104031573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47635044-T-C

http://identifiers.org/hco/10/GRCh38#104031614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47635087-A-C

104031686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47635169-G-T

104031841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47635298-G-A

104031841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47635298-G-T

104031913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47635370-G-T

104031951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47635414-A-G

104031958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47635421-A-G

http://identifiers.org/hco/10/GRCh38#104032009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47635472-C-A

104032009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47635472-C-T

http://identifiers.org/hco/10/GRCh38#104032294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47635721-A-C

104032333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47635756-G-T

104032361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47635782-T-C

http://identifiers.org/hco/10/GRCh38#104032381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47635802-C-A

104032388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47635808-G-T

104032414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47635833-G-C

104032414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47635833-G-T

http://identifiers.org/hco/10/GRCh38#104032475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47635890-C-A

104032539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47635931-G-A

104032539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47635931-G-T

104032595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47635980-A-G

104032625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47636009-G-A

104032625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47636009-G-C

104032625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47636009-G-T

104032630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47636014-G-T

http://identifiers.org/hco/10/GRCh38#104032642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47636022-A-C

104032823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636183-G-A

104032882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636214-G-T

104033067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636388-A-G

104033071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636392-T-C

104033082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636403-G-C

104033082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636403-G-T

104033108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636414-A-G

104033109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636415-A-G

104033109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636415-A-T

104033140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636443-A-G

104033211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636510-G-A

104033211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636510-G-T

104033230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 47636530-G-T

104033428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47636711-T-A

104033428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47636711-T-C

104033434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47636717-A-G

104033445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47636728-G-A

104033445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47636728-G-T

104033500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47636781-G-A

104033500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47636781-G-T

104033683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47636911-T-C

http://identifiers.org/hco/10/GRCh38#104033821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47637020-C-A

104033821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47637020-C-T

104033827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47637026-G-A

104033827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47637026-G-T

104034042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 47637267-G-A

104034068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 47637293-C-T

http://identifiers.org/hco/10/GRCh38#104034084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47637309-A-C

104034084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 47637309-A-G

104034163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47637382-G-C

104034225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47637429-G-A

104034230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47637434-C-T

104034343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47637538-T-C

104034343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47637538-T-G

104034352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47637547-G-A

104034352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47637547-G-T

104034584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47637729-G-A

104034584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47637729-G-C

104034584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47637729-G-T

104034607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47637751-G-A

104034607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47637751-G-T

http://identifiers.org/hco/10/GRCh38#104034637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47637781-C-A

104034637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47637781-C-G

104034637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47637781-C-T

104034639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47637783-G-T

104034655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47637799-G-A

104034658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47637802-G-A

104034658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47637802-G-T

104034661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47637805-G-A

104034664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47637808-T-C

104034721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47637865-G-C

104034751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47637895-G-T

104034775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47637920-G-T

104034855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638001-A-G

104034855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638001-A-T

104034885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638045-C-T

104034896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638056-G-T

104034952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638113-G-A

104035119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638323-A-G

104035119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638323-A-T

http://identifiers.org/hco/10/GRCh38#104035134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47638337-C-A

104035134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638337-C-G

104035134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638337-C-T

104035172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638382-A-G

104035172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638382-A-T

http://identifiers.org/hco/10/GRCh38#104035227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47638451-C-A

104035227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638451-C-G

104035227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638451-C-T

104035450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638673-C-T

http://identifiers.org/hco/10/GRCh38#104035529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47638751-C-A

104035529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47638751-C-T

http://identifiers.org/hco/10/GRCh38#104035541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47638763-A-C

104035541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47638763-A-G

104035542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47638764-A-G

104035621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638828-A-G

104035631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638838-G-A

104035631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638838-G-C

104035631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638838-G-T

http://identifiers.org/hco/10/GRCh38#104035679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47638879-A-C

104035679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638879-A-G

104035680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47638880-T-C

104036375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639073-G-A

104036375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639073-G-T

http://identifiers.org/hco/10/GRCh38#104036383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47639081-C-A

