http://identifiers.org/hco/4/GRCh38#108538202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130592320-C-A

http://identifiers.org/hco/4/GRCh38#108538215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130592301-C-A

108538215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130592301-C-T

http://identifiers.org/hco/4/GRCh38#108538238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130592278-A-C

108538275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130592243-A-G

108538362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130592193-G-T

http://identifiers.org/hco/4/GRCh38#108538365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130592190-C-A

108538365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130592190-C-T

http://identifiers.org/hco/4/GRCh38#108538705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130591727-C-A

108538706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591726-T-C

108538831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591478-G-T

108538858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591455-A-G

108538958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591358-T-C

108538965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591351-A-G

108539064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591267-G-T

108539147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591214-T-A

108539147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591214-T-C

108539199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591163-G-A

108539199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591163-G-T

108539384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130591008-T-C

108539407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130590986-T-C

108539490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130590915-T-C

http://identifiers.org/hco/4/GRCh38#108539562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130590843-A-C

http://identifiers.org/hco/4/GRCh38#108539573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130590832-C-A

108539573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130590832-C-T

108540738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130590405-G-T

108540751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130590392-T-C

108540764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130590380-G-A

108540791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130590354-G-C

108540791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130590354-G-T

http://identifiers.org/hco/4/GRCh38#108540855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130590311-C-A

108540855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130590311-C-T

108540880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130590285-C-T

http://identifiers.org/hco/4/GRCh38#108541025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130590153-A-C

108541025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130590153-A-G

108541222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130589951-G-T

108542075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130589835-G-A

108542102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130589807-G-T

108542115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130589798-C-T

108542126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130589787-T-C

108542186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130589728-A-G

108542273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130589649-G-T

108542294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130589633-T-C

108542318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130589609-T-C

108542377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130589562-C-G

108542390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130589549-A-G

108542427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130589512-G-A

108542427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130589512-G-T

http://identifiers.org/hco/4/GRCh38#108542546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130588683-C-A

108542603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130588649-T-A

108542683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130587826-T-C

108542819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130587676-T-A

108542875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130587608-G-C

108543467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130587362-C-G

108543471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130587358-T-C

108543511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130587318-G-A

108543694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130587170-C-T

108543763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130587099-A-T

http://identifiers.org/hco/4/GRCh38#108543998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130586924-A-C

108544034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130586889-T-C

108544058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130586865-G-A

108544720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130586526-A-G

108544893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130586352-G-A

108544920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130586325-T-C

108545093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130586182-A-G

108545112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130586157-G-A

108545127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130586142-A-G

http://identifiers.org/hco/4/GRCh38#108545179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130586094-A-C

108545339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130585530-G-T

108545349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130585520-G-C

108545371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130585498-T-C

108546563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130584876-G-A

108546570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130584869-A-T

108546594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130584845-T-C

108546645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130584803-C-T

108554854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130581842-C-G

http://identifiers.org/hco/4/GRCh38#108554971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130581751-C-A

108554971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130581751-C-T

108554985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130581737-C-G

108556608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130578727-A-G

108556608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130578727-A-T

108556621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130578714-A-T

108556625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130578710-A-G

http://identifiers.org/hco/4/GRCh38#108556644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130578696-C-A

108556644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130578696-C-T

108556836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130578532-T-C

108556850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130578518-T-C

108556928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130578442-G-A

108556928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130578442-G-T

108556979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non coding transcript exon variant
orthologous variants: 130578388-G-A

http://identifiers.org/hco/4/GRCh38#108557065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130578312-C-A

108557272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130577880-G-A

108557358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130577797-A-G

108557569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130577564-T-C

108557605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130577536-G-A

108557644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130577509-A-G

http://identifiers.org/hco/4/GRCh38#108557677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130577460-A-C

http://identifiers.org/hco/4/GRCh38#108557697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130577438-C-A

108557697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130577438-C-T

108557698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130577437-A-G

108557705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130577430-G-A

108558442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130577256-T-C

108558606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130577118-A-T

108558695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130577030-C-T

108558822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130576913-T-C

108558843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130576892-G-A

http://identifiers.org/hco/4/GRCh38#108558909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130576830-A-C

108558940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130576797-A-G

108559065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130576679-A-G

108559499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130576065-G-A

108559499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130576065-G-T

http://identifiers.org/hco/4/GRCh38#108559523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130575917-C-A

108559610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130575762-C-T

108559637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130575735-G-C

108559982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130575380-T-C

http://identifiers.org/hco/4/GRCh38#108560287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130574950-C-A

108560573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130574652-G-A

108560736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130574493-C-G

108560835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130567948-C-T

108561115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130567645-C-G

108561420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130567350-C-T

108561554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130567228-T-G

108561599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130567184-T-G

108561642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130567127-G-T

108562177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130566828-C-G

108562177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130566828-C-T

108562349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130566690-T-A

108562407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130566620-C-G

108562419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130566608-T-C

108562565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130566466-G-A

108562655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130566373-C-G

http://identifiers.org/hco/4/GRCh38#108563986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130565125-C-A

