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268847-T-A

33180922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268847-T-C

33180922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268847-T-G

33180991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: synonymous variant
orthologous variants: 34268780-C-T

33181036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268735-G-A

33181037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268734-A-T

33181083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268690-C-T

33181238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268524-T-G

33181252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268510-T-A

33181287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268465-T-C

33181287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268465-T-G

33181347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268398-C-T

33181373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34268376-C-T

33182792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34267745-G-A

33182903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34267632-A-G

33183136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34267403-C-T

33183346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34267206-C-T

33183407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34267144-T-A

33183809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34266753-G-A

33184016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34266558-G-A

33184016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34266558-G-T

33184017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34266557-A-G

33184049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34266400-G-T

33184069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34266352-G-A

33184069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34266352-G-T

33184079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34266326-A-G

33184206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant
orthologous variants: 34266188-T-C

33184304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 34266090-G-A

33184304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 34266090-G-T

http://identifiers.org/hco/6/GRCh38#33184331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34266063-A-C

33184331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 34266063-A-T

33184340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34266054-G-C

33184340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34266054-G-T

http://identifiers.org/hco/6/GRCh38#33184455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34265938-C-A

33184811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34265618-C-G

http://identifiers.org/hco/6/GRCh38#33184904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34265538-C-A

33184904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34265538-C-G

33184904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34265538-C-T

33184959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34265506-C-G

33185165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34265312-G-A

33185165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34265312-G-T

http://identifiers.org/hco/6/GRCh38#33185195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34265284-C-A

33185195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34265284-C-T

33185233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34265261-C-T

http://identifiers.org/hco/6/GRCh38#33185287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34265210-C-A

http://identifiers.org/hco/6/GRCh38#33185550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34264947-C-A

33185550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34264947-C-G

33185559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34264937-G-A

33185559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34264937-G-T

33185720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34264801-C-T

33185750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34264771-T-G

33185792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264729-G-A

33185792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264729-G-T

33185795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264726-G-A

33185795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264726-G-T

http://identifiers.org/hco/6/GRCh38#33185802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34264720-A-C

33185802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264720-A-G

33185869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264685-G-C

33185869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264685-G-T

33185896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264662-G-A

33185896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264662-G-T

33185917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264642-G-A

33185917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264642-G-C

33185917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264642-G-T

33185941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264614-T-A

33185970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264584-G-A

33186087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264475-A-G

http://identifiers.org/hco/6/GRCh38#33186288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34264344-C-A

33186369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264266-G-A

33186407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264241-G-A

33186407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264241-G-T

33186409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264239-A-G

33186413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34264232-G-A

33186542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34264087-G-A

33186557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34264051-G-A

33186617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34263992-G-A

33186617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34263992-G-C

33186852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34263743-T-C

33186985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34263490-T-C

http://identifiers.org/hco/6/GRCh38#33187089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34263382-C-A

http://identifiers.org/hco/6/GRCh38#33187220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34263242-A-C

33187227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34263236-T-A

33187297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34263156-C-T

33187473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34263013-G-A

33187722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262880-A-G

33187756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262870-T-C

33187914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262739-T-A

33188214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262500-G-T

http://identifiers.org/hco/6/GRCh38#33188286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34262430-C-A

33188290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262426-C-T

33188313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262406-A-G

33188319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262400-T-C

33188321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262398-G-A

33188332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262388-G-A

33188541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262189-A-G

33188637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262092-A-G

33188637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34262092-A-T

33188724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34261844-A-G

33188798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34261757-G-A

33188854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34261709-G-T

33188857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34261706-G-T

33188875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34261694-G-A

33188921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34261648-G-A

33189156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34261405-C-T

33189482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34261119-A-T

http://identifiers.org/hco/6/GRCh38#33189502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34261099-C-A

33189502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34261099-C-T

33189506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34261095-C-G

33189528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34261072-G-A

33189724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260919-C-T

33189725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260918-G-A

33189725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260918-G-T

33189768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260879-A-T

33189830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260826-T-C

33189890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260767-C-T

33190030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260629-G-A

33190117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260558-A-G

33190235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260448-C-T

33190257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260426-G-A

33190594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34260121-A-T

33190825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, undefined
orthologous variants: 34259896-G-A

33190825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, undefined
orthologous variants: 34259896-G-C

33190847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34259874-C-T

33190913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34259829-G-A

33191195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34259621-C-T

33191196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34259620-T-C

http://identifiers.org/hco/6/GRCh38#33191270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34259582-C-A

33191448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, undefined
orthologous variants: 34259347-A-T

33191480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, undefined
orthologous variants: 34259315-A-G

33191731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34259084-C-T

33191925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34258934-T-C

33192065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34258795-G-A

33192065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34258795-G-C

33192176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant
orthologous variants: 34258691-G-A

33192176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron_variant, missense_variant
orthologous variants: 34258691-G-T

http://identifiers.org/hco/6/GRCh38#33192352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34258551-C-A

33192357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34258547-G-A

33192357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34258547-G-C

33192357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34258547-G-T

33192439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34258469-T-C

33192439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34258469-T-G

33192446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34258462-T-A

33192446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34258462-T-C

http://identifiers.org/hco/6/GRCh38#33192447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34258461-C-A

http://identifiers.org/hco/6/GRCh38#33192501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34258409-C-A

33192501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34258409-C-T

33192503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34258407-C-G

33192535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34258374-G-A

33192535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34258374-G-C

33192536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34258373-C-T

33192547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34258362-C-T

33192570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: intron variant
orthologous variants: 34258339-C-T

33192590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34258320-G-T

http://identifiers.org/hco/6/GRCh38#33192612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34258290-A-C

33192612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2187
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34258290-A-G