104036383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639081-C-T

104036389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639086-G-C

104036389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639086-G-T

104036419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639126-G-A

104036691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639343-A-G

104036691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639343-A-T

http://identifiers.org/hco/10/GRCh38#104036714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47639359-C-A

104036714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639359-C-T

104036776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639415-G-C

104036776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639415-G-T

104036873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47639496-G-A

104036906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639532-A-G

http://identifiers.org/hco/10/GRCh38#104036920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47639547-C-A

104036920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639547-C-G

104036928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639555-C-G

http://identifiers.org/hco/10/GRCh38#104037030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47639635-C-A

104037030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639635-C-T

104037219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639811-G-A

104037219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47639811-G-T

104037455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640027-T-C

104037505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640076-A-G

104037505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640076-A-T

104037547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640110-C-T

104037797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640350-A-G

http://identifiers.org/hco/10/GRCh38#104037886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47640390-C-A

104037886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640390-C-G

http://identifiers.org/hco/10/GRCh38#104037908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47640409-C-A

104038217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640494-C-T

104038325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640501-G-A

104038388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640545-C-T

104038403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640560-C-T

104038445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47640602-C-T

http://identifiers.org/hco/10/GRCh38#104038488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47640645-C-A

104038488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47640645-C-G

104038488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47640645-C-T

104038524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47640681-T-C

104038524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47640681-T-G

http://identifiers.org/hco/10/GRCh38#104038525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47640682-C-A

104038525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47640682-C-T

104038641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640775-T-A

104038641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640775-T-C

104038768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640875-G-A

104038768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47640875-G-C

http://identifiers.org/hco/10/GRCh38#104039158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47641126-C-A

104039158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641126-C-T

104039172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641138-T-C

104039705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641220-A-G

http://identifiers.org/hco/10/GRCh38#104039779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47641286-C-A

104039779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641286-C-T

104039822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641328-T-A

104039822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641328-T-C

104039822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641328-T-G

104039824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641330-C-G

104039824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641330-C-T

104039844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641351-G-T

104039860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641367-C-T

104039882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641392-G-C

http://identifiers.org/hco/10/GRCh38#104040142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47641585-C-A

104040142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641585-C-G

104040142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641585-C-T

104040150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641591-G-A

104040150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641591-G-T

104040200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641638-T-C

104040298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641733-G-T

104040330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641767-T-C

104040446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641882-G-A

104040446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641882-G-T

104040453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641891-G-T

104040507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641930-T-C

104040523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641946-T-G

104040561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641979-G-A

104040561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641979-G-C

104040561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47641979-G-T

104040656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642073-G-A

104041188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642337-G-A

104041226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642374-G-C

104041226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642374-G-T

104041276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642422-C-T

104041282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642428-A-G

104041310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47642459-G-A

104041310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47642459-G-C

104041372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642513-T-C

104041440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642570-T-C

http://identifiers.org/hco/10/GRCh38#104041666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47642765-C-A

104041689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642784-G-A

104041689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642784-G-T

104041782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642863-T-C

http://identifiers.org/hco/10/GRCh38#104041826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47642907-C-A

104041826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642907-C-T

104041835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642916-C-T

104041849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642930-G-A

104041898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47642978-G-T

104042012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47643091-G-A

104042124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47643192-C-T

104042237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47643306-T-A

104042409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47644611-G-T

104042537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47644716-G-A

104042537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47644716-G-T

104042689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47644820-A-T

http://identifiers.org/hco/10/GRCh38#104042736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47644867-C-A

