47608198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782743-G-A

47608198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782743-G-T

http://identifiers.org/hco/19/GRCh38#47608218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15782720-C-A

47608218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782720-C-T

47608237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782701-G-A

47608433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782543-T-C

47608489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782486-G-A

47608489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782486-G-T

47608508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782477-G-A

47608557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782435-T-C

47608564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782428-G-A

47608564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15782428-G-T

47608814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15782179-T-C

47608915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15782089-T-G

47609083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15781904-C-T

47609402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15781563-G-C

47609402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15781563-G-T

http://identifiers.org/hco/19/GRCh38#47609478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15781486-C-A

47609478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15781486-C-T

47609557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15781414-T-C

47609634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15781332-C-T

47609993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15780981-T-C

http://identifiers.org/hco/19/GRCh38#47610041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15780932-A-C

47610122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15780850-C-T

47610420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15780525-C-T

47610489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15780455-C-T

47611093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15779949-G-A

47611093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15779949-G-T

47612961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15779091-T-G

47613157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15778864-C-T

47613411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15778622-G-A

http://identifiers.org/hco/19/GRCh38#47613413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15778620-A-C

47613482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15778544-G-C

47613482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15778544-G-T

http://identifiers.org/hco/19/GRCh38#47613589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15778478-C-A

47613589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15778478-C-T

47613665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15778398-G-A

47613667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15778396-T-C

47613759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15778330-C-T

47614014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15778081-G-T

47617701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15774900-C-T

47617775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15774843-A-T

47618103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15774523-G-C

47618103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15774523-G-T

47618300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15773626-C-T

47618472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15773460-A-G

47618736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15773223-G-A

47618762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15773197-G-A

http://identifiers.org/hco/19/GRCh38#47621417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15770098-A-C

47621457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15770058-T-A

47625631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15766906-C-G

http://identifiers.org/hco/19/GRCh38#47625669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15766886-A-C

47631992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15762925-A-G

47632287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15762628-T-A

47634139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15761629-G-A

47634139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15761629-G-T

47634216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15761588-G-A

47634249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15761555-C-T

47670293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733566-T-A

47670307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733552-T-A

47670307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733552-T-C

http://identifiers.org/hco/19/GRCh38#47670309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15733550-C-A

47670309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733550-C-T

http://identifiers.org/hco/19/GRCh38#47670342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15733517-C-A

47670342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733517-C-T

47670344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733515-T-C

47670361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733496-A-G

47670388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733471-T-C

47670400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733459-G-A

47670400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733459-G-T

47670512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 15733349-C-T

47670532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 15733329-G-A

47670532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 15733329-G-C

http://identifiers.org/hco/19/GRCh38#47670558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15733303-C-A

47670558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733303-C-T

47670666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733219-G-A

47670666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15733219-G-T

47671425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15732293-G-A

47672280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15732148-G-A

47672396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15732023-G-A

47672579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15731802-G-A

47672670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15731715-G-A

47672689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15731698-G-A

47673033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15731338-A-G

47673276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15730853-G-T

47673472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15730628-A-G

47673472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15730628-A-T

http://identifiers.org/hco/19/GRCh38#47673480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15730619-C-A

47673480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15730619-C-T

47673483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15730608-G-A

47673485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15730606-G-A

http://identifiers.org/hco/19/GRCh38#47673557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15730532-C-A

47673622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 15730467-A-G

http://identifiers.org/hco/19/GRCh38#47673632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15730457-C-A

47673632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15730457-C-T

http://identifiers.org/hco/19/GRCh38#47673653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15730432-A-C

http://identifiers.org/hco/19/GRCh38#47673695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15730391-A-C

47673813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15730273-T-A

47673813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15730273-T-G

47673822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15730264-G-A

http://identifiers.org/hco/19/GRCh38#47675573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15727325-C-A

47675573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15727325-C-G

47675708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15727194-A-G

47675946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15726974-G-A

47675946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15726974-G-T

47675970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15726957-G-A

http://identifiers.org/hco/19/GRCh38#47679266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15723417-A-C

