104268881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47853963-T-C

104268882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47853964-G-A

104268882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47853964-G-C

104268885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47853967-G-A

104268885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47853967-G-T

104268895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47853976-T-A

http://identifiers.org/hco/10/GRCh38#104268994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47854071-C-A

104268994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5 prime UTR variant
orthologous variants: 47854071-C-T

104269052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5 prime UTR variant
orthologous variants: 47854127-G-T

104269053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5 prime UTR variant
orthologous variants: 47854128-G-A

104269072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5 prime UTR variant
orthologous variants: 47854143-G-A

104269072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5 prime UTR variant
orthologous variants: 47854143-G-T

104269281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47854331-C-T

104269525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47854648-T-G

104269611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, undefined
orthologous variants: 47854717-G-T

http://identifiers.org/hco/10/GRCh38#104269850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47854945-C-A

104269905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47855024-G-T

http://identifiers.org/hco/10/GRCh38#104270404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47855491-A-C

http://identifiers.org/hco/10/GRCh38#104270535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47855590-A-C

104270609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47855725-T-C

104270801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47855927-A-T

104271088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47856696-C-T

104271181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47856808-A-G

104271243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47856868-G-C

104271384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47857005-T-C

104271463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47857070-C-G

104271463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47857070-C-T

104271967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47857693-A-G

104272011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47857743-G-C

http://identifiers.org/hco/10/GRCh38#104272030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47857757-C-A

http://identifiers.org/hco/10/GRCh38#104273763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47859251-C-A

104273881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859348-C-T

104273944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859409-C-T

104274016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859481-C-T

104274067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859519-G-A

104274085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859523-C-G

104274091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859529-G-A

104274091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859529-G-T

104274114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859545-G-T

104274142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859573-T-C

104274142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859573-T-G

104274193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859613-T-G

104274471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859858-G-C

104274537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, undefined
orthologous variants: 47859927-A-T

104274561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47859951-A-G

http://identifiers.org/hco/10/GRCh38#104274665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47860005-C-A

104274665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47860005-C-G

104274665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron variant
orthologous variants: 47860005-C-T

104274729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5 prime UTR variant
orthologous variants: 47860047-T-A

104274729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5 prime UTR variant
orthologous variants: 47860047-T-G

104274876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5 prime UTR variant
orthologous variants: 47860168-G-T

104274924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 47860217-G-A

104274924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 47860217-G-C

104274974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47860271-G-A

104275017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47860296-G-A

104275017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47860296-G-T

104275048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47860310-G-A

104275048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47860310-G-T

104275136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47860368-A-G

104275137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47860369-T-A

104275137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47860369-T-C

104275153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47860386-A-G

http://identifiers.org/hco/10/GRCh38#104275169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47860402-C-A

104275361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47860591-G-A

104275361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47860591-G-C

http://identifiers.org/hco/10/GRCh38#104275364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47860594-C-A

104275364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47860594-C-T

http://identifiers.org/hco/10/GRCh38#104275437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47860653-C-A

http://identifiers.org/hco/10/GRCh38#104275467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47860682-C-A

104275467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47860682-C-T

http://identifiers.org/hco/10/GRCh38#104275469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47860684-A-C

http://identifiers.org/hco/10/GRCh38#104275645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47860837-C-A

104275821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47861117-A-T

http://identifiers.org/hco/10/GRCh38#104275826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47861122-C-A

104275992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47861307-G-T

104276460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47861948-G-A

104276526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862011-T-G

104276621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862110-C-G

104276623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862158-A-G

104276796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862296-C-T

104277313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862850-G-T

104277314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47862851-G-T

104277646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863042-T-C

104277805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863187-T-A

104277814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863198-T-G

http://identifiers.org/hco/10/GRCh38#104277826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47863210-C-A

104277826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863210-C-T

104277853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863225-T-C

104277853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863225-T-G

104277939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47863314-C-T

http://identifiers.org/hco/10/GRCh38#104278124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47863499-C-A

http://identifiers.org/hco/10/GRCh38#104278145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47863520-C-A

104278146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863521-T-A

http://identifiers.org/hco/10/GRCh38#104278183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47863558-C-A

104278183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863558-C-T

104278207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47863576-A-G

http://identifiers.org/hco/10/GRCh38#104278239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47863607-A-C

http://identifiers.org/hco/10/GRCh38#104278943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47864459-A-C

104279218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864702-A-G

104279294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864761-C-T

104279295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864762-G-A

104279295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864762-G-T

104279308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864774-G-A

104279375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47864840-A-G

104279484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864949-G-A

104279484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864949-G-T

http://identifiers.org/hco/10/GRCh38#104279492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47864957-C-A

104279492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864957-C-T

http://identifiers.org/hco/10/GRCh38#104279493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47864958-C-A

104279493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864958-C-T

104279524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864982-G-A

104279524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864982-G-C

104279524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47864982-G-T

http://identifiers.org/hco/10/GRCh38#104279540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47864998-A-C

104279611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865072-A-G

104279611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865072-A-T

http://identifiers.org/hco/10/GRCh38#104279620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47865083-C-A

104280216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865279-A-G

104280514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865548-T-C

http://identifiers.org/hco/10/GRCh38#104280524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47865555-A-C

104280594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865676-G-A

104280664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865751-T-G

104280774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865862-A-G

104280876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47865960-C-T

104281206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47866144-C-T

104281314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47866374-T-A

http://identifiers.org/hco/10/GRCh38#104281342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47866470-A-C