104042843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47644966-C-T

104042889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645016-T-C

104043009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645128-T-C

104043171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645270-A-G

104043388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645414-T-C

104043388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645414-T-G

104043389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645415-C-T

104043416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645438-G-A

104043428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645450-G-A

104043598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645621-C-G

104043643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645656-C-G

104043643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645656-C-T

104043754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645817-G-A

104043754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645817-G-T

104043762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645834-G-A

104043762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645834-G-C

104043803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645881-G-A

104043803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645881-G-T

104043804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645882-G-T

104043859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 47645936-A-T

104043891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645961-T-C

104043904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47645971-A-T

104043941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646008-T-C

104044000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646064-T-A

104044000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646064-T-C

104044016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646077-G-C

104044131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646190-G-A

104044200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646257-T-C

104044482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646565-C-T

104044513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646595-G-A

104044513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646595-G-T

104044595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646659-G-A

http://identifiers.org/hco/10/GRCh38#104044697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47646750-C-A

104044697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646750-C-T

104044714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646766-T-C

http://identifiers.org/hco/10/GRCh38#104044746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47646797-C-A

104044746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646797-C-T

104044880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47646867-T-G

104045107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647071-C-G

104045173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647137-G-A

104045206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647170-C-T

104045210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647174-C-T

104045291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647234-C-T

104045441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647346-G-A

104045452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647356-C-T

104045544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47647440-G-A

104045567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47647449-A-G

http://identifiers.org/hco/10/GRCh38#104045606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47647475-C-A

104045606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647475-C-G

104045606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647475-C-T

104045705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47647574-T-C

104045722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647591-T-G

104045726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47647631-A-G

104045836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647744-C-G

104045836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647744-C-T

104045838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47647746-A-G

104046090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648002-A-G

104046113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648021-G-T

104046152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648048-C-T

http://identifiers.org/hco/10/GRCh38#104046155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47648051-C-A

104046262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648091-A-G

104046285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648110-A-G

104046512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648201-G-C

104046599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648283-G-A

104046599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648283-G-T

104046624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648312-G-A

104046624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648312-G-C

104046624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648312-G-T

104046663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648352-G-A

104046663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648352-G-T

104046664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648353-G-A

104046664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648353-G-C

104046684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648372-G-T

104046703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648389-G-T

104046726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648412-G-A

104046726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648412-G-T

http://identifiers.org/hco/10/GRCh38#104046851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47648583-A-C

104046851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648583-A-G

104046861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648593-A-G

http://identifiers.org/hco/10/GRCh38#104046866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47648598-A-C

104046866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648598-A-G

104046883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648615-G-A

104047259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648860-C-T

104047296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47648897-G-A

104047555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649090-G-T

http://identifiers.org/hco/10/GRCh38#104047595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649104-C-A

104047595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649104-C-T

http://identifiers.org/hco/10/GRCh38#104047607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649122-C-A

104047607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649122-C-T

http://identifiers.org/hco/10/GRCh38#104047622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649137-C-A

104047622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649137-C-T

http://identifiers.org/hco/10/GRCh38#104047624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649139-C-A

104047624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649139-C-T

104047626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649141-T-A

104047626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649141-T-C

http://identifiers.org/hco/10/GRCh38#104047645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649147-C-A

104047645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649147-C-T

http://identifiers.org/hco/10/GRCh38#104047648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649150-C-A

104047648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649150-C-T

104047657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649159-A-G

104047658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649160-C-T

104047659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649161-G-A

104047659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649161-G-T

104047671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649170-C-T

104047717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649200-C-G

104047718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649201-T-C

104047722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649205-T-C

104047726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649209-C-T

104047806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47649289-T-G

http://identifiers.org/hco/10/GRCh38#104047844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649326-C-A

104047906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649366-T-A

104047967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649415-G-A

104047967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649415-G-T

http://identifiers.org/hco/10/GRCh38#104048014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649461-C-A

104048047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649495-G-A

104048047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649495-G-C

104048146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47649650-G-T

104048191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649732-C-T

104048192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649733-A-G

104048206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649763-G-T

104048238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649793-G-A

104048238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649793-G-C

104048238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649793-G-T

http://identifiers.org/hco/10/GRCh38#104048248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649805-C-A

http://identifiers.org/hco/10/GRCh38#104048270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649826-C-A