47679266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 15723417-A-G

47679289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 15723394-G-A

47679289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 15723394-G-T

47679327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 15723357-G-A

47679327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 15723357-G-C

47679327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 15723357-G-T

47679381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 15723303-A-G

47679455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 15723229-G-T

47679657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 15723027-A-G

47679987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722697-G-A

47679987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722697-G-T

47680053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722631-G-A

47680053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722631-G-C

47680053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722631-G-T

47680083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722601-T-C

47680374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722307-G-A

47680374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722307-G-T

47680413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722268-C-T

47680488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722193-C-G

47680488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722193-C-T

47680534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15722147-G-A

47680604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15722077-G-A

47680604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15722077-G-C

47680604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15722077-G-T

47680785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15721893-G-A

http://identifiers.org/hco/19/GRCh38#47680869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15721809-C-A

47680869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15721809-C-T

47680923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15721755-G-A

47680923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15721755-G-C

47680923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15721755-G-T

http://identifiers.org/hco/19/GRCh38#47680936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15721742-C-A

47680936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15721742-C-G

47680936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15721742-C-T

47681184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15721494-T-C

47681213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15721465-G-A

47681213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15721465-G-T

http://identifiers.org/hco/19/GRCh38#47681214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15721464-C-A

47681214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15721464-C-T

47681325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721382-G-A

47681325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721382-G-T

47681331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721376-G-A

47681424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721328-A-T

47681630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721236-G-A

47681643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721225-C-T

47681738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721174-G-C

http://identifiers.org/hco/19/GRCh38#47681828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15721125-C-A

47681828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721125-C-T

47681834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721119-T-A

47681851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721107-G-A

47681851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721107-G-T

47681900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15721083-G-T

47681970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 15721018-T-A

47681970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 15721018-T-C

47682298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15720708-T-A

47682342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15720664-A-G

47682442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15720549-T-C

47683277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15719656-C-T

47692645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15715668-G-A

47692645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15715668-G-C

47692657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15715656-G-A

http://identifiers.org/hco/19/GRCh38#47692682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15715631-C-A

47693356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714578-C-T

http://identifiers.org/hco/19/GRCh38#47693360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15714574-C-A

47693364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714570-C-T

47693368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714566-T-C

47693372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714562-C-T

47693392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714542-C-T

47693791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714243-C-T

47693934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714111-T-A

47693934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714111-T-C

47693934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714111-T-G

47693979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714067-T-C

47694009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714033-G-C

47694009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15714033-G-T

47694033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15713988-G-T

http://identifiers.org/hco/19/GRCh38#47694054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15713967-A-C

47694255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15713745-G-A

http://identifiers.org/hco/19/GRCh38#47694340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15713660-A-C

47694340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15713660-A-G

47694340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15713660-A-T

http://identifiers.org/hco/19/GRCh38#47694393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15713607-C-A

47694393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15713607-C-G

47694393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15713607-C-T

http://identifiers.org/hco/19/GRCh38#47694462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15713538-C-A

47694462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15713538-C-G

47694462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15713538-C-T

47694494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15713506-T-C

47694515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15713485-C-T

http://identifiers.org/hco/19/GRCh38#47694530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15713470-C-A

47694622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15713378-G-A

http://identifiers.org/hco/19/GRCh38#47694686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15713314-C-A

47694686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15713314-C-T

47694770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15713220-T-A

47694770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15713220-T-C

47694770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15713220-T-G

http://identifiers.org/hco/19/GRCh38#47694775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15713215-C-A

47694775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15713215-C-G

47694775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15713215-C-T

47694864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15713151-T-C

47694938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15713080-G-A

47694938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 15713080-G-T

http://identifiers.org/hco/19/GRCh38#47695059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15712959-C-A

47695257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15712822-G-A

47695276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15712803-G-A

47695276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15712803-G-C

47695276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15712803-G-T

47695292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15712788-G-A

47695292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15712788-G-T

47695434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15712652-A-G

http://identifiers.org/hco/19/GRCh38#47695549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15712541-C-A

47695549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15712541-C-G

47695549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15712541-C-T

47696376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15711118-G-T

47696407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15711082-G-A

47696423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15711066-G-T

47698362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709972-A-T

47698447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709894-C-G

47698537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709821-G-T

47698543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709814-G-A

47698543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709814-G-T

http://identifiers.org/hco/19/GRCh38#47698544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15709813-C-A

47698544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709813-C-T

47698546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709811-T-C

http://identifiers.org/hco/19/GRCh38#47698565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15709793-A-C

http://identifiers.org/hco/19/GRCh38#47698597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15709765-C-A

47698597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709765-C-G

47698597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709765-C-T

http://identifiers.org/hco/19/GRCh38#47698677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15709693-C-A

