70902010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88868539-C-T

http://identifiers.org/hco/4/GRCh38#70902070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88868601-A-C

70902263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, undefined
orthologous variants: 88868722-G-A

http://identifiers.org/hco/4/GRCh38#70902293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88868755-C-A

70902293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, undefined
orthologous variants: 88868755-C-G

70902293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, undefined
orthologous variants: 88868755-C-T

70902297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, undefined
orthologous variants: 88868759-G-A

70902297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, undefined
orthologous variants: 88868759-G-T

70902322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, undefined
orthologous variants: 88868778-G-T

70902387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88868845-G-A

70902387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88868845-G-T

70902405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88868863-G-A

70902405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88868863-G-C

70902405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88868863-G-T

70902431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88868888-C-G

70902431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88868888-C-T

70902438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88868895-T-C

70902578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88869002-G-A

70902578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88869002-G-C

70902578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88869002-G-T

70902583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88869007-G-A

70902583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88869007-G-T

70902626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869060-G-A

70902626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869060-G-C

70902626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869060-G-T

70902628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869062-C-T

http://identifiers.org/hco/4/GRCh38#70902632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88869066-C-A

70902632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869066-C-G

70902632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869066-C-T

http://identifiers.org/hco/4/GRCh38#70902638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88869073-C-A

70902638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869073-C-G

70902638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869073-C-T

70902694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869117-C-G

70902694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869117-C-T

70902732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88869137-C-T

70902881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88870235-T-G

70902894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88870248-C-T

70903030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88870379-T-C

70903307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88870596-A-G

70903534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88870787-G-T

70903969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88871190-T-C

70905007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88871555-C-T

70906741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872519-G-A

70906860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872614-G-A

70906860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872614-G-C

70906860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872614-G-T

70906965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872712-C-T

70907033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872766-A-T

70908457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88873265-T-C

70914817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88879781-C-T

70914884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88879852-G-C

70914890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88879859-T-C

70924053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88880677-G-A

70926616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88881859-G-T

70948811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88885609-A-G

70948835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88885633-T-C

70951086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88886479-C-T

70951293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88886718-C-T

http://identifiers.org/hco/4/GRCh38#70957129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88890255-C-A

70957129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890255-C-T

70958488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890682-G-T

70958673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890891-G-T

70958744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890968-G-A

70958744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890968-G-T

70958748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890972-A-G

70958755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890979-A-G

70958755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890979-A-T

http://identifiers.org/hco/4/GRCh38#70958766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88890993-A-C

70958766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890993-A-G

70958807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891037-G-A

70958807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891037-G-T

70958991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88891280-T-C

70959015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88891304-T-G

70959067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891355-G-A

70959109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891397-G-C

70960707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891685-A-G

70960722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891700-C-T

70969494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88892519-T-C

70969552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88892573-C-T

70970199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88893286-C-T

70970388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88893457-C-G

70970388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88893457-C-T

70970923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88894173-T-C

70970996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88894223-C-T

70971027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88894255-G-A

70973277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88895463-A-G

70974543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88896708-T-C

70974576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88896733-G-A

http://identifiers.org/hco/4/GRCh38#70975005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88897268-C-A

70975005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897268-C-G

70975005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897268-C-T

70975020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897282-T-A

70975020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897282-T-C

70975044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897306-G-T

70975065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897327-G-A

70975065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897327-G-C

70975065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897327-G-T

http://identifiers.org/hco/4/GRCh38#70975068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88897330-C-A

70975110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897346-G-A

70975110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897346-G-T

70975293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88897524-T-C

70975355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88897587-C-G

70975366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88897598-A-G

http://identifiers.org/hco/4/GRCh38#70975559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88897767-A-C

http://identifiers.org/hco/4/GRCh38#70975566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88897774-C-A

70975566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88897774-C-T

70975741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88898574-T-C

70976399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88899207-C-G

70976399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88899207-C-T

70976470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88899277-T-G

70978829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88900754-G-T

70978854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88900778-T-G

70979309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901200-G-A

70979309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901200-G-T

http://identifiers.org/hco/4/GRCh38#70979359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88901253-C-A

70979359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901253-C-T

70979644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901786-G-T

70980116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88902341-T-C

70980747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88902888-G-C

70980985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88903128-A-G

70981041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88903184-C-T

70982223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88904186-A-G

70982246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88904208-A-G

http://identifiers.org/hco/4/GRCh38#70982278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88904239-C-A

70982341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88904339-A-G

70983155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88905221-G-T

70983306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88905360-T-C

70983468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88905513-A-G

http://identifiers.org/hco/4/GRCh38#70984017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88906051-C-A