104048270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649826-C-T

104048288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649841-C-G

104048361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47649904-T-A

http://identifiers.org/hco/10/GRCh38#104048451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47649994-A-C

104048477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47650052-T-C

104048543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47650146-G-A

104048659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47650329-C-G

104048659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47650329-C-T

104048704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47650373-G-A

104049428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47650794-G-A

104049428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47650794-G-C

104049470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: splice_region_variant, synonymous_variant, undefined
orthologous variants: 47650836-G-A

104049470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: splice_region_variant, synonymous_variant, undefined
orthologous variants: 47650836-G-T

104049543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47650927-C-T

104049552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47650941-A-G

104049552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47650941-A-T

http://identifiers.org/hco/10/GRCh38#104049583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47650976-C-A

104049583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47650976-C-T

104049593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47650986-G-A

104049593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47650986-G-C

104049617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47651019-G-T

104049704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47651102-T-C

104049766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47651163-G-A

104049780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651174-C-T

http://identifiers.org/hco/10/GRCh38#104049911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47651284-C-A

104049913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47651286-T-C

104049949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651322-T-C

104049997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651372-G-A

104049997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651372-G-C

104049997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651372-G-T

http://identifiers.org/hco/10/GRCh38#104050006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47651381-C-A

104050006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651381-C-T

104050049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651425-G-A

104050059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651435-G-A

104050078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47651449-G-C

104050175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651553-A-T

http://identifiers.org/hco/10/GRCh38#104050181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47651559-C-A

104050181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651559-C-G

104050192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651570-A-G

104050207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651585-G-A

104050489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651812-C-G

104050529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651879-G-A

104050567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651916-C-T

104050584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651932-G-A

104050593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651941-A-G

http://identifiers.org/hco/10/GRCh38#104050607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47651955-A-C

104050607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651955-A-T

104050612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47651962-G-A

104050613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47651963-T-G

http://identifiers.org/hco/10/GRCh38#104050685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47652035-A-C

104050694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652044-A-G

104050728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652078-C-G

104050737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652087-G-A

104050738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652088-G-C

104050738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652088-G-T

104051014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652383-G-A

104051014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652383-G-T

104051028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652397-A-G

104051040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652407-G-T

http://identifiers.org/hco/10/GRCh38#104051044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47652411-C-A

104051158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652527-C-G

104051420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652765-T-C

104051444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652789-G-T

http://identifiers.org/hco/10/GRCh38#104051462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47652807-C-A

104051462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652807-C-T

104051474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47652819-A-G

104051564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652907-G-A

104051565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652908-G-A

104051596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652941-G-C

104051607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652951-G-A

104051607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47652951-G-T

http://identifiers.org/hco/10/GRCh38#104051657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47653013-C-A

104051795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653111-G-C

104051870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653169-C-T

104052052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653318-G-T

104052138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653393-C-T

104052170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47653417-A-T

104052177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47653424-G-A

104052210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47653457-A-G

104052270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653497-C-T

104052303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653530-C-T

104052314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653541-G-C

104052314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653541-G-T

104052318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653545-G-T

http://identifiers.org/hco/10/GRCh38#104052454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47653637-A-C

104052454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47653637-A-G

104052544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653734-C-T

104052590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, undefined
orthologous variants: 47653781-T-C

104052745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47653982-C-T

104052802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654083-G-A

104052805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654086-G-A

http://identifiers.org/hco/10/GRCh38#104052892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47654187-A-C

104052892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654187-A-G

104052893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654188-G-C

104052893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654188-G-T

104052899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654194-G-A

104052899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654194-G-T

104053010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654275-G-A

104053010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654275-G-C

http://identifiers.org/hco/10/GRCh38#104053152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47654417-C-A