104281388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47866514-C-T

104281605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47866677-T-G

104281745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47866807-A-G

104283728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

104283777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

104284526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47869048-G-T

http://identifiers.org/hco/10/GRCh38#104284527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47869049-A-C

104284564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47869086-C-T

http://identifiers.org/hco/10/GRCh38#104284587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47869113-C-A

104284729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47869256-G-A

104284838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47869355-G-C

104285135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47869587-T-C

http://identifiers.org/hco/10/GRCh38#104288719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47870015-A-C

104288719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47870015-A-G

104288890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47870179-A-G

104288961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47870238-C-T

104289541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47870456-G-C

104291311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 47870816-G-A

104291311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 47870816-G-T

http://identifiers.org/hco/10/GRCh38#104291371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47870879-C-A

104291444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47870924-A-G

104291483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 47871025-T-C

http://identifiers.org/hco/10/GRCh38#104291495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47871042-C-A

104291495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 47871042-C-T

104291496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 47871043-A-T

104291531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 47871076-G-A

104291531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 47871076-G-T

http://identifiers.org/hco/10/GRCh38#104291544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47871090-C-A

104291611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 47871137-A-G

104291634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47871161-T-A

104291634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47871161-T-C

104291658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47871177-G-A

104291660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47871179-A-G

104291666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47871185-T-C

104291714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47871205-T-A

http://identifiers.org/hco/10/GRCh38#104294348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47871780-A-C

104294402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47871829-A-G

http://identifiers.org/hco/10/GRCh38#104297033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47872515-C-A

104297033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872515-C-T

104297042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872524-G-T

104297082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872568-T-A

104297082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872568-T-C

104297098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872584-T-A

104297134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872622-G-T

104297135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872623-G-A

104297135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872623-G-T

104297168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872653-G-A

104297177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872665-G-T

104297199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872688-T-C

104297289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872776-G-T

http://identifiers.org/hco/10/GRCh38#104297349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47872837-C-A

104297349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47872837-C-T

http://identifiers.org/hco/10/GRCh38#104297509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47873021-C-A

104297528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47873041-T-C

104297528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47873041-T-G

104297598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47873115-C-T

104297729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873236-G-T

104297757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873282-G-A

104297757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873282-G-T

http://identifiers.org/hco/10/GRCh38#104297759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47873284-C-A

http://identifiers.org/hco/10/GRCh38#104297761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47873286-C-A

104297761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873286-C-G

104297761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873286-C-T

104297826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873354-T-C

104298000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873543-C-T

104298150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873687-A-T

104298160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873697-A-G

104298365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873873-A-G

104298503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873925-C-T

104298556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873979-T-C

104298567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47873990-C-G

http://identifiers.org/hco/10/GRCh38#104299146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47874475-A-C

http://identifiers.org/hco/10/GRCh38#104299215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47874544-C-A

104299215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47874544-C-T

104299321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47874652-C-G

104299321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47874652-C-T

104299362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47874692-A-G

104299376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47874704-T-C

http://identifiers.org/hco/10/GRCh38#104299382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47874710-C-A

104299382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47874710-C-T

104299436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47874762-T-C

http://identifiers.org/hco/10/GRCh38#104299900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47874898-C-A

104299900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47874898-C-G

104299900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47874898-C-T

104299904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47874902-T-C

104299905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47874903-G-T

http://identifiers.org/hco/10/GRCh38#104299973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47874963-C-A

104299973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47874963-C-T

104299996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47874991-G-T

104300053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875139-A-G

http://identifiers.org/hco/10/GRCh38#104300072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47875158-C-A

104300072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875158-C-T

104300079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875165-G-A

http://identifiers.org/hco/10/GRCh38#104300309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47875397-C-A

104300309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875397-C-T

104300318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875406-T-C

104300321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875409-G-A

104300329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875417-C-G

http://identifiers.org/hco/10/GRCh38#104300407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47875489-A-C

http://identifiers.org/hco/10/GRCh38#104300428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47875510-C-A

104300434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875517-G-A

104300434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875517-G-C

104300434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875517-G-T

104300450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875533-T-C

104300450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875533-T-G

104300458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875541-G-T

104300464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875547-G-A

104300464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875547-G-T

104300475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875556-A-G

http://identifiers.org/hco/10/GRCh38#104300556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47875637-C-A

104300556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875637-C-T

104300567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875648-C-T

104300599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875691-G-T

104300621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875713-T-C

104300638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47875733-G-A

http://identifiers.org/hco/10/GRCh38#104300765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47875859-C-A

104300765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47875859-C-T

http://identifiers.org/hco/10/GRCh38#104300843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47875915-C-A

104300843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47875915-C-T

104300852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47875924-T-C

http://identifiers.org/hco/10/GRCh38#104300857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47875929-A-C

104300857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47875929-A-G

104300882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47875953-G-A

104300891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47875962-G-T

http://identifiers.org/hco/10/GRCh38#104300932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47876004-C-A

104300932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47876004-C-T

104301006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47876077-G-A

104301022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47876093-A-G

http://identifiers.org/hco/10/GRCh38#104301050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47876121-C-A

104301089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47876155-A-G

104301108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47876173-T-A

104301108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47876173-T-C

http://identifiers.org/hco/10/GRCh38#104301369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47876400-C-A

104301369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47876400-C-T

104301392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47876423-G-A

http://identifiers.org/hco/10/GRCh38#104301404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47876435-C-A

104301404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23064
most severe consequence: 3 prime UTR variant
orthologous variants: 47876435-C-T