47698677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15709693-C-G

47698689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15709681-A-T

47698710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15709660-G-A

47698819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709552-G-A

47698819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709552-G-T

47698852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709497-G-C

47698852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709497-G-T

47698867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709476-T-G

47698875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709468-G-A

47698875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709468-G-T

http://identifiers.org/hco/19/GRCh38#47698893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15709450-C-A

47698893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709450-C-T

47698900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709443-T-A

47698900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709443-T-C

47698903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709440-T-A

47698906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709437-C-T

47698908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709435-G-A

47698908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709435-G-T

http://identifiers.org/hco/19/GRCh38#47698914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15709429-C-A

47698914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709429-C-T

http://identifiers.org/hco/19/GRCh38#47698929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15709415-A-C

47698929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709415-A-G

47698929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709415-A-T

http://identifiers.org/hco/19/GRCh38#47698957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15709390-C-A

47698957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 15709390-C-G

47699103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709255-T-G

http://identifiers.org/hco/19/GRCh38#47699114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15709245-C-A

47699114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709245-C-T

47699135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709236-G-A

47699135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709236-G-C

47699135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709236-G-T

47699222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709177-T-C

47699228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709171-G-A

47699228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709171-G-C

47699228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709171-G-T

http://identifiers.org/hco/19/GRCh38#47699238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15709161-C-A

47699238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709161-C-T

47699289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15709122-T-C

47699315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15709096-T-A

47699315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 15709096-T-C

47699437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15708987-G-A

47699437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15708987-G-C

47699437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15708987-G-T

http://identifiers.org/hco/19/GRCh38#47699449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15708975-C-A

47699449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15708975-C-G

47699458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15708966-T-C

47699484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15708863-G-T

47699494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15708853-G-A

47699494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, undefined
orthologous variants: 15708853-G-T

http://identifiers.org/hco/19/GRCh38#47701220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15706903-A-C

47701384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706756-G-A

47701384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706756-G-C

47701384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706756-G-T

47701555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706573-T-C

47701561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706567-G-A

47701561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706567-G-T

47701570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706558-T-A

47701651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706477-G-A

47701651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706477-G-C

47701651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706477-G-T

47701678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706450-G-C

47701678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706450-G-T

http://identifiers.org/hco/19/GRCh38#47701735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15706393-C-A

http://identifiers.org/hco/19/GRCh38#47701783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15706345-C-A

47701783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706345-C-G

47701783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706345-C-T

http://identifiers.org/hco/19/GRCh38#47701946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15706174-C-A

47701946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706174-C-T

http://identifiers.org/hco/19/GRCh38#47702019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15706109-C-A

47702019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15706109-C-G

47702019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 15706109-C-T

http://identifiers.org/hco/19/GRCh38#47702026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15706102-C-A

47702026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 15706102-C-T

http://identifiers.org/hco/19/GRCh38#47702152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15705967-C-A

47702152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705967-C-T

http://identifiers.org/hco/19/GRCh38#47702417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15705699-A-C

47702417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705699-A-G

47702417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705699-A-T

47702472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705637-G-C

47702472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705637-G-T

http://identifiers.org/hco/19/GRCh38#47702486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15705623-C-A

47702486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705623-C-T

47702592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705525-G-A

47702592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705525-G-T

47702630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705474-A-G

47702863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705072-G-A

47702863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705072-G-T

47702865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705070-C-T

http://identifiers.org/hco/19/GRCh38#47702909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15705026-C-A

47702909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705026-C-T

http://identifiers.org/hco/19/GRCh38#47702920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15705010-C-A

47702920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15705010-C-T

http://identifiers.org/hco/19/GRCh38#47702960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15704912-C-A

http://identifiers.org/hco/19/GRCh38#47702970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15704897-A-C

47702970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15704897-A-G

47702970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15704897-A-T

47702987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15704880-T-A

http://identifiers.org/hco/19/GRCh38#47702995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15704872-A-C

47702995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15704872-A-T

47703009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15704852-T-C

http://identifiers.org/hco/19/GRCh38#47703011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15704850-C-A

47703011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15704850-C-T

http://identifiers.org/hco/19/GRCh38#47703014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15704847-A-C

47703014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15704847-A-G

http://identifiers.org/hco/19/GRCh38#47703017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15704844-C-A

47703017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15704844-C-T

http://identifiers.org/hco/19/GRCh38#47703020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#15704841-A-C

47703020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4332
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15704841-A-T