104053152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654417-C-T

104053173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654438-C-T

104053175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654440-T-C

http://identifiers.org/hco/10/GRCh38#104053192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47654447-C-A

http://identifiers.org/hco/10/GRCh38#104053212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47654468-C-A

104053225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654486-G-A

104053225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654486-G-T

104053557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654766-C-T

104053564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654771-G-A

104053595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654791-A-G

104053804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654831-C-T

104053853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654858-T-C

104053894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654895-T-C

104053899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47654900-A-G

104054008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655008-C-G

104054008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655008-C-T

104054015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655014-T-G

104054065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655058-G-C

104054127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655120-A-G

http://identifiers.org/hco/10/GRCh38#104054175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47655165-C-A

104054230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655295-G-A

104054230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655295-G-T

104054232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655297-A-T

104054564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655709-C-T

http://identifiers.org/hco/10/GRCh38#104054841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47655992-C-A

104054841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655992-C-G

104054841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47655992-C-T

http://identifiers.org/hco/10/GRCh38#104054966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47656118-C-A

104054966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656118-C-T

104055006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 47656158-A-G

104055073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656222-T-C

104055085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656234-A-G

104055092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656241-A-T

104055097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656246-G-A

104055097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656246-G-T

104055130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656273-C-T

104055131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656274-G-A

104055131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656274-G-C

104055131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656274-G-T

104055133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47656276-G-C

104055177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47656318-G-T

104055179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47656320-C-T

104055193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47656334-T-C

104055229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47656385-G-A

104055229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47656385-G-T

104055235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47656392-T-G

http://identifiers.org/hco/10/GRCh38#104055239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47656396-A-C

104055239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47656396-A-G

104055256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47656407-C-G

104055524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47656697-A-T

104055666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47656839-A-T

104055675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47656848-G-A

104055675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47656848-G-T

104055709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47656872-G-A

104055709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47656872-G-T

104055852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47657004-C-T

104056009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47657155-A-G

104056026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657170-G-A

104056128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657265-C-T

104056129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657266-T-A

104056202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657316-C-T

104056203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657317-T-G

104056353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657415-G-C

104056353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657415-G-T

104056396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657430-C-T

http://identifiers.org/hco/10/GRCh38#104057002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47657768-C-A

104057002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47657768-C-T

104057053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47657809-T-A

104057053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47657809-T-C

104057054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: stop gained
orthologous variants: 47657810-G-T

104057099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47657825-G-A

104057099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47657825-G-C

104057099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47657825-G-T

104057156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: synonymous variant
orthologous variants: 47657882-G-A

104057181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657907-G-C

http://identifiers.org/hco/10/GRCh38#104057200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47657926-A-C

104057200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657926-A-G

http://identifiers.org/hco/10/GRCh38#104057214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47657940-C-A

104057214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657940-C-G

104057214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47657940-C-T

104057448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658220-G-T

104057498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658253-T-A

104057498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658253-T-C

104057498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658253-T-G

104057523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658277-C-T

104057532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658287-A-G

104057747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658489-C-T

104057822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658563-T-C

104057918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658649-G-C

http://identifiers.org/hco/10/GRCh38#104057951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47658674-C-A

104057951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658674-C-T

104057974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658697-G-T

104058031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658741-G-A

104058031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658741-G-T

104058063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658761-A-G

104058065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658763-G-T

104058131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658823-G-A

104058131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron variant
orthologous variants: 47658823-G-C

104059456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47659195-T-A

104059456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47659195-T-C

104059456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47659195-T-G

http://identifiers.org/hco/10/GRCh38#104059473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47659212-C-A

104059473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47659212-C-T

104059484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47659223-T-A

104059484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47659223-T-C

104059513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47659248-C-T

104059558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47659280-G-A

104059565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47659287-G-T

104059609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 47659326-A-G

104059609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 47659326-A-T

104059667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense variant
orthologous variants: 47659382-G-A

http://identifiers.org/hco/10/GRCh38#104059714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47659429-A-C

