140175227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36481811-G-A

140175243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36481827-G-A

140175243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36481827-G-T

140175246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36481830-C-T

http://identifiers.org/hco/5/GRCh38#140175272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36481856-C-A

140175272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36481856-C-G

http://identifiers.org/hco/5/GRCh38#140175301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36481884-C-A

140175301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36481884-C-T

140175329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36481918-G-A

140175329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36481918-G-T

140175372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36481944-A-G

http://identifiers.org/hco/5/GRCh38#140175416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36481973-C-A

140175469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36482013-G-T

140175600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36482098-G-C

140175820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36482249-T-C

140176482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36482705-C-T

140176545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36482768-G-A

140177178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483281-G-A

140177602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483572-C-T

140177679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483694-G-A

140177737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483872-T-C

140177828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483958-T-C

140177899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36484028-G-A

140180142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36485758-C-G

140180154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36485770-G-A

140180154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36485770-G-C

140180260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36485867-C-G

140180439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36486070-C-T

http://identifiers.org/hco/5/GRCh38#140180564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36486187-C-A

140180649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36486246-A-G

http://identifiers.org/hco/5/GRCh38#140181102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36487190-C-A

140181348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36487368-C-T

140181375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36487397-T-G

140182007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36488533-A-T

140182029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36488556-G-A

140182115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36488641-T-C

140182291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36488803-A-G

140182519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36489041-G-A

140182632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36489149-T-A

140182643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36489160-A-T

140182857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36489336-A-G

140183218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36489679-C-G

140183711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36490374-A-T

140183874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36490511-G-C

140186600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492426-T-C

140186715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492535-T-A

140187178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492669-T-A

140187187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492672-C-G

140187187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492672-C-T

140187199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492684-G-C

140187199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492684-G-T

140187215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492699-A-G

140187215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492699-A-T

140187216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492700-T-A

140187327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492787-T-C

140187327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492787-T-G

140190356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36495662-G-A

140190754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36496217-G-A

140191183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36496633-A-G

140191269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36496714-G-A

140191301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36496744-G-A

http://identifiers.org/hco/5/GRCh38#140191638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36497044-A-C

140191698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36497109-G-C

140192279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36497869-T-G

140192365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36497941-A-G

140192455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36498033-G-A

140193070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36498547-A-G

http://identifiers.org/hco/5/GRCh38#140193656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36498813-C-A

http://identifiers.org/hco/5/GRCh38#140194034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36499180-C-A

140194034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36499180-C-T

140194214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36499357-A-G

http://identifiers.org/hco/5/GRCh38#140194464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36499585-C-A

140194464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36499585-C-T

http://identifiers.org/hco/5/GRCh38#140194488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36499609-C-A

140194489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36499610-A-G

140194545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36499666-G-T

140194661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36499803-C-T

http://identifiers.org/hco/5/GRCh38#140194775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36499914-C-A

140194782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36499924-A-G

140194940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36500069-G-A

140194996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36500108-G-C

140195228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36500302-T-C

140195275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36500343-G-A

140195371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36500435-A-G

140196999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36500699-G-A

140197394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36501058-G-A

140197395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36501059-T-G

140197593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36501222-G-A

140197740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36501368-C-T

http://identifiers.org/hco/5/GRCh38#140198150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36502133-C-A

140198150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36502133-C-G

140201451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36502870-C-T

140201540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36502953-C-T

140201754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36503135-G-T

140201778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36503153-T-C

http://identifiers.org/hco/5/GRCh38#140201786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36503161-C-A

140201786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36503161-C-T

140201872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36503228-A-G

140202428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36503449-A-G

140202658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36503812-A-G

140202658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36503812-A-T

140202854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36504025-T-C

140203018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36504319-G-T

140203989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36505540-G-A

140204500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36505858-T-C

140204534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36505880-A-G

140204574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36505918-C-T

140204797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36506382-G-A

http://identifiers.org/hco/5/GRCh38#140204927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36506500-C-A

