120760283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129123074-G-C

http://identifiers.org/hco/10/GRCh38#120760450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129123231-A-C

120760631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129123419-A-G

120760722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129123499-C-T

120760760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129123525-G-A

120760774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129123539-A-G

120761083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129123857-C-T

120761179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129123929-T-A

120761242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129123986-A-G

120761335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129124066-A-G

120761630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129124349-T-A

http://identifiers.org/hco/10/GRCh38#120761715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129124443-C-A

120761715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129124443-C-T

120761761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129124512-G-A

120761761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129124512-G-C

120761901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129124731-A-T

120762029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129124859-G-T

120762116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129124909-T-C

http://identifiers.org/hco/10/GRCh38#120762123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129124915-C-A

120762285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129125034-G-A

120762319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129125069-T-C

http://identifiers.org/hco/10/GRCh38#120765462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129126308-C-A

120765464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129126310-C-T

http://identifiers.org/hco/10/GRCh38#120765543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129126389-A-C

120765746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129126582-C-G

120766432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129127237-C-T

120766444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129127249-T-C

120766499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129127293-G-C

120766638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129127894-C-T

120766708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129127958-T-G

120766832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128086-T-C

120766912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128179-A-G

120766984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128226-G-C

120767465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128634-C-G

120767579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128750-A-G

120768088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128921-T-C

http://identifiers.org/hco/10/GRCh38#120768239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129129040-A-C

120768299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129088-A-G

120768416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129332-G-T

120768592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129841-G-A

120768684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129907-C-T

120768747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129959-G-A

120768850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130041-C-T

120768914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130099-G-A

120768963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130151-G-A

120769063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130264-A-G

120769087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130288-G-A

http://identifiers.org/hco/10/GRCh38#120769251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129130434-C-A

120769268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130452-C-T

120769269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130453-A-T

http://identifiers.org/hco/10/GRCh38#120774878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129131637-C-A

120774967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129131725-G-C

120775813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129134312-G-T

120775829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129134342-T-C

http://identifiers.org/hco/10/GRCh38#120775898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129134390-A-C

120775898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129134390-A-G

http://identifiers.org/hco/10/GRCh38#120776057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129134522-C-A

120776161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129134624-A-G

120776193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129134652-T-C

http://identifiers.org/hco/10/GRCh38#120776347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129134997-A-C

120776348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129134998-A-G

120776390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129135043-C-T

120776426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129135078-G-A

120776471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129135122-A-G

120776604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129135255-T-C

http://identifiers.org/hco/10/GRCh38#120776765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129135415-C-A

120776765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129135415-C-T

120776869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129135515-G-T

http://identifiers.org/hco/10/GRCh38#120776885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129135526-C-A

120776969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129135612-G-A

120777747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129137146-A-G

http://identifiers.org/hco/10/GRCh38#120777939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129137345-A-C

120777939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129137345-A-G

120778087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129137491-T-A

http://identifiers.org/hco/10/GRCh38#120778089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129137493-C-A

120778403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129138425-G-A

120778406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129138428-G-A

120778826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129138795-T-G

120778838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129138807-G-A

120779243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129139592-A-G

120779310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129139637-C-T

120779404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129139963-C-T

120779477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129140039-T-C

120780109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129140374-C-T

http://identifiers.org/hco/10/GRCh38#120780411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129140655-C-A

120780552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129140797-T-G

120780746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141036-C-T

http://identifiers.org/hco/10/GRCh38#120780830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129141116-C-A

120780887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141164-C-T

120780944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141225-A-G

120780945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141226-C-T

120781065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141360-G-A

120781075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141370-G-A

120781183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141472-C-T

120781220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141510-C-T

120781458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141725-G-A

120781546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141799-G-A

120781546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129141799-G-C

120782438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129142308-T-A

http://identifiers.org/hco/10/GRCh38#120782895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129142675-C-A

120782975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129142744-T-C

120783071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129142858-A-G

120783119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129142906-T-G

120783261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129143223-G-A

120783264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129143226-T-C

120783313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129143275-G-A

http://identifiers.org/hco/10/GRCh38#120783665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129143768-C-A

120784074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129144246-C-T

120784113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129144276-C-T

120784156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129144314-C-T

120784236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129144384-A-G

120784236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129144384-A-T

120786330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145382-T-C

120786422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145459-G-A

http://identifiers.org/hco/10/GRCh38#120786433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129145470-A-C