104059721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 47659436-A-G

104059734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47659449-A-G

http://identifiers.org/hco/10/GRCh38#104059804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47659496-C-A

104059804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47659496-C-T

http://identifiers.org/hco/10/GRCh38#104059830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47659525-C-A

104059830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47659525-C-T

104059834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47659529-T-A

104059834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47659529-T-C

104059883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47659583-C-T

104060049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47659732-G-A

104060049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47659732-G-T

http://identifiers.org/hco/10/GRCh38#104060064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47659747-C-A

104060064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47659747-C-T

104060105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47659790-A-G

104060144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47659832-T-C

104060329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660001-G-A

104060329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660001-G-T

104060390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660012-T-G

104060510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660109-T-A

104060853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660386-T-A

http://identifiers.org/hco/10/GRCh38#104060984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47660527-A-C

http://identifiers.org/hco/10/GRCh38#104060993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47660536-C-A

104060993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660536-C-T

104061087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660623-G-A

104061269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660749-G-T

104061284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660764-A-G

104061293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660773-A-G

104061314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660794-T-C

104061314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660794-T-G

104061369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660824-C-T

104061374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660829-C-T

104061463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 47660918-C-T

http://identifiers.org/hco/10/GRCh38#104061469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, missense_variant, stop_gained
orthologous variants: http://identifiers.org/mco/19/GRCm39#47660924-A-C

104061531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660984-G-A

104061531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47660984-G-T

104061621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661029-T-C

104061747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661236-T-G

104061790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661320-G-A

104061800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661331-G-A

104061800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661331-G-T

104061810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661343-C-G

104061949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661479-A-G

104061990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661522-C-T

104062119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661623-T-C

104062119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661623-T-G

104062132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661648-T-G

104062144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661660-G-T

104062213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661729-A-T

http://identifiers.org/hco/10/GRCh38#104062221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47661737-C-A

104062221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661737-C-G

104062221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661737-C-T

104062229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661744-C-G

104062229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661744-C-T

104062249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661764-C-G

104062262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 47661777-G-A

http://identifiers.org/hco/10/GRCh38#104062342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47661857-C-A

104062342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661857-C-T

104062389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661888-G-A

104062391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661890-A-G

104062399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661902-C-T

104062479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661988-G-A

104062479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47661988-G-T

104062525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47662015-T-C

104062651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47662118-T-C

104062684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47662151-T-C

104062748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47662197-C-T

104063653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47663087-G-A

104063898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663333-C-G

104063898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663333-C-T

104063907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663342-T-A

104063907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663342-T-C

104063923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663358-T-C

104063923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663358-T-G

104063945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663380-T-A

104063945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663380-T-C

104063956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663391-A-T

104064234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663681-T-C

104064296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663736-G-T

http://identifiers.org/hco/10/GRCh38#104064319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47663754-C-A

http://identifiers.org/hco/10/GRCh38#104064328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47663763-C-A

104064328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663763-C-T

104064344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663780-T-C

104064390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47663821-C-T

104064513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47663950-T-C

104064526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47663963-G-A

104064526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47663963-G-C

104064526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47663963-G-T

104064576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47664013-T-G

http://identifiers.org/hco/10/GRCh38#104064732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47664144-C-A

104065343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47664696-C-G

104065402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47664755-G-T

104065460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47664797-A-G

104065518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47664858-C-T

104065562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47664895-G-C

104065603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47664936-T-C

104065620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47664953-T-C

104065625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47664958-A-G

104065638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47664968-T-C

104065768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47665115-G-A

104070544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47665345-A-G

104070648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47665449-T-A

104070796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47665586-A-G

104070826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47665616-T-C

104070867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47665657-T-C

104071160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47665950-G-A

104071196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47665978-G-C

104071373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666147-G-A

104071427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666204-C-T

104071555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666319-A-G

104071624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666387-C-T

http://identifiers.org/hco/10/GRCh38#104071826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47666571-C-A

http://identifiers.org/hco/10/GRCh38#104071886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47666630-C-A