140204996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36506561-C-T

140204997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36506562-G-A

140205054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36506615-G-A

140205137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36506695-T-A

140205254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36506779-G-C

140205268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36506793-G-A

140205541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507119-A-T

140205542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507120-C-T

http://identifiers.org/hco/5/GRCh38#140206250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36507846-A-C

140206256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507852-G-A

140206310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507904-C-T

140207261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36509360-A-T

140207305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36509404-A-G

140207386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36509477-G-A

140207396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36509485-C-T

140207628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36509571-G-C

140207628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36509571-G-T

140210164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36510666-C-T

140210243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36510728-G-T

140210260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36510745-T-C

140210261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36510746-A-G

140210297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36510776-C-T

140210319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36510794-T-C

140210338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36510814-A-G

140210447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36510902-T-C

140210468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36510922-C-T

140210734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36511029-G-A

140210826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36511102-A-T

http://identifiers.org/hco/5/GRCh38#140210834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36511110-C-A

140211180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36511469-A-G

http://identifiers.org/hco/5/GRCh38#140211238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36511530-A-C

140211255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36511543-G-T

140211263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36511549-G-C

140214174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36512826-C-T

140214640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36513204-G-A

140215018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36513589-T-C

140215062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36513633-G-A

140215255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36513789-G-C

140215412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36513927-G-A

140215412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36513927-G-C

140215461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36513973-T-C

140217619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36514941-G-A

140217777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36515300-A-G

140218034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36515658-C-T

140218357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36515948-A-G

140218520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36516071-A-G

140218681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36516226-C-T

http://identifiers.org/hco/5/GRCh38#140218928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36516462-C-A

140218973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36516521-A-G

140219423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36516932-G-A

140219423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36516932-G-C

140219504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517011-C-T

140219722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517222-G-A

140219814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517315-A-G

140219892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517389-C-T

140220015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517514-C-T

140220784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517977-G-T

140220838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518027-G-A

140220838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518027-G-T

140221013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518154-G-A

140221296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518316-C-T

140221358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518355-G-A

140221380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518375-C-T

140221670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518664-T-C

140221682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518675-T-C

140222448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36519364-A-G

140222448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36519364-A-T

140223377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36519963-C-T

140223797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36520296-C-T

140223889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36520392-G-A

140225384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36520539-G-C

140227036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36524325-C-T

140227492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525191-G-A

140227503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525202-T-C

140227545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525242-G-A

140227635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525339-G-A

140227732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525382-G-A

140227887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525560-C-G

140227957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525617-G-T

140228081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525746-C-T

140228365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525948-C-T

http://identifiers.org/hco/5/GRCh38#140228596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36526137-C-A

140228596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526137-C-T

140228669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526197-C-T

http://identifiers.org/hco/5/GRCh38#140228672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36526200-C-A

140228673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526201-A-G

http://identifiers.org/hco/5/GRCh38#140228719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36526243-C-A

140229397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526873-A-G

140235793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36529122-A-G

140235812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36529142-G-A

140236754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36529875-G-A

140237651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36531655-G-A

140237909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36531915-G-A

140237978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36531972-C-G

140238160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36532160-G-A

140238795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36532644-G-A

140238990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36532803-G-C

140239013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36532826-C-G

http://identifiers.org/hco/5/GRCh38#140239081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36532856-C-A

140239366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533074-A-G

140239368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533076-G-A

140239442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533137-G-T

140239845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533488-A-G

140239901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533571-C-T

140239935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533607-G-A

140240584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533953-G-A

140240771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534149-C-T

140240780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534158-G-A

140240780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534158-G-T

140240870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534244-A-G

140241242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534486-C-T

140242981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535264-G-C

140242981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535264-G-T

140242984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535267-G-T

140243148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535410-C-T

140243193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535447-T-A

http://identifiers.org/hco/5/GRCh38#140243195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36535449-C-A

140243195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535449-C-T

http://identifiers.org/hco/5/GRCh38#140243198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36535452-A-C

140243198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535452-A-T

140243213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535462-G-T

http://identifiers.org/hco/5/GRCh38#140243267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36535512-C-A

140243267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535512-C-G

140243267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535512-C-T

140243282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535527-C-T

http://identifiers.org/hco/5/GRCh38#140243480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36535726-C-A