70984037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88906069-A-G

http://identifiers.org/hco/4/GRCh38#70984238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88906280-C-A

70984273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88906353-A-G

70984562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88906867-G-A

http://identifiers.org/hco/4/GRCh38#70984566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88906871-C-A

http://identifiers.org/hco/4/GRCh38#70984768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88907077-A-C

70984843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88907154-G-T

70984844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88907155-A-G

70984898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88907204-T-C

70984925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88907232-G-A

http://identifiers.org/hco/4/GRCh38#70985310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88907603-C-A

70986224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88908134-A-G

70986375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88908281-G-T

70986557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88908462-C-T

70986709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88908561-T-C

70986906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88908741-T-C

http://identifiers.org/hco/4/GRCh38#70986989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88908863-C-A

70987091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88908978-C-T

70987409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88909200-G-C

70987446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88909236-A-G

70987729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88909498-G-T

70987764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88909532-T-C

70987765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88909533-G-T

70987836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88909603-T-C

70987914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88909676-A-G

70988256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88910001-T-C

70988351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88910102-C-G

70988351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88910102-C-T

70992698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912149-T-C

70992739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912191-G-A

70992741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912193-C-G

70992774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912215-A-G

70992802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912246-A-G

70992986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912399-G-A

http://identifiers.org/hco/4/GRCh38#70992987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88912400-C-A

70992987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912400-C-T

http://identifiers.org/hco/4/GRCh38#70993043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88912444-C-A

70993053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88912454-C-T

70993074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88912483-G-A

70993074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88912483-G-T

70993328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912692-C-T

70993331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912695-A-G

70993365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912724-T-C

70993372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912732-G-A

70993372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912732-G-T

http://identifiers.org/hco/4/GRCh38#70993376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88912736-A-C

70993376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912736-A-T

70993385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912747-G-A

70993385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912747-G-T

70993392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912754-T-A

70993392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912754-T-C

70993409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912777-T-C

http://identifiers.org/hco/4/GRCh38#70993454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88912802-C-A

70993458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912806-T-C

70993468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912816-T-C

70993481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912828-G-A

70993481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912828-G-C

70993542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912877-T-C

70993543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912878-G-A

70993543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912878-G-C

70993543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912878-G-T

70993556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912891-C-T

70993561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912896-G-T

70993565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912900-G-A

70993565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912900-G-C

http://identifiers.org/hco/4/GRCh38#70993602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88912937-C-A

70993602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912937-C-T

70993725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 88913045-C-G

http://identifiers.org/hco/4/GRCh38#70993913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88913192-C-A

70993913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 88913192-C-T

70993987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88913248-T-A

http://identifiers.org/hco/4/GRCh38#70994001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88913250-C-A

70994009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88913258-A-G

http://identifiers.org/hco/4/GRCh38#70994141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88913299-C-A

70994176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88913331-C-T

70994312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88913433-C-G

70994486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88913606-C-T

70994520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88913636-A-T

70994792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88914031-T-G

70994929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88914165-A-G

70995090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88914311-T-C

70995179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88914379-T-C

70995179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88914379-T-G

70996560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88914884-G-A

70996637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88914955-T-C

70996953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88915413-T-C

70997030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88915486-T-C

70997227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88915653-C-G

70997274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88915679-T-C

70997330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88915729-A-G

70997388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88915784-T-C

70997460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88915862-C-T

70997494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88915907-G-A

70997613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88916096-C-T

70997674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88916156-A-G

70997677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88916159-T-C

70997959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88917356-G-T

70997972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88917366-G-T

70997976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88917370-G-T

70998017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88917412-T-C

70998125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 88917521-G-C

http://identifiers.org/hco/4/GRCh38#70998188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88917584-A-C

70998188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88917584-A-G

http://identifiers.org/hco/4/GRCh38#71006223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88918114-C-A

71006223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88918114-C-T

71006246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88918142-G-A

71006246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88918142-G-T

http://identifiers.org/hco/4/GRCh38#71006256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88918152-C-A

71006256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88918152-C-T

http://identifiers.org/hco/4/GRCh38#71006265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88918161-C-A

71006265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88918161-C-G

71006265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88918161-C-T

71006330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88918218-G-A

71006342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88918230-A-G

71006345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88918233-T-C

71022307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88920427-T-G

http://identifiers.org/hco/4/GRCh38#71022315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88920435-C-A

71022315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88920435-C-T

71022390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88920512-T-A

71022390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 88920512-T-C

71022390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88920512-T-G

71022396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 88920518-G-A

71022396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 88920518-G-C

71022396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29801
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 88920518-G-T