104071923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666669-C-T

104071928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666674-G-A

104071930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666676-G-A

104071930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666676-G-T

104071932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666678-G-A

104071932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666678-G-T

http://identifiers.org/hco/10/GRCh38#104071947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47666693-C-A

104071947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666693-C-T

104071952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666698-G-A

104071952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666698-G-T

104071956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666702-G-A

104071956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666702-G-T

104071961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666707-C-T

104072020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47666838-A-G

104072051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47666869-A-G

104072075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47666893-A-G

104072176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667002-C-T

104072180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667006-G-T

104072471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667243-C-T

104072561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667323-T-C

104072665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667442-C-T

104072683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667460-A-T

104073001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667677-C-G

http://identifiers.org/hco/10/GRCh38#104073075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47667749-C-A

104073075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667749-C-T

104073092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667760-G-A

104073092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667760-G-C

104073092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667760-G-T

104073117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667783-T-C

104073117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667783-T-G

104073274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667922-C-G

104073275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667923-A-G

104073279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667927-A-G

104073293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667936-G-A

104073293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667936-G-T

104073323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667952-A-G

http://identifiers.org/hco/10/GRCh38#104073353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47667975-C-A

104073364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47667986-T-A

104073388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668028-G-T

104073737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668405-G-A

104073772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668433-C-T

104073773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668434-A-G

104073804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668477-G-A

104073811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668483-T-C

http://identifiers.org/hco/10/GRCh38#104073837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47668508-C-A

104073904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668568-G-C

104073904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668568-G-T

http://identifiers.org/hco/10/GRCh38#104073914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47668578-C-A

104073914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668578-C-T

http://identifiers.org/hco/10/GRCh38#104073921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47668585-A-C

104073921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668585-A-G

http://identifiers.org/hco/10/GRCh38#104073967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47668633-C-A

104073967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668633-C-T

104074007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668673-T-A

104074007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668673-T-C

http://identifiers.org/hco/10/GRCh38#104074020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47668687-C-A

http://identifiers.org/hco/10/GRCh38#104074035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47668702-C-A

104074035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668702-C-T

104074037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668704-A-G

104074071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668731-T-C

104074092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668752-T-C

104074093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668753-G-T

104074114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668774-T-C

104074117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668777-A-G

104074117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668777-A-T

104074139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668796-G-A

104074172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668829-G-A

104074218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47668875-G-A

104074218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47668875-G-T

104074245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668902-G-T

104074249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668906-C-G

104074249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668906-C-T

104074258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668915-C-T

http://identifiers.org/hco/10/GRCh38#104074292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47668947-C-A

104074292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668947-C-T

104074338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668991-G-A

104074338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47668991-G-T

104075337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47669024-T-G

104075365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47669053-G-C

104075387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47669075-A-G

http://identifiers.org/hco/10/GRCh38#104075511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47669206-C-A

104075870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47669470-C-G

104076010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47669608-T-A

104076010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47669608-T-C

104076125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47669692-G-T

104076373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47669892-C-G

http://identifiers.org/hco/10/GRCh38#104076374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47669893-A-C

http://identifiers.org/hco/10/GRCh38#104076385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47669904-C-A

104076385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47669904-C-T

104076409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47669928-C-T

104076422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47669941-G-A

104076422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47669941-G-C

104076532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670071-C-T

104076542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670088-G-A

104076542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670088-G-T

http://identifiers.org/hco/10/GRCh38#104076562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47670103-C-A

104076741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47670278-C-T

104076809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670323-G-T

104077037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670535-T-C

104077060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47670557-T-C

104077250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670693-G-A

104077279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670722-G-T

104077298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670731-G-T

http://identifiers.org/hco/10/GRCh38#104077316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47670749-C-A

http://identifiers.org/hco/10/GRCh38#104077317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47670750-A-C