140243480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36535726-C-G

140243480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36535726-C-T

140243503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36535746-T-G

140243540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36535783-A-G

140243627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36535871-T-A

140243824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36536062-C-T

140243829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36536067-T-C

http://identifiers.org/hco/5/GRCh38#140243859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36536100-C-A

140243859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36536100-C-T

140244006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36536209-G-A

140244606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36536399-C-T

140244634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 36536427-G-A

140244634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 36536427-G-T

140244641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36536434-G-T

http://identifiers.org/hco/5/GRCh38#140244647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#36536440-C-A

140244647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36536440-C-T

140245132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36536795-T-C

140245177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36536837-T-G

140245214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36536858-T-C

http://identifiers.org/hco/5/GRCh38#140245270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36536890-C-A

140245271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36536891-T-G

140245301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36536914-G-A

140245301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36536914-G-T

http://identifiers.org/hco/5/GRCh38#140245461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36537050-C-A

http://identifiers.org/hco/5/GRCh38#140245660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36537164-C-A

http://identifiers.org/hco/5/GRCh38#140245739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36537248-C-A

140245739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36537248-C-T

http://identifiers.org/hco/5/GRCh38#140245751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36537260-C-A

140245751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36537260-C-T

140245853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36537344-T-C

http://identifiers.org/hco/5/GRCh38#140245918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36537376-C-A

140245918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36537376-C-T

140246031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36537487-G-A

140246031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36537487-G-T

http://identifiers.org/hco/5/GRCh38#140246049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36537505-C-A

140246049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36537505-C-T

140246091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537543-A-G

140246150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537591-T-A

140246150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537591-T-C

140246153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537594-G-A

140246153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537594-G-T

140246176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537614-T-C

140246176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537614-T-G

140246231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537670-T-C

140246388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537776-G-A

140248634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36539107-C-T

140248852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

140250657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36541542-A-G

140250705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36541596-T-G

140250777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36541665-T-C

140251695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36542101-T-G

140252551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36542904-C-T

http://identifiers.org/hco/5/GRCh38#140252706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36543652-C-A

140252858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36543788-G-A

140252928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36543851-C-T

140253041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36543924-C-T

140253399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544197-A-G

140253508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544272-A-G

140253561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544320-G-A

140253809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544451-C-T

140254245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544786-G-A

140254437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544916-T-A

140254437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544916-T-C

140254514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544971-A-G

140254527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544983-T-C

140254800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36545154-T-C

140254874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36545213-C-T

http://identifiers.org/hco/5/GRCh38#140255219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36545525-C-A

140255219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36545525-C-T

140255323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36545612-A-G

http://identifiers.org/hco/5/GRCh38#140261324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36549533-C-A

140261648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36549842-C-T

140261797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36549986-C-T

140261889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550061-G-C

140262032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550202-T-C

140262282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550443-C-T

140262303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550455-T-C

140262459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550686-C-T

140262900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

140263115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

140263117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/5/GRCh38#140263361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

140263377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

140263482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

140264415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552503-T-C

140267901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36554565-G-T

140267927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36554589-C-T

140268682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36555645-G-A

140268797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36555773-T-C

140268931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36556050-C-T

140268932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36556051-A-G

140270066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36556126-G-C

140270217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36556457-C-T

140270651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36556879-C-T

140273381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36559162-G-A

140273853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36559511-T-C

140273889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36559547-C-G

140280565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36564095-G-A

140280703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36564233-T-A

140280980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36564525-T-C

140281049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36564591-C-T

http://identifiers.org/hco/5/GRCh38#140281090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36564631-C-A

140281090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36564631-C-G

140281090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36564631-C-T

http://identifiers.org/hco/5/GRCh38#140281137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36564696-C-A

140281137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36564696-C-T

140281264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565019-T-G

140281268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565023-G-C

140281268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565023-G-T

140281302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565212-G-T

140281313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565223-G-A

140281313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565223-G-C

140281313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565223-G-T

140281700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565541-G-A

140281700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565541-G-T