120786443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145480-A-G

120786508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145543-G-A

120786593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145628-C-T

http://identifiers.org/hco/10/GRCh38#120786665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129145685-C-A

http://identifiers.org/hco/10/GRCh38#120786790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129145783-C-A

120786885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145847-A-T

120787011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129145977-T-C

http://identifiers.org/hco/10/GRCh38#120787189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129146152-A-C

120787203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129146166-T-A

120787246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129146214-T-A

120787269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129146235-T-A

http://identifiers.org/hco/10/GRCh38#120787403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129146383-C-A

120787403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129146383-C-T

http://identifiers.org/hco/10/GRCh38#120787476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129146451-A-C

120787588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129146535-C-T

120787604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129146551-G-A

http://identifiers.org/hco/10/GRCh38#120788322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129147237-A-C

120788322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129147237-A-G

120788411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129147340-G-C

120788474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129147403-C-T

120788750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129147672-A-T

http://identifiers.org/hco/10/GRCh38#120789002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129147903-A-C

120789011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129147912-C-T

120789667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129148456-T-G

120789749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129148537-G-C

120790234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129149839-T-A

120790482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129150088-G-T

120790483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129150089-G-A

120790538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129150167-A-G

120790642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129150267-G-A

120790840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129150449-G-A

120791239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129150883-T-C

120791289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129150920-G-T

120791333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129150966-G-T

120791356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129150989-G-A

120791356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129150989-G-C

120793698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129152031-G-T

120793809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129152141-C-T

http://identifiers.org/hco/10/GRCh38#120793852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129152183-C-A

120794011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129152337-C-T

120797092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129154347-A-T

120797099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129154354-G-C

http://identifiers.org/hco/10/GRCh38#120797127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129154386-A-C

http://identifiers.org/hco/10/GRCh38#120797232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129154498-A-C

http://identifiers.org/hco/10/GRCh38#120797322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129154614-A-C

http://identifiers.org/hco/10/GRCh38#120802964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129155545-A-C

120802964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129155545-A-G

120803582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129155918-G-A

120803605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129155942-T-C

120804011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129156247-T-C

120804322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129156559-T-A

120804322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129156559-T-C

120804449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129156685-A-T

120804817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129157076-A-G

120807682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129158502-T-C

120807794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129158614-G-A

http://identifiers.org/hco/10/GRCh38#120807951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129158756-C-A

120808085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129158891-C-T

120808223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129159013-G-A

120808223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129159013-G-C

120808464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129159248-G-T

120808688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129160020-G-A

120808754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129160086-T-A

120808754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129160086-T-C

120809313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129160300-C-G

120809313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129160300-C-T

120809314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129160301-A-G

120809331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129160318-G-T

http://identifiers.org/hco/10/GRCh38#120809394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129160385-A-C

120809394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129160385-A-G

120809562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129160554-C-T

120809584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129160576-C-T

120810342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129168724-G-A

120810346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129168728-G-A

120810551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129168939-C-T

120810634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129169014-T-G

120810639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129169019-G-C

http://identifiers.org/hco/10/GRCh38#120810640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129169020-A-C

120810677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129169068-G-A

120810713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129169097-T-C

120811011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129169409-G-A

120811078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129169472-T-C

http://identifiers.org/hco/10/GRCh38#120811295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129169676-A-C

120811464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129169828-A-G

http://identifiers.org/hco/10/GRCh38#120811482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129169839-A-C

120811484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129169841-A-G

120811645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129169990-A-G

120811771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129170096-C-T

120811964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129170268-T-C

120812036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129170368-T-A

120812036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129170368-T-C

120812079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129170405-C-T

120812128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129170459-A-G

120812248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129170582-A-G

http://identifiers.org/hco/10/GRCh38#120812251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129170585-A-C

120812383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129170718-C-T

120812500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129170816-T-G

120812519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129170835-C-T

http://identifiers.org/hco/10/GRCh38#120812530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129170846-A-C

120812798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129171102-C-T

120812877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129171158-G-C

120812878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129171159-G-C

120815492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129173783-G-A

120815635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129173901-G-A

120815635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129173901-G-T

120815641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129173907-T-A

120815641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129173907-T-C

http://identifiers.org/hco/10/GRCh38#120815698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129173968-C-A