104077317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670750-A-T

104077330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670763-T-C

104077330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670763-T-G

104077353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670765-A-G

104077353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670765-A-T

104077365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670777-G-T

104077381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670792-C-T

104077468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47670873-C-T

http://identifiers.org/hco/10/GRCh38#104077471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47670876-C-A

104077471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47670876-C-T

104077579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670977-T-A

104077585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670983-G-C

104077585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670983-G-T

104077587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47670985-T-C

http://identifiers.org/hco/10/GRCh38#104077620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47671012-C-A

104077620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671012-C-T

104077641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671033-G-A

104077676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671060-T-A

104077754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671103-G-A

104077763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671112-C-G

http://identifiers.org/hco/10/GRCh38#104077813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47671160-A-C

104077813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671160-A-G

104077944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671273-C-T

104078399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671523-G-A

104078399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671523-G-T

104078401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671525-A-G

104078401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671525-A-T

104078411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671536-A-G

104078502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671651-G-A

104078529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671664-G-A

104078652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671780-G-A

104078688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671809-G-A

104078688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671809-G-T

104078728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671848-G-C

104078728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671848-G-T

104078760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671884-C-G

104078760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671884-C-T

104078843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47671964-T-G

104079258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672442-C-T

104079276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672460-C-G

104079544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672834-C-T

104079582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672859-C-T

104079584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47672861-T-C

http://identifiers.org/hco/10/GRCh38#104079607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47672881-C-A

104079755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673002-G-A

104079866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673104-G-T

http://identifiers.org/hco/10/GRCh38#104080028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47673209-C-A

104080028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673209-C-T

104080213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673371-A-G

http://identifiers.org/hco/10/GRCh38#104080222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47673380-A-C

104080290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673475-G-C

104080339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673524-T-C

104080502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673887-A-G

104080502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673887-A-T

104080528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673916-G-T

104080531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47673919-G-T

http://identifiers.org/hco/10/GRCh38#104080723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47674053-C-A

104080723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47674053-C-T

104080806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47674156-C-T

104080824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47674175-G-A

104080824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47674175-G-C

104080824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47674175-G-T

104080877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47674228-A-G

http://identifiers.org/hco/10/GRCh38#104081005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47674333-C-A

104081005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47674333-C-T

104081191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47674887-T-A

104081191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47674887-T-G

104081275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47674974-C-T

104081475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47675090-G-A

104081538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47675151-A-G

104081765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47675348-G-A

104081793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47675672-G-T

104082054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47675928-T-C

104082055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47675929-G-A

104082076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47675952-C-G

104082101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47675978-G-T

104082160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47676025-A-G

104082338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47676202-T-C

104082413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47676307-C-T

104082798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47676726-G-T

104083033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47676969-C-T

104083060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47677000-G-A

104083061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47677001-T-C

http://identifiers.org/hco/10/GRCh38#104083277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47677213-A-C

104083277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47677213-A-G

104083389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47677325-G-A

104083405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47677342-T-C

104083430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47677367-C-G

104083451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47677388-A-T

104083486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47678019-C-T

104083642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47678181-C-T

104083694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47678231-G-A

http://identifiers.org/hco/10/GRCh38#104083735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47678239-A-C

http://identifiers.org/hco/10/GRCh38#104084031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47678563-C-A

104084048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47678577-G-A

http://identifiers.org/hco/10/GRCh38#104084097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47678625-A-C

http://identifiers.org/hco/10/GRCh38#104084718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47678914-C-A

104084820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47679009-G-A

http://identifiers.org/hco/10/GRCh38#104084850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47679039-C-A

104084965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47679133-A-G

104084989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47679160-A-G

104085159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47679723-G-T

104085163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47679727-C-T

104085296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47679878-A-T

104085480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47680006-C-T

104085664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47680186-C-T

http://identifiers.org/hco/10/GRCh38#104085676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47680198-C-A

104085676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47680198-C-T

104085730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47680259-G-T

104085788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2194
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47680317-T-G