108564569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130564620-A-G

108564598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130564592-A-T

108565059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130563343-T-A

108565163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130563263-G-A

108570626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130556047-C-T

108570907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130555800-C-T

108570973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130555705-G-T

http://identifiers.org/hco/4/GRCh38#108571040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130555634-C-A

108571156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130555559-C-T

108571216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130555497-G-C

108571501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130555423-G-A

108571573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130555389-C-T

108571655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130555318-A-G

108572051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130555002-C-T

108572129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130554878-A-T

http://identifiers.org/hco/4/GRCh38#108572166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130554824-C-A

108572178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130554812-G-A

108572178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130554812-G-C

108572189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130554801-T-C

108572283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130554724-T-A

108572283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130554724-T-C

108573083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130554404-A-T

108573105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130554382-G-C

108573191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130554313-G-C

108573921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130553042-C-T

108574020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130552949-T-C

108574085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130552888-A-T

108574762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130552234-G-T

108574848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130552145-T-C

108574993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130551995-C-T

108575061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130551927-T-C

108575244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130551736-T-A

108575245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130551735-T-A

108575245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130551735-T-C

108575259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130551734-A-G

108575618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130551563-T-C

108575644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130551537-T-C

http://identifiers.org/hco/4/GRCh38#108575721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130551463-C-A

108575721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130551463-C-G

108577485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130550862-C-T

108577555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130550791-T-A

108577653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130550694-G-A

108580819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130548891-G-A

108580819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130548891-G-C

http://identifiers.org/hco/4/GRCh38#108580986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130548743-C-A

108581083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130548658-G-A

108581124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130548618-T-A

108581128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130548614-A-G

108581280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130548452-G-A

108581298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130548435-T-A

108581695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130548145-G-C

108581959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130547750-G-A

108581982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130547728-G-A

108581987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130547723-G-A

108582142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130547611-C-T

108582161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130547592-C-T

108582428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130547297-A-G

108582468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130547246-G-C

http://identifiers.org/hco/4/GRCh38#108582477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130547237-A-C

108582667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130547056-C-T

108582886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130546824-T-C

108583198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130546525-T-C

108586318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130545175-T-C

108586389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130545116-T-A

108586445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130545061-A-T

108586454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130545052-T-G

http://identifiers.org/hco/4/GRCh38#108586499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130545007-A-C

108586517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130544989-A-G

108586834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130543388-T-G

108586860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130543362-T-C

http://identifiers.org/hco/4/GRCh38#108586900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130543323-C-A

108587096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130543161-G-A

108587259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130543009-G-A

108587437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130542862-C-G

108587751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130542582-A-G

108588529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130541595-T-C

108588607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130541519-G-T

108588802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130541318-G-A

108588848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130541276-G-T

108588937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130541208-G-C

108589010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130541134-C-T

http://identifiers.org/hco/4/GRCh38#108589013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130541131-C-A

108589064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130541100-C-T

108589343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130540831-A-G

108589382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130540793-A-T

108590041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130540154-C-G

108590041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130540154-C-T

http://identifiers.org/hco/4/GRCh38#108590145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130540059-C-A

108590153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130540051-C-G

108590235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130539976-T-C

108590466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130539815-T-G

108591256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130539226-T-C

108591308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130539173-G-A

108598371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130535742-T-C

108598378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130535735-T-C

108598414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130535714-A-G

http://identifiers.org/hco/4/GRCh38#108598430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130535698-C-A

108598430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130535698-C-G

108598451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130535677-G-A

108608653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 130535062-A-G

108609036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130534813-T-A

108609036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130534813-T-C

108609052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130534798-G-C

108609158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130534702-G-A

108610696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130532247-G-A

108610787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130532184-T-G

108610796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130532175-A-G

108610802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130532169-T-C

108610802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130532169-T-G

http://identifiers.org/hco/4/GRCh38#108612135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130530885-C-A

108612201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130530828-C-T

http://identifiers.org/hco/4/GRCh38#108612425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130530633-A-C

http://identifiers.org/hco/4/GRCh38#108612435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130530623-C-A

108612477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130530583-C-T

108612969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130530081-C-T

108612972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130530078-T-C

108613428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130529579-T-C

108619220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130524922-C-G

108619818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130524679-G-A

108619869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130524627-C-T

108620019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130524483-T-C

108620172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130524360-G-A

108620172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130524360-G-T

108620201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130524330-T-C

108620392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130524176-G-C

108620398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130524170-A-G

108620433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130524135-G-A

108620435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130524133-A-G

108620460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130524121-T-A

108620460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130524121-T-C

http://identifiers.org/hco/4/GRCh38#108620464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#130524117-C-A

108620464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130524117-C-G

108620464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26749
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130524117-C-T