120819172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129176651-C-T

120819219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129176694-T-A

120819352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129176878-G-C

120819352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129176878-G-T

http://identifiers.org/hco/10/GRCh38#120819367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129176892-A-C

120819367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129176892-A-G

120819464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129176978-T-C

120819483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129176997-G-T

http://identifiers.org/hco/10/GRCh38#120819507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129177020-C-A

120819529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177032-A-G

120819673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177176-C-T

120819674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177177-A-G

120819675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177178-A-G

120819711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177217-A-G

120819800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177301-G-A

120819860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177360-T-C

120820237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177728-A-G

120820313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177821-T-C

120820350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177859-A-G

120820482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129177987-A-G

http://identifiers.org/hco/10/GRCh38#120820527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129178041-C-A

120820610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178113-T-A

120820640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178143-T-C

120820641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178144-G-A

120820641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178144-G-T

120820643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178146-T-C

120820644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178147-T-A

120820644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178147-T-C

http://identifiers.org/hco/10/GRCh38#120820651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129178154-C-A

120820803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178168-G-A

120820803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178168-G-T

http://identifiers.org/hco/10/GRCh38#120820818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129178183-C-A

120820818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178183-C-G

120820818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178183-C-T

120820820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178185-G-A

120820820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178185-G-T

120820825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178190-T-C

120820826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178191-G-A

120820826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178191-G-T

http://identifiers.org/hco/10/GRCh38#120820860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129178216-C-A

120820860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178216-C-T

http://identifiers.org/hco/10/GRCh38#120820899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129178255-C-A

120820899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178255-C-T

120820920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178299-C-T

120823077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178528-G-A

120823136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129178586-G-A

http://identifiers.org/hco/10/GRCh38#120823430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129178795-C-A

http://identifiers.org/hco/10/GRCh38#120824227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129179208-C-A

120824227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129179208-C-T

120824329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129179347-C-T

120824332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129179350-G-T

120824366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129179384-G-A

120824366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129179384-G-T

120824380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129179397-C-T

120824469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129179485-C-T

120824525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129179542-T-G

http://identifiers.org/hco/10/GRCh38#120824545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129179562-C-A

120824646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129179649-A-G

120824752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129179741-C-T

http://identifiers.org/hco/10/GRCh38#120824818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129179808-C-A

120824953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129179986-T-C

120825046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129180080-G-A

http://identifiers.org/hco/10/GRCh38#120825057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129180090-C-A

120825059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129180092-G-T

120825153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129180179-G-A

120825229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129180229-C-G

120825323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129180313-G-T

http://identifiers.org/hco/10/GRCh38#120825334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129180324-C-A

120826308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129183918-G-C

120826308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129183918-G-T

120826370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129183984-C-T

120826527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129184098-A-T

120826538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129184109-T-C

120832435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129185801-G-A

120832557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129185915-G-A

120832557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129185915-G-T

120832675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129186031-A-G

120832676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129186032-G-T

120832719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129186068-G-A

120832895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129186279-G-A

120832895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129186279-G-C

120833064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129186450-C-T

120833321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129186683-A-G

120833670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129187016-G-A

120833777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129187089-G-A

120835801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129187354-A-G

120835833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129187384-C-T

120835849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129187400-T-G

120835879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129187429-T-C

http://identifiers.org/hco/10/GRCh38#120836181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129188561-A-C

120836235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129188615-C-T

120836279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129188657-G-A

120836444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129188808-T-A

120836560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129188989-G-C

120840805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129191298-G-A

120850993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129193327-A-G

120850996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129193330-G-A

120850996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129193330-G-T

http://identifiers.org/hco/10/GRCh38#120851160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129193482-C-A

120851162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: non coding transcript exon variant
orthologous variants: 129193484-G-T

http://identifiers.org/hco/10/GRCh38#120851265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#129193571-C-A

120851265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: non coding transcript exon variant
orthologous variants: 129193571-C-T

120851274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: non coding transcript exon variant
orthologous variants: 129193579-G-A

120851365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 129193652-G-T

120851369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 129193656-C-T

120851405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 129193688-T-A

120851405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27437
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 129193688-T-C